Literature DB >> 15977248

Recurrent mutations associated with isolation and passage of SARS coronavirus in cells from non-human primates.

Leo L M Poon1, Cynthia S W Leung, Kwok H Chan, Kwok Y Yuen, Yi Guan, Joseph S M Peiris.   

Abstract

Four clinical isolates of SARS coronavirus were serially passaged in two primate cell lines (FRhK4 and Vero E6). Viral genetic sequences encoding for structural proteins and open reading frames 6--8 were determined in the original clinical specimen, the initial virus isolate (passage 0) and at passages 5, 10, and 15. After 15 passages, a total of 15 different mutations were identified and 12 of them were non-synonymous mutations. Seven of these mutations were recurrent mutation and all located at the spike, membrane, and Orf 8a protein encoding sequences. Mutations in the membrane protein and a deletion in ORF 6--8 were already observed in passage 0, suggesting these amino acid substitutions are important in the adaptation of the virus isolate in primate cell culture. A mutation in the spike gene (residue 24079) appeared to be unique to adaptation in FRhK4 cells. It is important to be aware of cell culture associated mutations when interpreting data on molecular evolution of SARS coronavirus. (c) 2005 Wiley-Liss, Inc.

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Year:  2005        PMID: 15977248      PMCID: PMC7166449          DOI: 10.1002/jmv.20379

Source DB:  PubMed          Journal:  J Med Virol        ISSN: 0146-6615            Impact factor:   2.327


  19 in total

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Journal:  Proc Natl Acad Sci U S A       Date:  2004-10-20       Impact factor: 11.205

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Authors:  Xiaodong Xiao; Samitabh Chakraborti; Anthony S Dimitrov; Kosi Gramatikoff; Dimiter S Dimitrov
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Authors:  Wenhui Li; Michael J Moore; Natalya Vasilieva; Jianhua Sui; Swee Kee Wong; Michael A Berne; Mohan Somasundaran; John L Sullivan; Katherine Luzuriaga; Thomas C Greenough; Hyeryun Choe; Michael Farzan
Journal:  Nature       Date:  2003-11-27       Impact factor: 49.962

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  17 in total

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3.  Mouse-adapted MERS coronavirus causes lethal lung disease in human DPP4 knockin mice.

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6.  Amino acid substitutions in the s2 region enhance severe acute respiratory syndrome coronavirus infectivity in rat angiotensin-converting enzyme 2-expressing cells.

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7.  Synthetic reconstruction of zoonotic and early human severe acute respiratory syndrome coronavirus isolates that produce fatal disease in aged mice.

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8.  Human monoclonal antibody combination against SARS coronavirus: synergy and coverage of escape mutants.

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Journal:  PLoS Med       Date:  2006-07       Impact factor: 11.069

9.  The large 386-nt deletion in SARS-associated coronavirus: evidence for quasispecies?

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