Department of Pathology, University of California San Diego, La Jolla, CA, USA.
Department of Pediatrics, Division of Host-Microbe Systems and Therapeutics, University of California San Diego, LA Jolla, CA, USA.
Gut Microbes. 2021 Jan-Dec;13(1):1991776. doi: 10.1080/19490976.2021.1991776.
Host engulfment protein ELMO1 generates intestinal inflammation following internalization of enteric bacteria. In , bacterial effector IpgB1 interacts with ELMO1 and promotes bacterial invasion. IpgB1 belongs to the WxxxE effector family, a motif found in several effectors of enteric pathogens. Here, we have studied the role of WxxxE effectors, with emphasis on SifA and whether it interacts with ELMO1 to regulate inflammation. In-silico-analysis of WxxxE effectors was performed using BLAST search and Clustal W program. The interaction of ELMO1 with SifA was assessed by GST pulldown assay and co-immunoprecipitation. ELMO1 knockout mice, and ELMO1-depleted murine macrophage J774 cell lines were challenged with WT and mutant . Bacterial effectors containing the WxxxE motif were transfected in WT and ELMO1-depleted J774 cells to assess the inflammatory cytokines. ELMO1 generates differential pro-inflammatory cytokines between pathogenic and nonpathogenic bacteria. WxxxE motif is present in pathogens and in the TIR domain of host proteins. The C-terminal part of ELMO1 interacts with SifA where WxxxE motif is important for interaction. ELMO1-SifA interaction affects bacterial colonization, dissemination, and inflammatory cytokines . Moreover, ELMO1-SifA interaction increases TNF-α and IL-6 production from the macrophage cell line and is associated with enhanced Rac1 activity. ELMO1 also interacts with WxxxE effectors IpgB1, IpgB2, and Map and induces inflammation after challenge with microbes or microbial ligands. ELMO1 generates a differential response through interaction with the WxxxE motif, which is absent in commensals. ELMO1-WxxxE interaction plays a role in bacterial pathogenesis and induction of inflammatory response.
吞噬细胞 engulfment 蛋白 ELMO1 在摄取肠道细菌后会引发肠道炎症。在 ,细菌效应因子 IpgB1 与 ELMO1 相互作用并促进细菌入侵。IpgB1 属于 WxxxE 效应因子家族,该家族存在于几种肠道病原体的几种效应因子中。在这里,我们研究了 WxxxE 效应因子的作用,重点研究了 SifA 及其是否与 ELMO1 相互作用以调节炎症。使用 BLAST 搜索和 Clustal W 程序对 WxxxE 效应因子进行了计算机分析。通过 GST 下拉测定和共免疫沉淀评估了 ELMO1 与 SifA 的相互作用。用 WT 和 突变体 挑战 ELMO1 敲除小鼠和 ELMO1 耗尽的鼠巨噬细胞 J774 细胞系。将含有 WxxxE 基序的细菌效应因子转染到 WT 和 ELMO1 耗尽的 J774 细胞中,以评估炎症细胞因子。ELMO1 在病原体和宿主蛋白的 TIR 结构域中产生不同的促炎细胞因子。WxxxE 基序存在于病原体和宿主蛋白的 TIR 结构域中。ELMO1 的 C 末端与 SifA 相互作用,其中 WxxxE 基序对于相互作用很重要。ELMO1-SifA 相互作用影响细菌定植、传播和炎症细胞因子 。此外,ELMO1-SifA 相互作用增加了巨噬细胞系中 TNF-α 和 IL-6 的产生,并且与 Rac1 活性增强有关。ELMO1 还与 WxxxE 效应因子 IpgB1、IpgB2 和 Map 相互作用,并在受到微生物或微生物配体的挑战后引发炎症。ELMO1 通过与 WxxxE 基序相互作用产生不同的反应,而该基序在共生菌中不存在。ELMO1-WxxxE 相互作用在细菌发病机制和炎症反应诱导中起作用。