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Inventory of molecular markers affecting biological characteristics of avian influenza A viruses

Identifieur interne : 000247 ( Pmc/Corpus ); précédent : 000246; suivant : 000248

Inventory of molecular markers affecting biological characteristics of avian influenza A viruses

Auteurs : Annika Suttie ; Yi-Mo Deng ; Andrew R. Greenhill ; Philippe Dussart ; Paul F. Horwood ; Erik A. Karlsson

Source :

RBID : PMC:6831541

Abstract

Avian influenza viruses (AIVs) circulate globally, spilling over into domestic poultry and causing zoonotic infections in humans. Fortunately, AIVs are not yet capable of causing sustained human-to-human infection; however, AIVs are still a high risk as future pandemic strains, especially if they acquire further mutations that facilitate human infection and/or increase pathogenesis. Molecular characterization of sequencing data for known genetic markers associated with AIV adaptation, transmission, and antiviral resistance allows for fast, efficient assessment of AIV risk. Here we summarize and update the current knowledge on experimentally verified molecular markers involved in AIV pathogenicity, receptor binding, replicative capacity, and transmission in both poultry and mammals with a broad focus to include data available on other AIV subtypes outside of A/H5N1 and A/H7N9.


Url:
DOI: 10.1007/s11262-019-01700-z
PubMed: 31428925
PubMed Central: 6831541

Links to Exploration step

PMC:6831541

Le document en format XML

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<p id="Par1">Avian influenza viruses (AIVs) circulate globally, spilling over into domestic poultry and causing zoonotic infections in humans. Fortunately, AIVs are not yet capable of causing sustained human-to-human infection; however, AIVs are still a high risk as future pandemic strains, especially if they acquire further mutations that facilitate human infection and/or increase pathogenesis. Molecular characterization of sequencing data for known genetic markers associated with AIV adaptation, transmission, and antiviral resistance allows for fast, efficient assessment of AIV risk. Here we summarize and update the current knowledge on experimentally verified molecular markers involved in AIV pathogenicity, receptor binding, replicative capacity, and transmission in both poultry and mammals with a broad focus to include data available on other AIV subtypes outside of A/H5N1 and A/H7N9.</p>
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</TEI>
<pmc article-type="review-article">
<pmc-dir>properties open_access</pmc-dir>
<front>
<journal-meta>
<journal-id journal-id-type="nlm-ta">Virus Genes</journal-id>
<journal-id journal-id-type="iso-abbrev">Virus Genes</journal-id>
<journal-title-group>
<journal-title>Virus Genes</journal-title>
</journal-title-group>
<issn pub-type="ppub">0920-8569</issn>
<issn pub-type="epub">1572-994X</issn>
<publisher>
<publisher-name>Springer US</publisher-name>
<publisher-loc>New York</publisher-loc>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="pmid">31428925</article-id>
<article-id pub-id-type="pmc">6831541</article-id>
<article-id pub-id-type="publisher-id">1700</article-id>
<article-id pub-id-type="doi">10.1007/s11262-019-01700-z</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Review Paper</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>Inventory of molecular markers affecting biological characteristics of avian influenza A viruses</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Suttie</surname>
<given-names>Annika</given-names>
</name>
<xref ref-type="aff" rid="Aff1">1</xref>
<xref ref-type="aff" rid="Aff2">2</xref>
<xref ref-type="aff" rid="Aff3">3</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Deng</surname>
<given-names>Yi-Mo</given-names>
</name>
<xref ref-type="aff" rid="Aff3">3</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Greenhill</surname>
<given-names>Andrew R.</given-names>
</name>
<xref ref-type="aff" rid="Aff2">2</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Dussart</surname>
<given-names>Philippe</given-names>
</name>
<xref ref-type="aff" rid="Aff1">1</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Horwood</surname>
<given-names>Paul F.</given-names>
</name>
<xref ref-type="aff" rid="Aff4">4</xref>
</contrib>
<contrib contrib-type="author" corresp="yes">
<contrib-id contrib-id-type="orcid">http://orcid.org/0000-0001-6004-5671</contrib-id>
<name>
<surname>Karlsson</surname>
<given-names>Erik A.</given-names>
</name>
<address>
<email>ekarlsson@pasteur-kh.org</email>
</address>
<xref ref-type="aff" rid="Aff1">1</xref>
</contrib>
<aff id="Aff1">
<label>1</label>
<institution-wrap>
<institution-id institution-id-type="GRID">grid.418537.c</institution-id>
<institution>Virology Unit,</institution>
<institution>Institut Pasteur du Cambodge, Institut Pasteur International Network,</institution>
</institution-wrap>
5 Monivong Blvd, PO Box #983, Phnom Penh, Cambodia</aff>
<aff id="Aff2">
<label>2</label>
<institution-wrap>
<institution-id institution-id-type="GRID">grid.1040.5</institution-id>
<institution-id institution-id-type="ISNI">0000 0001 1091 4859</institution-id>
<institution>School of Health and Life Sciences,</institution>
<institution>Federation University,</institution>
</institution-wrap>
Churchill, Australia</aff>
<aff id="Aff3">
<label>3</label>
World Health Organization Collaborating Centre for Reference and Research on Influenza, Peter Doherty Institute for Infection and Immunity, Melbourne, Australia</aff>
<aff id="Aff4">
<label>4</label>
<institution-wrap>
<institution-id institution-id-type="GRID">grid.1011.1</institution-id>
<institution-id institution-id-type="ISNI">0000 0004 0474 1797</institution-id>
<institution>College of Public Health, Medical and Veterinary Sciences,</institution>
<institution>James Cook University,</institution>
</institution-wrap>
Townsville, QLD Australia</aff>
</contrib-group>
<author-notes>
<fn fn-type="com">
<p>Edited by William Dundon.</p>
</fn>
</author-notes>
<pub-date pub-type="epub">
<day>19</day>
<month>8</month>
<year>2019</year>
</pub-date>
<pub-date pub-type="pmc-release">
<day>19</day>
<month>8</month>
<year>2019</year>
</pub-date>
<pub-date pub-type="ppub">
<year>2019</year>
</pub-date>
<volume>55</volume>
<issue>6</issue>
<fpage>739</fpage>
<lpage>768</lpage>
<history>
<date date-type="received">
<day>9</day>
<month>6</month>
<year>2019</year>
</date>
<date date-type="accepted">
<day>9</day>
<month>8</month>
<year>2019</year>
</date>
</history>
<permissions>
<copyright-statement>© The Author(s) 2019</copyright-statement>
<license license-type="OpenAccess">
<license-p>
<bold>Open Access</bold>
This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (
<ext-link ext-link-type="uri" xlink:href="http://creativecommons.org/licenses/by/4.0/">http://creativecommons.org/licenses/by/4.0/</ext-link>
), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.</license-p>
</license>
</permissions>
<abstract id="Abs1">
<p id="Par1">Avian influenza viruses (AIVs) circulate globally, spilling over into domestic poultry and causing zoonotic infections in humans. Fortunately, AIVs are not yet capable of causing sustained human-to-human infection; however, AIVs are still a high risk as future pandemic strains, especially if they acquire further mutations that facilitate human infection and/or increase pathogenesis. Molecular characterization of sequencing data for known genetic markers associated with AIV adaptation, transmission, and antiviral resistance allows for fast, efficient assessment of AIV risk. Here we summarize and update the current knowledge on experimentally verified molecular markers involved in AIV pathogenicity, receptor binding, replicative capacity, and transmission in both poultry and mammals with a broad focus to include data available on other AIV subtypes outside of A/H5N1 and A/H7N9.</p>
</abstract>
<kwd-group xml:lang="en">
<title>Keywords</title>
<kwd>Avian influenza</kwd>
<kwd>Influenza virus</kwd>
<kwd>Molecular marker</kwd>
<kwd>Mutation</kwd>
<kwd>Risk assessment</kwd>
<kwd>Molecular inventory</kwd>
</kwd-group>
<funding-group>
<award-group>
<funding-source>
<institution-wrap>
<institution-id institution-id-type="FundRef">http://dx.doi.org/10.13039/100000016</institution-id>
<institution>U.S. Department of Health and Human Services</institution>
</institution-wrap>
</funding-source>
<award-id>IDSEP140020-01-00</award-id>
</award-group>
</funding-group>
<custom-meta-group>
<custom-meta>
<meta-name>issue-copyright-statement</meta-name>
<meta-value>© Springer Science+Business Media, LLC, part of Springer Nature 2019</meta-value>
</custom-meta>
</custom-meta-group>
</article-meta>
</front>
<body>
<sec id="Sec1" sec-type="introduction">
<title>Introduction</title>
<p id="Par2">Avian influenza viruses (AIVs) (Family:
<italic>Orthomyxoviridae</italic>
, genus:
<italic>Influenzavirus A</italic>
) are negative sense, single-stranded RNA viruses found globally in their natural reservoir hosts, wild waterfowl, and other aquatic birds (mainly of the orders
<italic>Anseriformes</italic>
and
<italic>Charadriiformes</italic>
). AIV genomes are composed of eight genomic RNA segments encoding at least twelve viral proteins. Viral nomenclature is based on combinations of the two surface glycoproteins, hemagglutinin (HA) and neuraminidase (NA). To date, sixteen HA (H1–H16) and nine NA (N1–N9) subtypes circulate in wild aquatic birds [
<xref ref-type="bibr" rid="CR1">1</xref>
], and two novel HA subtypes (H17 and H18) and two novel NA subtypes (N10 and N11) have recently been identified in bats [
<xref ref-type="bibr" rid="CR2">2</xref>
<xref ref-type="bibr" rid="CR6">6</xref>
]. AIVs are sporadically transmitted from waterfowl to domestic avian species, resulting in a number of stable AIV lineages in domestic poultry. These domestic lineages typically circulate in poultry flocks as low pathogenic (LPAIV) variants, causing little to no apparent illness; however, some subtypes (namely A/H5 and A/H7) have the potential to mutate to form highly pathogenic (HPAIV) variants capable of causing high mortality rates in domestic avian species. These HPAIV lineages then spread back to wild bird species, potentiating global spread [
<xref ref-type="bibr" rid="CR1">1</xref>
].</p>
<p id="Par3">Occasionally, AIVs spillover into mammalian species such as humans, swine, marine mammals, and various members of the Equidae, Felidae, and Canidae families [
<xref ref-type="bibr" rid="CR7">7</xref>
<xref ref-type="bibr" rid="CR10">10</xref>
], generally through close contact with domestic poultry, the primary intermediate host [
<xref ref-type="bibr" rid="CR11">11</xref>
]. These spillovers sometimes result in stable, mammalian-adapted lineages as have occurred with subtype A/H3N8 AIVs in equines and canines [
<xref ref-type="bibr" rid="CR9">9</xref>
]. A number of zoonotic infections with different AIV subtypes have occurred in humans, including: A/H5 (H5N1,H5N6), A/H6N1, A/H7 (H7N2, H7N3, H7N4, H7N7, H7N9), A/H9N2, and A/H10 (H10N7, H10N8) [
<xref ref-type="bibr" rid="CR12">12</xref>
]. Clinical symptoms vary in severity from asymptomatic infections, to conjunctivitis or influenza-like-illness, to severe acute respiratory illness. Infections with particularly virulent viral subtypes, such as A/H5 and A/H7, or infections in immunocompromised, high-risk hosts can cause high morbidity, respiratory distress and/or multiple-organ failure, and, in some cases, mortality [
<xref ref-type="bibr" rid="CR13">13</xref>
]. Fortunately, minimal human-to-human transmission occurs in human AIV cases; however, each zoonotic event in mammals represents a risk for AIVs to adapt replicative and transmissible properties in the mammalian host. Indeed, several studies using ferret models have shown that these AIVs have the potential to mutate into airborne transmissible forms, potentially with some mutations already present in nature [
<xref ref-type="bibr" rid="CR14">14</xref>
,
<xref ref-type="bibr" rid="CR15">15</xref>
]. However, while these observations are very important, point mutations associated with airborne transmission between ferrets are not universal, as they may not confer similar changes in biological characteristics of these viruses in other mammalian species, including humans.</p>
<p id="Par4">Given the continual circulation of AIVs in wild birds and domestic poultry, the potential for human spillover, and the mutable nature of AIV itself, it is paramount to understand the potential risk of any emerging AIV. Indeed, risk assessment tools are vital in pandemic preparedness planning [
<xref ref-type="bibr" rid="CR16">16</xref>
]. Genetic variation resulting in changes in viral properties such as receptor binding, replicative capacity, and transmission is a critical component of risk assessment. Historically, assessing these factors occurs in vivo; however, the ability to evaluate these properties in silico from sequence data allows for faster, more efficacious assessment of novel, emerging strains. Numerous studies identify molecular markers for AIV risk, and several previous papers compile markers of interest. Here, we summarize and update the current knowledge on experimentally verified molecular markers affecting biological characteristics of avian influenza viruses important for risk assessment and broaden the scope outside of the A/H5N1 and A/H7N9 subtypes.</p>
</sec>
<sec id="Sec2">
<title>Methodology</title>
<sec id="Sec3">
<title>Data collection</title>
<p id="Par5">All available information on AIV molecular markers/mutations was collected from: the CDC H5N1 Genetic changes inventory [
<xref ref-type="bibr" rid="CR17">17</xref>
], the WHO Working Group on Surveillance of Influenza Antiviral Susceptibility (WHO-AVWG) [
<xref ref-type="bibr" rid="CR18">18</xref>
], and publications summarizing AIV mutations and molecular markers affecting biological characteristics and potential risk [
<xref ref-type="bibr" rid="CR19">19</xref>
<xref ref-type="bibr" rid="CR21">21</xref>
]. Journal articles were sourced for each specific subtype using PubMed searches with MeSH Terms, Boolean operators and wild cards. For example, terms used to search for mutations in H6 AIVs: (influenza A virus[MeSH Terms]) AND (mutation OR mutagenesis OR virulence[MeSH Terms]) AND (H6[Title/Abstract] OR H6N*[Title/Abstract]).</p>
</sec>
<sec id="Sec4">
<title>Inclusion/exclusion</title>
<p id="Par6">All mutations/molecular markers from influenza viruses of avian origin were included in the initial screening and tabulation, including viruses isolated from humans AIV cases. However, we do not consider this inventory as an exhaustive list. Several studies computationally predict molecular markers of viral adaptation to humans [
<xref ref-type="bibr" rid="CR22">22</xref>
<xref ref-type="bibr" rid="CR26">26</xref>
]. While this work is extremely valuable, experimental validation of the majority of the markers described in these studies is not available and, therefore, necessitated exclusion from this data summary. In addition, since this inventory focuses on AIV and zoonotic infection, genome mutations in human seasonal influenza viruses were also excluded. As several publications observe the same mutations causing similar biological characteristics that could indicate risk markers, we excluded duplicate information from the tables.</p>
</sec>
<sec id="Sec5">
<title>Numbering</title>
<p id="Par7">For all data presented, HA mutations are numbered according to the H3 subtype to maintain consistency with available literature; however, H5 numbering was also included in the table. N2 numbering was used for NA as this is most commonly used in the current literature. Internal proteins (including deletions) and deletions in NA are numbered according to the full length of A/Goose/Guangdong/1/1996 genome segments.</p>
</sec>
</sec>
<sec id="Sec6">
<title>Surface proteins</title>
<sec id="Sec7">
<title>Hemagglutinin (HA; Table 
<xref rid="Tab1" ref-type="table">1</xref>
)</title>
<p id="Par8">Hemagglutinin is a homotrimeric transmembrane protein and is the most abundant protein present on the surface of influenza virions. For virions to successfully enter and replicate in host cells, host proteases cleave the HA0 precursor into two subunits, HA1 and HA2. The main role of the HA1 subunit is to initiate infection by recognizing and binding receptors on the host cell surface. After internalization and entrance into the endosomal pathway, the HA2 subunit fuses the viral and endosomal membranes, creating a pore for viral RNA entry into the host cell, and initiation of transcription and translation of viral products [
<xref ref-type="bibr" rid="CR27">27</xref>
,
<xref ref-type="bibr" rid="CR28">28</xref>
]. Several mutations in HA are associated with changes in viral fitness and transmissibility, as they affect viral receptor binding avidity/specificity or viral membrane fusion activities (Table 
<xref rid="Tab1" ref-type="table">1</xref>
).
