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| Research article summary (published 30 Aug 2009): |
Dual functions of Rift Valley fever virus NSs protein: inhibition of host mRNA transcription and post-transcriptional downregulation of protein kinase PKR.
Full Abstract
Rift Valley fever virus (RVFV), which belongs to the genus Phlebovirus, family Bunyaviridae, is a negative-stranded RNA virus carrying a single-stranded, tripartite RNA genome. RVFV is an important zoonotic pathogen transmitted by mosquitoes and causes large outbreaks among ruminants and humans in Africa and the Arabian Peninsula. Human patients develop an acute febrile illness, followed by a fatal hemorrhagic fever, encephalitis, or ocular diseases. A viral nonstructural protein, NSs, is a major viral virulence factor. Past studies showed that NSs suppresses the transcription of host mRNAs, including interferon-beta mRNAs. Here we demonstrated that the NSs protein induced post-transcriptional downregulation of dsRNA-dependent protein kinase (PKR), to prevent phosphorylation of eIF2alpha and promoted viral translation in infected cells. These two biological activities of the NSs most probably have a synergistic effect in suppressing host innate immune functions and facilitate efficient viral replication in infected mammalian hosts.
Author information
Author/s: Ikegami, Tetsuro (T); Narayanan, Krishna (K); Won, Sungyong (S); Kamitani, Wataru (W); Peters, C J (CJ); Makino, Shinji (S);
Affiliation: Department of Microbiology and Immunology, The University of Texas Medical Branch at Galveston, Galveston, Texas 77555-0438, USA. teikegam(-atsign-)utmb.edu
Grants: U54 AI057156 (Agency:NIAID NIH HHS)
Journal and publication information
Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
Journal: Annals of the New York Academy of Sciences (Ann N Y Acad Sci), published in United States. (Language: eng)
Reference: 2009-Sep; vol 1171 Suppl 1 (issue ) : pp E75-85
Dates: Created 2009/09/15; Completed 2009/10/23;
PMID: 19751406, status: MEDLINE (last retrieval date: 10/23/2009, IMS Date: )
Sourced from the National Library of Medicine. Abstract text and other information may be subject to copyright.
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