Department of Pathology, Cambridge University, Tennis Court Road, Cambridge, CB21QP, UK.
Cell Host Microbe. 2012 Feb 16;11(2):129-39. doi: 10.1016/j.chom.2012.01.006.
Salmonella virulence effectors elicit host cell membrane ruffling to facilitate pathogen invasion. The WAVE regulatory complex (WRC) governs the underlying membrane-localized actin polymerization, but how Salmonella manipulates WRC is unknown. We show that Rho GTPase activation by the Salmonella guanine nucleotide exchange factor (GEF) SopE efficiently triggered WRC recruitment but not its activation, which required host Arf GTPase activity. Invading Salmonella recruited and activated Arf1 to facilitate ruffling and uptake. Arf3 and Arf6 could also enhance invasion. RNAi screening of host Arf-family GEFs revealed a key role for ARNO in pathogen invasion and generation of pathogen-containing macropinosomes enriched in Arf1 and WRC. Salmonella recruited ARNO via Arf6 and the phosphoinositide phosphatase effector SopB-induced PIP3 generation. ARNO in turn triggered WRC recruitment and activation, which was dramatically enhanced when SopE and ARNO cooperated. Thus, we uncover a mechanism by which pathogen and host GEFs synergize to regulate WRC and trigger Salmonella invasion.
沙门氏菌毒力效应子引发宿主细胞膜皱襞,促进病原体入侵。WAVE 调节复合物(WRC)控制着潜在的膜定位肌动蛋白聚合,但沙门氏菌如何操纵 WRC 尚不清楚。我们表明,沙门氏菌鸟嘌呤核苷酸交换因子(GEF) SopE 的 Rho GTPase 激活有效地触发了 WRC 的募集,但不触发其激活,这需要宿主 Arf GTPase 活性。入侵的沙门氏菌募集并激活 Arf1 以促进皱襞和摄取。Arf3 和 Arf6 也可以增强入侵。宿主 Arf 家族 GEF 的 RNAi 筛选揭示了 ARNO 在病原体入侵和富含 Arf1 和 WRC 的含有病原体的大吞噬体形成中的关键作用。沙门氏菌通过 Arf6 和磷酸肌醇磷酸酶效应子 SopB 诱导的 PIP3 生成招募 ARNO。ARNO 反过来触发 WRC 的募集和激活,当 SopE 和 ARNO 合作时,这种激活显著增强。因此,我们揭示了一种机制,即病原体和宿主 GEFs 协同调节 WRC 并触发沙门氏菌入侵。