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Pathobiological Characterization of a Novel Reassortant Highly Pathogenic H5N1 Virus Isolated in British Columbia, Canada, 2015.

Identifieur interne : 000143 ( Main/Exploration ); précédent : 000142; suivant : 000144

Pathobiological Characterization of a Novel Reassortant Highly Pathogenic H5N1 Virus Isolated in British Columbia, Canada, 2015.

Auteurs : Yohannes Berhane [Canada] ; Darwyn Kobasa [Canada] ; Carissa Embury-Hyatt [Canada] ; Brad Pickering [Canada] ; Shawn Babiuk [Canada] ; Tomy Joseph [Canada] ; Victoria Bowes [Canada] ; Mathew Suderman [Canada] ; Anders Leung [Canada] ; Colleen Cottam-Birt [Canada] ; Tamiko Hisanaga [Canada] ; John Pasick [Canada]

Source :

RBID : pubmed:26988892

Descripteurs français

English descriptors

Abstract

In the current study, we describe the pathobiologic characteristics of a novel reassortant virus - A/chicken/BC/FAV-002/2015 (H5N1) belonging to clade 2.3.4.4 that was isolated from backyard chickens in British Columbia, Canada. Sequence analyses demonstrate PB1, PA, NA and NS gene segments were of North American lineage while PB2, HA, NP and M were derived from a Eurasian lineage H5N8 virus. This novel virus had a 19 amino acid deletion in the neuraminidase stalk. We evaluated the pathogenic potential of this isolate in various animal models. The virus was highly pathogenic to mice with a LD50 of 10 plaque forming units (PFU), but had limited tissue tropism. It caused only subclinical infection in pigs which did result in seroconversion. This virus was highly pathogenic to chickens, turkeys, juvenile Muscovy ducks (Cairnia moschata foma domestica) and adult Chinese geese (Anser cynoides domesticus) causing a systemic infection in all species. The virus was also efficiently transmitted and resulted in mortality in naïve contact ducks, geese and chickens. Our findings indicate that this novel H5N1 virus has a wide host range and enhanced surveillance of migratory waterfowl may be necessary in order to determine its potential to establish itself in the wild bird reservoir.

