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SARS coronavirus replicase proteins in pathogenesis
被引:111
作者:
Graham, Rachel L.
[1
,3
]
Sparks, Jennifer S.
[2
,3
]
Eckerle, Lance D.
[1
,2
,3
]
Sims, Amy C.
[4
]
Denison, Mark R.
[1
,2
,3
]
机构:
[1] Vanderbilt Univ, Med Ctr, Dept Pediat, Nashville, TN 37232 USA
[2] Vanderbilt Univ, Med Ctr, Dept Microbiol & Immunol, Nashville, TN USA
[3] Vanderbilt Univ, Med Ctr, Elizabeth B Lamb Ctr Pediat Res, Nashville, TN USA
[4] Univ N Carolina, Sch Publ Hlth, Dept Epidemiol, Chapel Hill, NC USA
基金:
美国国家卫生研究院;
关键词:
SARS coronavirus;
SARS-CoV;
replication;
pathogenesis;
reverse genetics;
protein processing;
temperature-sensitive mutants;
ts mutants;
D O I:
10.1016/j.virusres.2007.02.017
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
Much progress has been made in understanding the role of structural and accessory proteins in the pathogenesis of severe acute respiratory syndrome coronavirus (SARS-CoV) infections. The SARS epidemic also brought new attention to the proteins translated from ORF1a and ORF1b of the input genome RNA, also known as the replicase/transcriptase gene. Evidence for change within the ORF1ab coding sequence during the SARS epidemic, as well as evidence from studies with other coronaviruses, indicates that it is likely that the ORF1ab proteins play roles in virus pathogenesis distinct from or in addition to functions directly involved in viral replication. Recent reverse genetic studies have confirmed that proteins of ORF1ab may be involved in cellular signaling and modification of cellular gene expression, as well as virulence by mechanisms yet to be determined. Thus, the evolution of the OR-Flab proteins may be determined as much by issues of host range and virulence as they are by specific requirements for intracellular replication. (C) 2007 Published by Elsevier B.V.
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页码:88 / 100
页数:13
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