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Inhibition of autophagy by 3‐methyladenine restricts murine cytomegalovirus replication
Author(s) -
Zhang Xinyan,
Zhang Linlin,
Bi Yidan,
Xi Ting,
Zhang Zhan,
Huang Yuan,
Lu Yuan Yuan,
Liu Xinglou,
Shu Sainan,
Fang Feng
Publication year - 2021
Publication title -
journal of medical virology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.782
H-Index - 121
eISSN - 1096-9071
pISSN - 0146-6615
DOI - 10.1002/jmv.26787
Subject(s) - virology , cytomegalovirus , replication (statistics) , human cytomegalovirus , biology , viral replication , autophagy , virus , herpesviridae , viral disease , genetics , apoptosis
Cytomegalovirus (CMV) induced autophagy affects virus replication and survival of the infected cells. The purpose of this study was to investigate the role of autophagy inhibition by 3‐methyladenine (3‐MA) on murine cytomegalovirus (MCMV) replication and whether it is associated with caspase‐3 dependent apoptosis. The eyecup isolated from adult C57BL/6J mice (6–8 weeks old) and mouse embryo fibroblast cells (MEFs) were infected with MCMV K181 strain, followed by the treatment of 3‐methyladenine (3‐MA), chloroquine, or rapamycin to block or stimulate autophagy. In cultured MEFs, the ratio of LC3I/II was reduced at 24 hours post infection (hpi), but was increased at 48 hpi In the eyecup culture, LC3I/II ratio was also decreased at 4 and 7 days post infection (dpi). In addition, caspase‐3 cleavage was increased at 48 hpi in MEFs and also elevated in MCMV infected eyecups at 4, 7, 10, and 14 dpi. 3‐MA treatment significantly inhibited the virus replication in MEFs and eyecups. The expression of early antigen (EA) of MCMV was also decreased in MEFs and eyecups. Meanwhile, cleaved caspase‐3 dependent cell death was promoted with the presence of 3‐MA in MCMV infected MEFs and eyecups, while RIPK1/RIPK3/MLKL pathway was inhibited by 3‐MA in eyecups. Inhibition of autophagy by 3‐MA restricts virus replication and promotes caspase‐3 dependent apoptosis in the eyecup and MEFs with MCMV infection. It can be explained that during the early period of MCMV infection, the suppressed autophagy process directly reduced virus release, but later caspase‐3 dependent apoptosis dominated and resulted in decreased virus replication.