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- Publisher Website: 10.1016/S0140-6736(03)13967-0
- Scopus: eid_2-s2.0-0042198682
- PMID: 12892955
- WOS: WOS:000184413400007
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Article: Newly discovered coronavirus as the primary cause of severe acute respiratory syndrome
Title | Newly discovered coronavirus as the primary cause of severe acute respiratory syndrome |
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Authors | |
Issue Date | 2003 |
Publisher | The Lancet Publishing Group. The Journal's web site is located at http://www.elsevier.com/locate/lancet |
Citation | Lancet, 2003, v. 362 n. 9380, p. 263-270 How to Cite? |
Abstract | Background: The worldwide outbreak of severe acute respiratory syndrome (SARS) is associated with a newly discovered coronavirus, SARS-associated coronavirus (SARS-CoV). We did clinical and experimental studies to assess the role of this virus in the cause of SARS. Methods: We tested clinical and postmortem samples from 436 SARS patients in six countries for infection with SARS-CoV, human metapneumovirus, and other respiratory pathogens. We infected four cynomolgus macaques (Macaca fascicularis) with SARS-CoV in an attempt to replicate SARS and did necropsies on day 6 after infection. Findings: SARS-CoV infection was diagnosed in 329 (75%) of 436 patients fitting the case definition of SARS; human metapneumovirus was diagnosed in 41 (12%) of 335, and other respiratory pathogens were diagnosed only sporadically. SARS-CoV was, therefore, the most likely causal agent of SARS. The four SARS-CoV-infected macaques excreted SARS-CoV from nose, mouth, and pharynx from 2 days after infection. Three of four macaques developed diffuse alveolar damage, similar to that in SARS patients, and characterised by epithelial necrosis, serosanguineous exudate, formation of hyaline membranes, type 2 pneumocyte hyperplasia, and the presence of syncytia. SARS-CoV was detected in pneumonic areas by virus isolation and RT-PCR, and was localised to alveolar epithelial cells and syncytia by immunohistochemistry and transmission electron microscopy. Interpretation: Replication in SARS-CoV-infected macaques of pneumonia similar to that in human beings with SARS, combined with the high prevalence of SARS-CoV infection in SARS patients, fulfill the criteria required to prove that SARS-CoV is the primary cause of SARS. |
Persistent Identifier | http://hdl.handle.net/10722/79062 |
ISSN | 2023 Impact Factor: 98.4 2023 SCImago Journal Rankings: 12.113 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
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dc.contributor.author | Kuiken, T | en_HK |
dc.contributor.author | Fouchier, RAM | en_HK |
dc.contributor.author | Schutten, M | en_HK |
dc.contributor.author | Rimmelzwaan, GF | en_HK |
dc.contributor.author | Van Amerongen, G | en_HK |
dc.contributor.author | Van Riel, D | en_HK |
dc.contributor.author | Laman, JD | en_HK |
dc.contributor.author | De Jong, T | en_HK |
dc.contributor.author | Van Doornum, G | en_HK |
dc.contributor.author | Lim, W | en_HK |
dc.contributor.author | Ling, AE | en_HK |
dc.contributor.author | Chan, PKS | en_HK |
dc.contributor.author | Tam, JS | en_HK |
dc.contributor.author | Zambon, MC | en_HK |
dc.contributor.author | Gopal, R | en_HK |
dc.contributor.author | Drosten, C | en_HK |
dc.contributor.author | Van Der Werf, S | en_HK |
dc.contributor.author | Escriou, N | en_HK |
dc.contributor.author | Manuguerra, JC | en_HK |
dc.contributor.author | Stöhr, K | en_HK |
dc.contributor.author | Peiris, JSM | en_HK |
dc.contributor.author | Osterhaus, ADME | en_HK |
dc.date.accessioned | 2010-09-06T07:50:08Z | - |
dc.date.available | 2010-09-06T07:50:08Z | - |
dc.date.issued | 2003 | en_HK |
dc.identifier.citation | Lancet, 2003, v. 362 n. 9380, p. 263-270 | en_HK |
dc.identifier.issn | 0140-6736 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/79062 | - |
