Direct sequencing of SARS-coronavirus S and N genes from clinical specimens shows limited variation.
Identifieur interne : 002C09 ( PubMed/Curation ); précédent : 002C08; suivant : 002C10Direct sequencing of SARS-coronavirus S and N genes from clinical specimens shows limited variation.
Auteurs : Suxiang Tong [États-Unis] ; Jairam R. Lingappa ; Qi Chen ; Bo Shu ; Ashley C. Lamonte ; Byron T. Cook ; Charryse Birge ; Shur-Wern Wang Chern ; Xin Liu ; Renee Galloway ; Le Quynh Mai ; Wai Fu Ng ; Jyh-Yuan Yang ; Jagdish Butany ; James A. Comer ; Stephan S. Monroe ; Suzanne R. Beard ; Thomas G. Ksiazek ; Dean Erdman ; Paul A. Rota ; Mark A. Pallansch ; Larry J. AndersonSource :
- The Journal of infectious diseases [ 0022-1899 ] ; 2004.
Descripteurs français
- KwdFr :
- ARN viral (génétique), ARN viral (isolement et purification), Glycoprotéine de spicule des coronavirus, Glycoprotéines membranaires (génétique), Génome viral, Humains, Mutation faux-sens, Mutation ponctuelle, Polymorphisme génétique, Protéines de l'enveloppe virale (génétique), Protéines nucléocapside (génétique), Substitution d'acide aminé (génétique), Syndrome respiratoire aigu sévère (virologie), Virus du SRAS (génétique), Virus du SRAS (isolement et purification).
- MESH :
- génétique : ARN viral, Glycoprotéines membranaires, Protéines de l'enveloppe virale, Protéines nucléocapside, Substitution d'acide aminé, Virus du SRAS.
- isolement et purification : ARN viral, Virus du SRAS.
- virologie : Syndrome respiratoire aigu sévère.
- Glycoprotéine de spicule des coronavirus, Génome viral, Humains, Mutation faux-sens, Mutation ponctuelle, Polymorphisme génétique.
English descriptors
- KwdEn :
- Amino Acid Substitution (genetics), Genome, Viral, Humans, Membrane Glycoproteins (genetics), Mutation, Missense, Nucleocapsid Proteins (genetics), Point Mutation, Polymorphism, Genetic, RNA, Viral (genetics), RNA, Viral (isolation & purification), SARS Virus (genetics), SARS Virus (isolation & purification), Severe Acute Respiratory Syndrome (virology), Spike Glycoprotein, Coronavirus, Viral Envelope Proteins (genetics).
- MESH :
- chemical , genetics : Membrane Glycoproteins, Nucleocapsid Proteins, RNA, Viral, Viral Envelope Proteins.
- genetics : Amino Acid Substitution, SARS Virus.
- chemical , isolation & purification : RNA, Viral, SARS Virus.
- virology : Severe Acute Respiratory Syndrome.
- Genome, Viral, Humans, Mutation, Missense, Point Mutation, Polymorphism, Genetic, Spike Glycoprotein, Coronavirus.
Abstract
Severe acute respiratory syndrome-associated coronavirus (SARS-CoV) emerged, in November 2002, as a novel agent causing severe respiratory illness. To study sequence variation in the SARS-CoV genome, we determined the nucleic acid sequence of the S and N genes directly from clinical specimens from 10 patients--1 specimen with no matched SARS-CoV isolate, from 2 patients; multiple specimens from 3 patients; and matched clinical-specimen/cell-culture-isolate pairs from 6 patients. We identified 3 nucleotide substitutions that were most likely due to natural variation and 2 substitutions that arose after cell-culture passage of the virus. These data demonstrate the overall stability of the S and N genes of SARS-CoV over 3 months during which a minimum of 4 generations for transmission events occurred. These findings are a part of the expanding investigation of the evolution of how this virus adapts to a new host.
