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Article: Tropism and innate host responses of a novel avian influenza A H7N9 virus: an analysis of ex-vivo and in-vitro cultures of the human respiratory tract
Title | Tropism and innate host responses of a novel avian influenza A H7N9 virus: an analysis of ex-vivo and in-vitro cultures of the human respiratory tract |
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Authors | |
Issue Date | 2013 |
Publisher | The Lancet Publishing Group. The Journal's web site is located at http://www.elsevier.com/journals/the-lancet-respiratory-medicine/2213-2600 |
Citation | The Lancet Respiratory Medicine, 2013, v. 1 n. 7, p. 534-542 How to Cite? |
Abstract | BACKGROUND: Since March, 2013, an avian-origin influenza A H7N9 virus has caused severe pneumonia in China. The aim of this study was to investigate the pathogenesis of this new virus in human beings. METHODS: We obtained ex-vivo cultures of the human bronchus, lung, nasopharynx, and tonsil and in-vitro cultures of primary human alveolar epithelial cells and peripheral blood monocyte-derived macrophages. We compared virus tropism and induction of proinflammatory cytokine responses of two human influenza A H7N9 virus isolates, A/Shanghai/1/2013 and A/Shanghai/2/2013; a highly pathogenic avian influenza H5N1 virus; the highly pathogenic avian influenza H7N7 virus that infected human beings in the Netherlands in 2003; the 2009 pandemic influenza H1N1 virus, and a low pathogenic duck H7N9 virus that was genetically different to the human disease causing A H7N9 viruses. FINDINGS: Both human H7N9 viruses replicated efficiently in human bronchus and lung ex-vivo cultures, whereas duck/H7N9 virus failed to replicate in either. Both human A H7N9 viruses infected both ciliated and non-ciliated human bronchial epithelial cells and replicated to higher titres than did H5N1 (p<0·0001 to 0·0046) and A/Shanghai/1/2013 replicated to higher titres than did H7N7 (p=0·0002-0·01). Both human A H7N9 viruses predominantly infected type II alveolar epithelial cells and alveolar macrophages in the human lung and replicated to higher titres than did H5N1 (p<0·0001 to 0·0078); A/Shanghai/1/2013 replicated to higher titres than did H1N1 (p=0·0052-0·05) and H7N7 (p=0·0031-0·0151). Human H7N9 viruses were less potent inducers of proinflammatory cytokines compared with H5N1 virus. INTERPRETATION: Collectively, the results suggest that the novel H7N9 viruses are better adapted to infect and replicate in the human conducting and lower airways than are other avian influenza viruses, including H5N1, and pose an important pandemic threat. |
Persistent Identifier | http://hdl.handle.net/10722/194836 |
ISSN | 2023 Impact Factor: 38.7 2023 SCImago Journal Rankings: 7.965 |
ISI Accession Number ID | |
Grants |
DC Field | Value | Language |
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dc.contributor.author | Chan, MCW | en_US |
dc.contributor.author | Chan, WY | en_US |
dc.contributor.author | Chan, LY | en_US |
dc.contributor.author | Mok, KP | en_US |
dc.contributor.author | Hui, PY | en_US |
dc.contributor.author | Fong, JHM | en_US |
dc.contributor.author | Tao, KP | en_US |
dc.contributor.author | Poon, LLM | en_US |
dc.contributor.author | Nicholls, JM | en_US |
dc.contributor.author | Guan, Y | en_US |
dc.contributor.author | Peiris, JSM | en_US |
dc.date.accessioned | 2014-02-17T02:14:42Z | - |
dc.date.available | 2014-02-17T02:14:42Z | - |
dc.date.issued | 2013 | en_US |
dc.identifier.citation | The Lancet Respiratory Medicine, 2013, v. 1 n. 7, p. 534-542 | en_US |
dc.identifier.issn | 2213-2600 | - |
dc.identifier.uri | http://hdl.handle.net/10722/194836 | - |
