Type I Interferon Signaling Protects Mice From Lethal Henipavirus Infection

被引:63
作者
Dhondt, Kevin P. [1 ,2 ,3 ]
Mathieu, Cyrille [1 ,2 ,3 ]
Chalons, Marie [1 ,2 ,3 ]
Reynaud, Josephine M. [1 ,2 ,3 ]
Vallve, Audrey [4 ]
Raoul, Herve [4 ]
Horvat, Branka [1 ,2 ,3 ]
机构
[1] INSERM, U758, F-69365 Human Virology, France
[2] Ecole Normale Super Lyon, F-69364 Lyon, France
[3] Univ Lyon 1, F-69365 Lyon 07, France
[4] INSERM, Lab Jean Merieux P4, F-69365 Lyon, France
关键词
Nipah virus; Hendra virus; type I interferon; animal model; encephalitis; HENDRA VIRUS-INFECTION; NIPAH VIRUS; NEUTRALIZING ANTIBODIES; HAMSTER MODEL; PATHOGENESIS; MORBILLIVIRUS; CORONAVIRUS; RESPONSES; SURVIVAL; DEATH;
D O I
10.1093/infdis/jis653
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Hendra virus (HeV) and Nipah virus (NiV) are closely related, recently emerged paramyxoviruses that form Henipavirus genus and are capable of causing considerable morbidity and mortality in a number of mammalian species, including humans. However, in contrast to many other species and despite expression of functional virus entry receptors, mice are resistant to henipavirus infection. We report here the susceptibility of mice deleted for the type I interferon receptor (IFNAR-KO) to both HeV and NiV. Intraperitoneally infected mice developed fatal encephalitis, with pathology and immunohistochemical features similar to what was found in humans. Viral RNA was found in the majority of analyzed organs, and sublethally infected animals developed virus-specific neutralizing antibodies. Altogether, these results reveal IFNAR-KO mice as a new small animal model to study HeV and NiV pathogenesis, prophylaxis, and treatment and suggest the critical role of type I interferon signaling in the control of henipavirus infection.
引用
收藏
页码:142 / 151
页数:10
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