Autophagy postpones apoptotic cell death in PRRSV infection through Bad-Beclin1 interaction. Issue 2 (17th February 2016)

• Record Type: Journal Article
• Authors: Zhou, Ao; Li, Shuaifeng; Khan, Faheem Ahmed; Zhang, Shujun
• Is Part Of: Virulence. Volume 7:Issue 2(2016)
• Page Start: 98
• Page End: 109
• Publication Date: 2016-02-17
• Subjects: Apoptosis -- Autophagy -- Beclin1 -- Bad -- Porcine reproductive and respiratory syndrome virus; Virulence (Microbiology) -- Periodicals; Bacterial diseases -- Periodicals; Molecular microbiology -- Periodicals; 579.05
• DOI: 10.1080/21505594.2015.1131381
• Languages: English
• ISSNs: 2150-5608

Abstract

Abstract : Autophagy and apoptosis play significant roles in PRRSV infection and replication. However, the interaction between these 2 processes in PRRSV replication is still far from been completely understood. In our studies, the exposure of MARC-145 cells to PRRSV confirmed the activation of autophagy and subsequent induction of apoptosis. The inhibition of autophagy by 3-methyladenine (3-MA) caused a significant increase in PRRSV-induced apoptosis, showing a potential connection between both mechanisms. Moreover, we observed an increase in Bad expression (a pro-apoptotic protein) and Beclin1 (an autophagy regulator) in virus-infected cells up to 36h. Co-immunoprecipitation assays showed the formation of Bad and Beclin1 complex in PRRSV infected cells. Accordingly, Bad co-localized with Beclin1 in MARC-145 infected cells. Knockdown of Beclin1 significantly decreased PRRSV replication and PRRSV-induced autophagy, while Bad silencing resulted in increased autophagy and enhanced viral replication. Furthermore, PRRSV infection phosphorylated Bad (Ser112) to promote cellular survival. These results demonstrate that autophagy can favor PRRSV replication by postponing apoptosis through the formation of a Bad-Beclin1 complex.