The immunomodulating V and W proteins of Nipah virus determine disease course

被引:72
作者
Satterfield, Benjamin A. [1 ,2 ]
Cross, Robert W. [1 ,2 ]
Fenton, Karla A. [1 ,2 ]
Agans, Krystle N. [1 ,2 ]
Basler, Christopher F. [3 ]
Geisbert, Thomas W. [1 ,2 ]
Mire, Chad E. [1 ,2 ]
机构
[1] Univ Texas Med Branch, Galveston Natl Lab, Galveston, TX 77555 USA
[2] Univ Texas Med Branch, Dept Microbiol & Immunol, Galveston, TX 77555 USA
[3] Icahn Sch Med Mt Sinai, Dept Microbiol, New York, NY 10029 USA
基金
美国国家卫生研究院;
关键词
HENIPAVIRUS INFECTION; RECENT PROGRESS; HAMSTER MODEL; PIG-FARMERS; P GENE; RIG-I; INTERFERON; ENCEPHALITIS; STAT1; HOST;
D O I
10.1038/ncomms8483
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The viral determinants that contribute to Nipah virus (NiV)-mediated disease are poorly understood compared with other paramyxoviruses. Here we use recombinant NiVs ( rNiVs) to examine the contributions of the NiV V and W proteins to NiV pathogenesis in a ferret model. We show that a V-deficient rNiV is susceptible to the innate immune response in vitro and behaves as a replicating non-lethal virus in vivo. Remarkably, rNiV lacking W expression results in a delayed and altered disease course with decreased respiratory disease and increased terminal neurological disease associated with altered in vitro inflammatory cytokine production. This study confirms the V protein as the major determinant of pathogenesis, also being the first in vivo study to show that the W protein modulates the inflammatory host immune response in a manner that determines the disease course.
引用
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页数:15
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