DOI: 10.1038/srep23380
PubMed: 26988892
PubMed Central: PMC4796896


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

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<term>Amino Acid Sequence (MeSH)</term>
<term>Animals (MeSH)</term>
<term>Animals, Wild (MeSH)</term>
<term>British Columbia (MeSH)</term>
<term>Chickens (virology)</term>
<term>Ducks (virology)</term>
<term>Evolution, Molecular (MeSH)</term>
<term>Geese (virology)</term>
<term>Influenza A Virus, H5N1 Subtype (genetics)</term>
<term>Influenza A Virus, H5N1 Subtype (isolation & purification)</term>
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<term>Neuraminidase (genetics)</term>
<term>Orthomyxoviridae Infections (virology)</term>
<term>Phylogeny (MeSH)</term>
<term>Reassortant Viruses (genetics)</term>
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<keywords scheme="KwdFr" xml:lang="fr">
<term>Animaux (MeSH)</term>
<term>Animaux sauvages (MeSH)</term>
<term>Canards (virologie)</term>
<term>Charge virale (MeSH)</term>
<term>Colombie-Britannique (MeSH)</term>
<term>Délétion de séquence (MeSH)</term>
<term>Infections à Orthomyxoviridae (virologie)</term>
<term>Oies (virologie)</term>
<term>Phylogenèse (MeSH)</term>
<term>Poulets (virologie)</term>
<term>Sialidase (génétique)</term>
<term>Souris (MeSH)</term>
<term>Sous-type H5N1 du virus de la grippe A (génétique)</term>
<term>Sous-type H5N1 du virus de la grippe A (isolement et purification)</term>
<term>Suidae (MeSH)</term>
<term>Séquence d'acides aminés (MeSH)</term>
<term>Tropisme viral (MeSH)</term>
<term>Virus recombinants (génétique)</term>
<term>Virus recombinants (physiologie)</term>
<term>Évolution moléculaire (MeSH)</term>
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<term>Neuraminidase</term>
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<term>Sialidase</term>
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<term>Virus recombinants</term>
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<term>Influenza A Virus, H5N1 Subtype</term>
</keywords>
<keywords scheme="MESH" qualifier="isolement et purification" xml:lang="fr">
<term>Sous-type H5N1 du virus de la grippe A</term>
</keywords>
<keywords scheme="MESH" qualifier="physiologie" xml:lang="fr">
<term>Virus recombinants</term>
</keywords>
<keywords scheme="MESH" qualifier="physiology" xml:lang="en">
<term>Reassortant Viruses</term>
</keywords>
<keywords scheme="MESH" qualifier="virologie" xml:lang="fr">
<term>Canards</term>
<term>Infections à Orthomyxoviridae</term>
<term>Oies</term>
<term>Poulets</term>
</keywords>
<keywords scheme="MESH" qualifier="virology" xml:lang="en">
<term>Chickens</term>
<term>Ducks</term>
<term>Geese</term>
<term>Orthomyxoviridae Infections</term>
</keywords>
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<term>Amino Acid Sequence</term>
<term>Animals</term>
<term>Animals, Wild</term>
<term>British Columbia</term>
<term>Evolution, Molecular</term>
<term>Mice</term>
<term>Phylogeny</term>
<term>Sequence Deletion</term>
<term>Swine</term>
<term>Viral Load</term>
<term>Viral Tropism</term>
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<term>Charge virale</term>
<term>Colombie-Britannique</term>
<term>Délétion de séquence</term>
<term>Phylogenèse</term>
<term>Souris</term>
<term>Suidae</term>
<term>Séquence d'acides aminés</term>
<term>Tropisme viral</term>
<term>Évolution moléculaire</term>
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<front>
<div type="abstract" xml:lang="en">In the current study, we describe the pathobiologic characteristics of a novel reassortant virus - A/chicken/BC/FAV-002/2015 (H5N1) belonging to clade 2.3.4.4 that was isolated from backyard chickens in British Columbia, Canada. Sequence analyses demonstrate PB1, PA, NA and NS gene segments were of North American lineage while PB2, HA, NP and M were derived from a Eurasian lineage H5N8 virus. This novel virus had a 19 amino acid deletion in the neuraminidase stalk. We evaluated the pathogenic potential of this isolate in various animal models. The virus was highly pathogenic to mice with a LD50 of 10 plaque forming units (PFU), but had limited tissue tropism. It caused only subclinical infection in pigs which did result in seroconversion. This virus was highly pathogenic to chickens, turkeys, juvenile Muscovy ducks (Cairnia moschata foma domestica) and adult Chinese geese (Anser cynoides domesticus) causing a systemic infection in all species. The virus was also efficiently transmitted and resulted in mortality in naïve contact ducks, geese and chickens. Our findings indicate that this novel H5N1 virus has a wide host range and enhanced surveillance of migratory waterfowl may be necessary in order to determine its potential to establish itself in the wild bird reservoir. </div>
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<Day>18</Day>
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<Title>Scientific reports</Title>
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<ArticleTitle>Pathobiological Characterization of a Novel Reassortant Highly Pathogenic H5N1 Virus Isolated in British Columbia, Canada, 2015.</ArticleTitle>
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<MedlinePgn>23380</MedlinePgn>
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<AbstractText>In the current study, we describe the pathobiologic characteristics of a novel reassortant virus - A/chicken/BC/FAV-002/2015 (H5N1) belonging to clade 2.3.4.4 that was isolated from backyard chickens in British Columbia, Canada. Sequence analyses demonstrate PB1, PA, NA and NS gene segments were of North American lineage while PB2, HA, NP and M were derived from a Eurasian lineage H5N8 virus. This novel virus had a 19 amino acid deletion in the neuraminidase stalk. We evaluated the pathogenic potential of this isolate in various animal models. The virus was highly pathogenic to mice with a LD50 of 10 plaque forming units (PFU), but had limited tissue tropism. It caused only subclinical infection in pigs which did result in seroconversion. This virus was highly pathogenic to chickens, turkeys, juvenile Muscovy ducks (Cairnia moschata foma domestica) and adult Chinese geese (Anser cynoides domesticus) causing a systemic infection in all species. The virus was also efficiently transmitted and resulted in mortality in naïve contact ducks, geese and chickens. Our findings indicate that this novel H5N1 virus has a wide host range and enhanced surveillance of migratory waterfowl may be necessary in order to determine its potential to establish itself in the wild bird reservoir. </AbstractText>
