Serveur d'exploration H2N2

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In Silico Prediction and Experimental Confirmation of HA Residues Conferring Enhanced Human Receptor Specificity of H5N1 Influenza A Viruses

Identifieur interne : 000099 ( Pmc/Curation ); précédent : 000098; suivant : 000100

In Silico Prediction and Experimental Confirmation of HA Residues Conferring Enhanced Human Receptor Specificity of H5N1 Influenza A Viruses

Auteurs : Sonja Schmier [Allemagne] ; Ahmed Mostafa [Allemagne, Égypte] ; Thomas Haarmann [Allemagne] ; Norbert Bannert [Allemagne] ; John Ziebuhr [Allemagne] ; Veljko Veljkovic [Serbie] ; Ursula Dietrich [Allemagne] ; Stephan Pleschka [Allemagne]

Source :

RBID : PMC:4473683

Abstract

Newly emerging influenza A viruses (IAV) pose a major threat to human health by causing seasonal epidemics and/or pandemics, the latter often facilitated by the lack of pre-existing immunity in the general population. Early recognition of candidate pandemic influenza viruses (CPIV) is of crucial importance for restricting virus transmission and developing appropriate therapeutic and prophylactic strategies including effective vaccines. Often, the pandemic potential of newly emerging IAV is only fully recognized once the virus starts to spread efficiently causing serious disease in humans. Here, we used a novel phylogenetic algorithm based on the informational spectrum method (ISM) to identify potential CPIV by predicting mutations in the viral hemagglutinin (HA) gene that are likely to (differentially) affect critical interactions between the HA protein and target cells from bird and human origin, respectively. Predictions were subsequently validated by generating pseudotyped retrovirus particles and genetically engineered IAV containing these mutations and characterizing potential effects on virus entry and replication in cells expressing human and avian IAV receptors, respectively. Our data suggest that the ISM-based algorithm is suitable to identify CPIV among IAV strains that are circulating in animal hosts and thus may be a new tool for assessing pandemic risks associated with specific strains.


