Enterohaemorrhagic E. coli modulates an ARF6:Rab35 signaling axis to prevent recycling endosome maturation during infection

被引:16
作者
Furniss, R. Christopher D. [1 ]
Slater, Sabrina [1 ]
Frankel, Gad [1 ]
Clements, Abigail [1 ]
机构
[1] Imperial Coll London, Dept Life Sci, MRC Ctr Mol Bacteriol & Infect, London SW7 2AZ, England
基金
英国医学研究理事会;
关键词
Type 3 secretion system; EspG; host-pathogen interactions; small GTPase signaling; endosomal recycling; cargo trafficking; ENTEROPATHOGENIC ESCHERICHIA-COLI; III EFFECTORS ESPG; RAB GTPASES; PROTEIN; ARF6; MICROTUBULES; PERTURBATION; TRAFFICKING; RECRUITMENT; DISRUPTS;
D O I
10.1016/j.jmb.2016.05.023
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Enteropathogenic and enterohaemorrhagic Escherichia coli (EPEC/EHEC) manipulate a plethora of host cell processes to establish infection of the gut mucosa. This manipulation is achieved via the injection of bacterial effector proteins into host cells using a Type III secretion system. We have previously reported that the conserved EHEC and EPEC effector EspG disrupts recycling endosome function, reducing cell surface levels of host receptors through accumulation of recycling cargo within the host cell. Here we report that EspG interacts specifically with the small GTPases ARF6 and Rab35 during infection. These interactions target EspG to endosomes and prevent Rab35-mediated recycling of cargo to the host cell surface. Furthermore, we show that EspG has no effect on Rab35-mediated uncoating of newly formed endosomes, and instead leads to the formation of enlarged EspG/TfR/Rab11 positive, EEA1/Clathrin negative stalled recycling structures. Thus, this paper provides a molecular framework to explain how EspG disrupts recycling whilst also reporting the first known simultaneous targeting of ARF6 and Rab35 by a bacterial pathogen. (C) 2016 The Authors. Published by Elsevier Ltd. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
引用
收藏
页码:3399 / 3407
页数:9
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