dc.description.abstract | Background: The worldwide outbreak of severe acute respiratory syndrome (SARS) is associated with a newly discovered coronavirus, SARS-associated coronavirus (SARS-CoV). We did clinical and experimental studies to assess the role of this virus in the cause of SARS. Methods: We tested clinical and postmortem samples from 436 SARS patients in six countries for infection with SARS-CoV, human metapneumovirus, and other respiratory pathogens. We infected four cynomolgus macaques (Macaca fascicularis) with SARS-CoV in an attempt to replicate SARS and did necropsies on day 6 after infection. Findings: SARS-CoV infection was diagnosed in 329 (75%) of 436 patients fitting the case definition of SARS; human metapneumovirus was diagnosed in 41 (12%) of 335, and other respiratory pathogens were diagnosed only sporadically. SARS-CoV was, therefore, the most likely causal agent of SARS. The four SARS-CoV-infected macaques excreted SARS-CoV from nose, mouth, and pharynx from 2 days after infection. Three of four macaques developed diffuse alveolar damage, similar to that in SARS patients, and characterised by epithelial necrosis, serosanguineous exudate, formation of hyaline membranes, type 2 pneumocyte hyperplasia, and the presence of syncytia. SARS-CoV was detected in pneumonic areas by virus isolation and RT-PCR, and was localised to alveolar epithelial cells and syncytia by immunohistochemistry and transmission electron microscopy. Interpretation: Replication in SARS-CoV-infected macaques of pneumonia similar to that in human beings with SARS, combined with the high prevalence of SARS-CoV infection in SARS patients, fulfill the criteria required to prove that SARS-CoV is the primary cause of SARS. | en_HK |
dc.language | eng | en_HK |
dc.publisher | The Lancet Publishing Group. The Journal's web site is located at http://www.elsevier.com/locate/lancet | en_HK |
dc.relation.ispartof | Lancet | en_HK |
dc.title | Newly discovered coronavirus as the primary cause of severe acute respiratory syndrome | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0140-6736&volume=362 &issue=9380&spage=263&epage=70&date=2003&atitle=Newly+discovered+coronavirus+as+the+primary+cause+of+severe+acute+respiratory+syndrome. | en_HK |
dc.identifier.email | Peiris, JSM: malik@hkucc.hku.hk | en_HK |
dc.identifier.authority | Peiris, JSM=rp00410 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1016/S0140-6736(03)13967-0 | en_HK |
dc.identifier.pmid | 12892955 | - |
dc.identifier.scopus | eid_2-s2.0-0042198682 | en_HK |
dc.identifier.hkuros | 83116 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-0042198682&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 362 | en_HK |
dc.identifier.issue | 9380 | en_HK |
dc.identifier.spage | 263 | en_HK |
dc.identifier.epage | 270 | en_HK |
dc.identifier.isi | WOS:000184413400007 | - |
dc.publisher.place | United Kingdom | en_HK |
dc.identifier.scopusauthorid | Kuiken, T=26643529400 | en_HK |
dc.identifier.scopusauthorid | Fouchier, RAM=7006060466 | en_HK |
dc.identifier.scopusauthorid | Schutten, M=7004005251 | en_HK |
dc.identifier.scopusauthorid | Rimmelzwaan, GF=7005416180 | en_HK |
dc.identifier.scopusauthorid | Van Amerongen, G=7004695265 | en_HK |
dc.identifier.scopusauthorid | Van Riel, D=6602932722 | en_HK |
dc.identifier.scopusauthorid | Laman, JD=21635097100 | en_HK |
dc.identifier.scopusauthorid | De Jong, T=7201837394 | en_HK |
dc.identifier.scopusauthorid | Van Doornum, G=7005445921 | en_HK |
dc.identifier.scopusauthorid | Lim, W=7202378277 | en_HK |
dc.identifier.scopusauthorid | Ling, AE=7102194546 | en_HK |
dc.identifier.scopusauthorid | Chan, PKS=7403497792 | en_HK |
dc.identifier.scopusauthorid | Tam, JS=24788939600 | en_HK |
dc.identifier.scopusauthorid | Zambon, MC=7006818684 | en_HK |
dc.identifier.scopusauthorid | Gopal, R=7102284995 | en_HK |
dc.identifier.scopusauthorid | Drosten, C=7003813990 | en_HK |
dc.identifier.scopusauthorid | Van Der Werf, S=7005851162 | en_HK |
dc.identifier.scopusauthorid | Escriou, N=6603606703 | en_HK |
dc.identifier.scopusauthorid | Manuguerra, JC=7003610543 | en_HK |
dc.identifier.scopusauthorid | Stöhr, K=7004827453 | en_HK |
dc.identifier.scopusauthorid | Peiris, JSM=7005486823 | en_HK |
dc.identifier.scopusauthorid | Osterhaus, ADME=7202908501 | en_HK |
dc.identifier.issnl | 0140-6736 | - |