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Direct sequencing of SARS-coronavirus S and N genes from clinical specimens shows limited variation.
Tong, Suxiang; Lingappa, Jairam R; Chen, Qi; Shu, Bo; LaMonte, Ashley C; Cook, Byron T; Birge, Charryse; Chern, Shur-wern Wang; Liu, Xin; Galloway, Renee; Mai, Le Quynh; Ng, Wai Fu; Yang, Jyh-Yuan; Butany, Jagdish; Comer, James A; Monroe, Stephan S; Beard, Suzanne R; Ksiazek, Thomas G; Erdman, Dean; Rota, Paul A; Pallansch, Mark A; Anderson, Larry J.
Affiliation
  • Tong S; National Center for Infectious Diseases, Centers for Disease Control and Prevention, 1600 Clifton Road NE, MS-G17, Atlanta, GA 30333, USA. sot1@cdc.gov
J Infect Dis ; 190(6): 1127-31, 2004 Sep 15.
Article in En | MEDLINE | ID: mdl-15319863
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.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: RNA, Viral / Membrane Glycoproteins / Viral Envelope Proteins / Nucleocapsid Proteins / Severe Acute Respiratory Syndrome / Severe acute respiratory syndrome-related coronavirus Type of study: Prognostic_studies Limits: Humans Language: En Journal: J Infect Dis Year: 2004 Document type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: RNA, Viral / Membrane Glycoproteins / Viral Envelope Proteins / Nucleocapsid Proteins / Severe Acute Respiratory Syndrome / Severe acute respiratory syndrome-related coronavirus Type of study: Prognostic_studies Limits: Humans Language: En Journal: J Infect Dis Year: 2004 Document type: Article Affiliation country: United States
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