<table-wrap id="Tab1">
<label>Table 1</label>
<caption>
<p>Molecular markers/motifs in the hemagglutinin (HA; segment 4) gene of influenza virus experimentally verified molecular markers involved in AIV pathogenicity, receptor binding, replicative capacity, and transmission in both poultry and mammals</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" colspan="2">Mutation/motif</th>
<th align="left" rowspan="2">Phenotype</th>
<th align="left" rowspan="2">Subtypes tested</th>
<th align="left" rowspan="2">References</th>
</tr>
<tr>
<th align="left">H3 numbering
<sup>a</sup>
</th>
<th align="left">H5 numbering
<sup>b</sup>
</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left">D101N</td>
<td align="left">D94N</td>
<td align="left">Increased virus binding to α2–6</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR200">200</xref>
]</td>
</tr>
<tr>
<td align="left">S126N</td>
<td align="left">S121N</td>
<td align="left">Increased virus binding to α2–6</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR201">201</xref>
]</td>
</tr>
<tr>
<td align="left">S137A</td>
<td align="left">S133A</td>
<td align="left">Increased pseudovirus binding to α2–6</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR44">44</xref>
]</td>
</tr>
<tr>
<td align="left">A138V</td>
<td align="left">A134V</td>
<td align="left">Increased infectivity in SIAT Cells</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR202">202</xref>
,
<xref ref-type="bibr" rid="CR203">203</xref>
]</td>
</tr>
<tr>
<td align="left">G143R</td>
<td align="left">G139R</td>
<td align="left">Increased virus binding to α2–6</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR204">204</xref>
]</td>
</tr>
<tr>
<td align="left">S158N</td>
<td align="left">S154N</td>
<td align="left">Increased virus binding to α2–6</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR201">201</xref>
]</td>
</tr>
<tr>
<td align="left">N158D</td>
<td align="left">N154D</td>
<td align="left">Decreased virulence in mice</td>
<td align="left">H9N2</td>
<td align="left">[
<xref ref-type="bibr" rid="CR205">205</xref>
]</td>
</tr>
<tr>
<td align="left">S159N</td>
<td align="left">S155N</td>
<td align="left">Increased virus binding to α2–6</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR201">201</xref>
]</td>
</tr>
<tr>
<td align="left">T160A</td>
<td align="left">T156A</td>
<td align="left">Increased virus binding to α2–6, increased transmission in guinea pigs</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR201">201</xref>
,
<xref ref-type="bibr" rid="CR206">206</xref>
]</td>
</tr>
<tr>
<td align="left">G186V</td>
<td align="left">G182V</td>
<td align="left">Increased virus binding to α2–3</td>
<td align="left">H7N9</td>
<td align="left">[
<xref ref-type="bibr" rid="CR207">207</xref>
]</td>
</tr>
<tr>
<td align="left">N186K/D</td>
<td align="left">N182K/D</td>
<td align="left">Increased virus binding to α2–6</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR201">201</xref>
,
<xref ref-type="bibr" rid="CR203">203</xref>
,
<xref ref-type="bibr" rid="CR204">204</xref>
,
<xref ref-type="bibr" rid="CR206">206</xref>
]</td>
</tr>
<tr>
<td align="left">V186N</td>
<td align="left">V182N</td>
<td align="left">Increased binding to α2–6, decreased binding to α2–3</td>
<td align="left">H13N6</td>
<td align="left">[
<xref ref-type="bibr" rid="CR208">208</xref>
]</td>
</tr>
<tr>
<td align="left">P186L</td>
<td align="left">P182L</td>
<td align="left">Decreased binding to α2–3</td>
<td align="left">H6N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR209">209</xref>
]</td>
</tr>
<tr>
<td align="left">D187G</td>
<td align="left">D183G</td>
<td align="left">Increased virus binding to α2–6</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR47">47</xref>
]</td>
</tr>
<tr>
<td align="left">E190G</td>
<td align="left">E186G</td>
<td align="left">Increased virus binding to α2–6, maintained α2–3 binding, decreased virulence in mice</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR47">47</xref>
,
<xref ref-type="bibr" rid="CR210">210</xref>
]</td>
</tr>
<tr>
<td align="left">E190V</td>
<td align="left">E186V</td>
<td align="left">Decreased binding to α2–3 and α2–6</td>
<td align="left">H6N2</td>
<td align="left">[
<xref ref-type="bibr" rid="CR211">211</xref>
]</td>
</tr>
<tr>
<td align="left">T190V</td>
<td align="left">T186V</td>
<td align="left">Enhances binding affinity to mammalian cells and replication in mammalian cells</td>
<td align="left">H9N2</td>
<td align="left">[
<xref ref-type="bibr" rid="CR212">212</xref>
]</td>
</tr>
<tr>
<td align="left">T192I</td>
<td align="left">T188I</td>
<td align="left">Increased pseudovirus binding to α2–6</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR44">44</xref>
]</td>
</tr>
<tr>
<td align="left">K193R/T</td>
<td align="left">K189R/T</td>
<td align="left">Increased virus binding to α2–6</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR201">201</xref>
,
<xref ref-type="bibr" rid="CR213">213</xref>
]</td>
</tr>
<tr>
<td align="left">Q196R/H</td>
<td align="left">Q192R/H</td>
<td align="left">Increased virus binding to α2–6</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR47">47</xref>
,
<xref ref-type="bibr" rid="CR204">204</xref>
,
<xref ref-type="bibr" rid="CR214">214</xref>
]</td>
</tr>
<tr>
<td align="left">N197K</td>
<td align="left">N193K</td>
<td align="left">Increased virus binding to α2–6</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR204">204</xref>
]</td>
</tr>
<tr>
<td align="left">V214I</td>
<td align="left">V210I</td>
<td align="left">Increased virus binding to α2–6</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR214">214</xref>
]</td>
</tr>
<tr>
<td align="left">G225D</td>
<td align="left">G221D</td>
<td align="left">Increased virus binding to α2,6</td>
<td align="left">H6N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR43">43</xref>
]</td>
</tr>
<tr>
<td align="left" rowspan="6">Q226L</td>
<td align="left" rowspan="6">Q222L</td>
<td align="left">Increased virus binding to α2–6</td>
<td align="left">H4N6</td>
<td align="left">[
<xref ref-type="bibr" rid="CR50">50</xref>
]</td>
</tr>
<tr>
<td align="left">Increased virus binding to α2–6</td>
<td align="left">H6N2</td>
<td align="left">[
<xref ref-type="bibr" rid="CR211">211</xref>
]</td>
</tr>
<tr>
<td align="left">Increased virus binding to α2–6, decreased binding to α2–3</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR46">46</xref>
]</td>
</tr>
<tr>
<td align="left">Increased virus binding to α2–3, decreased binding to α2–6</td>
<td align="left">H7N9</td>
<td align="left">[
<xref ref-type="bibr" rid="CR52">52</xref>
,
<xref ref-type="bibr" rid="CR215">215</xref>
]</td>
</tr>
<tr>
<td align="left">Increased virus binding to α2–6, enhanced replication in mammalian cells and ferrets, enhanced contact transmission in ferrets</td>
<td align="left">H9N2</td>
<td align="left">[
<xref ref-type="bibr" rid="CR49">49</xref>
,
<xref ref-type="bibr" rid="CR54">54</xref>
]</td>
</tr>
<tr>
<td align="left">Loss of binding to α2–3</td>
<td align="left">H10N8 (human isolate)</td>
<td align="left">[
<xref ref-type="bibr" rid="CR53">53</xref>
,
<xref ref-type="bibr" rid="CR216">216</xref>
,
<xref ref-type="bibr" rid="CR217">217</xref>
]</td>
</tr>
<tr>
<td align="left">L226I</td>
<td align="left">L222I</td>
<td align="left">Decreased binding to α2–3</td>
<td align="left">H7N9</td>
<td align="left">[
<xref ref-type="bibr" rid="CR52">52</xref>
]</td>
</tr>
<tr>
<td align="left">S227N</td>
<td align="left">S223N</td>
<td align="left">Increased virus binding to α2–6</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR46">46</xref>
,
<xref ref-type="bibr" rid="CR47">47</xref>
,
<xref ref-type="bibr" rid="CR203">203</xref>
,
<xref ref-type="bibr" rid="CR218">218</xref>
,
<xref ref-type="bibr" rid="CR219">219</xref>
]</td>
</tr>
<tr>
<td align="left">G228A/S</td>
<td align="left">G224A/S</td>
<td align="left">Increased binding to α2–6, dual receptor specificity</td>
<td align="left">H4N6</td>
<td align="left">[
<xref ref-type="bibr" rid="CR50">50</xref>
]</td>
</tr>
<tr>
<td align="left" rowspan="5">G228S</td>
<td align="left" rowspan="5">G224S</td>
<td align="left">Increased viral replication in mammalian cells and virulence in mice</td>
<td align="left">H1N2</td>
<td align="left">[
<xref ref-type="bibr" rid="CR220">220</xref>
]</td>
</tr>
<tr>
<td align="left">Increased virus binding to α2–6</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR45">45</xref>
,
<xref ref-type="bibr" rid="CR46">46</xref>
,
<xref ref-type="bibr" rid="CR201">201</xref>
,
<xref ref-type="bibr" rid="CR209">209</xref>
]</td>
</tr>
<tr>
<td align="left">Decreased virus binding to α2–3</td>
<td align="left">H6N2</td>
<td align="left">[
<xref ref-type="bibr" rid="CR211">211</xref>
]</td>
</tr>
<tr>
<td align="left">Decreased binding to α2–3 and α2–6 receptors</td>
<td align="left">H7N9</td>
<td align="left">[
<xref ref-type="bibr" rid="CR51">51</xref>
]</td>
</tr>
<tr>
<td align="left">Decreased binding to α2–3, no binding to α2–6</td>
<td align="left">H10N8 (human isolate)</td>
<td align="left">[
<xref ref-type="bibr" rid="CR53">53</xref>
,
<xref ref-type="bibr" rid="CR217">217</xref>
]</td>
</tr>
<tr>
<td align="left">P239S</td>
<td align="left">P235S</td>
<td align="left">Increased virus binding to α2–6</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR214">214</xref>
]</td>
</tr>
<tr>
<td align="left">E255K</td>
<td align="left">E251K</td>
<td align="left">Increased virus binding to α2–6</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR47">47</xref>
]</td>
</tr>
<tr>
<td align="left" rowspan="2">326 to 329</td>
<td align="left" rowspan="2">323 to 330 (R-X-R, K-R)</td>
<td align="left" rowspan="2">Polybasic cleavage motif sequence required for high pathogenicity avian influenza viruses</td>
<td align="left">H5Nx</td>
<td align="left">[
<xref ref-type="bibr" rid="CR221">221</xref>
<xref ref-type="bibr" rid="CR228">228</xref>
]</td>
</tr>
<tr>
<td align="left">H7Nx</td>
<td align="left">[
<xref ref-type="bibr" rid="CR229">229</xref>
<xref ref-type="bibr" rid="CR231">231</xref>
]</td>
</tr>
<tr>
<td align="left">K387I</td>
<td align="left">K388I</td>
<td align="left">Decreased pH of fusion, increased HA stability, increased replication efficiency and virulence in mice</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR130">130</xref>
,
<xref ref-type="bibr" rid="CR232">232</xref>
,
<xref ref-type="bibr" rid="CR233">233</xref>
]</td>
</tr>
<tr>
<td align="left">K393E</td>
<td align="left">K394E</td>
<td align="left">Increased pH of fusion, decreased HA stability, decreased virulence in mice</td>
<td align="left">H7N9</td>
<td align="left">[
<xref ref-type="bibr" rid="CR234">234</xref>
]</td>
</tr>
<tr>
<td align="left">E83K, S128P</td>
<td align="left">E75K, S123P</td>
<td align="left">Increased virus binding to α2–6</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR204">204</xref>
]</td>
</tr>
<tr>
<td align="left">E83K, S128P, R496K</td>
<td align="left">E75K, S123P, R497K</td>
<td align="left">Increased virus binding to α2–6</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR204">204</xref>
]</td>
</tr>
<tr>
<td align="left">E83K, S128P, N197K, R496K</td>
<td align="left">E75K, S123P, N193K, R497K</td>
<td align="left">Increased virus binding to α2–6</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR204">204</xref>
]</td>
</tr>
<tr>
<td align="left">E83K, N197K</td>
<td align="left">E75K, N193K</td>
<td align="left">Increased virus binding to α2–6</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR204">204</xref>
]</td>
</tr>
<tr>
<td align="left">E83K, N197K, R496K</td>
<td align="left">E75K, N193K, R497K</td>
<td align="left">Increased virus binding to α2–6</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR204">204</xref>
]</td>
</tr>
<tr>
<td align="left">E83K, R496K</td>
<td align="left">E75K, R497K</td>
<td align="left">Increased virus binding to α2–6</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR204">204</xref>
]</td>
</tr>
<tr>
<td align="left">H110Y, T160A, Q226L, G228S</td>
<td align="left">H103Y, T156A, Q222L, G224S (with PB2: E627K; PB1: H99Y)</td>
<td align="left">Airborne transmissible in ferrets</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR15">15</xref>
,
<xref ref-type="bibr" rid="CR58">58</xref>
]</td>
</tr>
<tr>
<td align="left">S114R, T115I</td>
<td align="left">S107R, T108I</td>
<td align="left">Increased virulence in chickens and mice, increased pH of fusion</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR235">235</xref>
]</td>
</tr>
<tr>
<td align="left">S128P, N197K</td>
<td align="left">S123P, N193K</td>
<td align="left">Increased virus binding to α2–6</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR204">204</xref>
]</td>
</tr>
<tr>
<td align="left">S128P, N197K, R496K</td>
<td align="left">S123P, N193K, R497K</td>
<td align="left">Increased virus binding to α2–6</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR204">204</xref>
]</td>
</tr>
<tr>
<td align="left">S128P, R496K</td>
<td align="left">S123P, R497K</td>
<td align="left">Increased virus binding to α2–6</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR204">204</xref>
]</td>
</tr>
<tr>
<td align="left">
<sup>c</sup>
, A138V</td>
<td align="left">L129V, A134V</td>
<td align="left">Increased virus binding to α2–6</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR236">236</xref>
]</td>
</tr>
<tr>
<td align="left">∆, I155T</td>
<td align="left">L129del, I151T</td>
<td align="left">Increased virus binding to α2–6</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR214">214</xref>
,
<xref ref-type="bibr" rid="CR236">236</xref>
]</td>
</tr>
<tr>
<td align="left">S137A, T192I</td>
<td align="left">S133A, T188I</td>
<td align="left">Increased pseudovirus binding to α2–6</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR44">44</xref>
]</td>
</tr>
<tr>
<td align="left">G143R, N186K</td>
<td align="left">G139R, N182K</td>
<td align="left">Decreased binding to α2–3, increased virus binding to α2–6</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR46">46</xref>
,
<xref ref-type="bibr" rid="CR204">204</xref>
]</td>
</tr>
<tr>
<td align="left">N158D, N224K, Q226L, T318I</td>
<td align="left">N154D, N220K, Q222L, T315I</td>
<td align="left">Transmissible among ferrets</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR14">14</xref>
]</td>
</tr>
<tr>
<td align="left">N158S, Q226L</td>
<td align="left">N154S, Q222L</td>
<td align="left">Increased virus binding to α2–6</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR237">237</xref>
]</td>
</tr>
<tr>
<td align="left">N158S, Q226L, N248D</td>
<td align="left">N154S, Q222L, N244D</td>
<td align="left">Increased virus binding to α2–6</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR237">237</xref>
]</td>
</tr>
<tr>
<td align="left">S159N, T160A</td>
<td align="left">S155N, T156A</td>
<td align="left">Increased virus binding to α2–6</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR201">201</xref>
,
<xref ref-type="bibr" rid="CR209">209</xref>
]</td>
</tr>
<tr>
<td align="left">S159N, T160A, S227N</td>
<td align="left">S155N, T156A, S223N</td>
<td align="left">Increased virus binding to α2–6, reduced lethality and systemic spread in mice</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR238">238</xref>
]</td>
</tr>
<tr>
<td align="left">T160A, K193T, N224K, Q226L</td>
<td align="left">T156A, K189T, N220K, Q222L</td>
<td align="left">Increased virus binding to α2–6</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR213">213</xref>
]</td>
</tr>
<tr>
<td align="left">T160A, Q226L</td>
<td align="left">T156A, Q222L</td>
<td align="left">Increased virus binding to α2–6</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR201">201</xref>
,
<xref ref-type="bibr" rid="CR209">209</xref>
]</td>
</tr>
<tr>
<td align="left">T160A, Q226L, G228S</td>
<td align="left">T156A, Q222L, G224S</td>
<td align="left">Increased virus binding to α2–6</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR201">201</xref>
,
<xref ref-type="bibr" rid="CR209">209</xref>
,
<xref ref-type="bibr" rid="CR239">239</xref>
]</td>
</tr>
<tr>
<td align="left">T160A, S227N</td>
<td align="left">T156A, S223N</td>
<td align="left">Increased virus binding to α2–6</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR201">201</xref>
,
<xref ref-type="bibr" rid="CR209">209</xref>
]</td>
</tr>
<tr>
<td align="left">V186N, N228K</td>
<td align="left">V182N, N224K</td>
<td align="left">Increased virus binding to α2–6</td>
<td align="left">H7N9</td>
<td align="left">[
<xref ref-type="bibr" rid="CR51">51</xref>
]</td>
</tr>
<tr>
<td align="left">V186K/G, K193T, G228S</td>
<td align="left">V182 K/G, K189T, G224S</td>
<td align="left">Increased virus binding to α2–6</td>
<td align="left">H7N9</td>
<td align="left">[
