Serveur d'exploration SRAS

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Genomic diversity of SARS-CoV-2 in Coronavirus Disease 2019 patients.

Identifieur interne : 000482 ( PubMed/Checkpoint ); précédent : 000481; suivant : 000483

Genomic diversity of SARS-CoV-2 in Coronavirus Disease 2019 patients.

Auteurs : Zijie Shen [République populaire de Chine] ; Yan Xiao [République populaire de Chine] ; Lu Kang [République populaire de Chine] ; Wentai Ma [République populaire de Chine] ; Leisheng Shi [République populaire de Chine] ; Li Zhang [République populaire de Chine] ; Zhuo Zhou [République populaire de Chine] ; Jing Yang [République populaire de Chine] ; Jiaxin Zhong [République populaire de Chine] ; Donghong Yang [République populaire de Chine] ; Li Guo [République populaire de Chine] ; Guoliang Zhang [République populaire de Chine] ; Hongru Li [République populaire de Chine] ; Yu Xu [République populaire de Chine] ; Mingwei Chen [République populaire de Chine] ; Zhancheng Gao [République populaire de Chine] ; Jianwei Wang [République populaire de Chine] ; Lili Ren [République populaire de Chine] ; Mingkun Li [République populaire de Chine]

Source :

RBID : pubmed:32129843

Abstract

A novel coronavirus (SARS-CoV-2) has infected more than 75,000 individuals and spread to over 20 countries. It is still unclear how fast the virus evolved and how the virus interacts with other microorganisms in the lung.

DOI: 10.1093/cid/ciaa203
PubMed: 32129843


Affiliations:


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pubmed:32129843

Le document en format XML

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<nlm:affiliation>Department of Respiratory and Critical Care Medicine, the First Affiliated Hospital of Xi'an Jiaotong University, Shaanxi Province, P.R. China.</nlm:affiliation>
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<name sortKey="Gao, Zhancheng" sort="Gao, Zhancheng" uniqKey="Gao Z" first="Zhancheng" last="Gao">Zhancheng Gao</name>
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<nlm:affiliation>Department of Respiratory and Critical Care Medicine, Peking University People's Hospital, Beijing, China.</nlm:affiliation>
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<name sortKey="Wang, Jianwei" sort="Wang, Jianwei" uniqKey="Wang J" first="Jianwei" last="Wang">Jianwei Wang</name>
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<name sortKey="Ren, Lili" sort="Ren, Lili" uniqKey="Ren L" first="Lili" last="Ren">Lili Ren</name>
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<name sortKey="Li, Mingkun" sort="Li, Mingkun" uniqKey="Li M" first="Mingkun" last="Li">Mingkun Li</name>
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<country xml:lang="fr">République populaire de Chine</country>
<wicri:regionArea>Key Laboratory of Genomic and Precision Medicine, Beijing Institute of Genomics, Chinese Academy of Sciences, and China National Center for Bioinformation, Beijing</wicri:regionArea>
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<title level="j">Clinical infectious diseases : an official publication of the Infectious Diseases Society of America</title>
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<date when="2020" type="published">2020</date>
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<div type="abstract" xml:lang="en">A novel coronavirus (SARS-CoV-2) has infected more than 75,000 individuals and spread to over 20 countries. It is still unclear how fast the virus evolved and how the virus interacts with other microorganisms in the lung.</div>
</front>
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<DateRevised>
<Year>2020</Year>
<Month>04</Month>
<Day>03</Day>
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<ISSN IssnType="Electronic">1537-6591</ISSN>
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<Year>2020</Year>
<Month>Mar</Month>
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<Title>Clinical infectious diseases : an official publication of the Infectious Diseases Society of America</Title>
<ISOAbbreviation>Clin. Infect. Dis.</ISOAbbreviation>
</Journal>
<ArticleTitle>Genomic diversity of SARS-CoV-2 in Coronavirus Disease 2019 patients.</ArticleTitle>
<ELocationID EIdType="pii" ValidYN="Y">ciaa203</ELocationID>
<ELocationID EIdType="doi" ValidYN="Y">10.1093/cid/ciaa203</ELocationID>
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<AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">A novel coronavirus (SARS-CoV-2) has infected more than 75,000 individuals and spread to over 20 countries. It is still unclear how fast the virus evolved and how the virus interacts with other microorganisms in the lung.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">We have conducted metatranscriptome sequencing for the bronchoalveolar lavage fluid of eight SARS-CoV-2 patients, 25 community-acquired pneumonia (CAP) patients, and 20 healthy controls.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">The median number of intra-host variants was 1-4 in SARS-CoV-2 infected patients, which ranged between 0 and 51 in different samples. The distribution of variants on genes was similar to those observed in the population data (110 sequences). However, very few intra-host variants were observed in the population as polymorphism, implying either a bottleneck or purifying selection involved in the transmission of the virus, or a consequence of the limited diversity represented in the current polymorphism data. Although current evidence did not support the transmission of intra-host variants in a person-to-person spread, the risk should not be overlooked. The microbiota in SARS-CoV-2 infected patients was similar to those in CAP, either dominated by the pathogens or with elevated levels of oral and upper respiratory commensal bacteria.</AbstractText>
<AbstractText Label="CONCLUSION" NlmCategory="CONCLUSIONS">SARS-CoV-2 evolves in vivo after infection, which may affect its virulence, infectivity, and transmissibility. Although how the intra-host variant spreads in the population is still elusive, it is necessary to strengthen the surveillance of the viral evolution in the population and associated clinical changes.</AbstractText>
<CopyrightInformation>© The Author(s) 2020. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com.</CopyrightInformation>
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<AffiliationInfo>
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