Actin Assembly around the Shigella-Containing Vacuole Promotes Successful Infection.

Abstract:

:The enteroinvasive bacterium Shigella flexneri forces its uptake into non-phagocytic host cells through the translocation of T3SS effectors that subvert the actin cytoskeleton. Here, we report de novo actin polymerization after cellular entry around the bacterium-containing vacuole (BCV) leading to the formation of a dynamic actin cocoon. This cocoon is thicker than any described cellular actin structure and functions as a gatekeeper for the cytosolic access of the pathogen. Host CDC42, TOCA-1, N-WASP, WIP, the Arp2/3 complex, cortactin, coronin, and cofilin are recruited to the actin cocoon. They are subverted by T3SS effectors, such as IpgD, IpgB1, and IcsB. IcsB immobilizes components of the actin polymerization machinery at the BCV dependent on its fatty acyltransferase activity. This represents a unique microbial subversion strategy through localized entrapment of host actin regulators causing massive actin assembly. We propose that the cocoon promotes subsequent invasion steps for successful Shigella infection.

journal_name

Cell Rep

journal_title

Cell reports

authors

Kühn S,Bergqvist J,Gil M,Valenzuela C,Barrio L,Lebreton S,Zurzolo C,Enninga J

doi

10.1016/j.celrep.2020.107638

subject

Has Abstract

pub_date

2020-05-12 00:00:00

pages

107638

issue

6

issn

2211-1247

pii

S2211-1247(20)30591-X

journal_volume

31

pub_type

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