<xref ref-type="bibr" rid="CR51">51</xref>
]</td>
</tr>
<tr>
<td align="left">V186N, N224K, G228S</td>
<td align="left">V182N, N220K, G224S</td>
<td align="left">Increased virus binding to α2–6</td>
<td align="left">H7N9</td>
<td align="left">[
<xref ref-type="bibr" rid="CR51">51</xref>
]</td>
</tr>
<tr>
<td align="left">N186K, Q196R, Q226L, S227N, G228S</td>
<td align="left">N182K, Q192R, Q222L, S223N, G224S</td>
<td align="left">Increased virus binding to α2–6</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR46">46</xref>
]</td>
</tr>
<tr>
<td align="left">N186K, Q226L, S227N, G228S</td>
<td align="left">N182K, Q222L, S223N, G224S</td>
<td align="left">Increased virus binding to α2–6</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR46">46</xref>
]</td>
</tr>
<tr>
<td align="left">N186K, Q226L, G228S</td>
<td align="left">N182K, Q222L, G224S</td>
<td align="left">Increased virus binding to α2–6</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR46">46</xref>
]</td>
</tr>
<tr>
<td align="left">E187G, E190D, K193S, Q226L, G228S</td>
<td align="left">E183G, E186D, K189S, Q222L, G224S</td>
<td align="left">Increased virus binding to α2–6</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR240">240</xref>
]</td>
</tr>
<tr>
<td align="left">E187G, Q226L,G228S</td>
<td align="left">E183G, Q222L,G224S</td>
<td align="left">Increased virus binding to α2–6</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR47">47</xref>
]</td>
</tr>
<tr>
<td align="left">D187G, S227N</td>
<td align="left">D183G, S223N</td>
<td align="left">Increased virus binding to α2–6</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR47">47</xref>
]</td>
</tr>
<tr>
<td align="left">T189A, G192R</td>
<td align="left">T185A, G188R</td>
<td align="left">Enhanced replication in ferrets, transmitted via aerosols among ferrets</td>
<td align="left">H9N2 (with human H3N2 backbone)</td>
<td align="left">[
<xref ref-type="bibr" rid="CR241">241</xref>
]</td>
</tr>
<tr>
<td align="left">E190G, Q226E, G228S</td>
<td align="left">E186G, Q222E, G224S</td>
<td align="left">Increased virus binding to α2–6</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR47">47</xref>
]</td>
</tr>
<tr>
<td align="left">K193T, G228S</td>
<td align="left">K189T, G224S</td>
<td align="left">Dual α2–3 and α2–6 binding</td>
<td align="left">H7N9</td>
<td align="left">[
<xref ref-type="bibr" rid="CR51">51</xref>
]</td>
</tr>
<tr>
<td align="left">K193R, Q226L, G228S</td>
<td align="left">K189R, Q222L, G224S</td>
<td align="left">Increased virus binding to α2–6</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR239">239</xref>
,
<xref ref-type="bibr" rid="CR240">240</xref>
]</td>
</tr>
<tr>
<td align="left">Q196R, Q226L, S227N, G228S</td>
<td align="left">Q192R, Q222L, S223N, G224S</td>
<td align="left">Increased virus binding to α2–6</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR46">46</xref>
]</td>
</tr>
<tr>
<td align="left">Q196R, Q226L, G228S</td>
<td align="left">Q192R, Q222L, G224S</td>
<td align="left">Increased virus binding to α2–6</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR46">46</xref>
,
<xref ref-type="bibr" rid="CR47">47</xref>
]</td>
</tr>
<tr>
<td align="left">Q196R, S227N</td>
<td align="left">Q192R, S223N</td>
<td align="left">Increased virus binding to α2–6</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR46">46</xref>
,
<xref ref-type="bibr" rid="CR47">47</xref>
]</td>
</tr>
<tr>
<td align="left">N197K, R496K</td>
<td align="left">N193K, R497K</td>
<td align="left">Increased virus binding to α2–6</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR204">204</xref>
]</td>
</tr>
<tr>
<td align="left">K222Q, S227R</td>
<td align="left">K218Q, S223R</td>
<td align="left">Increased virus binding to α2–3 and α2–6</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR242">242</xref>
]</td>
</tr>
<tr>
<td align="left">N224K, G228S</td>
<td align="left">N220K, G224S</td>
<td align="left">Increased virus binding to α2–6</td>
<td align="left">H7N9</td>
<td align="left">[
<xref ref-type="bibr" rid="CR51">51</xref>
]</td>
</tr>
<tr>
<td align="left">Q226L, S227N, G228S</td>
<td align="left">Q222L, S223N, G224S</td>
<td align="left">Increased virus binding to α2–6</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR46">46</xref>
]</td>
</tr>
<tr>
<td align="left" rowspan="4">Q226L, G228S</td>
<td align="left" rowspan="4">Q222L, G224S</td>
<td align="left">Increased virus binding to α2–6</td>
<td align="left">H4N6</td>
<td align="left">[
<xref ref-type="bibr" rid="CR50">50</xref>
]</td>
</tr>
<tr>
<td align="left">Increased virus binding to α2–6; decreased antiviral response in host; reduced tissue tropism in guinea pigs</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR45">45</xref>
<xref ref-type="bibr" rid="CR47">47</xref>
,
<xref ref-type="bibr" rid="CR201">201</xref>
,
<xref ref-type="bibr" rid="CR206">206</xref>
,
<xref ref-type="bibr" rid="CR209">209</xref>
,
<xref ref-type="bibr" rid="CR215">215</xref>
,
<xref ref-type="bibr" rid="CR237">237</xref>
,
<xref ref-type="bibr" rid="CR239">239</xref>
,
<xref ref-type="bibr" rid="CR240">240</xref>
,
<xref ref-type="bibr" rid="CR243">243</xref>
,
<xref ref-type="bibr" rid="CR244">244</xref>
]</td>
</tr>
<tr>
<td align="left">Increased virus binding to α2–6</td>
<td align="left">H7N7 (human isolate)</td>
<td align="left">[
<xref ref-type="bibr" rid="CR245">245</xref>
]</td>
</tr>
<tr>
<td align="left">Loss of binding to α2–3, no gain of binding to α2–6</td>
<td align="left">H10N8 (human isolate)</td>
<td align="left">[
<xref ref-type="bibr" rid="CR53">53</xref>
,
<xref ref-type="bibr" rid="CR216">216</xref>
,
<xref ref-type="bibr" rid="CR217">217</xref>
]</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<p>Single mutations are presented first followed by motifs involving multiple mutations. Individual markers and motifs are listed in numerical order for ease of identifying mutation of interest</p>
<p>
<sup>a</sup>
Mutation/location H3 numbering relative to A/Aichi/2/1968 (H3N2)</p>
<p>
<sup>b</sup>
Mutation/location H5 numbering relative to A/Vietnam/1203/2004 (H5N1)</p>
<p>
<sup>c</sup>
∆ indicates amino acids present in A/H5 but are deleted compared to A/H3</p>
</table-wrap-foot>
</table-wrap>
</p>
<sec id="Sec8">
<title>Receptor binding specificity</title>
<p id="Par9">The HA protein initiates influenza virus infections by recognizing and binding to sialylated glycans on the surface of host cells. Distribution and type of sialic acid residues in the host respiratory tract and the receptor binding preference of AIVs are major determinants of viral host range and transmissibility [
<xref ref-type="bibr" rid="CR29">29</xref>
<xref ref-type="bibr" rid="CR32">32</xref>
]. AIVs typically bind to sialic acids in α2,3 linkage to galactose, whereas human adapted viruses bind sialic acids in α2,6 linkage. While the respiratory tract of humans contains both linkages of sialic acids, α2,6 linkages are more abundant on the surface of epithelial cells lining the upper respiratory tract, allowing for the spread of human adapted viruses through the production of aerosols by sneezing and coughing [
<xref ref-type="bibr" rid="CR33">33</xref>
,
<xref ref-type="bibr" rid="CR34">34</xref>
]. α2,3 linkages are mainly found in the lower respiratory tract of humans, permitting infection with AIVs but restricting transmission [
<xref ref-type="bibr" rid="CR35">35</xref>
]. In contrast, avian species have both α2,6 and α2,3 linked sialic acids in their respiratory and intestinal tracts, though abundance and distribution differs between species [
<xref ref-type="bibr" rid="CR36">36</xref>
<xref ref-type="bibr" rid="CR39">39</xref>
]. Generally, epithelial cells with α2,3 linkages are more abundant in the avian intestinal tract, facilitating transmission via the fecal–oral route.</p>
<p id="Par10">A switch in binding preference from α2,3 “avian-type” receptors to α2,6 “human-type” receptors is considered a key factor for pandemic potential of AIVs. There are numerous HA mutations that, individually or in combination, affect viral receptor binding preference, pathogenicity and transmissibility [
<xref ref-type="bibr" rid="CR40">40</xref>
]. Two mutations, E190D and G225D, increase the preference for “human-type” receptors in both the 1918, “Spanish” A/H1N1 pandemic virus and the 2009 A/H1N1 “Swine Flu” pandemic virus [
<xref ref-type="bibr" rid="CR41">41</xref>
,
<xref ref-type="bibr" rid="CR42">42</xref>
]. However, the impact of these mutations on other AIVs appears to be subtype specific [
<xref ref-type="bibr" rid="CR43">43</xref>
<xref ref-type="bibr" rid="CR45">45</xref>
]. A single G225D mutation alters the receptor preference of an A/H6N1 virus isolated from a human in Taiwan to bind α2,6 human-type receptors [
<xref ref-type="bibr" rid="CR43">43</xref>
] In contrast, while the same single substitution in A/H5 viruses does not increase affinity for α2,6 glycans [
<xref ref-type="bibr" rid="CR44">44</xref>
<xref ref-type="bibr" rid="CR46">46</xref>
], E190G produces a dual α2,3/α2,6 receptor binding phenotype [
<xref ref-type="bibr" rid="CR47">47</xref>
]. Double E190D/G225D mutants have minimal binding to either α2,3 or α2,6 glycans in both A/H5 and A/H6 subtypes [
<xref ref-type="bibr" rid="CR43">43</xref>
<xref ref-type="bibr" rid="CR45">45</xref>
].</p>
<p id="Par11">Unlike the 1918 and “Swine Flu” pandemic viruses, the 1957 “Asian” pandemic A/H2N2 virus and the 1968 “Hong Kong” A/H3N2 pandemic virus gained dual Q226L/G228S mutations [
<xref ref-type="bibr" rid="CR31">31</xref>
,
<xref ref-type="bibr" rid="CR48">48</xref>
]. Both Q226L and G228S mutations have a profound effect on the HA receptor specificity for a large range of AIV subtypes. Individually, Q226L decreases, or completely negates, HA affinity for α2,3 “avian-type” receptors in several subtypes, namely A/H4, A/H5, A/H7, A/H9, and A/H10 [
<xref ref-type="bibr" rid="CR46">46</xref>
,
<xref ref-type="bibr" rid="CR49">49</xref>
<xref ref-type="bibr" rid="CR53">53</xref>
]. However, the effect of Q226L on α2,6 binding preference varies. In A/H5, A/H7, and A/H10 subtype AIVs, Q226L either mildly enhances, or does not influence, α2,6 binding [
<xref ref-type="bibr" rid="CR45">45</xref>
,
<xref ref-type="bibr" rid="CR46">46</xref>
,
<xref ref-type="bibr" rid="CR52">52</xref>
,
<xref ref-type="bibr" rid="CR53">53</xref>
]. Conversely, Q226L substantially increases HA preference for α2,6 “human-type” receptors in A/H4 and A/H9 subtype AIVs [
<xref ref-type="bibr" rid="CR49">49</xref>
,
<xref ref-type="bibr" rid="CR50">50</xref>
,
<xref ref-type="bibr" rid="CR54">54</xref>
]. In contrast to Q226L, a singular G228S mutation in A/H5 subtype isolates produces a dual binding phenotype, increasing α2,6 binding and maintaining α2,3. Therefore, the combination of Q226L/G228S dual mutations decreases, or even ablates, α2,3 binding while simultaneously increasing affinity for α2,6. However, this elegant switch does not hold true for all subtypes. For instance, single Q226L or dual Q226L/G228S mutations in a human A/H10N8 isolate significantly decrease α2,3 binding with only a minimal increase in α2,6 affinity [33, 34]. In addition, a number of other HA mutations, individually or in combination, affect viral receptor binding preference, pathogenicity and transmissibility, and more work is necessary to understand the risk of these mutations in all subtypes of concern.</p>
<p id="Par12">Overall, the variable effect of HA mutations on AIV receptor binding preference between different AIV subtypes likely occurs due to differences in the HA receptor binding site (RBS). Four key structural elements are present in the HA RBS of all AIV subtypes: the 130-loop, 150-loop, 190-helix, and 220-loop. Conformation and amino acid composition of these structures is a primary determinant of HA receptor specify. Therefore, the variability of RBS loop length and amino acid composition between AIV subtypes could account for the variable effects observed with the same mutations in the RBS [
<xref ref-type="bibr" rid="CR40">40</xref>
].</p>
</sec>
<sec id="Sec9">
<title>pH of fusion and HA stability</title>
<p id="Par13">HA stability, or pH of fusion, refers to the pH required to trigger an irreversible conformational change in the HA1/HA2 trimer that activates the HA2 fusion peptide to mediate the fusion of the viral and endosomal membranes. This fusion creates pores through which viral ribonucleoproteins (RNPs) can exit the endosome, initiating AIV infection in the cytoplasm of the host cell. Following internalization, the endosome progressively becomes more acidic until the contents are destroyed in the host lysosome [
<xref ref-type="bibr" rid="CR55">55</xref>
]. Therefore, pH of fusion dictates the efficient timing of the release of viral RNPs. If released too early, host cell recognition of viral products heightens host antiviral response, attenuating viral infection [
<xref ref-type="bibr" rid="CR56">56</xref>
,
<xref ref-type="bibr" rid="CR57">57</xref>
]. If released too late, endosomal contents are destroyed, preventing release of viral products. The optimal pH of fusion varies substantially. In avian species, optimal pH of fusion can differ dramatically; however, a pH of fusion above 5.5 is believed to enhance AIV replication and transmission. In humans and ferrets, increased stability with a pH of fusion of less than 5.5 favors replication [
<xref ref-type="bibr" rid="CR28">28</xref>
].</p>
<p id="Par14">Understanding mutations affecting HA stability is vitally important since pH of fusion may partly contribute to the ability of AIVs to transmit by aerosol droplet in the ferret model [
<xref ref-type="bibr" rid="CR14">14</xref>
,
<xref ref-type="bibr" rid="CR15">15</xref>
]. In subtype A/H5, a H103Y mutation stabilizes the HA, possibly increasing transmissibility [
<xref ref-type="bibr" rid="CR58">58</xref>
]. A separate mutation, K387I, decreases the pH of fusion, increasing viral replication efficiency and virulence in mice while attenuating virulence in ducks [
<xref ref-type="bibr" rid="CR59">59</xref>
]. A comprehensive list of mutations affecting HA stability can be found in publications by Russell [
<xref ref-type="bibr" rid="CR60">60</xref>
] and Mair et al. [
<xref ref-type="bibr" rid="CR61">61</xref>
]; however, the overall biological significance of pH of fusion requires further investigation. Therefore, mutations that affect pH stability without experimentally verified effects on viral replication efficiency, transmissibility, or pathogenicity have not been included in the inventory.</p>
</sec>
</sec>
<sec id="Sec10">
<title>Neuraminidase (NA; Table 
<xref rid="Tab2" ref-type="table">2</xref>
)</title>
<sec id="Sec11">
<title>Viral infectivity and release from host cells</title>
<p id="Par15">Neuraminidase (NA) is the second major transmembrane protein present on the influenza virus surface [
<xref ref-type="bibr" rid="CR62">62</xref>
]. NA is a sialidase, cleaving sialic acid from glycoproteins, which enables virions to move through the mucus lining epithelial cells to initiate viral infections [
<xref ref-type="bibr" rid="CR63">63</xref>
,
<xref ref-type="bibr" rid="CR64">64</xref>
], as well as mediating the release of progeny virions from the surface of infected cells [
<xref ref-type="bibr" rid="CR65">65</xref>
]. HA and NA need to operate in equilibrium for efficient viral replication (reviewed in [
<xref ref-type="bibr" rid="CR66">66</xref>
]) and perturbations can result in decreased viral infectivity and replication. For instance, a reduction in NA expression on seasonal human influenza viruses by experimentally introduced mutations in the viral promoter decreases virulence in mice [
<xref ref-type="bibr" rid="CR67">67</xref>
]. Additionally, deletions in the NA stalk domain, the area between the enzymatically active head and the hydrophobic, envelope region, inhibit sialidase activity of NA, and alter HA binding and viral infectivity [
<xref ref-type="bibr" rid="CR68">68</xref>
<xref ref-type="bibr" rid="CR70">70</xref>
]. NA stalk length varies considerably between AIVs and a shortening of this domain is associated with adaptation of AIVs from wild birds to domestic poultry [
<xref ref-type="bibr" rid="CR71">71</xref>
,
<xref ref-type="bibr" rid="CR72">72</xref>
]. A nineteen amino acid NA stalk deletion is commonly observed in highly pathogenic A/H5N1 viruses, and this deletion associates with enhanced replication capacity in mice [
<xref ref-type="bibr" rid="CR53">53</xref>
,
<xref ref-type="bibr" rid="CR54">54</xref>
]. Similarly, experimentally introduced NA stalk deletions in A/H1N1, A/H7N1, A/H9N2 and A/H7N9 subtypes increase viral pathogenicity in mice and/or chickens [
<xref ref-type="bibr" rid="CR71">71</xref>
,
<xref ref-type="bibr" rid="CR73">73</xref>
<xref ref-type="bibr" rid="CR78">78</xref>
].