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<LastName>Berhane</LastName>
<ForeName>Yohannes</ForeName>
<Initials>Y</Initials>
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<Affiliation>Canadian Food Inspection Agency, National Centre for Foreign Animal Disease, Winnipeg, Manitoba, Canada R3E 3M4.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Department of Animal Science, University of Manitoba, Winnipeg, Canada.</Affiliation>
</AffiliationInfo>
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<ForeName>Darwyn</ForeName>
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<AffiliationInfo>
<Affiliation>Public Health Agency of Canada, National Microbiology Laboratory, 1015 Arlington Street, Winnipeg, Manitoba, Canada.</Affiliation>
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<AffiliationInfo>
<Affiliation>Department of Medical Microbiology, University of Manitoba, Winnipeg, Canada.</Affiliation>
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<ForeName>Carissa</ForeName>
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<Affiliation>Canadian Food Inspection Agency, National Centre for Foreign Animal Disease, Winnipeg, Manitoba, Canada R3E 3M4.</Affiliation>
</AffiliationInfo>
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<Affiliation>Canadian Food Inspection Agency, National Centre for Foreign Animal Disease, Winnipeg, Manitoba, Canada R3E 3M4.</Affiliation>
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<Affiliation>Canadian Food Inspection Agency, National Centre for Foreign Animal Disease, Winnipeg, Manitoba, Canada R3E 3M4.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Department of Immunology, University of Manitoba, Winnipeg, Canada.</Affiliation>
</AffiliationInfo>
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<LastName>Joseph</LastName>
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<Initials>T</Initials>
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<Affiliation>Animal Health Centre, Ministry of Agriculture, Abbotsford, British Columbia, Canada V3G 2M3.</Affiliation>
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<LastName>Bowes</LastName>
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<Affiliation>Canadian Food Inspection Agency, National Centre for Foreign Animal Disease, Winnipeg, Manitoba, Canada R3E 3M4.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Leung</LastName>
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<Initials>A</Initials>
<AffiliationInfo>
<Affiliation>Public Health Agency of Canada, National Microbiology Laboratory, 1015 Arlington Street, Winnipeg, Manitoba, Canada.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Cottam-Birt</LastName>
<ForeName>Colleen</ForeName>
<Initials>C</Initials>
<AffiliationInfo>
<Affiliation>Canadian Food Inspection Agency, National Centre for Foreign Animal Disease, Winnipeg, Manitoba, Canada R3E 3M4.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Hisanaga</LastName>
<ForeName>Tamiko</ForeName>
<Initials>T</Initials>
<AffiliationInfo>
<Affiliation>Canadian Food Inspection Agency, National Centre for Foreign Animal Disease, Winnipeg, Manitoba, Canada R3E 3M4.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Pasick</LastName>
<ForeName>John</ForeName>
<Initials>J</Initials>
<AffiliationInfo>
<Affiliation>Canadian Food Inspection Agency, National Centre for Foreign Animal Disease, Winnipeg, Manitoba, Canada R3E 3M4.</Affiliation>
</AffiliationInfo>
</Author>
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<PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType>
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<Year>2016</Year>
<Month>03</Month>
<Day>18</Day>
</ArticleDate>
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<Country>England</Country>
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<NlmUniqueID>101563288</NlmUniqueID>
<ISSNLinking>2045-2322</ISSNLinking>
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<MeshHeading>
<DescriptorName UI="D000595" MajorTopicYN="N">Amino Acid Sequence</DescriptorName>
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<MeshHeading>
<DescriptorName UI="D000818" MajorTopicYN="N">Animals</DescriptorName>
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<MeshHeading>
<DescriptorName UI="D000835" MajorTopicYN="N">Animals, Wild</DescriptorName>
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<MeshHeading>
<DescriptorName UI="D001955" MajorTopicYN="N">British Columbia</DescriptorName>
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<DescriptorName UI="D002645" MajorTopicYN="N">Chickens</DescriptorName>
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</MeshHeading>
<MeshHeading>
<DescriptorName UI="D053124" MajorTopicYN="N">Influenza A Virus, H5N1 Subtype</DescriptorName>
<QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName>
<QualifierName UI="Q000302" MajorTopicYN="Y">isolation & purification</QualifierName>
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<QualifierName UI="Q000821" MajorTopicYN="Y">virology</QualifierName>
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<MeshHeading>
<DescriptorName UI="D010802" MajorTopicYN="N">Phylogeny</DescriptorName>
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