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

Identifieur interne : 000033 ( PascalFrancis/Curation ); précédent : 000032; suivant : 000034

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

Auteurs : This Kuiken [Pays-Bas] ; Ron A. M. Fouchier [Pays-Bas] ; Martin Schutten [Pays-Bas] ; Guus F. Rimmelzwaan [Pays-Bas] ; Geert Van Amerongen [Pays-Bas] ; Debby Van Riel [Pays-Bas] ; Jon D. Laman [Pays-Bas] ; Ton De Jong [Pays-Bas] ; Gerard Van Doornum [Pays-Bas] ; Wilina Lim [République populaire de Chine] ; AI EE LING [Singapour] ; Paul K. S. Chan [Hong Kong] ; John S. Tam [Hong Kong] ; Maria C. Zambon [Royaume-Uni] ; Robin Gopal [Royaume-Uni] ; Christian Drosten [Allemagne] ; Sylvie Van Der Werf [France] ; Nicolas Escriou [France] ; Jean-Claude Manuguerra [France] ; Klaus Stöhr [Suisse] ; J. S. Malik Peiris [Hong Kong] ; Albert D. M. E. Osterhaus [Pays-Bas]

Source :

RBID : Pascal:03-0484722

Descripteurs français

English descriptors

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.
pA  
A01 01  1    @0 0140-6736
A02 01      @0 LANCAO
A03   1    @0 Lancet : (Br. ed.)
A05       @2 362
A06       @2 9380
A08 01  1  ENG  @1 Newly discovered coronavirus as the primary cause of severe acute respiratory syndrome
A11 01  1    @1 KUIKEN (This)
A11 02  1    @1 FOUCHIER (Ron A. M.)
A11 03  1    @1 SCHUTTEN (Martin)
A11 04  1    @1 RIMMELZWAAN (Guus F.)
A11 05  1    @1 VAN AMERONGEN (Geert)
A11 06  1    @1 VAN RIEL (Debby)
A11 07  1    @1 LAMAN (Jon D.)
A11 08  1    @1 DE JONG (Ton)
A11 09  1    @1 VAN DOORNUM (Gerard)
A11 10  1    @1 LIM (Wilina)
A11 11  1    @1 AI EE LING
A11 12  1    @1 CHAN (Paul K. S.)
A11 13  1    @1 TAM (John S.)
A11 14  1    @1 ZAMBON (Maria C.)
A11 15  1    @1 GOPAL (Robin)
A11 16  1    @1 DROSTEN (Christian)
A11 17  1    @1 VAN DER WERF (Sylvie)
A11 18  1    @1 ESCRIOU (Nicolas)
A11 19  1    @1 MANUGUERRA (Jean-Claude)
A11 20  1    @1 STÖHR (Klaus)
A11 21  1    @1 PEIRIS (J. S. Malik)
A11 22  1    @1 OSTERHAUS (Albert D. M. E.)
A14 01      @1 Department of Virology, Erasmus Medical Centre, PO Box 1738 @2 3000 DR Rotterdam @3 NLD @Z 1 aut. @Z 2 aut. @Z 3 aut. @Z 4 aut. @Z 5 aut. @Z 9 aut. @Z 22 aut.
A14 02      @1 Department of Immunology, Erasmus Medical Centre, PO Box 1738 @2 3000 DR Rotterdam @3 NLD @Z 6 aut. @Z 7 aut.
A14 03      @1 Department of Pathology, Erasmus Medical Centre, PO Box 1738 @2 3000 DR Rotterdam @3 NLD @Z 8 aut.