<table-wrap id="Tab2">
<label>Table 2</label>
<caption>
<p>Experimentally verified molecular markers/motifs in the neuraminidase (NA; segment 6) gene of avian influenza viruses associated with enhanced virulence and antiviral resistance</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left">Mutation/motif (N2 numbering
<sup>a</sup>
)</th>
<th align="left">Phenotype</th>
<th align="left">Subtypes tested</th>
<th align="left">References</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" rowspan="3">49–68 deletion
<sup>b</sup>
</td>
<td align="left" rowspan="2">Enhanced virulence in mice</td>
<td align="left" rowspan="2">H5N1 (with H1N1 backbone)</td>
<td align="left">[
<xref ref-type="bibr" rid="CR73">73</xref>
]</td>
</tr>
<tr>
<td align="left">[
<xref ref-type="bibr" rid="CR74">74</xref>
]</td>
</tr>
<tr>
<td align="left">Enhanced virulence in mice</td>
<td align="left">H7N9 (human isolate)</td>
<td align="left">[
<xref ref-type="bibr" rid="CR75">75</xref>
]</td>
</tr>
<tr>
<td align="left" rowspan="3">54–72 deletion</td>
<td align="left">Enhanced virulence in mice but not chickens</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR72">72</xref>
]</td>
</tr>
<tr>
<td align="left">Enhanced virulence in mice</td>
<td align="left">H7N9 (human isolate)</td>
<td align="left">[
<xref ref-type="bibr" rid="CR75">75</xref>
]</td>
</tr>
<tr>
<td align="left">Enhanced virulence in mice and chickens</td>
<td align="left">H1N1 (avian)</td>
<td align="left">[
<xref ref-type="bibr" rid="CR71">71</xref>
]</td>
</tr>
<tr>
<td align="left">54–73 deletion</td>
<td align="left">Enhanced virulence in mice</td>
<td align="left">H7N9 (human isolate)</td>
<td align="left">[
<xref ref-type="bibr" rid="CR75">75</xref>
]</td>
</tr>
<tr>
<td align="left">54–75 deletion</td>
<td align="left">Enhanced virulence in chickens but not ducks</td>
<td align="left">H7N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR76">76</xref>
]</td>
</tr>
<tr>
<td align="left">54–81 deletion</td>
<td align="left">Enhanced replication in chicken, but not duck, cell line. Enhanced replication in respiratory tract of chickens.</td>
<td align="left">H2N2</td>
<td align="left">[
<xref ref-type="bibr" rid="CR246">246</xref>
]</td>
</tr>
<tr>
<td align="left">57–65 deletion</td>
<td align="left">Enhanced virulence in mice</td>
<td align="left">H7N9 (human isolate)</td>
<td align="left">[
<xref ref-type="bibr" rid="CR77">77</xref>
]</td>
</tr>
<tr>
<td align="left">V116A</td>
<td align="left">Reduced susceptibility to oseltamivir and zanamivir</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR247">247</xref>
,
<xref ref-type="bibr" rid="CR248">248</xref>
]</td>
</tr>
<tr>
<td align="left">I117T</td>
<td align="left">Reduced susceptibility to oseltamivir and zanamivir</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR249">249</xref>
]</td>
</tr>
<tr>
<td align="left" rowspan="3">E119A</td>
<td align="left">Reduced susceptibility to zanamivir</td>
<td align="left">H4N2</td>
<td align="left">[
<xref ref-type="bibr" rid="CR250">250</xref>
]</td>
</tr>
<tr>
<td align="left">Reduced susceptibility to oseltamivir and zanamivir</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR251">251</xref>
,
<xref ref-type="bibr" rid="CR252">252</xref>
]</td>
</tr>
<tr>
<td align="left">Reduced susceptibility to oseltamivir, zanamivir, peramivir, and laninamivir</td>
<td align="left">H7N9</td>
<td align="left">[
<xref ref-type="bibr" rid="CR253">253</xref>
]</td>
</tr>
<tr>
<td align="left" rowspan="4">E119D</td>
<td align="left">Reduced susceptibility to zanamivir</td>
<td align="left">H4N2</td>
<td align="left">[
<xref ref-type="bibr" rid="CR250">250</xref>
]</td>
</tr>
<tr>
<td align="left">Reduced susceptibility to oseltamivir, zanamivir, and peramivir</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR251">251</xref>
]</td>
</tr>
<tr>
<td align="left">Reduced susceptibility to oseltamivir, zanamivir, peramivir, and laninamivir</td>
<td align="left">H7N9</td>
<td align="left">[
<xref ref-type="bibr" rid="CR253">253</xref>
]</td>
</tr>
<tr>
<td align="left">Reduced susceptibility to zanamivir</td>
<td align="left">H9N2</td>
<td align="left">[
<xref ref-type="bibr" rid="CR254">254</xref>
]</td>
</tr>
<tr>
<td align="left" rowspan="3">E119G</td>
<td align="left">Reduced susceptibility to zanamivir</td>
<td align="left">H4N2</td>
<td align="left">[
<xref ref-type="bibr" rid="CR250">250</xref>
]</td>
</tr>
<tr>
<td align="left">Reduced susceptibility to zanamivir and peramivir</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR251">251</xref>
]</td>
</tr>
<tr>
<td align="left">Reduced susceptibility to zanamivir, peramivir, and laninamivir</td>
<td align="left">H7N9</td>
<td align="left">[
<xref ref-type="bibr" rid="CR253">253</xref>
]</td>
</tr>
<tr>
<td align="left" rowspan="2">Q136L</td>
<td align="left">Reduced susceptibility to oseltamivir and zanamivir</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR255">255</xref>
]</td>
</tr>
<tr>
<td align="left">Reduced susceptibility to zanamivir, permaivir, and laninamivir</td>
<td align="left">H7N9</td>
<td align="left">[
<xref ref-type="bibr" rid="CR253">253</xref>
]</td>
</tr>
<tr>
<td align="left">R152K</td>
<td align="left">Reduced susceptibility to laninamivir</td>
<td align="left">H7N9</td>
<td align="left">[
<xref ref-type="bibr" rid="CR253">253</xref>
]</td>
</tr>
<tr>
<td align="left">D198G</td>
<td align="left">Reduced susceptibility to oseltamivir and zanamivir</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR256">256</xref>
]</td>
</tr>
<tr>
<td align="left">I222M</td>
<td align="left">Reduced susceptibility to oseltamivir</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR256">256</xref>
]</td>
</tr>
<tr>
<td align="left">I222K</td>
<td align="left">Reduced susceptibility to oseltamivir, zanamivir, peramivir, and laninamivir</td>
<td align="left">H7N9</td>
<td align="left">[
<xref ref-type="bibr" rid="CR253">253</xref>
]</td>
</tr>
<tr>
<td align="left">I222R</td>
<td align="left">Reduced susceptibility to oseltamivir and laninamivir</td>
<td align="left">H7N9</td>
<td align="left">[
<xref ref-type="bibr" rid="CR253">253</xref>
]</td>
</tr>
<tr>
<td align="left">S246N</td>
<td align="left">Reduced susceptibility to oseltamivir</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR248">248</xref>
]</td>
</tr>
<tr>
<td align="left">T247P</td>
<td align="left">Reduced susceptibility to oseltamivir and zanamivir</td>
<td align="left">H7N9</td>
<td align="left">[
<xref ref-type="bibr" rid="CR253">253</xref>
]</td>
</tr>
<tr>
<td align="left" rowspan="2">H274Y</td>
<td align="left">Reduced susceptibility to oseltamivir and peramivir</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR251">251</xref>
<xref ref-type="bibr" rid="CR253">253</xref>
,
<xref ref-type="bibr" rid="CR256">256</xref>
<xref ref-type="bibr" rid="CR258">258</xref>
]</td>
</tr>
<tr>
<td align="left">Reduced susceptibility to oseltamivir</td>
<td align="left">H7N9</td>
<td align="left">[
<xref ref-type="bibr" rid="CR253">253</xref>
]</td>
</tr>
<tr>
<td align="left">E276D</td>
<td align="left">Reduced susceptibility to oseltamivir, zanamivir, peramivir, and laninamivir</td>
<td align="left">H7N9</td>
<td align="left">[
<xref ref-type="bibr" rid="CR253">253</xref>
]</td>
</tr>
<tr>
<td align="left">E277Q</td>
<td align="left">Reduced susceptibility to oseltamivir</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR259">259</xref>
]</td>
</tr>
<tr>
<td align="left" rowspan="4">R292K</td>
<td align="left">Reduced susceptibility to zanamivir</td>
<td align="left">H4N2</td>
<td align="left">[
<xref ref-type="bibr" rid="CR250">250</xref>
]</td>
</tr>
<tr>
<td align="left">Reduced susceptibility to oseltamivir</td>
<td align="left">H6N2</td>
<td align="left">[
<xref ref-type="bibr" rid="CR260">260</xref>
]</td>
</tr>
<tr>
<td align="left">Reduced susceptibility to oseltamivir, zanamivir, peramivir, and laninamivir</td>
<td align="left">H7N9</td>
<td align="left">[
<xref ref-type="bibr" rid="CR261">261</xref>
,
<xref ref-type="bibr" rid="CR262">262</xref>
]</td>
</tr>
<tr>
<td align="left">Reduced susceptibility to oseltamivir</td>
<td align="left">H9N2</td>
<td align="left">[
<xref ref-type="bibr" rid="CR254">254</xref>
]</td>
</tr>
<tr>
<td align="left" rowspan="2">N294S</td>
<td align="left">Reduced susceptibility to oseltamivir, zanamivir, and peramivir</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR251">251</xref>
,
<xref ref-type="bibr" rid="CR252">252</xref>
,
<xref ref-type="bibr" rid="CR257">257</xref>
,
<xref ref-type="bibr" rid="CR263">263</xref>
]</td>
</tr>
<tr>
<td align="left">Reduced susceptibility to zanamivir</td>
<td align="left">H7N9</td>
<td align="left">[
<xref ref-type="bibr" rid="CR253">253</xref>
]</td>
</tr>
<tr>
<td align="left">R371K</td>
<td align="left">Reduced susceptibility to oseltamivir, zanamivir, peramivir, and laninamivir</td>
<td align="left">H7N9</td>
<td align="left">[
<xref ref-type="bibr" rid="CR253">253</xref>
]</td>
</tr>
<tr>
<td align="left">A401T</td>
<td align="left">Increased virus binding to α2–3</td>
<td align="left">H7N9</td>
<td align="left">[
<xref ref-type="bibr" rid="CR264">264</xref>
]</td>
</tr>
<tr>
<td align="left">K432T</td>
<td align="left">Reduced susceptibility to zanamivir</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR265">265</xref>
]</td>
</tr>
<tr>
<td align="left">I117V, I314V</td>
<td align="left">Reduced susceptibility to oseltamivir</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR247">247</xref>
]</td>
</tr>
<tr>
<td align="left">E119V, E222V</td>
<td align="left">Reduced susceptibility to oseltamivir</td>
<td align="left">H7N9</td>
<td align="left">[
<xref ref-type="bibr" rid="CR266">266</xref>
]</td>
</tr>
<tr>
<td align="left">E119A/D/G, H274Y</td>
<td align="left">Reduced susceptibility to oseltamivir, zanamivir, and peramivir</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR251">251</xref>
]</td>
</tr>
<tr>
<td align="left">I222L, S246N</td>
<td align="left">Reduced susceptibility to oseltamivir</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR265">265</xref>
]</td>
</tr>
<tr>
<td align="left">I222M/V, H274Y</td>
<td align="left">Reduced susceptibility to oseltamivir and peramivir</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR256">256</xref>
]</td>
</tr>
<tr>
<td align="left">K150N, I222L, S246N</td>
<td align="left">Reduced susceptibility to oseltamivir</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR248">248</xref>
]</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<p>Single mutations are presented first followed by motifs involving multiple mutations. Individual markers and motifs are listed in numerical order for ease of identifying mutation of interest</p>
<p>
<sup>a</sup>
Mutation/location N2 numbering relative to A/Aichi/2/1968 (H3N2)</p>
<p>
<sup>b</sup>
Deletions are numbered according to alignments with A/Goose/Guangdong/1/1996 (H5N1)</p>
</table-wrap-foot>
</table-wrap>
</p>
</sec>
<sec id="Sec12">
<title>Antiviral susceptibility and resistance</title>
<p id="Par16">The function of NA is essential for productive AIV infection, as exemplified by conserved NA catalytic sites across influenza virus strains. Developed as antivirals in the 1990s, neuraminidase inhibitors (NAIs) bind to this active site of NA and prevent the release of new viruses from the surface of the infected host cell. While these antiviral compounds have been used successfully for several decades, the prevalence of NAI resistance is increasing [
<xref ref-type="bibr" rid="CR79">79</xref>
]. Environmental contamination with NAIs is also a recent concern, increasing the possibility of NAI resistance in AIVs from wild birds and domestic poultry [
<xref ref-type="bibr" rid="CR80">80</xref>
]. The majority of NA mutations in this updated inventory are markers associated with resistance to the major NAIs currently in use globally: oseltamivir, zanamivir, laninamivir, and peramivir. The WHO-AVWG periodically releases a comprehensive table of mutations shown to affect NAI susceptibility in seasonal human influenza viruses (including both A and B genera viruses) as well as in subtype A/H5N1 and A/H7N9 AIVs [
<xref ref-type="bibr" rid="CR18">18</xref>
]. The NA table (Table 
<xref rid="Tab2" ref-type="table">2</xref>
) provides a summary of WHO-AVWG NAI susceptibility markers for A/H5N1 and A/H7N9 viruses.</p>
</sec>
</sec>
</sec>
<sec id="Sec13">
<title>Proteins of the ribonucleoprotein complex: PB2, PB1, PA, and NP</title>
<p id="Par17">Inside the viral envelope, the eight genomic viral RNA (vRNA) segments of influenza A viruses form part of the viral ribonucleoprotein complex (vRNP). The vRNP consists of vRNA associated with multiple copies of the nucleoprotein (NP), and an RNA-dependent RNA polymerase sub-complex (RdRP), formed by polymerase basic protein 2 (PB2), polymerase basic protein 1 (PB1), and the polymerase acidic protein (PA). Cryo-EM and crystal structures of the RdRP show that PB1 forms the core of the structure, associating with PA via its N-terminal and PB2 via it’s C-terminal [
<xref ref-type="bibr" rid="CR81">81</xref>
<xref ref-type="bibr" rid="CR83">83</xref>
]. Subunits of the RdRP associate with the 5′ and 3′ ends of viral RNA and with NP. The RdRP is crucial for viral transcription and replication, producing vRNA, complementary RNA and viral messenger RNA (mRNA) (reviewed in [
<xref ref-type="bibr" rid="CR84">84</xref>
,
<xref ref-type="bibr" rid="CR85">85</xref>
]). The synthesis of viral mRNA is dependent on RdRP cap snatching. Whereby, PB2 binds the 5′ cap of host RNA polymerase II transcripts [
<xref ref-type="bibr" rid="CR86">86</xref>
<xref ref-type="bibr" rid="CR89">89</xref>
], 10–13 nucleotides are cleaved by the endonuclease site of PA, and PB1 uses the cleaved fragment as a primer to initiate transcription [
<xref ref-type="bibr" rid="CR90">90</xref>
]. Cap snatching not only facilitates the translation of viral mRNA, it also inhibits the production of host mRNA, referred to as host shutoff [
<xref ref-type="bibr" rid="CR91">91</xref>
,
<xref ref-type="bibr" rid="CR92">92</xref>
]. Mutations that hinder AIV cap snatching ability affinity of vRNP proteins can affect viral replicative capacity and, consequently, AIV virulence.</p>
<p id="Par18">Mutations that increase the polymerase activity of AIVs are important for the adaptation of AIVs to mammalian hosts [
<xref ref-type="bibr" rid="CR84">84</xref>
]. In a number of studies, the polymerase activity of AIVs is impaired in mammalian cell lines [
<xref ref-type="bibr" rid="CR93">93</xref>
]. This reduction in polymerase activity limits the transcription of viral RNA resulting in less viral material available to be packaged into progeny viruses. Additionally, limited replication capacity reduces viral genomic mutation, hindering the ability of AIVs to create progeny with beneficial mutations. A number of mutations in proteins of the polymerase complex enhance the replicative capacity of AIVs in mammalian cells. However, these increases in polymerase activity and/or replicative capacity do not always correlate with an increase in viral pathogenicity [
<xref ref-type="bibr" rid="CR94">94</xref>
].</p>
<sec id="Sec14">
<title>Polymerase basic protein 2 (PB2; Table 
<xref rid="Tab3" ref-type="table">3</xref>
)</title>
<p id="Par19">Mutations in the PB2 protein, namely one mutation—the substitution of glutamate with lysine at position 627 (E627K)—are, by far, the best-known mutations in the polymerase complex proteins to be associated with increases in viral fitness [
<xref ref-type="bibr" rid="CR95">95</xref>
]. Avian viruses typically have glutamate at this position and the substitution with lysine arises during adaptation to replication in mammalian species and supports transmission [
<xref ref-type="bibr" rid="CR96">96</xref>
,
<xref ref-type="bibr" rid="CR97">97</xref>
]. E627K increases viral polymerase activity and replication in mammalian cell lines at temperatures similar to those of the upper respiratory tract of humans (~ 33 °C), a trait that increases transmissibility of AIVs in mammals [
<xref ref-type="bibr" rid="CR98">98</xref>
<xref ref-type="bibr" rid="CR100">100</xref>
]. This mutation increases virulence of A/H5N1, A/H6N1, A/H7N7, A/H7N9, and A/H9N2 AIVs in mammalian models of disease [
<xref ref-type="bibr" rid="CR101">101</xref>
<xref ref-type="bibr" rid="CR105">105</xref>
]. In contrast, E627K decreases, or has no effect, on AIV virulence in chickens [
<xref ref-type="bibr" rid="CR106">106</xref>
<xref ref-type="bibr" rid="CR108">108</xref>
]. Interestingly, position 627 is situated on the surface of PB2 [
<xref ref-type="bibr" rid="CR84">84</xref>
,
<xref ref-type="bibr" rid="CR95">95</xref>
,
<xref ref-type="bibr" rid="CR109">109</xref>
], and, therefore, mutations at this position influence the association of PB2 with interacting partners e.g., NP, importin α, and ANP32A [
<xref ref-type="bibr" rid="CR110">110</xref>
<xref ref-type="bibr" rid="CR112">112</xref>
]. However, the exact mechanism behind the influence of position 627 on AIV host range remains unknown. Indeed, other mutations in PB2 aside from E627K include, but are not limited to: T271A, K526R, A588V, Q591K, E627V, D701N, D701V, and S714R. All of these mutations increase viral polymerase activity in mammalian cell lines for multiple AIV subtypes. Combinations of these mutations, such as E627K/D701N/S714R, can also further enhance viral polymerase activity, replication and virulence [
<xref ref-type="bibr" rid="CR102">102</xref>
].
