Determination of the henipavirus phosphoprotein gene mRNA editing frequencies and detection of the C, V and W proteins of Nipah virus in virus-infected cells

被引:59
作者
Lo, Michael K. [1 ,2 ,4 ,5 ]
Harcourt, Brian H. [1 ]
Mungall, Bruce A. [3 ]
Tamin, Azaibi [1 ]
Peeples, Mark E. [4 ,5 ]
Bellini, William J. [1 ]
Rota, Paul A. [1 ]
机构
[1] Measles Mumps Rubella & Herpesviruses Lab Branch, Atlanta, GA 30333 USA
[2] Emory Univ, Sch Med, Dept Microbiol & Immunol, Atlanta, GA 30322 USA
[3] Commonwealth Sci Ind Res Org, Australian Anim Hlth Lab, Geelong, Vic, Australia
[4] Nationwide Childrens Hosp, Res Inst, Ctr Vaccines & Immun, Columbus, OH 43205 USA
[5] Ohio State Univ, Coll Med, Dept Pediat, Columbus, OH 43205 USA
关键词
MEASLES-VIRUS; SENDAI-VIRUS; HENDRA-VIRUS; MINIGENOME REPLICATION; WILD-TYPE; NUCLEAR ACCUMULATION; ABATTOIR WORKERS; PREVENTING STAT1; P-PROTEIN; INTERFERON;
D O I
10.1099/vir.0.007294-0
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The henipaviruses, Nipah virus (NiV) and Hendra virus (HeV), are highly pathogenic zoonotic paramyxoviruses. Like many other paramyxoviruses, henipaviruses employ a process of co-transcriptional mRNA editing during transcription of the phosphoprotein (P) gene to generate additional mRNAs encoding the V and W proteins. The C protein is translated from the P mRNA, but in an alternate reading frame. Sequence analysis of multiple, cloned mRNAs showed that the mRNA editing frequencies of the P genes of the henipaviruses are higher than those reported for other paramyxoviruses. Antisera to synthetic peptides from the P, V, W and C proteins of NiV were generated to study their expression in infected cells. All proteins were detected in both infected cells and purified virions. In infected cells, the W protein was detected in the nucleus while P, V and C were found in the cytoplasm.
引用
收藏
页码:398 / 404
页数:7
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