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Article: Receptor binding and transmission studies of H5N1 influenza virus in mammals

TitleReceptor binding and transmission studies of H5N1 influenza virus in mammals
Authors
KeywordsReceptor binding
Transmission
H5N1
Mammal
Influenza A virus
Issue Date2013
PublisherNature Publishing Group. The Journal's web site is located at http://www.nature.com/emi/marketing/index.html
Citation
Emerging Microbes & Infections, 2013, v. 2, article no. e85 How to Cite?
AbstractThe H5N1 influenza A virus that is currently circulating in Asia, Africa and Europe has resulted in persistent outbreaks in poultry with sporadic transmission to humans. Thus far, it is believed that H5N1 does not possess sufficient ability for human-to-human transmission and subsequent pandemic infection. Both receptor binding specificity and virus infectivity are key factors in determining whether influenza A virus becomes pandemic. The use of human viral isolates in various studies has helped to illustrate the changes in receptor binding specificity and virulence as a result of adaptation in humans. In this review, we highlight the important amino acids and domains of viral proteins related to receptor binding specificity that have been reported for humans and avians using mammalian models. Thus, this review will consolidate findings from studies that have shed light on the receptor binding and transmission characteristics of the H5N1 influenza virus, with the goal of improving our ability to predict the transmission efficiency or pandemic potential of new viral strains.
Persistent Identifierhttp://hdl.handle.net/10722/231189
ISSN
2021 Impact Factor: 19.568
2020 SCImago Journal Rankings: 2.475
PubMed Central ID
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorZhao, H-
dc.contributor.authorZhou, J-
dc.contributor.authorJiang, S-
dc.contributor.authorZheng, B-
dc.date.accessioned2016-09-20T05:21:18Z-
dc.date.available2016-09-20T05:21:18Z-
dc.date.issued2013-
dc.identifier.citationEmerging Microbes & Infections, 2013, v. 2, article no. e85-
dc.identifier.issn2222-1751-
dc.identifier.urihttp://hdl.handle.net/10722/231189-
dc.description.abstractThe H5N1 influenza A virus that is currently circulating in Asia, Africa and Europe has resulted in persistent outbreaks in poultry with sporadic transmission to humans. Thus far, it is believed that H5N1 does not possess sufficient ability for human-to-human transmission and subsequent pandemic infection. Both receptor binding specificity and virus infectivity are key factors in determining whether influenza A virus becomes pandemic. The use of human viral isolates in various studies has helped to illustrate the changes in receptor binding specificity and virulence as a result of adaptation in humans. In this review, we highlight the important amino acids and domains of viral proteins related to receptor binding specificity that have been reported for humans and avians using mammalian models. Thus, this review will consolidate findings from studies that have shed light on the receptor binding and transmission characteristics of the H5N1 influenza virus, with the goal of improving our ability to predict the transmission efficiency or pandemic potential of new viral strains.-
dc.languageeng-
dc.publisherNature Publishing Group. The Journal's web site is located at http://www.nature.com/emi/marketing/index.html-
dc.relation.ispartofEmerging Microbes & Infections-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectReceptor binding-
dc.subjectTransmission-
dc.subjectH5N1-
dc.subjectMammal-
dc.subjectInfluenza A virus-
dc.titleReceptor binding and transmission studies of H5N1 influenza virus in mammals-
dc.typeArticle-
dc.identifier.emailZhao, H: hjzhao13@hku.hk-
dc.identifier.emailZhou, J: jiezhou@hku.hk-
dc.identifier.emailZheng, B: bzheng@hkucc.hku.hk-
dc.identifier.authorityZhou, J=rp01412-
dc.identifier.authorityZheng, B=rp00353-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1038/emi.2013.89-
dc.identifier.pmid26038448-
dc.identifier.pmcidPMC3880874-
dc.identifier.scopuseid_2-s2.0-84920878316-
dc.identifier.hkuros266780-
dc.identifier.volume2-
dc.identifier.spagearticle no. e85-
dc.identifier.epagearticle no. e85-
dc.identifier.isiWOS:000339193900001-
dc.publisher.placeUnited Kingdom-
dc.identifier.issnl2222-1751-

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