<table-wrap id="Tab3">
<label>Table 3</label>
<caption>
<p>Experimentally verified molecular markers/motifs in the polymerase basic protein 2 (PB2; segment 1) gene of avian influenza virus associated with polymerase activity, virulence, and transmissibility</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left">Mutation/motif</th>
<th align="left">Phenotype</th>
<th align="left">Subtypes tested</th>
<th align="left">References</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left">D9N
<sup>a</sup>
</td>
<td align="left">Increased virulence in mice</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR115">115</xref>
,
<xref ref-type="bibr" rid="CR116">116</xref>
]</td>
</tr>
<tr>
<td align="left">V25A</td>
<td align="left">Increased virulence in mice</td>
<td align="left">H5N1 backbone with H1N1 NS</td>
<td align="left">[
<xref ref-type="bibr" rid="CR267">267</xref>
]</td>
</tr>
<tr>
<td align="left">I63T</td>
<td align="left">Decreased pathogenicity in mice</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR72">72</xref>
]</td>
</tr>
<tr>
<td align="left" rowspan="2">E158G</td>
<td align="left" rowspan="2">Increased polymerase activity in mammalian cell line, increased virulence in mice</td>
<td align="left">H5N2</td>
<td align="left">[
<xref ref-type="bibr" rid="CR268">268</xref>
]</td>
</tr>
<tr>
<td align="left">H5N9</td>
<td align="left">[
<xref ref-type="bibr" rid="CR268">268</xref>
]</td>
</tr>
<tr>
<td align="left">E158K</td>
<td align="left">Increased polymerase activity and replication in mammalian cell line, increase virulence in mice</td>
<td align="left">H4N6</td>
<td align="left">[
<xref ref-type="bibr" rid="CR269">269</xref>
]</td>
</tr>
<tr>
<td align="left">E192K</td>
<td align="left">Increased polymerase activity in mammalian and avian cell line, increased virulence in mice</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR117">117</xref>
]</td>
</tr>
<tr>
<td align="left">A199S</td>
<td align="left">Increased virulence in mice</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR116">116</xref>
]</td>
</tr>
<tr>
<td align="left">D253N</td>
<td align="left">Increased polymerase activity in mammalian cell line</td>
<td align="left">H9N2</td>
<td align="left">[
<xref ref-type="bibr" rid="CR270">270</xref>
]</td>
</tr>
<tr>
<td align="left">D256G</td>
<td align="left">Increased polymerase activity in mammalian cell line</td>
<td align="left">H5N1 backbone with pH1N1 PB2</td>
<td align="left">[
<xref ref-type="bibr" rid="CR271">271</xref>
]</td>
</tr>
<tr>
<td align="left" rowspan="3">T271A</td>
<td align="left" rowspan="3">Increase polymerase activity in avian and mammalian cell line</td>
<td align="left">H3N2 (avian)</td>
<td align="left">[
<xref ref-type="bibr" rid="CR272">272</xref>
]</td>
</tr>
<tr>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR273">273</xref>
]</td>
</tr>
<tr>
<td align="left">H7N9</td>
<td align="left">[
<xref ref-type="bibr" rid="CR274">274</xref>
]</td>
</tr>
<tr>
<td align="left" rowspan="2">I292V</td>
<td align="left">Increased polymerase activity in mammalian cell line, increased virulence in mice</td>
<td align="left">H9N2</td>
<td align="left">[
<xref ref-type="bibr" rid="CR275">275</xref>
]</td>
</tr>
<tr>
<td align="left">Increased polymerase activity in mammalian cell line</td>
<td align="left">H10N8</td>
<td align="left">[
<xref ref-type="bibr" rid="CR276">276</xref>
]</td>
</tr>
<tr>
<td align="left">E358V</td>
<td align="left">Decreased virulence in mice</td>
<td align="left">H7N3</td>
<td align="left">[
<xref ref-type="bibr" rid="CR277">277</xref>
]</td>
</tr>
<tr>
<td align="left">K389R</td>
<td align="left">Increased polymerase activity and replication in mammalian cell line</td>
<td align="left">H7N9</td>
<td align="left">[
<xref ref-type="bibr" rid="CR278">278</xref>
]</td>
</tr>
<tr>
<td align="left">L339T</td>
<td align="left">Decreased polymerase activity and decreased virulence in mice</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR279">279</xref>
]</td>
</tr>
<tr>
<td align="left">K482R</td>
<td align="left">Increased polymerase activity in mammalian cell line</td>
<td align="left">H7N9</td>
<td align="left">[
<xref ref-type="bibr" rid="CR280">280</xref>
,
<xref ref-type="bibr" rid="CR281">281</xref>
]</td>
</tr>
<tr>
<td align="left" rowspan="2">K526R</td>
<td align="left" rowspan="2">Increased polymerase activity in mammalian cell line</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR282">282</xref>
]</td>
</tr>
<tr>
<td align="left">H7N9</td>
<td align="left">[
<xref ref-type="bibr" rid="CR282">282</xref>
]</td>
</tr>
<tr>
<td align="left">M535L</td>
<td align="left">Increased polymerase activity in mammalian cell line</td>
<td align="left">H7N9</td>
<td align="left">[
<xref ref-type="bibr" rid="CR25">25</xref>
]</td>
</tr>
<tr>
<td align="left" rowspan="3">A588V</td>
<td align="left" rowspan="3">Increased polymerase activity and replication in mammalian and avian cell lines, increased virulence in mice</td>
<td align="left">H7N9</td>
<td align="left">[
<xref ref-type="bibr" rid="CR276">276</xref>
]</td>
</tr>
<tr>
<td align="left">H9N2</td>
<td align="left">[
<xref ref-type="bibr" rid="CR276">276</xref>
]</td>
</tr>
<tr>
<td align="left">H10N8</td>
<td align="left">[
<xref ref-type="bibr" rid="CR276">276</xref>
]</td>
</tr>
<tr>
<td align="left" rowspan="3">Q591K</td>
<td align="left">Increased polymerase activity in mammalian and avian cell line, increased replication in mammalian cell line, increased virulence in mice</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR117">117</xref>
,
<xref ref-type="bibr" rid="CR283">283</xref>
]</td>
</tr>
<tr>
<td align="left">Increased polymerase activity in mammalian and avian cell lines</td>
<td align="left">H7N9</td>
<td align="left">[
<xref ref-type="bibr" rid="CR25">25</xref>
,
<xref ref-type="bibr" rid="CR274">274</xref>
]</td>
</tr>
<tr>
<td align="left">Increased polymerase activity and replication in mammalian cell line, increased virulence in mice</td>
<td align="left">H9N2</td>
<td align="left">[
<xref ref-type="bibr" rid="CR284">284</xref>
]</td>
</tr>
<tr>
<td align="left">V598T/I</td>
<td align="left">Increased polymerase activity and replication in mammalian cells, increased virulence in mice</td>
<td align="left">H7N9</td>
<td align="left">[
<xref ref-type="bibr" rid="CR278">278</xref>
]</td>
</tr>
<tr>
<td align="left" rowspan="6">E627K</td>
<td align="left">Increased polymerase activity and replication in mammalian cell line, increase virulence in mice</td>
<td align="left">H4N6</td>
<td align="left">[
<xref ref-type="bibr" rid="CR269">269</xref>
]</td>
</tr>
<tr>
<td align="left">Enhanced polymerase activity, increased virulence in mice, contributes to airborne pathogenicity of IAVs in ferrets and contact transmission in guinea pigs. Decreases polymerase activity and replication in avian cell lines. Decreases virulence in chickens.</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR15">15</xref>
,
<xref ref-type="bibr" rid="CR100">100</xref>
,
<xref ref-type="bibr" rid="CR101">101</xref>
,
<xref ref-type="bibr" rid="CR106">106</xref>
<xref ref-type="bibr" rid="CR108">108</xref>
,
<xref ref-type="bibr" rid="CR116">116</xref>
,
<xref ref-type="bibr" rid="CR257">257</xref>
,
<xref ref-type="bibr" rid="CR271">271</xref>
,
<xref ref-type="bibr" rid="CR285">285</xref>
<xref ref-type="bibr" rid="CR289">289</xref>
]</td>
</tr>
<tr>
<td align="left">Increased polymerase activity in mammalian cell line, increased virulence in mice</td>
<td align="left">H6N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR103">103</xref>
]</td>
</tr>
<tr>
<td align="left">Increased polymerase activity in mammalian cell lines, increase virulence in mice</td>
<td align="left">H7N7</td>
<td align="left">[
<xref ref-type="bibr" rid="CR102">102</xref>
,
<xref ref-type="bibr" rid="CR104">104</xref>
]</td>
</tr>
<tr>
<td align="left">Increased polymerase activity and replication in mammalian cell lines, increased virulence in mice</td>
<td align="left">H7N9</td>
<td align="left">[
<xref ref-type="bibr" rid="CR102">102</xref>
,
<xref ref-type="bibr" rid="CR105">105</xref>
]</td>
</tr>
<tr>
<td align="left">Increased polymerase activity in mammalian cell line, increased virulence in mice</td>
<td align="left">H9N2</td>
<td align="left">[
<xref ref-type="bibr" rid="CR102">102</xref>
,
<xref ref-type="bibr" rid="CR290">290</xref>
]</td>
</tr>
<tr>
<td align="left">E627V</td>
<td align="left">Increased polymerase activity and replication in mammalian cell lines, increased virulence in mice</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR117">117</xref>
]</td>
</tr>
<tr>
<td align="left">K627E</td>
<td align="left">Increased virulence in chickens</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR291">291</xref>
]</td>
</tr>
<tr>
<td align="left" rowspan="4">D701N</td>
<td align="left">Increased viral replication in mammalian cells and virulence in mice</td>
<td align="left">H1N2</td>
<td align="left">[
<xref ref-type="bibr" rid="CR220">220</xref>
]</td>
</tr>
<tr>
<td align="left">Increased polymerase activity, enhanced replication efficiency, increased virulence and contact transmission in guinea pigs, increased virulence in mice</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR96">96</xref>
,
<xref ref-type="bibr" rid="CR117">117</xref>
,
<xref ref-type="bibr" rid="CR206">206</xref>
,
<xref ref-type="bibr" rid="CR292">292</xref>
,
<xref ref-type="bibr" rid="CR293">293</xref>
]</td>
</tr>
<tr>
<td align="left">Increased polymerase activity in mammalian cell line</td>
<td align="left">H7N9</td>
<td align="left">[
<xref ref-type="bibr" rid="CR25">25</xref>
,
<xref ref-type="bibr" rid="CR274">274</xref>
]</td>
</tr>
<tr>
<td align="left">Increased polymerase activity in mammalian cell line</td>
<td align="left">H9N2</td>
<td align="left">[
<xref ref-type="bibr" rid="CR102">102</xref>
]</td>
</tr>
<tr>
<td align="left">D701V</td>
<td align="left">Increased polymerase activity and replication in mammalian cell lines, increased virulence in mice</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR117">117</xref>
]</td>
</tr>
<tr>
<td align="left" rowspan="2">S714R</td>
<td align="left">Increased polymerase activity and replication in mammalian cell line</td>
<td align="left">H7N7</td>
<td align="left">[
<xref ref-type="bibr" rid="CR94">94</xref>
,
<xref ref-type="bibr" rid="CR102">102</xref>
,
<xref ref-type="bibr" rid="CR124">124</xref>
]</td>
</tr>
<tr>
<td align="left">Increased polymerase activity in mammalian cell line</td>
<td align="left">H9N2</td>
<td align="left">[
<xref ref-type="bibr" rid="CR102">102</xref>
]</td>
</tr>
<tr>
<td align="left">S715N</td>
<td align="left">Decreased virulence in mice</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR294">294</xref>
]</td>
</tr>
<tr>
<td align="left">M28I, A274T, K526R, I553V, L607V</td>
<td align="left">Decreased polymerase activity in mammalian cell line</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR295">295</xref>
]</td>
</tr>
<tr>
<td align="left">L89V, G309D</td>
<td align="left">Increased polymerase activity in mammalian cell line and increased virulence in mice</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR296">296</xref>
]</td>
</tr>
<tr>
<td align="left">L89V, G309D, T339K, R477G, I495V, K627E, A676T</td>
<td align="left">Increased polymerase activity in mammalian cell line and increased virulence in mice</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR296">296</xref>
]</td>
</tr>
<tr>
<td align="left">M147L, E627K</td>
<td align="left">Increased polymerase activity in mammalian cell line and virulence in mice</td>
<td align="left">H9N2</td>
<td align="left">[
<xref ref-type="bibr" rid="CR297">297</xref>
]</td>
</tr>
<tr>
<td align="left">I147T, K339T, A588T</td>
<td align="left">Increased polymerase activity in mammalian cell line and virulence in mice</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR298">298</xref>
]</td>
</tr>
<tr>
<td align="left" rowspan="2">K526R, E627K</td>
<td align="left" rowspan="2">Increased polymerase activity and viral replication in mammalian cell lines, increased virulence in mice</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR282">282</xref>
]</td>
</tr>
<tr>
<td align="left">H7N9</td>
<td align="left">[
<xref ref-type="bibr" rid="CR282">282</xref>
]</td>
</tr>
<tr>
<td align="left">E627K, D701N</td>
<td align="left">Increased polymerase activity in mammalian cell line</td>
<td align="left">H7N9</td>
<td align="left">[
<xref ref-type="bibr" rid="CR299">299</xref>
]</td>
</tr>
<tr>
<td align="left" rowspan="3">E627K, S714R</td>
<td align="left" rowspan="3">Increased polymerase activity in mammalian cell lines</td>
<td align="left">H7N7</td>
<td align="left">[
<xref ref-type="bibr" rid="CR102">102</xref>
]</td>
</tr>
<tr>
<td align="left">H7N9</td>
<td align="left">[
<xref ref-type="bibr" rid="CR102">102</xref>
]</td>
</tr>
<tr>
<td align="left">H9N2</td>
<td align="left">[
<xref ref-type="bibr" rid="CR102">102</xref>
]</td>
</tr>
<tr>
<td align="left">E627K, D701N, S714R</td>
<td align="left">Increased polymerase activity in mammalian cells, increased virulence in mice</td>
<td align="left">H9N2</td>
<td align="left">[
<xref ref-type="bibr" rid="CR102">102</xref>
]</td>
</tr>
<tr>
<td align="left" rowspan="4">D701N, S714R</td>
<td align="left">Increased polymerase activity in mammalian cell line, increased virulence in mice</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR300">300</xref>
]</td>
</tr>
<tr>
<td align="left">Increased polymerase activity in mammalian cell lines</td>
<td align="left">H7N7</td>
<td align="left">[
<xref ref-type="bibr" rid="CR102">102</xref>
]</td>
</tr>
<tr>
<td align="left">Increased polymerase activity in mammalian cell lines</td>
<td align="left">H7N9</td>
<td align="left">[
<xref ref-type="bibr" rid="CR102">102</xref>
]</td>
</tr>
<tr>
<td align="left">Increased polymerase activity in mammalian cell lines</td>
<td align="left">H9N2</td>
<td align="left">[
<xref ref-type="bibr" rid="CR102">102</xref>
]</td>
</tr>
<tr>
<td align="left">E627K (with HA: H110Y, T160A, Q226L, G228S; PB1: H99Y)</td>
<td align="left">Enable airborne transmissibility between ferrets and contact transmission between guinea pigs</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR15">15</xref>
,
<xref ref-type="bibr" rid="CR58">58</xref>
]</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<p>Single mutations are presented first followed by motifs involving multiple mutations. Individual markers and motifs are listed in numerical order for ease of identifying mutation of interest</p>
<p>
<sup>a</sup>
Mutations/motifs are numbered according to alignments with A/Goose/Guangdong/1/1996 (H5N1)</p>
</table-wrap-foot>
</table-wrap>
</p>
<p id="Par20">PB2 also potentially antagonizes the host interferon (IFN) response. A subset of AIVs contain PB2 proteins with an N-terminal mitochondrial targeting signal (MTS) that facilitates import of PB2 into the mitochondrial matrix [
<xref ref-type="bibr" rid="CR66">66</xref>
,
<xref ref-type="bibr" rid="CR67">67</xref>
]. Mitochondrial PB2 then antagonizes host IFN production by interfering with the action of mitochondrial antiviral signaling proteins (MAVS) [
<xref ref-type="bibr" rid="CR113">113</xref>
,
<xref ref-type="bibr" rid="CR114">114</xref>
]. Disruption of the MTS through a single amino acid substitution at position 9 prevents mitochondrial localization of PB2, heightening host IFN response and attenuating viral virulence [
<xref ref-type="bibr" rid="CR115">115</xref>
,
<xref ref-type="bibr" rid="CR116">116</xref>
]. Asparagine (N9) or threonine (T9) at position 9 facilitates import of PB2 into the mitochondrial matrix. N9 is typically present in human seasonal viruses (A/H1N1 prior to 2009, A/H2N2, and A/H3N2). In contrast, AIVs typically have aspartic acid at positon 9 (D9), and AIV PB2s are non-mitochondrial and predominantly found in the nucleus. Experimentally mutating seasonal human influenza viruses to contain the non-mitochondrial D9 heightens production of IFN-β and attenuates pathogenicity in mice [
<xref ref-type="bibr" rid="CR115">115</xref>
]. Conversely, mutating avian A/H5N1 to contain N9 increases pathogenicity in mice, though specific cellular localization was not investigated [
<xref ref-type="bibr" rid="CR116">116</xref>
].</p>
</sec>
<sec id="Sec15">
<title>Polymerase basic protein 1 (PB1; Table 
<xref rid="Tab4" ref-type="table">4</xref>
) and polymerase protein (PA; Table 
<xref rid="Tab5" ref-type="table">5</xref>
)</title>
<p id="Par21">Mutations in PB1 and PA affect viral replicative capacity and polymerase activity by altering the affinity between components of the RdRP [
<xref ref-type="bibr" rid="CR86">86</xref>
<xref ref-type="bibr" rid="CR92">92</xref>
]. A number of single amino acid substitutions increase AIV virulence in mice, PB1: K577E, D622G; PA: V63I, T97I, K142N/E, K356R, S421I, R443K, and K615N. Of these mutations PB1: N105S, K577E and PA: T97I, K356R also increase AIV polymerase activity in mammalian cell lines at 33 °C (a number of mutations were only tested at 37 °C) [
<xref ref-type="bibr" rid="CR117">117</xref>
<xref ref-type="bibr" rid="CR119">119</xref>
]. The mechanism behind changes in viral replication and virulence caused by these substitutions is not always clear. PA substitutions at positions 63, 97 and 142 could hinder RdRP cap snatching by reducing cleavage of host mRNA caps. Interestingly, four substitutions in PA at positions 142, 147, 171 and 182 that are associated with low polymerase activity of AIVs can drive the emergence of compensatory mutations in other RdRP proteins, as demonstrated for the emergence of PB2 E627K in A(H7N9) viruses [
<xref ref-type="bibr" rid="CR120">120</xref>
].
