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Newly discovered coronavirus as the primary cause of severe acute respiratory syndrome.

Identifieur interne : 000109 ( Hal/Corpus ); précédent : 000108; suivant : 000110

Newly discovered coronavirus as the primary cause of severe acute respiratory syndrome.

Auteurs : Thijs Kuiken ; Ron A M. Fouchier ; Martin Schutten ; Guus F. Rimmelzwaan ; Geert Van Amerongen ; Debby Van Riel ; Jon D. Laman ; Ton De Jong ; Gerard Van Doornum ; Wilina Lim ; Ai Ee Ling ; Paul K S. Chan ; John S. Tam ; Maria C. Zambon ; Robin Gopal ; Christian Drosten ; Sylvie Van Der Werf ; Nicolas Escriou ; Jean-Claude Manuguerra ; Klaus Stöhr ; J S Malik Peiris ; Albert D M E. Osterhaus

Source :

RBID : Hal:pasteur-00167032

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.


Url:
DOI: 10.1016/S0140-6736(03)13967-0

Links to Exploration step

Hal:pasteur-00167032

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<name sortKey="Osterhaus, Albert D M E" sort="Osterhaus, Albert D M E" uniqKey="Osterhaus A" first="Albert D M E" last="Osterhaus">Albert D M E. Osterhaus</name>
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<orgName>Department of Virology</orgName>
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<idno type="DOI">10.1016/S0140-6736(03)13967-0</idno>
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<title level="j">The Lancet</title>
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<p>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.</p>
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<persName>
<forename type="first">Thijs</forename>
<surname>Kuiken</surname>
</persName>
<idno type="halauthorid">202066</idno>
<affiliation ref="#struct-42281"></affiliation>
</author>
<author role="aut">
<persName>
<forename type="first">Ron A M</forename>
<surname>Fouchier</surname>
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<idno type="halauthorid">202067</idno>
<affiliation ref="#struct-42281"></affiliation>
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<author role="aut">
<persName>
<forename type="first">Martin</forename>
<surname>Schutten</surname>
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<idno type="halauthorid">202068</idno>
<affiliation ref="#struct-42281"></affiliation>
</author>
<author role="aut">
<persName>
<forename type="first">Guus F</forename>
<surname>Rimmelzwaan</surname>
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<idno type="halauthorid">202069</idno>
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<persName>
<forename type="first">Geert</forename>
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<persName>
<forename type="first">Debby</forename>
<surname>Van Riel</surname>
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<idno type="halauthorid">202071</idno>
<affiliation ref="#struct-42282"></affiliation>
</author>
<author role="aut">
<persName>
<forename type="first">Jon D</forename>
<surname>Laman</surname>
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<idno type="halauthorid">202072</idno>
<affiliation ref="#struct-42282"></affiliation>
</author>
<author role="aut">
<persName>
<forename type="first">Ton</forename>
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<persName>
<forename type="first">Gerard</forename>
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<idno type="halauthorid">202074</idno>
<affiliation ref="#struct-42281"></affiliation>
</author>
<author role="aut">
<persName>
<forename type="first">Wilina</forename>
<surname>Lim</surname>
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<idno type="halauthorid">202075</idno>
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<persName>
<forename type="first">Ai Ee</forename>
<surname>Ling</surname>
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<idno type="halauthorid">202076</idno>
<affiliation ref="#struct-42305"></affiliation>
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<author role="aut">
<persName>
<forename type="first">Paul K S</forename>
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<idno type="halauthorid">202077</idno>
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<persName>
<forename type="first">John S</forename>
<surname>Tam</surname>
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<idno type="halauthorid">202078</idno>
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<author role="aut">
<persName>
<forename type="first">Maria C</forename>
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<forename type="first">Robin</forename>
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<idno type="halauthorid">202080</idno>
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<author role="aut">
<persName>
<forename type="first">Christian</forename>
<surname>Drosten</surname>
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<idno type="halauthorid">202081</idno>
</author>
<author role="aut">
<persName>
<forename type="first">Sylvie</forename>
<surname>Van Der Werf</surname>
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<idno type="halauthorid">202082</idno>
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<author role="aut">
<persName>
<forename type="first">Nicolas</forename>
<surname>Escriou</surname>
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<idno type="halauthorid">202083</idno>
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<author role="aut">
<persName>
<forename type="first">Jean-Claude</forename>
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<author role="aut">
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<forename type="first">Klaus</forename>
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<idno type="halauthorid">202085</idno>
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<forename type="first">J S Malik</forename>
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<author role="aut">
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<forename type="first">Albert D M E</forename>
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<idno type="halauthorid">202087</idno>
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<forename>Christiane</forename>
<surname>Goisnard</surname>
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<email type="md5">47e9ba613cd3dd92b058a58331201dea</email>
<email type="domain">aol.com</email>
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<date type="whenSubmitted">2007-08-14 10:52:37</date>
<date type="whenModified">2020-03-27 03:47:18</date>
<date type="whenReleased">2007-08-16 14:29:33</date>
<date type="whenProduced">2003-07-26</date>
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<idno type="stamp" n="RIIP_PARIS">Institut Pasteur de Paris</idno>
<idno type="stamp" n="UNIV-PARIS7" corresp="UNIV-PARIS">Université Denis Diderot - Paris VII</idno>
<idno type="stamp" n="USPC">Université Sorbonne Paris Cité</idno>
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<forename type="first">Jon D</forename>
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<forename type="first">John S</forename>
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<forename type="first">Maria C</forename>
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<forename type="first">Robin</forename>
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<forename type="first">Jean-Claude</forename>
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<forename type="first">Albert D M E</forename>
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<biblScope unit="pp">263-70</biblScope>
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</imprint>
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<idno type="doi">10.1016/S0140-6736(03)13967-0</idno>
<idno type="pubmed">12892955</idno>
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<langUsage>
<language ident="en">English</language>
</langUsage>
<textClass>
<classCode scheme="mesh">Animals</classCode>
<classCode scheme="mesh">China</classCode>
<classCode scheme="mesh">World Health</classCode>
<classCode scheme="mesh">Communicable Diseases, Emerging</classCode>
<classCode scheme="mesh">Disease Models, Animal</classCode>
<classCode scheme="mesh">Disease Outbreaks</classCode>
<classCode scheme="mesh">Humans</classCode>
<classCode scheme="mesh">Macaca fascicularis</classCode>
<classCode scheme="mesh">Pulmonary Alveoli</classCode>
<classCode scheme="mesh">SARS Virus</classCode>
<classCode scheme="mesh">Severe Acute Respiratory Syndrome</classCode>
<classCode scheme="halDomain" n="sdv.bbm.bm">Life Sciences [q-bio]/Biochemistry, Molecular Biology/Molecular biology</classCode>
<classCode scheme="halTypology" n="ART">Journal articles</classCode>
</textClass>
<abstract xml:lang="en">
<p>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.</p>
</abstract>
</profileDesc>
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