A Bacterial Effector Reveals the V-ATPase-ATG16L1 Axis that Initiates Xenophagy
Author(s) -
Yue Xu,
PingKun Zhou,
Sen Cheng,
Qiuhe Lu,
Kathrin Nowak,
Ann-Katrin Hopp,
Lin Li,
Xuyan Shi,
Zhiwei Zhou,
Wenqing Gao,
Da Li,
Huabin He,
Xiaoyun Liu,
Jingjin Ding,
Michael O. Hottiger,
Feng Shao
Publication year - 2019
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2019.06.007
Subject(s) - autophagy , atg16l1 , biology , vacuole , effector , intracellular parasite , microbiology and biotechnology , intracellular , bag3 , biochemistry , cytoplasm , apoptosis
Antibacterial autophagy (xenophagy) is an important host defense, but how it is initiated is unclear. Here, we performed a bacterial transposon screen and identified a T3SS effector SopF that potently blocked Salmonella autophagy. SopF was a general xenophagy inhibitor without affecting canonical autophagy. S. Typhimurium ΔsopF resembled S. flexneri ΔvirAΔicsB with the majority of intracellular bacteria targeted by autophagy, permitting a CRISPR screen that identified host V-ATPase as an essential factor. Upon bacteria-caused vacuolar damage, the V-ATPase recruited ATG16L1 onto bacteria-containing vacuole, which was blocked by SopF. Mammalian ATG16L1 bears a WD40 domain required for interacting with the V-ATPase. Inhibiting autophagy by SopF promoted S. Typhimurium proliferation in vivo. SopF targeted Gln124 of ATP6V0C in the V-ATPase for ADP-ribosylation. Mutation of Gln124 also blocked xenophagy, but not canonical autophagy. Thus, the discovery of SopF reveals the V-ATPase-ATG16L1 axis that critically mediates autophagic recognition of intracellular pathogen.
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