Unknown

Dataset Information

0

V. cholerae MakA is a cholesterol-binding pore-forming toxin that induces non-canonical autophagy.


ABSTRACT: Pore-forming toxins (PFTs) are important virulence factors produced by many pathogenic bacteria. Here, we show that the Vibrio cholerae toxin MakA is a novel cholesterol-binding PFT that induces non-canonical autophagy in a pH-dependent manner. MakA specifically binds to cholesterol on the membrane at pH < 7. Cholesterol-binding leads to oligomerization of MakA on the membrane and pore formation at pH 5.5. Unlike other cholesterol-dependent cytolysins (CDCs) which bind cholesterol through a conserved cholesterol-binding motif (Thr-Leu pair), MakA contains an Ile-Ile pair that is essential for MakA-cholesterol interaction. Following internalization, endosomal acidification triggers MakA pore-assembly followed by ESCRT-mediated membrane repair and V-ATPase-dependent unconventional LC3 lipidation on the damaged endolysosomal membranes. These findings characterize a new cholesterol-binding toxin that forms pores in a pH-dependent manner and reveals the molecular mechanism of host autophagy manipulation.

SUBMITTER: Jia X 

PROVIDER: S-EPMC9536202 | biostudies-literature | 2022 Dec

REPOSITORIES: biostudies-literature

altmetric image

Publications

V. cholerae MakA is a cholesterol-binding pore-forming toxin that induces non-canonical autophagy.

Jia Xiaotong X   Knyazeva Anastasia A   Zhang Yu Y   Castro-Gonzalez Sergio S   Nakamura Shuhei S   Carlson Lars-Anders LA   Yoshimori Tamotsu T   Corkery Dale P DP   Wu Yao-Wen YW  

The Journal of cell biology 20221004 12


Pore-forming toxins (PFTs) are important virulence factors produced by many pathogenic bacteria. Here, we show that the Vibrio cholerae toxin MakA is a novel cholesterol-binding PFT that induces non-canonical autophagy in a pH-dependent manner. MakA specifically binds to cholesterol on the membrane at pH < 7. Cholesterol-binding leads to oligomerization of MakA on the membrane and pore formation at pH 5.5. Unlike other cholesterol-dependent cytolysins (CDCs) which bind cholesterol through a cons  ...[more]

Similar Datasets

| S-EPMC1794277 | biostudies-literature
| S-EPMC10262753 | biostudies-literature
| S-EPMC8818996 | biostudies-literature
2010-07-29 | E-GEOD-19337 | biostudies-arrayexpress
2010-06-29 | GSE19337 | GEO
| S-EPMC8824476 | biostudies-literature
| S-EPMC8009392 | biostudies-literature
| S-EPMC6613103 | biostudies-literature
| S-EPMC10159106 | biostudies-literature
| S-EPMC7914777 | biostudies-literature