Partial direct contact transmission in ferrets of a mallard H7N3 influenza virus with typical avian-like receptor specificity.
Identifieur interne : 000736 ( Main/Exploration ); précédent : 000735; suivant : 000737Partial direct contact transmission in ferrets of a mallard H7N3 influenza virus with typical avian-like receptor specificity.
Auteurs : Haichen Song [États-Unis] ; Hongquan Wan ; Yonas Araya ; Daniel R. PerezSource :
- Virology journal [ 1743-422X ] ; 2009.
Descripteurs français
- KwdFr :
- Animaux (MeSH), Attachement viral (MeSH), Canada (MeSH), Données de séquences moléculaires (MeSH), Femelle (MeSH), Furets (MeSH), Grippe chez les oiseaux (métabolisme), Grippe chez les oiseaux (transmission), Grippe chez les oiseaux (virologie), Grippe humaine (métabolisme), Grippe humaine (transmission), Grippe humaine (virologie), Humains (MeSH), Liaison aux protéines (MeSH), Lignée cellulaire (MeSH), Modèles animaux de maladie humaine (MeSH), Oiseaux (MeSH), Récepteurs viraux (composition chimique), Récepteurs viraux (métabolisme), Réplication virale (MeSH), Souris (MeSH), Souris de lignée BALB C (MeSH), Spécificité d'espèce (MeSH), Virus de la grippe A (génétique), Virus de la grippe A (isolement et purification), Virus de la grippe A (physiologie).
- MESH :
- composition chimique : Récepteurs viraux.
- génétique : Virus de la grippe A.
- isolement et purification : Virus de la grippe A.
- métabolisme : Grippe chez les oiseaux, Grippe humaine, Récepteurs viraux.
- physiologie : Virus de la grippe A.
- virologie : Grippe chez les oiseaux, Grippe humaine.
- Animaux, Attachement viral, Canada, Données de séquences moléculaires, Femelle, Furets, Grippe chez les oiseaux, Grippe humaine, Humains, Liaison aux protéines, Lignée cellulaire, Modèles animaux de maladie humaine, Oiseaux, Réplication virale, Souris, Souris de lignée BALB C, Spécificité d'espèce.
- Wicri :
- geographic : Canada.
English descriptors
- KwdEn :
- Animals (MeSH), Birds (MeSH), Canada (MeSH), Cell Line (MeSH), Disease Models, Animal (MeSH), Female (MeSH), Ferrets (MeSH), Humans (MeSH), Influenza A virus (genetics), Influenza A virus (isolation & purification), Influenza A virus (physiology), Influenza in Birds (metabolism), Influenza in Birds (transmission), Influenza in Birds (virology), Influenza, Human (metabolism), Influenza, Human (transmission), Influenza, Human (virology), Mice (MeSH), Mice, Inbred BALB C (MeSH), Molecular Sequence Data (MeSH), Protein Binding (MeSH), Receptors, Virus (chemistry), Receptors, Virus (metabolism), Species Specificity (MeSH), Virus Attachment (MeSH), Virus Replication (MeSH).
- MESH :
- chemical , chemistry : Receptors, Virus.
- chemical , metabolism : Receptors, Virus.
- geographic : Canada.
- genetics : Influenza A virus.
- isolation & purification : Influenza A virus.
- metabolism : Influenza in Birds, Influenza, Human.
- physiology : Influenza A virus.
- transmission : Influenza in Birds, Influenza, Human.
- virology : Influenza in Birds, Influenza, Human.
- Animals, Birds, Cell Line, Disease Models, Animal, Female, Ferrets, Humans, Mice, Mice, Inbred BALB C, Molecular Sequence Data, Protein Binding, Species Specificity, Virus Attachment, Virus Replication.
Abstract
BACKGROUND
Avian influenza viruses of the H7 subtype have caused multiple outbreaks in domestic poultry and represent a significant threat to public health due to their propensity to occasionally transmit directly from birds to humans. In order to better understand the cross species transmission potential of H7 viruses in nature, we performed biological and molecular characterizations of an H7N3 virus isolated from mallards in Canada in 2001.
