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Porcine Reproductive and Respiratory Syndrome Virus nsp5 Induces Incomplete Autophagy by Impairing the Interaction of STX17 and SNAP29

Yanrong Zhou, Yang Li, Ran Tao, Jia Li, Liurong Fang, Shaobo Xiao

2023Microbiology Spectrum23 citationsDOIOpen Access PDF

Abstract

A substantial number of viruses have been demonstrated to utilize or hijack autophagy to benefit their replication. In the case of porcine reproductive and respiratory syndrome virus (PRRSV), previous studies have demonstrated the proviral effects of autophagy on PRRSV proliferation. Thus, an investigation of the mechanism by which PRRSV regulates the autophagy processes can provide new insight into viral pathogenesis. Autophagic flux is a dynamic process that consists of autophagosome formation and subsequent lysosomal degradation. However, the exact effect of PRRSV infection on the autophagic flux remains disputed. In this study, we demonstrated that PRRSV infection, as well as PRRSV nsp5 overexpression, inhibited the interaction of STX17 with SNAP29 to impair the fusion of autophagosomes with lysosomes, thereby blocking autophagic flux. This information will help us to understand PRRSV-host interactions and unravel new targets for PRRS prevention and control.

Topics & Concepts

AutophagyRespiratory systemBiologyVirusPorcine reproductive and respiratory syndrome virusCell biologyVirologyGeneticsAnatomyApoptosisAnimal Virus Infections StudiesPlant Virus Research StudiesVirus-based gene therapy research