Url:
DOI: 10.1038/srep11434
PubMed: 26091504
PubMed Central: 4473683

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PMC:4473683

Le document en format XML

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Prediction and Experimental Confirmation of HA Residues Conferring Enhanced Human Receptor Specificity of H5N1 Influenza A Viruses</title>
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<p>Newly emerging influenza A viruses (IAV) pose a major threat to human health by causing seasonal epidemics and/or pandemics, the latter often facilitated by the lack of pre-existing immunity in the general population. Early recognition of candidate pandemic influenza viruses (CPIV) is of crucial importance for restricting virus transmission and developing appropriate therapeutic and prophylactic strategies including effective vaccines. Often, the pandemic potential of newly emerging IAV is only fully recognized once the virus starts to spread efficiently causing serious disease in humans. Here, we used a novel phylogenetic algorithm based on the informational spectrum method (ISM) to identify potential CPIV by predicting mutations in the viral hemagglutinin (HA) gene that are likely to (differentially) affect critical interactions between the HA protein and target cells from bird and human origin, respectively. Predictions were subsequently validated by generating pseudotyped retrovirus particles and genetically engineered IAV containing these mutations and characterizing potential effects on virus entry and replication in cells expressing human and avian IAV receptors, respectively. Our data suggest that the ISM-based algorithm is suitable to identify CPIV among IAV strains that are circulating in animal hosts and thus may be a new tool for assessing pandemic risks associated with specific strains.</p>
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</TEI>
<pmc article-type="research-article">
<pmc-dir>properties open_access</pmc-dir>
<front>
<journal-meta>
<journal-id journal-id-type="nlm-ta">Sci Rep</journal-id>
<journal-id journal-id-type="iso-abbrev">Sci Rep</journal-id>
<journal-title-group>
<journal-title>Scientific Reports</journal-title>
</journal-title-group>
<issn pub-type="epub">2045-2322</issn>
<publisher>
<publisher-name>Nature Publishing Group</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="pmid">26091504</article-id>
<article-id pub-id-type="pmc">4473683</article-id>
<article-id pub-id-type="pii">srep11434</article-id>
<article-id pub-id-type="doi">10.1038/srep11434</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Article</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>
<italic>In Silico</italic>
Prediction and Experimental Confirmation of HA Residues Conferring Enhanced Human Receptor Specificity of H5N1 Influenza A Viruses</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Schmier</surname>
<given-names>Sonja</given-names>
</name>
<xref ref-type="aff" rid="a1">1</xref>
<xref ref-type="author-notes" rid="n1">*</xref>
<xref ref-type="author-notes" rid="n3"></xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Mostafa</surname>
<given-names>Ahmed</given-names>
</name>
<xref ref-type="aff" rid="a2">2</xref>
<xref ref-type="aff" rid="a3">3</xref>
<xref ref-type="author-notes" rid="n3"></xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Haarmann</surname>
<given-names>Thomas</given-names>
</name>
<xref ref-type="aff" rid="a1">1</xref>
<xref ref-type="author-notes" rid="n2"></xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Bannert</surname>
<given-names>Norbert</given-names>
</name>
<xref ref-type="aff" rid="a4">4</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Ziebuhr</surname>
<given-names>John</given-names>
</name>
<xref ref-type="aff" rid="a2">2</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Veljkovic</surname>
<given-names>Veljko</given-names>
</name>
<xref ref-type="aff" rid="a5">5</xref>
<xref ref-type="author-notes" rid="n4">§</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Dietrich</surname>
<given-names>Ursula</given-names>
</name>
<xref ref-type="aff" rid="a1">1</xref>
<xref ref-type="author-notes" rid="n4">§</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Pleschka</surname>
<given-names>Stephan</given-names>
</name>
<xref ref-type="corresp" rid="c1">a</xref>
<xref ref-type="aff" rid="a2">2</xref>
<xref ref-type="author-notes" rid="n4">§</xref>
</contrib>
<aff id="a1">
<label>1</label>
<institution>Georg-Speyer-Haus, Institute for Tumor Biology and Experimental Therapy</institution>
, Paul-Ehrlich-Str. 42-44, Frankfurt,
<country>Germany</country>
</aff>
<aff id="a2">
<label>2</label>
<institution>Institute of Medical Virology, Justus Liebig University Giessen</institution>
, Schubertstrasse 81, Giessen,
<country>Germany</country>
</aff>
<aff id="a3">
<label>3</label>
<institution>Center of Scientific Excellence for Influenza Viruses, National Research Centre (NRC)</institution>
, Dokki, Giza,
<country>Egypt</country>
</aff>
<aff id="a4">
<label>4</label>
<institution>Robert-Koch-Institute, Division for HIV and other Retroviruses</institution>
, Nordufer 20, Berlin,
<country>Germany</country>
</aff>
<aff id="a5">
<label>5</label>
<institution>Centre for Multidisciplinary Research, Institute of Nuclear Sciences VINCA</institution>
