posted on 2016-01-27, 00:00authored byAM Yakoub, D. Shukla
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.
Funding
This study was supported by a NIH grant (EY023058) to D.S. and a core grant (EY01792).
The authors claim no conflicts of interest.