dc.description.abstract | BACKGROUND: Since March, 2013, an avian-origin influenza A H7N9 virus has caused severe pneumonia in China. The aim of this study was to investigate the pathogenesis of this new virus in human beings. METHODS: We obtained ex-vivo cultures of the human bronchus, lung, nasopharynx, and tonsil and in-vitro cultures of primary human alveolar epithelial cells and peripheral blood monocyte-derived macrophages. We compared virus tropism and induction of proinflammatory cytokine responses of two human influenza A H7N9 virus isolates, A/Shanghai/1/2013 and A/Shanghai/2/2013; a highly pathogenic avian influenza H5N1 virus; the highly pathogenic avian influenza H7N7 virus that infected human beings in the Netherlands in 2003; the 2009 pandemic influenza H1N1 virus, and a low pathogenic duck H7N9 virus that was genetically different to the human disease causing A H7N9 viruses. FINDINGS: Both human H7N9 viruses replicated efficiently in human bronchus and lung ex-vivo cultures, whereas duck/H7N9 virus failed to replicate in either. Both human A H7N9 viruses infected both ciliated and non-ciliated human bronchial epithelial cells and replicated to higher titres than did H5N1 (p<0·0001 to 0·0046) and A/Shanghai/1/2013 replicated to higher titres than did H7N7 (p=0·0002-0·01). Both human A H7N9 viruses predominantly infected type II alveolar epithelial cells and alveolar macrophages in the human lung and replicated to higher titres than did H5N1 (p<0·0001 to 0·0078); A/Shanghai/1/2013 replicated to higher titres than did H1N1 (p=0·0052-0·05) and H7N7 (p=0·0031-0·0151). Human H7N9 viruses were less potent inducers of proinflammatory cytokines compared with H5N1 virus. INTERPRETATION: Collectively, the results suggest that the novel H7N9 viruses are better adapted to infect and replicate in the human conducting and lower airways than are other avian influenza viruses, including H5N1, and pose an important pandemic threat. | en_US |
dc.language | eng | en_US |
dc.publisher | The Lancet Publishing Group. The Journal's web site is located at http://www.elsevier.com/journals/the-lancet-respiratory-medicine/2213-2600 | - |
dc.relation.ispartof | The Lancet Respiratory Medicine | en_US |
dc.rights | NOTICE: this is the author’s version of a work that was accepted for publication in The Lancet Respiratory Medicine. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in The Lancet Respiratory Medicine, 2013, v. 1 n. 7, p. 534-542. DOI: 10.1016/S2213-2600(13)70138-3 | - |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.title | Tropism and innate host responses of a novel avian influenza A H7N9 virus: an analysis of ex-vivo and in-vitro cultures of the human respiratory tract | en_US |
dc.type | Article | en_US |
dc.identifier.email | Chan, MCW: mchan@hku.hk | en_US |
dc.identifier.email | Chan, WY: reneewy@hku.hk | en_US |
dc.identifier.email | Chan, LY: louisa12@hku.hk | en_US |
dc.identifier.email | Mok, KP: ch02mkp@hkucc.hku.hk | en_US |
dc.identifier.email | Hui, PY: kenrie@hkucc.hku.hk | en_US |
dc.identifier.email | Fong, JHM: fongjhm@hku.hk | en_US |
dc.identifier.email | Tao, KP: marstao@hku.hk | en_US |
dc.identifier.email | Poon, LLM: llmpoon@hkucc.hku.hk | en_US |
dc.identifier.email | Nicholls, JM: jmnichol@hkucc.hku.hk | en_US |
dc.identifier.email | Guan, Y: yguan@hkucc.hku.hk | en_US |
dc.identifier.email | Peiris, JSM: malik@hkucc.hku.hk | en_US |
dc.identifier.authority | Chan, MCW=rp00420 | en_US |
dc.identifier.authority | Chan, WY=rp01596 | en_US |
dc.identifier.authority | Mok, KP=rp01805 | en_US |
dc.identifier.authority | Poon, LLM=rp00484 | en_US |
dc.identifier.authority | Nicholls, JM=rp00364 | en_US |
dc.identifier.authority | Guan, Y=rp00397 | en_US |
dc.identifier.authority | Peiris, JSM=rp00410 | en_US |
dc.description.nature | postprint | - |
dc.identifier.doi | 10.1016/S2213-2600(13)70138-3 | en_US |
dc.identifier.pmid | 24461614 | - |
dc.identifier.scopus | eid_2-s2.0-84883454591 | - |
dc.identifier.hkuros | 227935 | en_US |
dc.identifier.hkuros | 217207 | - |
dc.identifier.volume | 1 | en_US |
dc.identifier.issue | 7 | - |
dc.identifier.spage | 534 | en_US |
dc.identifier.epage | 542 | en_US |
dc.identifier.isi | WOS:000342690100018 | - |
dc.publisher.place | United Kingdom | - |
dc.relation.project | Control of Pandemic and Inter-pandemic Influenza | - |
dc.identifier.issnl | 2213-2600 | - |