Yakoub Abraam M, Shukla Deepak
1] Department of Microbiology and Immunology, University of Illinois, Chicago. IL USA, 60612 [2] Department of Ophthalmology and Visual Sciences, University of Illinois Medical Center, Chicago. IL USA, 60612.
Sci Rep. 2015 Apr 9;5:9730. doi: 10.1038/srep09730.
Herpes simplex virus-1 (HSV-1) is a double-stranded DNA virus that causes life-long infections. HSV-1 infections may lead to herpetic stromal keratitis that may advance to corneal blindness. HSV-1 infections can also cause fatal conditions, such as herpes encephalitis, or neonatal disease. A major virulence mechanism of HSV-1 is the control of autophagy, an innate immune defense strategy that could otherwise degrade viral particles. Here, to investigate a new mechanism for antiviral therapy, we tested the effect of various autophagy inducers (physiological and pharmacological) on infection. Autophagy stimulation was confirmed to significantly suppress HSV-1 infection in various cell types, without affecting cell viability. This study establishes the importance of autophagy for regulating HSV-1 infection, and provides a proof-of-principle evidence for a novel antiviral mechanism.
单纯疱疹病毒1型(HSV-1)是一种双链DNA病毒,可导致终身感染。HSV-1感染可能会引发疱疹性基质性角膜炎,进而发展为角膜盲。HSV-1感染还可能导致致命疾病,如疱疹性脑炎或新生儿疾病。HSV-1的一种主要致病机制是对自噬的控制,自噬是一种先天性免疫防御策略,否则可能会降解病毒颗粒。在此,为了研究抗病毒治疗的新机制,我们测试了各种自噬诱导剂(生理性和药理学性)对感染的影响。自噬刺激被证实可显著抑制多种细胞类型中的HSV-1感染,而不影响细胞活力。本研究确立了自噬对调节HSV-1感染的重要性,并为一种新型抗病毒机制提供了原理性证据。