A14 04      @1 Government Virus Unit, Public Health Laboratory Centre, Shek Kip Mei, Kowloon, Hong Kong Special Administrative Region @2 Kowloon @3 CHN @Z 10 aut.
A14 05      @1 Department of Pathology, Singapore General Hospital @3 SGP @Z 11 aut.
A14 06      @1 Department of Microbiology, Chinese University of Hong Kong, Prince of Wales Hospital @3 HKG @Z 12 aut. @Z 13 aut.
A14 07      @1 Enteric Respiratory and Neurological Virus Laboratory, Health Protection Agency @2 London @3 GBR @Z 14 aut. @Z 15 aut.
A14 08      @1 Department of Virology, Bernhard-Nocht Institute for Tropical Medicine @2 Hamburg @3 DEU @Z 16 aut.
A14 09      @1 Unité de Génétique Moléculaire des Virus Respiratoires, Institut Pasteur @2 Paris @3 FRA @Z 17 aut. @Z 18 aut. @Z 19 aut.
A14 10      @1 SARS Aetiology Study Group, WHO @2 Geneva @3 CHE @Z 20 aut.
A14 11      @1 Department of Microbiology and Medicine, Queen Mary Hospital, University of Hong Kong @3 HKG @Z 21 aut.
A20       @1 263-270
A21       @1 2003
A23 01      @0 ENG
A43 01      @1 INIST @2 5004 @5 354000111380480040
A44       @0 0000 @1 © 2003 INIST-CNRS. All rights reserved.
A45       @0 30 ref.
A47 01  1    @0 03-0484722
A60       @1 P
A61       @0 A
A64 01  1    @0 Lancet : (British edition)
A66 01      @0 GBR
C01 01    ENG  @0 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.
C02 01  X    @0 002B05C02C
C03 01  X  FRE  @0 Coronavirus @2 NW @5 02
C03 01  X  ENG  @0 Coronavirus @2 NW @5 02
C03 01  X  SPA  @0 Coronavirus @2 NW @5 02
C03 02  X  FRE  @0 Homme @5 03
C03 02  X  ENG  @0 Human @5 03
C03 02  X  SPA  @0 Hombre @5 03
C03 03  X  FRE  @0 Syndrome respiratoire aigu sévère @4 CD @5 96
C03 03  X  ENG  @0 Severe acute respiratory syndrome @4 CD @5 96
C07 01  X  FRE  @0 Coronaviridae @2 NW
C07 01  X  ENG  @0 Coronaviridae @2 NW
C07 01  X  SPA  @0 Coronaviridae @2 NW
C07 02  X  FRE  @0 Nidovirales @2 NW
C07 02  X  ENG  @0 Nidovirales @2 NW
C07 02  X  SPA  @0 Nidovirales @2 NW
C07 03  X  FRE  @0 Virus @2 NW
C07 03  X  ENG  @0 Virus @2 NW
C07 03  X  SPA  @0 Virus @2 NW
C07 04  X  FRE  @0 Appareil respiratoire pathologie @5 37
C07 04  X  ENG  @0 Respiratory disease @5 37
C07 04  X  SPA  @0 Aparato respiratorio patología @5 37
C07 05  X  FRE  @0 Poumon pathologie @5 38
C07 05  X  ENG  @0 Lung disease @5 38
C07 05  X  SPA  @0 Pulmón patología @5 38
C07 06  X  FRE  @0 Virose @5 39
C07 06  X  ENG  @0 Viral disease @5 39
C07 06  X  SPA  @0 Virosis @5 39
C07 07  X  FRE  @0 Infection
C07 07  X  ENG  @0 Infection
C07 07  X  SPA  @0 Infección
N21       @1 328
N82       @1 PSI