RESULTS
Sequence analysis that the HA gene of the mallard H7N3 virus shares 97% identity with the highly pathogenic avian influenza (HPAI) H7N3 virus isolated from a human case in British Columbia, Canada in 2004. The mallard H7N3 virus was able to replicate in quail and chickens, and transmitted efficiently in quail but not in chickens. Interestingly, although this virus showed preferential binding to analogs of avian-like receptors with sialic acid (SA) linked to galactose in an alpha2-3 linkage (SAalpha2-3Gal), it replicated to high titers in cultures of primary human airway epithelial (HAE) cells, comparable to an avian H9N2 influenza virus with human-like alpha2-6 linkage receptors (SAalpha2-6Gal). In addition, the virus replicated in mice and ferrets without prior adaptation and was able to transmit partially among ferrets.
CONCLUSION
Our findings highlight the importance and need for systematic in vitro and in vivo analysis of avian influenza viruses isolated from the natural reservoir in order to define their zoonotic potential.
DOI: 10.1186/1743-422X-6-126
PubMed: 19682381
PubMed Central: PMC2743663
Affiliations:
Links toward previous steps (curation, corpus...)
Le document en format XML
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Sequence Data (MeSH)</term><term>Protein Binding (MeSH)</term><term>Receptors, Virus (chemistry)</term><term>Receptors, Virus (metabolism)</term><term>Species Specificity (MeSH)</term><term>Virus Attachment (MeSH)</term><term>Virus Replication (MeSH)</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Animaux (MeSH)</term><term>Attachement viral (MeSH)</term><term>Canada (MeSH)</term><term>Données de séquences moléculaires (MeSH)</term><term>Femelle (MeSH)</term><term>Furets (MeSH)</term><term>Grippe chez les oiseaux (métabolisme)</term><term>Grippe chez les oiseaux (transmission)</term><term>Grippe chez les oiseaux (virologie)</term><term>Grippe humaine (métabolisme)</term><term>Grippe humaine (transmission)</term><term>Grippe humaine (virologie)</term><term>Humains (MeSH)</term><term>Liaison aux protéines (MeSH)</term><term>Lignée cellulaire (MeSH)</term><term>Modèles animaux de maladie humaine (MeSH)</term><term>Oiseaux (MeSH)</term><term>Récepteurs viraux (composition 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oiseaux</term><term>Grippe humaine</term></keywords><keywords scheme="MESH" qualifier="virology" xml:lang="en"><term>Influenza in Birds</term><term>Influenza, Human</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Animals</term><term>Birds</term><term>Cell Line</term><term>Disease Models, Animal</term><term>Female</term><term>Ferrets</term><term>Humans</term><term>Mice</term><term>Mice, Inbred BALB C</term><term>Molecular Sequence Data</term><term>Protein Binding</term><term>Species Specificity</term><term>Virus Attachment</term><term>Virus Replication</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Animaux</term><term>Attachement viral</term><term>Canada</term><term>Données de séquences moléculaires</term><term>Femelle</term><term>Furets</term><term>Grippe chez les oiseaux</term><term>Grippe humaine</term><term>Humains</term><term>Liaison aux protéines</term><term>Lignée cellulaire</term><term>Modèles animaux de maladie humaine</term><term>Oiseaux</term><term>Réplication virale</term><term>Souris</term><term>Souris de lignée BALB C</term><term>Spécificité d'espèce</term></keywords><keywords scheme="Wicri" type="geographic" xml:lang="fr"><term>Canada</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><p><b>BACKGROUND</b></p><p>Avian influenza viruses of the H7 subtype have caused multiple outbreaks in domestic poultry and represent a significant threat to public health due to their propensity to occasionally transmit directly from birds to humans. In order to better understand the cross species transmission potential of H7 viruses in nature, we performed biological and molecular characterizations of an H7N3 virus isolated from mallards in Canada in 2001.