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Article: Cross-species spill-over potential of the H9N2 bat influenza A virus

TitleCross-species spill-over potential of the H9N2 bat influenza A virus
Authors
Issue Date25-Apr-2024
PublisherNature Portfolio
Citation
Nature Communications, 2024, v. 15, n. 1 How to Cite?
Abstract

In 2017, a novel influenza A virus (IAV) was isolated from an Egyptian fruit bat. In contrast to other bat influenza viruses, the virus was related to avian A(H9N2) viruses and was probably the result of a bird-to-bat transmission event. To determine the cross-species spill-over potential, we biologically characterize features of A/bat/Egypt/381OP/2017(H9N2). The virus has a pH inactivation profile and neuraminidase activity similar to those of human-adapted IAVs. Despite the virus having an avian virus–like preference for α2,3 sialic acid receptors, it is unable to replicate in male mallard ducks; however, it readily infects ex-vivo human respiratory cell cultures and replicates in the lungs of female mice. A/bat/Egypt/381OP/2017 replicates in the upper respiratory tract of experimentally-infected male ferrets featuring direct-contact and airborne transmission. These data suggest that the bat A(H9N2) virus has features associated with increased risk to humans without a shift to a preference for α2,6 sialic acid receptors.


Persistent Identifierhttp://hdl.handle.net/10722/353851
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorEl-Shesheny, Rabeh-
dc.contributor.authorFranks, John-
dc.contributor.authorKandeil, Ahmed-
dc.contributor.authorBadra, Rebecca-
dc.contributor.authorTurner, Jasmine-
dc.contributor.authorSeiler, Patrick-
dc.contributor.authorMarathe, Bindumadhav M.-
dc.contributor.authorJeevan, Trushar-
dc.contributor.authorKercher, Lisa-
dc.contributor.authorHu, Meng-
dc.contributor.authorSim, Yul Eum-
dc.contributor.authorHui, Kenrie P.Y.-
dc.contributor.authorChan, Michael C.W.-
dc.contributor.authorThompson, Andrew J.-
dc.contributor.authorMcKenzie, Pamela-
dc.contributor.authorGovorkova, Elena A.-
dc.contributor.authorRussell, Charles J.-
dc.contributor.authorVogel, Peter-
dc.contributor.authorPaulson, James C.-
dc.contributor.authorPeiris, J. S.Malik-
dc.contributor.authorWebster, Robert G.-
dc.contributor.authorAli, Mohamed A.-
dc.contributor.authorKayali, Ghazi-
dc.contributor.authorWebby, Richard J.-
dc.date.accessioned2025-01-28T00:35:25Z-
dc.date.available2025-01-28T00:35:25Z-
dc.date.issued2024-04-25-
dc.identifier.citationNature Communications, 2024, v. 15, n. 1-
dc.identifier.urihttp://hdl.handle.net/10722/353851-
dc.description.abstract<p>In 2017, a novel influenza A virus (IAV) was isolated from an Egyptian fruit bat. In contrast to other bat influenza viruses, the virus was related to avian A(H9N2) viruses and was probably the result of a bird-to-bat transmission event. To determine the cross-species spill-over potential, we biologically characterize features of A/bat/Egypt/381OP/2017(H9N2). The virus has a pH inactivation profile and neuraminidase activity similar to those of human-adapted IAVs. Despite the virus having an avian virus–like preference for α2,3 sialic acid receptors, it is unable to replicate in male mallard ducks; however, it readily infects ex-vivo human respiratory cell cultures and replicates in the lungs of female mice. A/bat/Egypt/381OP/2017 replicates in the upper respiratory tract of experimentally-infected male ferrets featuring direct-contact and airborne transmission. These data suggest that the bat A(H9N2) virus has features associated with increased risk to humans without a shift to a preference for α2,6 sialic acid receptors.</p>-
dc.languageeng-
dc.publisherNature Portfolio-
dc.relation.ispartofNature Communications-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.titleCross-species spill-over potential of the H9N2 bat influenza A virus-
dc.typeArticle-
dc.identifier.doi10.1038/s41467-024-47635-4-
dc.identifier.pmid38664384-
dc.identifier.scopuseid_2-s2.0-85191503470-
dc.identifier.volume15-
dc.identifier.issue1-
dc.identifier.eissn2041-1723-
dc.identifier.isiWOS:001211008800007-
dc.identifier.issnl2041-1723-

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