Direct sequencing of SARS-coronavirus S and N genes from clinical specimens shows limited variation

  • Suxiang Tong
  • , Jairam R. Lingappa
  • , Qi Chen
  • , Bo Shu
  • , Ashley C. LaMonte
  • , Byron T. Cook
  • , Charryse Birge
  • , Wang Chern Shur-Wern
  • , Xin Liu
  • , Renee Galloway
  • , Quynh Mai Le
  • , Fu Ng Wai
  • , 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. Anderson

Research output: Contribution to journalArticlepeer-review

9 Scopus citations

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.

Original languageEnglish (US)
Pages (from-to)1127-1131
Number of pages5
JournalJournal of Infectious Diseases
Volume190
Issue number6
DOIs
StatePublished - Sep 15 2004
Externally publishedYes

ASJC Scopus subject areas

  • General Medicine

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