共 19 条
Rift Valley fever virus NSs mRNA is transcribed from an incoming anti-viral-sense S RNA segment
被引:70
作者:

Ikegami, T
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机构: Univ Texas, Med Branch, Dept Microbiol & Immunol, Galveston, TX 77555 USA

Won, S
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机构: Univ Texas, Med Branch, Dept Microbiol & Immunol, Galveston, TX 77555 USA

Peters, CJ
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机构: Univ Texas, Med Branch, Dept Microbiol & Immunol, Galveston, TX 77555 USA

Makino, S
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h-index: 0
机构:
Univ Texas, Med Branch, Dept Microbiol & Immunol, Galveston, TX 77555 USA Univ Texas, Med Branch, Dept Microbiol & Immunol, Galveston, TX 77555 USA
机构:
[1] Univ Texas, Med Branch, Dept Microbiol & Immunol, Galveston, TX 77555 USA
[2] Univ Texas, Med Branch, Dept Pathol, Galveston, TX 77550 USA
关键词:
D O I:
10.1128/JVI.79.18.12106-12111.2005
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
Analysis of purified Rift Valley fever virus (RVFV) particles demonstrated the presence of three negativesense RNA genomes, plus three anti-viral-sense RNA segments. The virion-associated anti-viral-sense S segment served as a template for the synthesis of NSs mRNA immediately after infection. NSs protein synthesis also occurred early in infection, suggesting that NSs protein produced early in infection probably has biologically significant roles in virus replication and/or survival in the host. Translation inhibitor treatment of mammalian cells infected with viruses belonging to the Bunyaviridae family generally inhibits viral mRNA synthesis. However, RVFV NSs mRNA synthesis, but not N mRNA synthesis, was resistant to puromycin treatment during primary transcription, pointing to the uniqueness of RVFV NSs mRNA synthesis.
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页码:12106 / 12111
页数:6
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