, Mihaila Petrovica 14, Belgrade,
<country>Serbia</country>
</aff>
</contrib-group>
<author-notes>
<corresp id="c1">
<label>a</label>
<email>stephan.pleschka@viro.med.uni-giessen.de</email>
</corresp>
<fn id="n1">
<label>*</label>
<p>Current address: B.Braun Melsungen AG, Carl-Braun-Str. 1, Melsungen, Germany.</p>
</fn>
<fn id="n2">
<label></label>
<p>Current address: AB Enzymes GmbH, Feldbergstrasse 78, Darmstadt, Germany.</p>
</fn>
<fn id="n3">
<label></label>
<p>These authors contributed eqully to this work.</p>
</fn>
<fn id="n4">
<label>§</label>
<p>These authors jointly supervised this work.</p>
</fn>
</author-notes>
<pub-date pub-type="epub">
<day>19</day>
<month>06</month>
<year>2015</year>
</pub-date>
<pub-date pub-type="collection">
<year>2015</year>
</pub-date>
<volume>5</volume>
<elocation-id>11434</elocation-id>
<history>
<date date-type="received">
<day>25</day>
<month>11</month>
<year>2014</year>
</date>
<date date-type="accepted">
<day>27</day>
<month>05</month>
<year>2015</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright © 2015, Macmillan Publishers Limited</copyright-statement>
<copyright-year>2015</copyright-year>
<copyright-holder>Macmillan Publishers Limited</copyright-holder>
<license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by/4.0/">
<pmc-comment>author-paid</pmc-comment>
<license-p>This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit
<ext-link ext-link-type="uri" xlink:href="http://creativecommons.org/licenses/by/4.0/">http://creativecommons.org/licenses/by/4.0/</ext-link>
</license-p>
</license>
</permissions>
<abstract>
<p>Newly emerging influenza A viruses (IAV) pose a major threat to human health by causing seasonal epidemics and/or pandemics, the latter often facilitated by the lack of pre-existing immunity in the general population. Early recognition of candidate pandemic influenza viruses (CPIV) is of crucial importance for restricting virus transmission and developing appropriate therapeutic and prophylactic strategies including effective vaccines. Often, the pandemic potential of newly emerging IAV is only fully recognized once the virus starts to spread efficiently causing serious disease in humans. Here, we used a novel phylogenetic algorithm based on the informational spectrum method (ISM) to identify potential CPIV by predicting mutations in the viral hemagglutinin (HA) gene that are likely to (differentially) affect critical interactions between the HA protein and target cells from bird and human origin, respectively. Predictions were subsequently validated by generating pseudotyped retrovirus particles and genetically engineered IAV containing these mutations and characterizing potential effects on virus entry and replication in cells expressing human and avian IAV receptors, respectively. Our data suggest that the ISM-based algorithm is suitable to identify CPIV among IAV strains that are circulating in animal hosts and thus may be a new tool for assessing pandemic risks associated with specific strains.</p>
</abstract>
</article-meta>
</front>
<floats-group>
<fig id="f1">
<label>Figure 1</label>
<caption>
<title>Effects of combined mutations K153D, S223N and G272S in H5-HA of A/Thailand/KAN-1/2004 (KAN-1) on the informational spectra (IS).</title>
<p>
<bold>a</bold>
) IS of HA1 of the wildtype KAN-1 virus,
<bold>b</bold>
) IS of HA1 from the KAN-1 virus-derived triple mutant. Frequencies at 0.076 and 0.236 for avian and human receptor specificity are indicated.</p>
</caption>
<graphic xlink:href="srep11434-f1"></graphic>
</fig>
<fig id="f2">
<label>Figure 2</label>
<caption>
<title>Characterization of HA-pseudotyped KAN-1 wildtype PRPs.</title>
<p>
<bold>a</bold>
) FACS analysis of eGFP expression in A549 cells untransduced (left) or transduced (right) with wildtype HA/NA/M/eGFP pseudotyped retroviral particles.
<bold>b</bold>
) Electron microscopic images of wildtype H5N1 PRPs produced from 293T cells. A free immature PRP (left panel), as well as a mature PRP (right panel) are marked by an arrow. An electron lucent core characterizes the immature particle on the left panel, whereas the more mature particle on the right panel has an electron dense core.</p>
</caption>
<graphic xlink:href="srep11434-f2"></graphic>
</fig>
<fig id="f3">
<label>Figure 3</label>
<caption>
<title>Determination of α2,6- and α2,3 receptors on MDCK-SIAT1, A549 and QT6 cells with specific lectins.</title>
<p>
<bold>a,b)</bold>
The binding of varying amounts of biotinylated lectins MAAII (specific for avian α2,3 receptors) and SNA/EBL (specific for human α2,6 receptors) to QT6 and MDCK-SIAT1 cells as well as A549 control cells was determined by FACS analysis using streptavidine-PE. The differences of binding of varying amounts of biotinylated lectins to different cell lines were statistically compared to QT6 for MAAII-lectin binding or A549 for SNA/EBL-lectin binding using two-way ANOVA, followed by Bonferroni
<italic>post hoc</italic>
test. Significant differences between data sets are indicated by asterisks (
<bold>*</bold>
), whilst (ns) indicates non-significant differences.
<bold>c</bold>
) Formaldehyde-fixed monolayers of the indicated cell types were incubated with fluorescein-labelled SNA lectin to detect α2,6-linked sialic acids and biotinylated MAAII lectin and streptavidin-Cy3 to detect α2,3-linked sialic acids. The cellular membrane was permeabilized, the nuclei were stained with DAPI and analyzed using confocal microscopy.</p>