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Pascal:03-0484722

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<name sortKey="Van Der Werf, Sylvie" sort="Van Der Werf, Sylvie" uniqKey="Van Der Werf S" first="Sylvie" last="Van Der Werf">Sylvie Van Der Werf</name>
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<name sortKey="Manuguerra, Jean Claude" sort="Manuguerra, Jean Claude" uniqKey="Manuguerra J" first="Jean-Claude" last="Manuguerra">Jean-Claude Manuguerra</name>
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<title xml:lang="en" level="a">Newly discovered coronavirus as the primary cause of severe acute respiratory syndrome</title>
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<name sortKey="Laman, Jon D" sort="Laman, Jon D" uniqKey="Laman J" first="Jon D." last="Laman">Jon D. Laman</name>
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<name sortKey="De Jong, Ton" sort="De Jong, Ton" uniqKey="De Jong T" first="Ton" last="De Jong">Ton De Jong</name>
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<s1>Department of Pathology, Erasmus Medical Centre, PO Box 1738</s1>
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<name sortKey="Van Doornum, Gerard" sort="Van Doornum, Gerard" uniqKey="Van Doornum G" first="Gerard" last="Van Doornum">Gerard Van Doornum</name>
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<s1>Department of Virology, Erasmus Medical Centre, PO Box 1738</s1>
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<name sortKey="Lim, Wilina" sort="Lim, Wilina" uniqKey="Lim W" first="Wilina" last="Lim">Wilina Lim</name>
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<country>République populaire de Chine</country>
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<name sortKey="Ai Ee Ling" sort="Ai Ee Ling" uniqKey="Ai Ee Ling" last="Ai Ee Ling">AI EE LING</name>
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<s1>Department of Pathology, Singapore General Hospital</s1>
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<name sortKey="Chan, Paul K S" sort="Chan, Paul K S" uniqKey="Chan P" first="Paul K. S." last="Chan">Paul K. S. Chan</name>
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<inist:fA14 i1="06">
<s1>Department of Microbiology, Chinese University of Hong Kong, Prince of Wales Hospital</s1>
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<country>Hong Kong</country>
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<name sortKey="Tam, John S" sort="Tam, John S" uniqKey="Tam J" first="John S." last="Tam">John S. Tam</name>
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<inist:fA14 i1="06">
<s1>Department of Microbiology, Chinese University of Hong Kong, Prince of Wales Hospital</s1>
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<sZ>13 aut.</sZ>
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<country>Hong Kong</country>
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<name sortKey="Zambon, Maria C" sort="Zambon, Maria C" uniqKey="Zambon M" first="Maria C." last="Zambon">Maria C. Zambon</name>
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<s1>Enteric Respiratory and Neurological Virus Laboratory, Health Protection Agency</s1>
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<country>Royaume-Uni</country>
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<author>
<name sortKey="Gopal, Robin" sort="Gopal, Robin" uniqKey="Gopal R" first="Robin" last="Gopal">Robin Gopal</name>
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<inist:fA14 i1="07">
<s1>Enteric Respiratory and Neurological Virus Laboratory, Health Protection Agency</s1>
<s2>London</s2>
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<sZ>14 aut.</sZ>
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<country>Royaume-Uni</country>
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<name sortKey="Drosten, Christian" sort="Drosten, Christian" uniqKey="Drosten C" first="Christian" last="Drosten">Christian Drosten</name>
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<s1>Department of Virology, Bernhard-Nocht Institute for Tropical Medicine</s1>
<s2>Hamburg</s2>
<s3>DEU</s3>
<sZ>16 aut.</sZ>
</inist:fA14>
<country>Allemagne</country>
</affiliation>
</author>
<author>
<name sortKey="Van Der Werf, Sylvie" sort="Van Der Werf, Sylvie" uniqKey="Van Der Werf S" first="Sylvie" last="Van Der Werf">Sylvie Van Der Werf</name>
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<s1>Unité de Génétique Moléculaire des Virus Respiratoires, Institut Pasteur</s1>
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<country>France</country>
