Esterase D enhances type I interferon signal transduction to suppress foot-and-mouth disease virus replication. (July 2016)

• Record Type: Journal Article
• Authors: Li, Weiwei; Zhu, Zixiang; Cao, Weijun; Yang, Fan; Zhang, Xiangle; Li, Dan; Zhang, Keshan; Li, Pengfei; Mao, Ruoqing; Liu, Xiangtao; Zheng, Haixue
• Is Part Of: Molecular immunology. Volume 75(2016:Jul.)
• Page Start: 112
• Page End: 121
• Publication Date: 2016-07
• Subjects: Foot-and-mouth disease virus -- Esterase D -- IRF3 -- Interferon-stimulated genes -- Antiviral response; Immunochemistry -- Periodicals; Molecular biology -- Periodicals; Immunochemistry -- Periodicals; Allergy and Immunology -- Periodicals; Molecular Biology -- Periodicals; Immunochimie -- Périodiques; Biologie moléculaire -- Périodiques; Immunochemistry; Molecular biology; Periodicals; Electronic journals; 571.96
• DOI: 10.1016/j.molimm.2016.05.016
• Languages: English
• ISSNs: 0161-5890

Abstract

Highlights: FMDV infection induces the expression of esterase D (ESD) in PK-15 cells. ESD restricts FMDV replication in PK-15 cells. ESD enhances IFN-β signal transduction through promoting phosphorylation of IRF3. ESD suppresses FMDV replication through upregulation of various interferon-stimulated genes (ISGs). Abstract: The enzymatic activities of esterase D (ESD) are involved in many human diseases. However, no antiviral property of ESD has been described to date. Foot-and-mouth disease virus (FMDV) is the etiological agent of foot-and-mouth disease. In this study, we showed that FMDV infection triggered ESD expression. Overexpression of ESD significantly suppressed FMDV replication and knockdown of ESD expression enhanced virus replication, showing an essential antiviral role of ESD. Furthermore, we found that Sendai-virus-induced interferon (IFN) signaling was enhanced by upregulation of ESD, and ESD promoted activation of the IFN-β promoter simulated by IFN regulatory factor (IRF)3 or its upstream molecules (retinoic acid-inducible gene-I, melanoma differentiation-associated protein 5, virus-induced signaling adaptor and TANK binding kinase 1). Detailed analysis revealed that ESD protein enhanced IRF3 phosphorylation during FMDV infection. Overexpression of ESD also promoted the expression of various antiviral interferon-stimulated genes (ISGs) and knockdown of ESD impaired the expression of these antiviral genes during FMDV infection. Our findings demonstrate a new mechanism evolved by ESD to enhance type I IFN signal transduction and suppress viral replication during FMDV infection.