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- Publisher Website: 10.1038/s41467-024-47635-4
- Scopus: eid_2-s2.0-85191503470
- PMID: 38664384
- WOS: WOS:001211008800007
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Article: Cross-species spill-over potential of the H9N2 bat influenza A virus
| Title | Cross-species spill-over potential of the H9N2 bat influenza A virus |
|---|---|
| Authors | El-Shesheny, RabehFranks, JohnKandeil, AhmedBadra, RebeccaTurner, JasmineSeiler, PatrickMarathe, Bindumadhav M.Jeevan, TrusharKercher, LisaHu, MengSim, Yul EumHui, Kenrie P.Y.Chan, Michael C.W.Thompson, Andrew J.McKenzie, PamelaGovorkova, Elena A.Russell, Charles J.Vogel, PeterPaulson, James C.Peiris, J. S.MalikWebster, Robert G.Ali, Mohamed A.Kayali, GhaziWebby, Richard J. |
| Issue Date | 25-Apr-2024 |
| Publisher | Nature 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 Identifier | http://hdl.handle.net/10722/353851 |
| ISI Accession Number ID |
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | El-Shesheny, Rabeh | - |
| dc.contributor.author | Franks, John | - |
| dc.contributor.author | Kandeil, Ahmed | - |
| dc.contributor.author | Badra, Rebecca | - |
| dc.contributor.author | Turner, Jasmine | - |
| dc.contributor.author | Seiler, Patrick | - |
| dc.contributor.author | Marathe, Bindumadhav M. | - |
| dc.contributor.author | Jeevan, Trushar | - |
| dc.contributor.author | Kercher, Lisa | - |
| dc.contributor.author | Hu, Meng | - |
| dc.contributor.author | Sim, Yul Eum | - |
| dc.contributor.author | Hui, Kenrie P.Y. | - |
| dc.contributor.author | Chan, Michael C.W. | - |
| dc.contributor.author | Thompson, Andrew J. | - |
| dc.contributor.author | McKenzie, Pamela | - |
| dc.contributor.author | Govorkova, Elena A. | - |
| dc.contributor.author | Russell, Charles J. | - |
| dc.contributor.author | Vogel, Peter | - |
| dc.contributor.author | Paulson, James C. | - |
| dc.contributor.author | Peiris, J. S.Malik | - |
| dc.contributor.author | Webster, Robert G. | - |
| dc.contributor.author | Ali, Mohamed A. | - |
| dc.contributor.author | Kayali, Ghazi | - |
| dc.contributor.author | Webby, Richard J. | - |
| dc.date.accessioned | 2025-01-28T00:35:25Z | - |
| dc.date.available | 2025-01-28T00:35:25Z | - |
| dc.date.issued | 2024-04-25 | - |
| dc.identifier.citation | Nature Communications, 2024, v. 15, n. 1 | - |
| dc.identifier.uri | http://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.language | eng | - |
| dc.publisher | Nature Portfolio | - |
| dc.relation.ispartof | Nature Communications | - |
| dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
| dc.title | Cross-species spill-over potential of the H9N2 bat influenza A virus | - |
| dc.type | Article | - |
| dc.identifier.doi | 10.1038/s41467-024-47635-4 | - |
| dc.identifier.pmid | 38664384 | - |
| dc.identifier.scopus | eid_2-s2.0-85191503470 | - |
| dc.identifier.volume | 15 | - |
| dc.identifier.issue | 1 | - |
| dc.identifier.eissn | 2041-1723 | - |
| dc.identifier.isi | WOS:001211008800007 | - |
| dc.identifier.issnl | 2041-1723 | - |
