Cell Entry of Porcine Epidemic Diarrhea Coronavirus Is Activated by Lysosomal Proteases

• Published in: The Journal of biological chemistry 2016-11, Vol.291 (47), p.24779-24786
• Main Authors: Liu, Chang, Ma, Yuanmei, Yang, Yang, Zheng, Yuan, Shang, Jian, Zhou, Yusen, Jiang, Shibo, Du, Lanying, Li, Jianrong, Li, Fang
• Format: Article
• Language: English
• Subjects: Animals; Cathepsin B - metabolism; Cathepsin L - metabolism; Cell Line; cysteine protease; Humans; Lysosomes - enzymology; Lysosomes - virology; membrane fusion; Microbiology; Porcine epidemic diarrhea virus - physiology; protease inhibitor; proteolysis; Spike Glycoprotein, Coronavirus - metabolism; Swine; virus entry; Virus Internalization
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1074/jbc.M116.740746

Porcine epidemic diarrhea coronavirus (PEDV) is currently devastating the United States pork industry by causing an 80–100% fatality rate in infected piglets. Coronavirus spike proteins mediate virus entry into cells, a process that requires the spike proteins to be proteolytically activated. It has been a conundrum which proteases activate PEDV entry. Here we systematically investigated the roles of different proteases in PEDV entry using pseudovirus entry, biochemical, and live virus infection assays. We found that the PEDV spike is activated by lysosomal cysteine proteases but not proprotein convertases or cell surface serine proteases. Extracellular trypsin activates PEDV entry when lysosomal cysteine proteases are inhibited. We further pinpointed cathepsin L and cathepsin B as the lysosomal cysteine proteases that activate the PEDV spike. These results advance our understanding of the molecular mechanism for PEDV entry and identify potential antiviral targets for curbing the spread of PEDV.