Basal Autophagy Is Required for Herpes simplex Virus-2 Infection

被引:37
作者
Yakoub, Abraam M. [1 ,2 ]
Shukla, Deepak [1 ,2 ]
机构
[1] Univ Illinois, Dept Microbiol & Immunol, Chicago, IL 60612 USA
[2] Univ Illinois, Med Ctr, Dept Ophthalmol & Visual Sci, Chicago, IL 60612 USA
关键词
CONSTITUTIVE AUTOPHAGY; MAMMALIAN AUTOPHAGY; INHIBITION; TYPE-2; NEUROVIRULENCE; MICE; EPIDEMIOLOGY; PROTEINS; GROWTH; ENTRY;
D O I
10.1038/srep12985
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
Autophagy is a conserved catabolic process of the cell, which plays an important role in regulating plethora of infections. The role of autophagy in Herpes simplex virus-2 (HSV-2) infection is unknown. Here, we found that HSV-2 does not allow induction of an autophagic response to infection, but maintains basal autophagy levels mostly unchanged during productive infection. Thus, we investigated the importance of basal autophagy for HSV-2 infection, using pharmacological autophagy suppression or cells genetically deficient in an autophagy-essential gene (ATG5). Interference with basal autophagy flux in cells significantly reduced viral replication and diminished the infection. These results indicate that basal autophagy plays an indispensable role required for a productive infection. Importantly, this study draws a sharp distinction between induced and basal autophagy, where the former acts as a viral clearance mechanism abrogating infection, while the latter supports infection.
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页数:13
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