</p></div><div type="abstract" xml:lang="en"><p><b>RESULTS</b></p><p>Sequence analysis that the HA gene of the mallard H7N3 virus shares 97% identity with the highly pathogenic avian influenza (HPAI) H7N3 virus isolated from a human case in British Columbia, Canada in 2004. The mallard H7N3 virus was able to replicate in quail and chickens, and transmitted efficiently in quail but not in chickens. Interestingly, although this virus showed preferential binding to analogs of avian-like receptors with sialic acid (SA) linked to galactose in an alpha2-3 linkage (SAalpha2-3Gal), it replicated to high titers in cultures of primary human airway epithelial (HAE) cells, comparable to an avian H9N2 influenza virus with human-like alpha2-6 linkage receptors (SAalpha2-6Gal). In addition, the virus replicated in mice and ferrets without prior adaptation and was able to transmit partially among ferrets.</p></div><div type="abstract" xml:lang="en"><p><b>CONCLUSION</b></p><p>Our findings highlight the importance and need for systematic in vitro and in vivo analysis of avian influenza viruses isolated from the natural reservoir in order to define their zoonotic potential.</p></div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">19682381</PMID><DateCompleted><Year>2009</Year><Month>11</Month><Day>03</Day></DateCompleted><DateRevised><Year>2018</Year><Month>11</Month><Day>13</Day></DateRevised><Article PubModel="Electronic"><Journal><ISSN IssnType="Electronic">1743-422X</ISSN><JournalIssue CitedMedium="Internet"><Volume>6</Volume><PubDate><Year>2009</Year><Month>Aug</Month><Day>14</Day></PubDate></JournalIssue><Title>Virology journal</Title><ISOAbbreviation>Virol. J.</ISOAbbreviation></Journal><ArticleTitle>Partial direct contact transmission in ferrets of a mallard H7N3 influenza virus with typical avian-like receptor specificity.</ArticleTitle><Pagination><MedlinePgn>126</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1186/1743-422X-6-126</ELocationID><Abstract><AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">Avian influenza viruses of the H7 subtype have caused multiple outbreaks in domestic poultry and represent a significant threat to public health due to their propensity to occasionally transmit directly from birds to humans. In order to better understand the cross species transmission potential of H7 viruses in nature, we performed biological and molecular characterizations of an H7N3 virus isolated from mallards in Canada in 2001.</AbstractText><AbstractText Label="RESULTS" NlmCategory="RESULTS">Sequence analysis that the HA gene of the mallard H7N3 virus shares 97% identity with the highly pathogenic avian influenza (HPAI) H7N3 virus isolated from a human case in British Columbia, Canada in 2004. The mallard H7N3 virus was able to replicate in quail and chickens, and transmitted efficiently in quail but not in chickens. Interestingly, although this virus showed preferential binding to analogs of avian-like receptors with sialic acid (SA) linked to galactose in an alpha2-3 linkage (SAalpha2-3Gal), it replicated to high titers in cultures of primary human airway epithelial (HAE) cells, comparable to an avian H9N2 influenza virus with human-like alpha2-6 linkage receptors (SAalpha2-6Gal). In addition, the virus replicated in mice and ferrets without prior adaptation and was able to transmit partially among ferrets.</AbstractText><AbstractText Label="CONCLUSION" NlmCategory="CONCLUSIONS">Our findings highlight the importance and need for systematic in vitro and in vivo analysis of avian influenza viruses isolated from the natural reservoir in order to define their zoonotic potential.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Song</LastName><ForeName>Haichen</ForeName><Initials>H</Initials><AffiliationInfo><Affiliation>Department of Veterinary Medicine, University of Maryland, Virginia-Maryland Regional College of Veterinary Medicine, College Park, MD 20742, USA. songhc@umd.edu</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Wan</LastName><ForeName>Hongquan</ForeName><Initials>H</Initials></Author><Author ValidYN="Y"><LastName>Araya</LastName><ForeName>Yonas</ForeName><Initials>Y</Initials></Author><Author ValidYN="Y"><LastName>Perez</LastName><ForeName>Daniel R</ForeName><Initials>DR</Initials></Author></AuthorList><Language>eng</Language><GrantList