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首页> 外文期刊>Journal of Molecular Biology >Enterohaemorrhagic E. coli modulates an ARF6:Rab35 signaling axis to prevent recycling endosome maturation during infection
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Enterohaemorrhagic E. coli modulates an ARF6:Rab35 signaling axis to prevent recycling endosome maturation during infection

机译:肠出血性大肠杆菌调节ARF6:Rab35信号转导轴,以防止感染期间内体成熟的再循环

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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/).
机译:肠致病性和肠出血性大肠杆菌(EPEC / EHEC)操纵大量宿主细胞过程以建立肠道粘膜感染。这种操纵是通过使用III型分泌系统将细菌效应蛋白注入宿主细胞来实现的。我们以前曾报道过,保守的EHEC和EPEC效应子EspG破坏了回收内体功能,通过在宿主细胞内积聚回收货物来降低宿主受体的细胞表面水平。在这里,我们报道EspG在感染过程中与小GTPases ARF6和Rab35特异性相互作用。这些相互作用将EspG靶向内体,并阻止Rab35介导的货物再循环到宿主细胞表面。此外,我们显示EspG对Rab35介导的新形成的内体的脱膜没有作用,而是导致形成扩大的EspG / TfR / Rab11阳性,EEA1 / Clathrin阴性失速的再循环结构。因此,本文提供了一个分子框架来解释EspG如何破坏回收,同时还报告了细菌病原体首次同时靶向ARF6和Rab35。 (C)2016作者。由Elsevier Ltd.发行。这是CC BY许可下的开放访问文章(http://creativecommons.org/licenses/by/4.0/)。

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