<table-wrap id="Tab4">
<label>Table 4</label>
<caption>
<p>Experimentally verified molecular markers/motifs in the polymerase basic protein 1 (PB1; segment 2) gene of influenza virus associated with polymerase activity, replication, virulence, and transmissibility</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left">Protein</th>
<th align="left">Mutation/motif</th>
<th align="left">Phenotype</th>
<th align="left">Subtypes tested</th>
<th align="left">References</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" rowspan="13">PB1</td>
<td align="left">D3V
<sup>a</sup>
</td>
<td align="left">Increased polymerase activity and viral replication in avian and mammalian cell lines</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR301">301</xref>
]</td>
</tr>
<tr>
<td align="left">N105S</td>
<td align="left">Increase polymerase activity and replication in mammalian cell line, increased virulence in mice</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR117">117</xref>
]</td>
</tr>
<tr>
<td align="left">K207R</td>
<td align="left">Decreased polymerase activity in mammalian cell line</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR302">302</xref>
]</td>
</tr>
<tr>
<td align="left">Y436H</td>
<td align="left">Decreased polymerase activity in mammalian cell line; decreased virulence in ducks, ferrets and mice</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR302">302</xref>
]</td>
</tr>
<tr>
<td align="left">V473L</td>
<td align="left">Decreased polymerase activity and replication efficiency in mammalian cells</td>
<td align="left">H1N1 with PB2, PB1, PA NP from H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR303">303</xref>
]</td>
</tr>
<tr>
<td align="left">K577E</td>
<td align="left">Increased polymerase activity and virulence in mice</td>
<td align="left">H9N2</td>
<td align="left">[
<xref ref-type="bibr" rid="CR118">118</xref>
]</td>
</tr>
<tr>
<td align="left">V598P</td>
<td align="left">Decreased polymerase activity and replication efficiency in mammalian cells</td>
<td align="left">H1N1 with PB2, PB1, PA NP from H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR303">303</xref>
]</td>
</tr>
<tr>
<td align="left">D622G</td>
<td align="left">Increased polymerase activity and virulence in mice</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR304">304</xref>
]</td>
</tr>
<tr>
<td align="left">T677M</td>
<td align="left">Increased polymerase activity in mammalian cell line, decreased replication efficiency, decreased virulence in mice</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR72">72</xref>
]</td>
</tr>
<tr>
<td align="left">S678N</td>
<td align="left">Increased replication in avian and mammalian cell lines</td>
<td align="left">H7N7</td>
<td align="left">[
<xref ref-type="bibr" rid="CR124">124</xref>
]</td>
</tr>
<tr>
<td align="left">V3A, N328K, N375S</td>
<td align="left">Decreased replication efficiency and virulence in ferrets</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR93">93</xref>
]</td>
</tr>
<tr>
<td align="left">V473L, P598L</td>
<td align="left">Decreased polymerase activity and replication in mammalian cells</td>
<td align="left">H1N1 with PB2, PB1, PA NP from H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR303">303</xref>
]</td>
</tr>
<tr>
<td align="left">H99Y (with HA: H110Y, T160A, G226L, G228S; PB2: E627K)</td>
<td align="left">Airborne transmissible in ferrets</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR15">15</xref>
,
<xref ref-type="bibr" rid="CR58">58</xref>
]</td>
</tr>
<tr>
<td align="left" rowspan="2">PB1-F2</td>
<td align="left">N66S</td>
<td align="left">Enhanced replication, virulence and antiviral response in mice</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR171">171</xref>
,
<xref ref-type="bibr" rid="CR305">305</xref>
]</td>
</tr>
<tr>
<td align="left">T51M, V56A, E87G</td>
<td align="left">Decrease polymerase activity, replication and virulence in ducks</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR173">173</xref>
]</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<p>Single mutations are presented first followed by motifs involving multiple mutations. Individual markers and motifs are listed in numerical order for ease of identifying mutation of interest</p>
<p>
<sup>a</sup>
Mutations/motifs in both PB1 and PB1-F2 proteins are numbered according to alignments with A/Goose/Guangdong/1/1996 (H5N1)</p>
</table-wrap-foot>
</table-wrap>
<table-wrap id="Tab5">
<label>Table 5</label>
<caption>
<p>Experimentally verified molecular markers/motifs in the polymerase (PA; segment 3) gene of avian influenza viruses associated with polymerase activity, replication, virulence, and host inflammatory response</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left">Protein</th>
<th align="left">Mutation/motif</th>
<th align="left">Phenotype</th>
<th align="left">Subtypes tested</th>
<th align="left">References</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" rowspan="25">PA</td>
<td align="left">S37A
<sup>a</sup>
</td>
<td align="left">Increased polymerase activity in mammalian cell line</td>
<td align="left">H7N9</td>
<td align="left">[
<xref ref-type="bibr" rid="CR280">280</xref>
]</td>
</tr>
<tr>
<td align="left">A37S</td>
<td align="left">Decreased polymerase activity in mammalian cell line</td>
<td align="left">H7N7</td>
<td align="left">[
<xref ref-type="bibr" rid="CR306">306</xref>
]</td>
</tr>
<tr>
<td align="left">V63I</td>
<td align="left">Increase polymerase activity and enhanced replication in mammalian cell line, increased virulence in mice</td>
<td align="left">H7N7</td>
<td align="left">[
<xref ref-type="bibr" rid="CR306">306</xref>
,
<xref ref-type="bibr" rid="CR307">307</xref>
]</td>
</tr>
<tr>
<td align="left" rowspan="3">T97I</td>
<td align="left">Increased polymerase activity and replication in mammalian cell line, increased virulence in mice</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR117">117</xref>
]</td>
</tr>
<tr>
<td align="left">Increased polymerase activity in mammalian cell line and enhanced replication in mice</td>
<td align="left">H5N2</td>
<td align="left">[
<xref ref-type="bibr" rid="CR308">308</xref>
]</td>
</tr>
<tr>
<td align="left">Increased polymerase activity in mammalian cells</td>
<td align="left">H6N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR103">103</xref>
]</td>
</tr>
<tr>
<td align="left">K142N/E</td>
<td align="left">Increased virulence in mice</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR116">116</xref>
]</td>
</tr>
<tr>
<td align="left">K158R</td>
<td align="left">Increased polymerase activity in mammalian cell line</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR301">301</xref>
]</td>
</tr>
<tr>
<td align="left">P190S</td>
<td align="left">Decreased virulence in mice</td>
<td align="left">H7N3</td>
<td align="left">[
<xref ref-type="bibr" rid="CR277">277</xref>
]</td>
</tr>
<tr>
<td align="left">K356R</td>
<td align="left">Increase polymerase activity and enhanced replication in mammalian cell line, increased virulence in mice</td>
<td align="left">H9N2</td>
<td align="left">[
<xref ref-type="bibr" rid="CR119">119</xref>
]</td>
</tr>
<tr>
<td align="left">N383D</td>
<td align="left">Increased polymerase activity in mammalian and avian cell lines</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR121">121</xref>
,
<xref ref-type="bibr" rid="CR122">122</xref>
]</td>
</tr>
<tr>
<td align="left">Q400P</td>
<td align="left">Decreased virulence in mice</td>
<td align="left">H7N3</td>
<td align="left">[
<xref ref-type="bibr" rid="CR277">277</xref>
]</td>
</tr>
<tr>
<td align="left">N409S</td>
<td align="left">Increased polymerase activity and replication in mammalian cell line</td>
<td align="left">H7N9</td>
<td align="left">[
<xref ref-type="bibr" rid="CR280">280</xref>
]</td>
</tr>
<tr>
<td align="left">S421I</td>
<td align="left">Increased virulence in mice</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR116">116</xref>
]</td>
</tr>
<tr>
<td align="left">R443K</td>
<td align="left">Increased virulence in mice</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR267">267</xref>
]</td>
</tr>
<tr>
<td align="left">K497R</td>
<td align="left">Increased polymerase activity in mammalian cell line</td>
<td align="left">H7N9 (human isolate)</td>
<td align="left">[
<xref ref-type="bibr" rid="CR281">281</xref>
]</td>
</tr>
<tr>
<td align="left">T515A</td>
<td align="left">Decreased polymerase activity in mammalian cell line, decreased virulence in ducks</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR302">302</xref>
]</td>
</tr>
<tr>
<td align="left">K615N</td>
<td align="left">Increased polymerase activity in mammalian cell line and increased virulence in mice</td>
<td align="left">H7N7</td>
<td align="left">[
<xref ref-type="bibr" rid="CR94">94</xref>
,
<xref ref-type="bibr" rid="CR124">124</xref>
]</td>
</tr>
<tr>
<td align="left">A343S, D347E</td>
<td align="left">Increased polymerase activity in mammalian cell line, increase virulence in mice</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR309">309</xref>
]</td>
</tr>
<tr>
<td align="left">P103H, S659L</td>
<td align="left">Decreased polymerase activity replication in mammalian cell line, decreased virulence in mice</td>
<td align="left">H7N7</td>
<td align="left">[
<xref ref-type="bibr" rid="CR310">310</xref>
]</td>
</tr>
<tr>
<td align="left">S224P, N383D</td>
<td align="left">Increased polymerase activity and enhanced viral replication in duck and mouse cell lines, increased virulence in mice and ducks</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR121">121</xref>
,
<xref ref-type="bibr" rid="CR122">122</xref>
]</td>
</tr>
<tr>
<td align="left">K142R, I147V, I171V, M182L</td>
<td align="left">Increased polymerase activity in mammalian cell line</td>
<td align="left">H7N9</td>
<td align="left">[
<xref ref-type="bibr" rid="CR120">120</xref>
]</td>
</tr>
<tr>
<td align="left">V44I, V127A, C241Y, A343T, I573V</td>
<td align="left">Increased replication in mammalian cell line virulence in mice</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR311">311</xref>
]</td>
</tr>
<tr>
<td align="left">S149P, H266R, I357K, S515T</td>
<td align="left">Increased polymerase activity in mammalian cell line</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR295">295</xref>
]</td>
</tr>
<tr>
<td align="left">K356R (with PB2 E627K)</td>
<td align="left">Increase polymerase activity, enhanced replication capacity in mammalian cell line, increased virulence in mice</td>
<td align="left">H9N2</td>
<td align="left">[
<xref ref-type="bibr" rid="CR119">119</xref>
]</td>
</tr>
<tr>
<td align="left" rowspan="2">PA-X</td>
<td align="left" rowspan="2">Truncations resulting in loss of PA-X expression</td>
<td align="left">Increased viral replication in mammalian and avian cell lines; increased inflammatory response in mice; increased virulence in mice, chickens, and ducks</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR121">121</xref>
,
<xref ref-type="bibr" rid="CR177">177</xref>
,
<xref ref-type="bibr" rid="CR178">178</xref>
,
<xref ref-type="bibr" rid="CR182">182</xref>
,
<xref ref-type="bibr" rid="CR183">183</xref>
]</td>
</tr>
<tr>
<td align="left">Decreased virulence in mice, inhibited host inflammatory response</td>
<td align="left">H9N2</td>
<td align="left">[
<xref ref-type="bibr" rid="CR183">183</xref>
]</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<p>Single mutations are presented first followed by motifs involving multiple mutations. Individual markers and motifs are listed in numerical order for ease of identifying mutation of interest</p>
<p>
<sup>a</sup>
Mutations/motifs in both PA and PA-X proteins are numbered according to alignments with A/Goose/Guangdong/1/1996 (H5N1)</p>
</table-wrap-foot>
</table-wrap>
</p>
<p id="Par22">Interestingly, a combination of two mutations in PA, S224P and N383D, increase polymerase activity of a A/H5N1 subtype virus and enhance viral replication in both mammalian and avian cell lines [
<xref ref-type="bibr" rid="CR121">121</xref>
,
<xref ref-type="bibr" rid="CR122">122</xref>
]. This dual mutation also increases A/H5N1 AIV virulence in both mice and ducks. The mutations act in synergy, N383D increases AIV polymerase activity alone while the combination of S224P and N383D significantly increases AIV virulence. This combination differs from previously mentioned mutations as single point mutations in polymerase proteins typically affect viral virulence in mammalian species, with minimal changes in the polymerase activity, replication or virulence in avian species. Some mutations reportedly increase polymerase activity in avian and mammalian cell lines (PB2: A588V, Q591K; PB1: D3V, S678N). However, in these reports, only murine models were utilized to test AIV virulence.</p>
</sec>
<sec id="Sec16">
<title>Nucleoprotein (NP; Table 
<xref rid="Tab6" ref-type="table">6</xref>
)</title>
<p id="Par23">The NP protein encapsulates viral genomic RNA and mediates import into the nucleus to initiate viral replication through nuclear localization signals and the importin-α/importin-β nuclear import pathway. Mutations that affect the functions of NP have not been extensively investigated; however, substitutions I41V, R91K, R198K, E210D, K227R, K229R, N319K, E434K, K470R enhance polymerase activity in mammalian cell lines [
<xref ref-type="bibr" rid="CR53">53</xref>
,
<xref ref-type="bibr" rid="CR94">94</xref>
,
<xref ref-type="bibr" rid="CR111">111</xref>
,
<xref ref-type="bibr" rid="CR123">123</xref>
]. These mutations do not always increase AIV virulence and the mechanism behind the increase in viral replication is not always clear. One particular mutation, N319K, improves A/H7N7 viral replication in mammalian cells by enhancing the interaction between NP and importin-α isoforms [
<xref ref-type="bibr" rid="CR94">94</xref>
,
<xref ref-type="bibr" rid="CR111">111</xref>
,
<xref ref-type="bibr" rid="CR124">124</xref>
]. M105V, I109T, and A184K enhance viral replication and increase AIV virulence in chickens [
<xref ref-type="bibr" rid="CR125">125</xref>
<xref ref-type="bibr" rid="CR127">127</xref>
]. Interestingly, the M105V mutation may be involved in spillover adaption from ducks to chickens as M105V affects viral replication in embryo fibroblasts from chickens but not from ducks [
<xref ref-type="bibr" rid="CR127">127</xref>
].