CompleteYN="Y"><Grant><GrantID>R01AI052155</GrantID><Acronym>AI</Acronym><Agency>NIAID NIH HHS</Agency><Country>United States</Country></Grant><Grant><GrantID>U01 CI000355</GrantID><Acronym>CI</Acronym><Agency>NCPDCID CDC HHS</Agency><Country>United States</Country></Grant><Grant><GrantID>1U01CI000355</GrantID><Acronym>CI</Acronym><Agency>NCPDCID CDC HHS</Agency><Country>United States</Country></Grant><Grant><GrantID>GM62116</GrantID><Acronym>GM</Acronym><Agency>NIGMS NIH HHS</Agency><Country>United States</Country></Grant><Grant><GrantID>R01 AI052155</GrantID><Acronym>AI</Acronym><Agency>NIAID NIH HHS</Agency><Country>United States</Country></Grant><Grant><GrantID>U54 GM062116</GrantID><Acronym>GM</Acronym><Agency>NIGMS NIH HHS</Agency><Country>United States</Country></Grant><Grant><GrantID>HHSN266200700010C</GrantID><Acronym>AI</Acronym><Agency>NIAID NIH HHS</Agency><Country>United States</Country></Grant></GrantList><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D052061">Research Support, N.I.H., Extramural</PublicationType><PublicationType UI="D013486">Research Support, U.S. Gov't, Non-P.H.S.</PublicationType><PublicationType UI="D013487">Research Support, U.S. Gov't, P.H.S.</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2009</Year><Month>08</Month><Day>14</Day></ArticleDate></Article><MedlineJournalInfo><Country>England</Country><MedlineTA>Virol J</MedlineTA><NlmUniqueID>101231645</NlmUniqueID><ISSNLinking>1743-422X</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D011991">Receptors, Virus</NameOfSubstance></Chemical></ChemicalList><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D000818" MajorTopicYN="N">Animals</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D001717" MajorTopicYN="N">Birds</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D002170" MajorTopicYN="N" Type="Geographic">Canada</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D002460" MajorTopicYN="N">Cell Line</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D004195" MajorTopicYN="Y">Disease Models, Animal</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D005260" MajorTopicYN="N">Female</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D005289" MajorTopicYN="Y">Ferrets</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D009980" MajorTopicYN="N">Influenza A virus</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName><QualifierName UI="Q000302" MajorTopicYN="N">isolation & purification</QualifierName><QualifierName UI="Q000502" MajorTopicYN="Y">physiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D005585" MajorTopicYN="N">Influenza in Birds</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName><QualifierName UI="Q000635" MajorTopicYN="Y">transmission</QualifierName><QualifierName UI="Q000821" MajorTopicYN="N">virology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D007251" MajorTopicYN="N">Influenza, Human</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName><QualifierName UI="Q000635" MajorTopicYN="Y">transmission</QualifierName><QualifierName UI="Q000821" MajorTopicYN="N">virology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D051379" MajorTopicYN="N">Mice</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D008807" MajorTopicYN="N">Mice, Inbred BALB C</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D008969" MajorTopicYN="N">Molecular Sequence Data</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D011485" MajorTopicYN="N">Protein Binding</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D011991" MajorTopicYN="N">Receptors, Virus</DescriptorName><QualifierName UI="Q000737" MajorTopicYN="N">chemistry</QualifierName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D013045" MajorTopicYN="N">Species Specificity</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D053585" MajorTopicYN="N">Virus Attachment</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D014779" MajorTopicYN="N">Virus 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sort="Araya, Yonas" uniqKey="Araya Y" first="Yonas" last="Araya">Yonas Araya</name><name sortKey="Perez, Daniel R" sort="Perez, Daniel R" uniqKey="Perez D" first="Daniel R" last="Perez">Daniel R. 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