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Ferredoxin Is Involved in Secretion of Cytotoxic Necrotizing Factor 1 across the Cytoplasmic Membrane in Escherichia coli K1

机译:铁氧还蛋白参与大肠埃希菌K1细胞质膜中细胞毒性坏死因子1的分泌。

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We previously showed that cytotoxic necrotizing factor 1 (CNF1) contributes to Escherichia coli K1 invasion of human brain microvascular endothelial cells (HBMEC) and interacts with the receptor on the surface of HBMEC. CNF1 is the cytoplasmic protein, and it remains incompletely understood how CNF1 is secreted across the inner and outer membranes in E. coli K1. In order to investigate the genetic determinants for secretion of CNF1 in E. coli K1, we performed Tn5 mutagenesis screening by applying β-lactamase as a reporter to monitor secretion of CNF1. We identified a Tn5 mutant that exhibited no β-lactamase activity in the culture supernatant and in which the mutated gene encodes a ferredoxin gene (fdx). In the fdx deletion mutant, there was no evidence of translocation of CNF1 into HBMEC. Western blot analysis of the fdx deletion mutant revealed that ferredoxin is involved in translocation of CNF1 across the cytoplasmic membrane. The fdx mutant exhibited significantly decreased invasion of HBMEC, similar to the decreased HBMEC invasion observed with the CNF1 mutant. The failures to secrete CNF1 and invade HBMEC of the fdx mutant were restored to the levels of the parent strain by complementation with fdx. These findings demonstrate for the first time that ferredoxin is involved in secretion of CNF1 across the inner membrane in meningitis-causing E. coli K1.
机译:我们先前显示,细胞毒性坏死因子1(CNF1)导致人脑微血管内皮细胞(HBMEC)侵染大肠杆菌K1,并与HBMEC表面的受体相互作用。 CNF1是细胞质蛋白,至今仍未完全了解CNF1如何在E中跨内膜和外膜分泌。大肠杆菌 K1。为了调查 E中CNF1分泌的遗传决定因素。在大肠杆菌K1中,我们以β-内酰胺酶为报告基因,监测CNF1的分泌,进行Tn 5 诱变筛选。我们鉴定出一个Tn 5 突变体,该突变体在培养上清液中不显示β-内酰胺酶活性,并且其中的突变基因编码一个铁氧还蛋白基因( fdx )。在 fdx 缺失突变体中,没有证据表明CNF1易位到HBMEC。对 fdx 缺失突变体的蛋白质印迹分析表明,铁氧还蛋白与CNF1跨细胞质膜的转运有关。 fdx 突变体对HBMEC的侵袭显着降低,类似于CNF1突变体对HBMEC侵袭的降低。通过与 fdx 互补,将分泌 fdx 突变体的CNF1和入侵HBMEC的失败恢复到亲本菌株的水平。这些发现首次证明铁氧还蛋白在引起脑膜炎的 E中参与CNF1跨内膜的分泌。大肠杆菌 K1。

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