<table-wrap id="Tab6">
<label>Table 6</label>
<caption>
<p>Experimentally verified molecular markers/motifs in the nucleoprotein (NP; segment 5) gene of influenza virus associated with polymerase activity, virulence, and transmissibility</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left">Mutation/motif</th>
<th align="left">Phenotype</th>
<th align="left">Subtypes tested</th>
<th align="left">References</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left">I41V
<sup>a</sup>
</td>
<td align="left">Increased polymerase activity in mammalian cell line</td>
<td align="left">H7N9</td>
<td align="left">[
<xref ref-type="bibr" rid="CR299">299</xref>
]</td>
</tr>
<tr>
<td align="left">K91R</td>
<td align="left">Decreased polymerase activity in mammalian cell line</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR123">123</xref>
]</td>
</tr>
<tr>
<td align="left">M105V</td>
<td align="left">Increased virulence in chickens</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR126">126</xref>
,
<xref ref-type="bibr" rid="CR127">127</xref>
]</td>
</tr>
<tr>
<td align="left">I109T</td>
<td align="left">Increased polymerase activity and viral replication in chickens (but not ducks), increased virulence in chickens</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR126">126</xref>
,
<xref ref-type="bibr" rid="CR127">127</xref>
]</td>
</tr>
<tr>
<td align="left">A184K</td>
<td align="left">Increased replication in avian cells and virulence in chickens, enhanced IFN response</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR125">125</xref>
]</td>
</tr>
<tr>
<td align="left">K198R</td>
<td align="left">Decreased polymerase activity in mammalian cell line</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR123">123</xref>
]</td>
</tr>
<tr>
<td align="left">E210D</td>
<td align="left">Increased polymerase activity in mammalian cell line</td>
<td align="left">H7N9</td>
<td align="left">[
<xref ref-type="bibr" rid="CR299">299</xref>
]</td>
</tr>
<tr>
<td align="left">K227R</td>
<td align="left">Increased polymerase activity in mammalian cell line</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR123">123</xref>
]</td>
</tr>
<tr>
<td align="left">K229R</td>
<td align="left">Increased polymerase activity in mammalian cell line</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR123">123</xref>
]</td>
</tr>
<tr>
<td align="left">N319K</td>
<td align="left">Increased polymerase activity and replication in mammalian cell line</td>
<td align="left">H7N7</td>
<td align="left">[
<xref ref-type="bibr" rid="CR94">94</xref>
,
<xref ref-type="bibr" rid="CR111">111</xref>
]</td>
</tr>
<tr>
<td align="left">E434K</td>
<td align="left">Increased polymerase activity in mammalian cell line</td>
<td align="left">H9N2</td>
<td align="left">[
<xref ref-type="bibr" rid="CR53">53</xref>
]</td>
</tr>
<tr>
<td align="left">K470R</td>
<td align="left">Increased polymerase activity and replication in mammalian cell line, increased virulence in mice</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR123">123</xref>
]</td>
</tr>
<tr>
<td align="left">Q357L (with PB2: E627K)</td>
<td align="left">Increased virulence in mice</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR116">116</xref>
]</td>
</tr>
<tr>
<td align="left">E434K (with HA: Q227P, D375E)</td>
<td align="left">Enhanced contact transmission in guinea pigs</td>
<td align="left">H9N2</td>
<td align="left">[
<xref ref-type="bibr" rid="CR53">53</xref>
]</td>
</tr>
<tr>
<td align="left">E434K (with HA: Q227P, PB2: D195N)</td>
<td align="left">Enhanced contact transmission in guinea pigs</td>
<td align="left">H9N2</td>
<td align="left">[
<xref ref-type="bibr" rid="CR53">53</xref>
]</td>
</tr>
<tr>
<td align="left">R99K, S345N (with HA: H110Y, T160A, Q226L, G228S; PB2: E627K; PB1: H99Y, I368V</td>
<td align="left">Airborne transmissible in ferrets</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR15">15</xref>
]</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<p>Single mutations are presented first followed by motifs involving multiple mutations. Individual markers and motifs are listed in numerical order for ease of identifying mutation of interest</p>
<p>
<sup>a</sup>
Mutations/motifs are numbered according to alignments with A/Goose/Guangdong/1/1996 (H5N1)</p>
</table-wrap-foot>
</table-wrap>
</p>
</sec>
<sec id="Sec17">
<title>Non-structural proteins 1 and 2 (NS1/NS2; Table 
<xref rid="Tab7" ref-type="table">7</xref>
)</title>
<p id="Par24">Influenza virus genomic segment 8 encodes for three viral proteins: NS1, NS2 (Nuclear Export Protein; NEP), and NS3. The NS3 protein was only recently identified and its function remains largely unknown, therefore, mutations in this protein are not included in the inventory [
<xref ref-type="bibr" rid="CR128">128</xref>
]. The NS1 protein performs multiple functions that affect AIV replication and virulence (reviewed in [
<xref ref-type="bibr" rid="CR129">129</xref>
]). Typically 230 amino acids in length, NS1 ranges between 202 and 238 amino acids in length as the C-terminus is frequently truncated or, occasionally, elongated [
<xref ref-type="bibr" rid="CR130">130</xref>
]. Structurally, NS1 proteins contain an RNA-binding domain (RBD) at the N-terminus with a flexible linker region connecting the RBD to a C-terminal effector domain (ED). The RBD and ED are functional domains that mediate the associations between NS1 and interacting partners. NS1 interacts with the vRNP complex, specifically NP and PA, as well as a number of proteins involved in cellular signaling pathways, the host antiviral response, and nuclear/cytoplasmic trafficking or translation of mRNA. Overall,NS1 is the major viral antagonist of the host IFN response and plays a role in host cell shutoff and viral replication [
<xref ref-type="bibr" rid="CR129">129</xref>
].
<table-wrap id="Tab7">
<label>Table 7</label>
<caption>
<p>Experimentally verified molecular markers/motifs in the non-structural protein (NS; segment 8) gene of influenza virus associated with replication, virulence, pathogenicity, and antiviral response</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left">Protein</th>
<th align="left">Mutation/motif</th>
<th align="left">Phenotype</th>
<th align="left">Subtypes tested</th>
<th align="left">References</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" rowspan="25">NS1</td>
<td align="left">P42S
<sup>a</sup>
</td>
<td align="left">Increased virulence and decreased antiviral response in mice</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR131">131</xref>
]</td>
</tr>
<tr>
<td align="left">D74N</td>
<td align="left">Enhanced replication in mammalian cells and pathogenicity in mice</td>
<td align="left">H7N1 backbone with H5N1 NS</td>
<td align="left">[
<xref ref-type="bibr" rid="CR312">312</xref>
]</td>
</tr>
<tr>
<td align="left" rowspan="3">80–84 deletion</td>
<td align="left">Increased virulence in chickens</td>
<td align="left">H1N1 (avian)</td>
<td align="left">[
<xref ref-type="bibr" rid="CR313">313</xref>
]</td>
</tr>
<tr>
<td align="left">Increased virulence in chickens and mice</td>
<td align="left">H1N1 backbone with H5N1 HA, NA and NS</td>
<td align="left">[
<xref ref-type="bibr" rid="CR134">134</xref>
]</td>
</tr>
<tr>
<td align="left">Increased virulence in swine</td>
<td align="left">H1N1 backbone with H5N1 NS</td>
<td align="left">[
<xref ref-type="bibr" rid="CR314">314</xref>
]</td>
</tr>
<tr>
<td align="left">Y84F</td>
<td align="left">Decreases replication in mammalian cells and enhances interferon response</td>
<td align="left">H1N1 with H5N1 NS</td>
<td align="left">[
<xref ref-type="bibr" rid="CR132">132</xref>
]</td>
</tr>
<tr>
<td align="left" rowspan="2">D92E [D87E]
<sup>b</sup>
</td>
<td align="left">Increased virulence in swine and mice</td>
<td align="left">H1N1 backbone with H5N1 NS</td>
<td align="left">[
<xref ref-type="bibr" rid="CR314">314</xref>
,
<xref ref-type="bibr" rid="CR315">315</xref>
]</td>
</tr>
<tr>
<td align="left">Increased virulence in chickens and mice</td>
<td align="left">H1N1 backbone with H5N1 HA, NA and NS</td>
<td align="left">[
<xref ref-type="bibr" rid="CR134">134</xref>
]</td>
</tr>
<tr>
<td align="left">I106M [I101M]</td>
<td align="left">Increased viral replication in mammalian cells virulence in mice</td>
<td align="left">H1N1 with all internal genes from H7N9</td>
<td align="left">[
<xref ref-type="bibr" rid="CR316">316</xref>
]</td>
</tr>
<tr>
<td align="left">C138F</td>
<td align="left">Increased replication in mammalian cells, decreased interferon response</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR317">317</xref>
]</td>
</tr>
<tr>
<td align="left">V149A</td>
<td align="left">Increased virulence and decreased interferon response in chickens</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR318">318</xref>
]</td>
</tr>
<tr>
<td align="left">L103F, I106M [L98F, I101M]</td>
<td align="left">Increased virulence in mice</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR319">319</xref>
,
<xref ref-type="bibr" rid="CR320">320</xref>
]</td>
</tr>
<tr>
<td align="left">N205S (with NS2: T47A)</td>
<td align="left">Decreased antiviral response in ferrets</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR133">133</xref>
]</td>
</tr>
<tr>
<td align="left">G210R (with: NS2 M51I)</td>
<td align="left">Decreased antiviral response in ferrets</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR133">133</xref>
]</td>
</tr>
<tr>
<td align="left">P3S, R41K, D74N</td>
<td align="left">Enhanced replication in mammalian cells and pathogenicity in mice</td>
<td align="left">H7N1 backbone with H5N1 NS</td>
<td align="left">[
<xref ref-type="bibr" rid="CR312">312</xref>
]</td>
</tr>
<tr>
<td align="left">R38A, K41A</td>
<td align="left">Decreased replication in mammalian and avian cell line</td>
<td align="left">H7N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR321">321</xref>
]</td>
</tr>
<tr>
<td align="left">K55E, K66E, C138F</td>
<td align="left">Enhanced replication in mammalian cells, decrease IF response</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR317">317</xref>
]</td>
</tr>
<tr>
<td align="left">222–230 deletion</td>
<td align="left">Increased replication in mammalian and avian cell lines</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR138">138</xref>
]</td>
</tr>
<tr>
<td align="left" rowspan="2">225–230 deletion</td>
<td align="left">Increased viral replication in avian cell line</td>
<td align="left">H7N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR130">130</xref>
,
<xref ref-type="bibr" rid="CR322">322</xref>
]</td>
</tr>
<tr>
<td align="left">No impact on viral replication in avian cell lines</td>
<td align="left">H7N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR140">140</xref>
]</td>
</tr>
<tr>
<td align="left" rowspan="3">
<sup>227</sup>
ESEV
<sup>230</sup>
(PDZ domain)</td>
<td align="left">Increased virulence in mice</td>
<td align="left">H1N1 pdm09 virus with ‘avian’ PDZ motif</td>
<td align="left">[
<xref ref-type="bibr" rid="CR323">323</xref>
]</td>
</tr>
<tr>
<td align="left">Decreased viral replication in mammalian and avian cell lines</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR138">138</xref>
]</td>
</tr>
<tr>
<td align="left">Increased viral replication and virulence in mice, decreased viral replication in human and duck cell lines</td>
<td align="left">H7N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR137">137</xref>
]</td>
</tr>
<tr>
<td align="left">
<sup>227</sup>
RSKV
<sup>230</sup>
(PDZ domain)</td>
<td align="left">Increased viral replication in human and duck cell lines but no effect in murine cells</td>
<td align="left">H7N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR137">137</xref>
]</td>
</tr>
<tr>
<td align="left">230–237 elongation</td>
<td align="left">Increased replication and inflammatory cytokine production in chickens</td>
<td align="left">H9N2</td>
<td align="left">[
<xref ref-type="bibr" rid="CR324">324</xref>
]</td>
</tr>
<tr>
<td align="left" rowspan="4">NS2/NEP</td>
<td align="left">M16I</td>
<td align="left">Increased polymerase activity in mammalian cell line</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR325">325</xref>
]</td>
</tr>
<tr>
<td align="left">M16I, Y41C, E75G</td>
<td align="left">Increased polymerase activity in mammalian cell line</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR325">325</xref>
]</td>
</tr>
<tr>
<td align="left">T47A (with NS1: N205S)</td>
<td align="left">Decreased antiviral response in ferrets</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR133">133</xref>
]</td>
</tr>
<tr>
<td align="left">M51I (with NS1: G2010R)</td>
<td align="left">Decreased antiviral response in ferrets</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR133">133</xref>
]</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<p>Single mutations are presented first followed by motifs involving multiple mutations. Individual markers and motifs are listed in numerical order for ease of identifying mutation of interest</p>
<p>
<sup>a</sup>
Mutations/motifs in NS1 and NEP are presented with numbering relative to A/goose/Guangdong/1/1996 (H5N1)</p>
<p>
<sup>b</sup>
The CDC molecular inventory numbers NS1 mutations relative to A/Vietnam/1203/2014 (H5N1) which contains an NS1 deletion. For entries from the CDC inventory that uses alternate numbering, the numbering according to A/Vietnam/1203/2014 (H5N1) is included in brackets</p>
</table-wrap-foot>
</table-wrap>
</p>
<p id="Par25">Single amino acid substitutions, deletions, and C-terminal truncations in NS1 affect AIV replicative capacity and pathogenicity. Point mutations in NS1 decreasing the host antiviral response (in chickens, ferrets or mice), include: P42S, F89Y, V149A, N200S (with NS2: T47A—see below) and G205R (with NS2: M51I—see below) [
<xref ref-type="bibr" rid="CR131">131</xref>
<xref ref-type="bibr" rid="CR133">133</xref>
]. Deletions and C-terminal truncations of NS1 occur commonly. Contemporary A/H5N1 subtype viruses have five amino acids deleted from position 80 to 84 (relative to A/goose/Guangdong/1996) associated with an increase in virulence in mice and chickens [
<xref ref-type="bibr" rid="CR134">134</xref>
]. C-terminal truncations result in deletion of the NS1 PDZ domain, a four amino acid motif that modulates protein–protein interactions with PDZ proteins important for cellular signaling pathways [
<xref ref-type="bibr" rid="CR135">135</xref>
]. Human influenza viruses typically contain the PDZ motifs RSKV or RSEV whereas avian viruses have ESEV or EPEV [
<xref ref-type="bibr" rid="CR136">136</xref>
] and the influence of PDZ motifs on viral phenotype is host and strain specific. The “avian” ESEV motif decreases viral replication in human and duck cell lines compared to the “human” RSKV motif, whereas these substitutions do not affect virulence in chickens [
<xref ref-type="bibr" rid="CR137">137</xref>
,
<xref ref-type="bibr" rid="CR138">138</xref>
]. Overall, the PDZ domain does not appear to be a major determinant of AIV pathogenicity. Indeed, PDZ deletions in the 2009 pandemic A/H1N1 virus as well as in avian A/H5N1 and A/H7N1 subtype AIVs do not significantly affect viral virulence [
<xref ref-type="bibr" rid="CR139">139</xref>
,
<xref ref-type="bibr" rid="CR140">140</xref>
].</p>
<p id="Par26">The NS2 protein, also referred to as the nuclear export protein (NEP) [
<xref ref-type="bibr" rid="CR141">141</xref>
], regulates several factors, including: transcription and translation of viral products [
<xref ref-type="bibr" rid="CR142">142</xref>
]; nuclear export of vRNP complexes [
<xref ref-type="bibr" rid="CR143">143</xref>
]; and viral budding from host cells [
<xref ref-type="bibr" rid="CR144">144</xref>
,
<xref ref-type="bibr" rid="CR145">145</xref>
]. NS2 regulates viral polymerase activity, enhancing the synthesis of viral cRNA, vRNA, and, in some cases, mRNA [
<xref ref-type="bibr" rid="CR142">142</xref>
,
<xref ref-type="bibr" rid="CR146">146</xref>
]. Very few NS2 mutations that affect viral fitness and host adaptation are characterized in AIVs. Adaptive mutations described in a human A/H5N1 isolate include M16I that, individually or in combination with Y41C and E75G, increase viral polymerase activity in mammalian cell lines [
<xref ref-type="bibr" rid="CR146">146</xref>
,
<xref ref-type="bibr" rid="CR147">147</xref>
]. Additionally, two combinations of NS1 and NS2 mutations, T47A with NS1 N200S and M51I with NS1 G205R, decrease the host antiviral response in ferrets [
<xref ref-type="bibr" rid="CR133">133</xref>
]. However, the effect of these mutations on AIV pathogenicity is either negligible or unclear [
<xref ref-type="bibr" rid="CR146">146</xref>
,
<xref ref-type="bibr" rid="CR147">147</xref>
].</p>
</sec>
<sec id="Sec18">
<title>Matrix protein (MP; Table 
<xref rid="Tab8" ref-type="table">8</xref>
)</title>
<p id="Par27">Influenza virus genomic segment 7 (MP) encodes for the matrix 1 and 2 proteins (M1 and M2, respectively). M1 is located beneath the viral envelope where it associates with the lipid membrane and viral RNPs. This interaction needs to be ablated for viral RNP to enter the host cell cytoplasm [
<xref ref-type="bibr" rid="CR148">148</xref>
,
<xref ref-type="bibr" rid="CR149">149</xref>
]. In the nucleus, M1 associates with vRNPs and mediates export into the cytoplasm [
<xref ref-type="bibr" rid="CR149">149</xref>
]. M1 is also involved in viral assembly and budding [
<xref ref-type="bibr" rid="CR150">150</xref>
]. M2 is a transmembrane protein present on the surface of influenza virions that acts as an ion channel, acidifying endosomes and contributing to the release of viral RNP into the cytoplasm [
<xref ref-type="bibr" rid="CR151">151</xref>
]. The cytoplasmic domain of M2 is also involved in viral genome packaging for progeny viruses [
<xref ref-type="bibr" rid="CR152">152</xref>
,
<xref ref-type="bibr" rid="CR153">153</xref>
]. Three more M proteins have also recently been identified: M3, M4 and M42 [
<xref ref-type="bibr" rid="CR154">154</xref>
]; however, the functional roles of these proteins are not well established and currently no mutations have been shown to affect viral fitness so they are not included in this inventory.