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<name sortKey="Escriou, Nicolas" sort="Escriou, Nicolas" uniqKey="Escriou N" first="Nicolas" last="Escriou">Nicolas Escriou</name>
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<author>
<name sortKey="Manuguerra, Jean Claude" sort="Manuguerra, Jean Claude" uniqKey="Manuguerra J" first="Jean-Claude" last="Manuguerra">Jean-Claude Manuguerra</name>
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<inist:fA14 i1="09">
<s1>Unité de Génétique Moléculaire des Virus Respiratoires, Institut Pasteur</s1>
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<country>France</country>
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<author>
<name sortKey="Stohr, Klaus" sort="Stohr, Klaus" uniqKey="Stohr K" first="Klaus" last="Stöhr">Klaus Stöhr</name>
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<s1>SARS Aetiology Study Group, WHO</s1>
<s2>Geneva</s2>
<s3>CHE</s3>
<sZ>20 aut.</sZ>
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<country>Suisse</country>
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</author>
<author>
<name sortKey="Peiris, J S Malik" sort="Peiris, J S Malik" uniqKey="Peiris J" first="J. S. Malik" last="Peiris">J. S. Malik Peiris</name>
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<s1>Department of Microbiology and Medicine, Queen Mary Hospital, University of Hong Kong</s1>
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<country>Hong Kong</country>
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</author>
<author>
<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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<s1>Department of Virology, Erasmus Medical Centre, PO Box 1738</s1>
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<title level="j" type="main">Lancet : (British edition)</title>
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<term>Coronavirus</term>
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<term>Severe acute respiratory syndrome</term>
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<term>Coronavirus</term>
<term>Homme</term>
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<div type="abstract" xml:lang="en">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.</div>
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<s0>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.</s0>
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<s0>Homme</s0>
<s5>03</s5>
</fC03>
<fC03 i1="02" i2="X" l="ENG">
<s0>Human</s0>
<s5>03</s5>
</fC03>
<fC03 i1="02" i2="X" l="SPA">
<s0>Hombre</s0>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="X" l="FRE">
<s0>Syndrome respiratoire aigu sévère</s0>
<s4>CD</s4>
<s5>96</s5>
</fC03>
<fC03 i1="03" i2="X" l="ENG">
<s0>Severe acute respiratory syndrome</s0>
<s4>CD</s4>
<s5>96</s5>
</fC03>
<fC07 i1="01" i2="X" l="FRE">
<s0>Coronaviridae</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="01" i2="X" l="ENG">
<s0>Coronaviridae</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="01" i2="X" l="SPA">
<s0>Coronaviridae</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="02" i2="X" l="FRE">
<s0>Nidovirales</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="02" i2="X" l="ENG">
<s0>Nidovirales</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="02" i2="X" l="SPA">
<s0>Nidovirales</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="03" i2="X" l="FRE">
<s0>Virus</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="03" i2="X" l="ENG">
<s0>Virus</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="03" i2="X" l="SPA">
<s0>Virus</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="04" i2="X" l="FRE">
<s0>Appareil respiratoire pathologie</s0>
<s5>37</s5>
</fC07>
<fC07 i1="04" i2="X" l="ENG">
<s0>Respiratory disease</s0>
<s5>37</s5>
</fC07>
<fC07 i1="04" i2="X" l="SPA">
<s0>Aparato respiratorio patología</s0>
<s5>37</s5>
</fC07>
<fC07 i1="05" i2="X" l="FRE">
<s0>Poumon pathologie</s0>
<s5>38</s5>
</fC07>
<fC07 i1="05" i2="X" l="ENG">
<s0>Lung disease</s0>
<s5>38</s5>
</fC07>
<fC07 i1="05" i2="X" l="SPA">
<s0>Pulmón patología</s0>
<s5>38</s5>
</fC07>
<fC07 i1="06" i2="X" l="FRE">
<s0>Virose</s0>
<s5>39</s5>
</fC07>
<fC07 i1="06" i2="X" l="ENG">
<s0>Viral disease</s0>
<s5>39</s5>
</fC07>
<fC07 i1="06" i2="X" l="SPA">
<s0>Virosis</s0>
<s5>39</s5>
</fC07>
<fC07 i1="07" i2="X" l="FRE">
<s0>Infection</s0>
</fC07>
<fC07 i1="07" i2="X" l="ENG">
<s0>Infection</s0>
</fC07>
<fC07 i1="07" i2="X" l="SPA">
<s0>Infección</s0>
</fC07>
<fN21>
<s1>328</s1>
</fN21>
<fN82>
<s1>PSI</s1>
</fN82>
</pA>
</standard>
</inist>
</record>

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