Highly permissive infection of microglial cells by Japanese encephalitis virus: a possible role as a viral reservoir

被引:56
作者
Thongtan, Thananya [2 ]
Cheepsunthorn, Poonlarp [3 ]
Chaiworakul, Voravasa [4 ]
Rattanarungsan, Chutima [2 ]
Wikan, Nitwara [1 ]
Smith, Duncan R. [1 ]
机构
[1] Mahidol Univ, Inst Mol Biosci, Mol Pathol Lab, Nakhon Pathom 73170, Thailand
[2] Chulalongkorn Univ, Dept Biochem, Bangkok 10330, Thailand
[3] Chulalongkorn Univ, Dept Anat, Bangkok 10330, Thailand
[4] Chulalongkorn Univ, Program Biomed Sci, Fac Med, Bangkok 10330, Thailand
关键词
Apoptosis; Japanese encephalitis virus; Microglia; Mouse; NEURONAL DEATH; INDUCED APOPTOSIS; NERVOUS-SYSTEM; HOST-CELLS; EXPRESSION; DENGUE; PERSISTENCE; ACTIVATION; MEDIATORS; CYTOKINE;
D O I
10.1016/j.micinf.2009.09.013
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Japanese encephalitis virus (JEV), a mosquito-borne Flavivirus, is a major cause of acute encephalitis, and neurons have been proposed to be the principle JEV target cells in the central nervous system. However, clinically, infection with JEV leads to increased levels of cytokines and chemokines in the serum and cerebrospinal fluid (CSF) the levels of which correlate with the mortality rate of patients. This research aimed to study the role of microglial cells in JEV infection. Mouse microglial cells (BV-2) supported the replication of JEV with extracellular production of virus by 10 h post-infection, and virus titer reached a maximum (2.55 x 10(10) pfu/ml) by day 3 post-infection. While apoptosis was induced in response to virus infection, no alteration in nitric oxide production was observed. Microglial cells remained productively infected with JEV for up to 16 weeks without significant morphological alterations, and the released virions were infectious to mouse neuroblastoma (NA) cells. The high virus production and long persistence of JEV in microglial cells suggests that these cells may serve as viral reservoirs for the infection of neurons in the CNS. (C) 2009 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:37 / 45
页数:9
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