<table-wrap id="Tab8">
<label>Table 8</label>
<caption>
<p>Experimentally verified molecular markers/motifs in the matrix (M; segment 7) gene of influenza virus associated with virulence and antiviral resistance</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left">Protein</th>
<th align="left">Mutation/motif</th>
<th align="left">Phenotype</th>
<th align="left">Subtypes tested</th>
<th align="left">References</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" rowspan="3">M1</td>
<td align="left">N30D
<sup>a</sup>
</td>
<td align="left">Increased virulence in mice</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR156">156</xref>
]</td>
</tr>
<tr>
<td align="left">I43M</td>
<td align="left">Increased virulence in mice, chickens and ducks</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR157">157</xref>
]</td>
</tr>
<tr>
<td align="left">T215A</td>
<td align="left">Increased virulence in mice</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR156">156</xref>
]</td>
</tr>
<tr>
<td align="left" rowspan="5">M2</td>
<td align="left">L26F</td>
<td align="left">Increased resistance to amantadine and rimantadine</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR159">159</xref>
,
<xref ref-type="bibr" rid="CR160">160</xref>
,
<xref ref-type="bibr" rid="CR326">326</xref>
]</td>
</tr>
<tr>
<td align="left">I/V27A/T/S</td>
<td align="left">Increased resistance to amantadine and rimantadine</td>
<td align="left">
<p>H5N1</p>
<p>H5N2</p>
</td>
<td align="left">[
<xref ref-type="bibr" rid="CR159">159</xref>
<xref ref-type="bibr" rid="CR161">161</xref>
,
<xref ref-type="bibr" rid="CR326">326</xref>
,
<xref ref-type="bibr" rid="CR327">327</xref>
]</td>
</tr>
<tr>
<td align="left">A30V/T/S</td>
<td align="left">Increased resistance to amantadine and rimantadine</td>
<td align="left">
<p>H5N1</p>
<p>H5N2</p>
<p>H7N2</p>
</td>
<td align="left">[
<xref ref-type="bibr" rid="CR161">161</xref>
,
<xref ref-type="bibr" rid="CR326">326</xref>
,
<xref ref-type="bibr" rid="CR327">327</xref>
]</td>
</tr>
<tr>
<td align="left">S31N/G</td>
<td align="left">Increased resistance to amantadine and rimantadine</td>
<td align="left">
<p>H5N1</p>
<p>H5N2</p>
<p>H9N2</p>
</td>
<td align="left">[
<xref ref-type="bibr" rid="CR160">160</xref>
,
<xref ref-type="bibr" rid="CR161">161</xref>
,
<xref ref-type="bibr" rid="CR326">326</xref>
<xref ref-type="bibr" rid="CR330">330</xref>
]</td>
</tr>
<tr>
<td align="left">G34E</td>
<td align="left">Increased resistance to amantadine and rimantadine</td>
<td align="left">H5N1</td>
<td align="left">[
<xref ref-type="bibr" rid="CR159">159</xref>
]</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<p>Single mutations are presented first followed by motifs involving multiple mutations. Individual markers and motifs are listed in numerical order for ease of identifying mutation of interest</p>
<p>
<sup>a</sup>
Mutations/motifs in M1 and M2 proteins are presented with numbering relative to A/goose/Guangdong/1/1996 (H5N1)</p>
</table-wrap-foot>
</table-wrap>
</p>
<p id="Par28">Only a small number of mutations in segment 7 are associated with host adaptation. All occur in the region encoding the M1 protein. Four mutations, namely N30D, I43M, T139A and T215A, increase the virulence of A/H5N1 subtype AIVs in mice [
<xref ref-type="bibr" rid="CR155">155</xref>
<xref ref-type="bibr" rid="CR157">157</xref>
]. I43M also increases virulence in chickens and ducks; however, the underlying mechanisms remain unclear [
<xref ref-type="bibr" rid="CR157">157</xref>
]. The M2 protein is an important target of antiviral compounds and mutations in this region contribute to antiviral resistance phenotypes. Adamantanes (amantadine and rimantadine) block the M2 ion channel and inhibit early stages of virus replication. This class of drugs is no longer recommended against seasonal human influenza as these viruses display a high degree of adamantine resistance. In addition, adamantine resistance is increasing in AIVs globally, including subtypes of major concern, such as A/H5 and A/H7 [
<xref ref-type="bibr" rid="CR158">158</xref>
]. Well-known mutations associated with adamantane resistance in M2 include: L26F, V27A, A30V/T/S, S31N/G, and G34E [
<xref ref-type="bibr" rid="CR159">159</xref>
<xref ref-type="bibr" rid="CR161">161</xref>
].</p>
</sec>
</sec>
<sec id="Sec19">
<title>Auxiliary proteins</title>
<sec id="Sec20">
<title>PB1-F2 (Table 
<xref rid="Tab4" ref-type="table">4</xref>
)</title>
<p id="Par29">PB1-F2 is an auxiliary protein expressed in a majority of influenza A viruses and produced from a + 1 alternate reading frame of PB1 [
<xref ref-type="bibr" rid="CR162">162</xref>
]. Full-length PB1-F2 is approximately 90 amino acids in length, with frequent variation by truncation. Overall expression and length of PB1-F2 affect influenza virus pathogenicity in both a host and strain dependent manner [
<xref ref-type="bibr" rid="CR163">163</xref>
]. PB1-F2 induces host cell apoptosis, antagonizes the host antiviral innate immunity, enhances the production of pro-inflammatory cytokines, and affects viral polymerase activity (reviewed in [
<xref ref-type="bibr" rid="CR164">164</xref>
]). Pro-apoptotic activity of PB1-F2 has been reported in human seasonal A/H1N1 influenza viruses but not in A/H5N1 subtype AIVs [
<xref ref-type="bibr" rid="CR165">165</xref>
]. The association between PB1-F2, mitochondrial-associated proteins, and cellular factors also inhibits antiviral responses and enhances production of pro-inflammatory cytokines. Interaction of PB1-F2 with MAVS, TBK1 and IRF3. PB1-F2 inhibits the action of TBK1 and IRF3, downregulating host production of type 1 interferon [
<xref ref-type="bibr" rid="CR166">166</xref>
,
<xref ref-type="bibr" rid="CR167">167</xref>
]. Additionally, interaction between PB1-F2 and MAVS enhances TRAF6-mediated NF-kB activation, promoting the production of pro-inflammatory cytokines [
<xref ref-type="bibr" rid="CR168">168</xref>
,
<xref ref-type="bibr" rid="CR169">169</xref>
]. In A/H5N1 subtype AIVs and human pandemic influenza viruses from 1918, 1957 and 1968, expression of full-length PB1-F2 heightens the inflammatory response to infection in mice, rendering them more susceptible to secondary bacterial pneumonia [
<xref ref-type="bibr" rid="CR170">170</xref>
].</p>
<p id="Par30">Only a few PB1-F2 mutations in AIVs subtypes affect viral pathogenicity. Truncation of the A/H5N1 PB1-F2 protein increases pathogenicity in mice [
<xref ref-type="bibr" rid="CR165">165</xref>
,
<xref ref-type="bibr" rid="CR171">171</xref>
], but complete deletion of A/H5N1 PB1-F2 does not significantly alter viral virulence [
<xref ref-type="bibr" rid="CR163">163</xref>
,
<xref ref-type="bibr" rid="CR171">171</xref>
]. Perhaps the best-known PB1-F2 mutation, N66S, inhibits host interferon production, increasing pro-inflammatory cytokine responses. However, these effects remain strain and host specific. For example, N66S in A/H5N1 subtype AIV enhances viral replication and pathogenicity in mice but not ducks [
<xref ref-type="bibr" rid="CR171">171</xref>
]. Indeed, the few reports that analyze the effect of PB1-F2 expression in avian species show viral attenuation. PB1-F2 expression in A/H5N1 and A/H9N2 subtype AIVs decreases viral pathogenicity in chickens, possibly through inducing the host immune response earlier in chickens compared to mice [
<xref ref-type="bibr" rid="CR172">172</xref>
]. Additionally, a combination of mutations T51M/V56A/E87G in PB1-F2 decrease viral polymerase activity, replication, and virulence in mallard ducks [
<xref ref-type="bibr" rid="CR173">173</xref>
].</p>
</sec>
<sec id="Sec21">
<title>PA-X (Table 
<xref rid="Tab5" ref-type="table">5</xref>
)</title>
<p id="Par31">PA-X is a fusion protein comprised of 191N-terminal amino acids (including the endonuclease domain) and 61 amino acids from the C-terminus from segment 3 (PA) formed as the result of ribosomal frameshifting [
<xref ref-type="bibr" rid="CR174">174</xref>
]. PA-X has plays a role in host shutoff [
<xref ref-type="bibr" rid="CR174">174</xref>
<xref ref-type="bibr" rid="CR176">176</xref>
], modulating the host immune response [
<xref ref-type="bibr" rid="CR174">174</xref>
,
<xref ref-type="bibr" rid="CR177">177</xref>
<xref ref-type="bibr" rid="CR179">179</xref>
], viral polymerase activity, viral replication, viral induced apoptosis, and virulence (reviewed in [
<xref ref-type="bibr" rid="CR180">180</xref>
]). Approximately 75% of all influenza virus isolates possess a full-length PA-X sequence, with the remaining 25% expressing PA-X truncations. These truncations of up to 41 amino acids in length most commonly occur in the PA-X C-terminus and are most commonly found in the 2009 pandemic A/H1N1, canine A/H3N2 and A/H3N8, equine A/H7N7, and bat influenza viruses. However, they also occur in some A/H5N1 and A/H9N2 subtype AIVs [
<xref ref-type="bibr" rid="CR181">181</xref>
]. Overall, the function of PA-X appears to be subtype specific. In A/H5N1 subtype AIV, loss of PA-X expression increases viral replication, host inflammatory response, and virulence in mice, chickens, and ducks [
<xref ref-type="bibr" rid="CR177">177</xref>
,
<xref ref-type="bibr" rid="CR178">178</xref>
,
<xref ref-type="bibr" rid="CR182">182</xref>
]. In contrast, loss of PA-X in the A/H9N2 subtype limits the host inflammatory response and decreases virulence in mice [
<xref ref-type="bibr" rid="CR183">183</xref>
].</p>
</sec>
</sec>
<sec id="Sec22">
<title>Limitations and usage considerations of this molecular inventory</title>
<p id="Par32">As stated in the methodology, this inventory was not intended as an exhaustive list so several caveats and limitations need to be considered when utilizing these tables. First, the inventory only includes experimentally validated (in vitro or in vivo) markers/mutations. As stated previously, several studies utilize in silico approaches to predict molecular markers of viral adaptation to humans [
<xref ref-type="bibr" rid="CR22">22</xref>
<xref ref-type="bibr" rid="CR26">26</xref>
]. This work is extremely valuable and findings from these computational studies guide future research. Indeed, novel machine learning approaches have helped to identify novel markers and amino acid positions in human and avian influenza strains associated with pandemic potential [
<xref ref-type="bibr" rid="CR184">184</xref>
,
<xref ref-type="bibr" rid="CR185">185</xref>
]. Further work on these novel mutations should be conducted in vitro and in vivo. Second, as stated in the text, changes in biological characteristics for specific point mutations and motifs are sometimes only associated with specific viral subtypes or hosts, so caution should be made when generalizing findings for novel strains or hosts. Finally, consideration must be made for viral sequences themselves. Influenza viruses, like many other RNA viruses, replicate as a quasispecies, allowing for rapid changes in diversity and viral adaptation in response to environmental pressures [
<xref ref-type="bibr" rid="CR186">186</xref>
]. The majority of molecular markers/motifs described in these studies come from consensus sequences which may not adequately reflect the entire population of viruses in a given sample. With the continual advancement of Next Generation Sequencing (NGS) and bioinformatics we are better able to understand how minority variants could contribute to pandemic potential of influenza strains. Indeed, recent work by Welkers et al. using NGS on human respiratory A/H5N1 samples identifies multiple single amino acid variants in all three polymerase subunits. In vitro analysis of these markers shows substantial increases in polymerase activity [
<xref ref-type="bibr" rid="CR187">187</xref>
]. Therefore, we must move towards consideration of the influenza viral quasispecies as a whole when considering the dynamic evolutionary and adaptive pathways/processes and the meaning and predictive power for zoonotic and/or pandemic potential.</p>
</sec>
<sec id="Sec23">
<title>Discussion/conclusions</title>
<p id="Par33">Since the discovery of the Goose/Guangdong-lineage A/H5 viruses in China in 1996, HPAIV of the A/H5N1 subtype have spread globally, causing numerous outbreaks in wild birds and poultry. Overall, 861 confirmed human A/H5N1 infections have been reported with a case fatality rate of 52.8% [
<xref ref-type="bibr" rid="CR188">188</xref>
]. In addition, newly emerged and emerging AIVs with zoonotic potential continue to appear, including subtypes A/H7N9, A/H7N4, A/H5Nx, A/H9N2, A/H10N7, and A/H10N8 [
<xref ref-type="bibr" rid="CR189">189</xref>
<xref ref-type="bibr" rid="CR193">193</xref>
]. As of June 2019, there have been 1,568 human A/H7N9 cases reported with 616 deaths (CFR: 39%) [
<xref ref-type="bibr" rid="CR194">194</xref>
]. There have been 23 human cases of A/H5N6 infection reported from 10 different provinces across mainland China, of which 15 were fatal (CFR 65.2%) [
<xref ref-type="bibr" rid="CR195">195</xref>
]. A single human non-fatal infection with an A/H7N4 subtype virus occurred in an elderly woman in Jiangsu, China in December 2017 [
<xref ref-type="bibr" rid="CR192">192</xref>
,
<xref ref-type="bibr" rid="CR196">196</xref>
]. This virus is antigenically distinct from formerly circulating A/H7 strains, and, concerningly, appears to be spreading across Southeast Asia, continually reassorting with other viruses in the region [
<xref ref-type="bibr" rid="CR197">197</xref>
,
<xref ref-type="bibr" rid="CR198">198</xref>
]. To date, none of the novel A/H7N4 viruses contains known amino acid mutations that confer adaptation of AIV to humans (e.g., PB2 627/701 or HA 186/226/228) or antiviral resistance. However, A/H7N4 isolated from Cambodia does contain the M gene amino acid mutations N30D and T215A that increase pathogenicity of A/H5N1 virus in mice [
<xref ref-type="bibr" rid="CR198">198</xref>
]. Due to the antigenic differences between the A/H7N4 viruses and other H7 lineages, including the A/Anhui/1/2013-like A/H7N9 lineage, the continual spread, and risk for human infection, this newly detected A/H7N4 lineage is now in preparation as a candidate vaccine virus for pandemic preparedness [
<xref ref-type="bibr" rid="CR199">199</xref>
]. To date, no avian origin influenza viruses can transmit efficiently from human-to-human via aerosols. Given the ongoing spillover of avian influenza viruses into domestic poultry, as well as the risk of human infection and potential for adaptation, continual, vigilant surveillance and risk assessment is vital to combat endemic and emerging AIVs. This inventory provides a list of the currently known, experimentally verified mutations/molecular markers affecting host adaptation in AIVs and can be utilized for molecular characterization and risk assessment of novel AIV strains.</p>
</sec>
</body>
<back>
<fn-group>
<fn>
<p>
<bold>Publisher's Note</bold>
</p>
<p>Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.</p>
</fn>
</fn-group>
<ack>
<title>Acknowledgements</title>
<p>The authors would like to thank all of the members of the Influenza Team in the Virology Unit at the Institute Pasteur in Cambodia, as well as at the WHO Collaborating Center and Peter Doherty Institute at the University of Melbourne for their insightful discussions and input.</p>
</ack>
<notes notes-type="funding-information">
<title>Funding</title>
<p>This publication is the result, in part, of work conducted under a cooperative agreement with the Office of the Assistant Secretary for Preparedness and Response in the U.S. Department of Health and Human Services (HHS), grant number IDSEP140020-01-00 awarded to Dr. Philippe Dussart and Dr. Erik Karlsson. Its contents and conclusions are solely the responsibility of the authors and do not represent the official views of HHS. Annika Suttie is funded by an Australian Government Research Training Program Scholarship and a Faculty of Science and Technology Research Scholarship from Federation University. The Melbourne WHO Collaborating Centre for Reference and Research on Influenza is supported by the Australian Government Department of Health.</p>
</notes>
<notes>
<title>Compliance with Ethical Standards</title>
<notes notes-type="COI-statement">
<title>Conflict of Interest</title>
<p id="Par34">All authors declare that they have no conflicts of interest.</p>
</notes>
<notes>
<title>Ethical approval</title>
<p id="Par35">This article does not contain any studies with human participants or animals performed by any of the authors.</p>
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