</caption>
<graphic xlink:href="srep11434-f3"></graphic>
</fig>
<fig id="f4">
<label>Figure 4</label>
<caption>
<title>Infectivity of wildtype and HA-mutated PRPs on QT6 and MDCK-SIAT1 cells.</title>
<p>Equal numbers of MDCK-SIAT and QT6 cells, respectively, were transduced with the indicated PRPs at an MOI of 0.2 and GFP-positive cells were counted by FACS analysis at 72 h post transduction. The ratio of GFP-positive MDCK-SIAT/QT6 cells is shown for the mutants compared to wildtype. Shown are the results of a representative experiment. The MDCK-SIAT/QT6 ratio was calculated from median values determined from triplicate cultures performed for each of the mutants.</p>
</caption>
<graphic xlink:href="srep11434-f4"></graphic>
</fig>
<fig id="f5">
<label>Figure 5</label>
<caption>
<title>Location of the studied amino acid (aa) in the H5-HA of avian influenza A/Thailand/1(KAN-1)/2004 (H5N1) virus.</title>
<p>
<bold>a</bold>
) The schematic representation shows the relative locations of H5-HA mutations in HA1 at aa positions 153, 223 and 272 (indicated in blue). The multibasic protease cleavage site present in the original KAN-1 isolate was removed in all recombinant viruses generated in this study (Wt-LP and Mut-I to -III). SP: signal peptide; TM: transmembrane domain; CT: cytoplasmic tail.
<bold>b</bold>
) and
<bold>c</bold>
) 3D structure model of H5 HA1 (for details, see Materials and Methods). Amino acid residues at positions 153, 223 and 272 (blue, spheres) are shown in side and top view in relation to the receptor-binding sites (red side chains). The other 7 aa that were previously identified by ISM in H5N1 viruses circulating in Egypt between 2006 and 2012, which also increase the A(0.236)/A(0.076) ratio (74, 110, 127, 143, 188, 234, 275), are shown as green side chains.</p>
</caption>
<graphic xlink:href="srep11434-f5"></graphic>
</fig>
<fig id="f6">
<label>Figure 6</label>
<caption>
<title>Focus phenotypes of recombinant KAN-1 (Wt-LP) and H5-HA mutant KAN-1 viruses on MDCK cells.</title>
<p>
<bold>a</bold>
) Focus assay showing different focus sizes. MDCK-II cells were infected with the parental and mutated viruses at an MOI of 0.001 for 24 h and then stained using a monoclonal antibody against NP.
<bold>b</bold>
) Average focus sizes were determined from 50 foci for each virus. Asterisks (*) indicate a significant difference (p < 0.05) compared to the parental KAN-1 (Wt-LP) virus, while (ns) indicates non-significant difference. Statistical analysis was performed using one-way ANOVA, followed by Turkey’s
<italic>post hoc</italic>
test.</p>
</caption>
<graphic xlink:href="srep11434-f6"></graphic>
</fig>
<fig id="f7">
<label>Figure 7</label>
<caption>
<title>
<italic>In vitro</italic>
growth kinetics of KAN-1 (Wt-LP) and H5-HA mutant KAN-1 viruses.</title>
<p>
<bold>a</bold>
) MDCK-SIAT1,
<bold>b</bold>
) QT6, or
<bold>c</bold>
) A549 cells were infected at an MOI of 0.001. The infectious virus and HA titers were determined at the indicated time points in MDCK-II cells by focus assay (FFU/ml) and standardized hemagglutination assay (HAU/ml). Mean values of results represent the averages from three independent experiments and are presented with standard deviations (SDs) indicated by error bars. Asterisks (*) indicate a significant difference (p < 0.05) compared to the parental KAN-1 (Wt-LP) virus while (ns) indicates a non-significant difference. Statistical analysis was performed using repeated measures ANOVA, followed by Bonferroni
<italic>post hoc</italic>
test.</p>
</caption>
<graphic xlink:href="srep11434-f7"></graphic>
</fig>
<table-wrap position="float" id="t1">
<label>Table 1</label>
<caption>
<title>Infectious titers of the different HA pseudotyped retroviral particles on A549 cells.</title>
</caption>
<table frame="hsides" rules="groups" border="1">
<colgroup>
<col align="left"></col>
<col align="center"></col>
</colgroup>
<tbody valign="top">
<tr>
<td align="left" valign="top" charoff="50">WT</td>
<td align="center" valign="top" charoff="50">5.1 × 10
<sup>5</sup>
/ml</td>
</tr>
<tr>
<td align="left" valign="top" charoff="50">K153D</td>
<td align="center" valign="top" charoff="50">2.2 × 10
<sup>6</sup>
/ml</td>
</tr>
<tr>
<td align="left" valign="top" charoff="50">S223N</td>
<td align="center" valign="top" charoff="50">8.3 × 10
<sup>6</sup>
/ml</td>
</tr>
<tr>
<td align="left" valign="top" charoff="50">G272S</td>
<td align="center" valign="top" charoff="50">3.5 × 10
<sup>6</sup>
/ml</td>
</tr>
<tr>
<td align="left" valign="top" charoff="50">K153D/S223N</td>
<td align="center" valign="top" charoff="50">2.4 × 10
<sup>4</sup>
/ml</td>
</tr>
<tr>
<td align="left" valign="top" charoff="50">K153D/G272S</td>
<td align="center" valign="top" charoff="50">not analyzed</td>
</tr>
<tr>
<td align="left" valign="top" charoff="50">S223N/G272S</td>
<td align="center" valign="top" charoff="50">2.3 × 10
<sup>7</sup>
/ml</td>
</tr>
<tr>
<td align="left" valign="top" charoff="50">K153D/S223N/G272S</td>
<td align="center" valign="top" charoff="50">4.3 × 10
<sup>5</sup>
/ml</td>
</tr>
</tbody>
</table>
</table-wrap>
</floats-group>
</pmc>
</record>

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