DOI: 10.1086/422849
PubMed: 15319863
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pubmed:15319863Le document en format XML
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<front><div type="abstract" xml:lang="en">Severe acute respiratory syndrome-associated coronavirus (SARS-CoV) emerged, in November 2002, as a novel agent causing severe respiratory illness. To study sequence variation in the SARS-CoV genome, we determined the nucleic acid sequence of the S and N genes directly from clinical specimens from 10 patients--1 specimen with no matched SARS-CoV isolate, from 2 patients; multiple specimens from 3 patients; and matched clinical-specimen/cell-culture-isolate pairs from 6 patients. We identified 3 nucleotide substitutions that were most likely due to natural variation and 2 substitutions that arose after cell-culture passage of the virus. These data demonstrate the overall stability of the S and N genes of SARS-CoV over 3 months during which a minimum of 4 generations for transmission events occurred. These findings are a part of the expanding investigation of the evolution of how this virus adapts to a new host.</div>
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<Month>04</Month>
<Day>15</Day>
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<Issue>6</Issue>
<PubDate><Year>2004</Year>
<Month>Sep</Month>
<Day>15</Day>
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<Title>The Journal of infectious diseases</Title>
<ISOAbbreviation>J. Infect. Dis.</ISOAbbreviation>
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<ArticleTitle>Direct sequencing of SARS-coronavirus S and N genes from clinical specimens shows limited variation.</ArticleTitle>
<Pagination><MedlinePgn>1127-31</MedlinePgn>
</Pagination>
<Abstract><AbstractText>Severe acute respiratory syndrome-associated coronavirus (SARS-CoV) emerged, in November 2002, as a novel agent causing severe respiratory illness. To study sequence variation in the SARS-CoV genome, we determined the nucleic acid sequence of the S and N genes directly from clinical specimens from 10 patients--1 specimen with no matched SARS-CoV isolate, from 2 patients; multiple specimens from 3 patients; and matched clinical-specimen/cell-culture-isolate pairs from 6 patients. We identified 3 nucleotide substitutions that were most likely due to natural variation and 2 substitutions that arose after cell-culture passage of the virus. These data demonstrate the overall stability of the S and N genes of SARS-CoV over 3 months during which a minimum of 4 generations for transmission events occurred. These findings are a part of the expanding investigation of the evolution of how this virus adapts to a new host.</AbstractText>
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<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Tong</LastName>
<ForeName>Suxiang</ForeName>
<Initials>S</Initials>
<AffiliationInfo><Affiliation>National Center for Infectious Diseases, Centers for Disease Control and Prevention, 1600 Clifton Road NE, MS-G17, Atlanta, GA 30333, USA. sot1@cdc.gov</Affiliation>
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<Author ValidYN="Y"><LastName>Lingappa</LastName>
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<Author ValidYN="Y"><LastName>Anderson</LastName>
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<MeshHeading><DescriptorName UI="D045473" MajorTopicYN="N">SARS Virus</DescriptorName>
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<MeshHeading><DescriptorName UI="D045169" MajorTopicYN="N">Severe Acute Respiratory Syndrome</DescriptorName>
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<MeshHeading><DescriptorName UI="D064370" MajorTopicYN="N">Spike Glycoprotein, Coronavirus</DescriptorName>
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<MeshHeading><DescriptorName UI="D014759" MajorTopicYN="N">Viral Envelope Proteins</DescriptorName>
<QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName>
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<PubmedData><History><PubMedPubDate PubStatus="received"><Year>2004</Year>
<Month>01</Month>
<Day>13</Day>
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<PubMedPubDate PubStatus="accepted"><Year>2004</Year>
<Month>03</Month>
<Day>15</Day>
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<PubMedPubDate PubStatus="medline"><Year>2004</Year>
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<ArticleIdList><ArticleId IdType="pubmed">15319863</ArticleId>
<ArticleId IdType="doi">10.1086/422849</ArticleId>
<ArticleId IdType="pii">JID32367</ArticleId>
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