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

机译:铁氧还蛋白涉及大肠埃希氏大肠杆菌K1细胞质膜中细胞毒性坏死因子1的分泌。

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摘要

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)有助于大肠杆菌K1侵袭人脑微血管内皮细胞(HBMEC),并与HBMEC表面的受体相互作用。 CNF1是胞质蛋白,至今仍未完全了解CNF1是如何在大肠杆菌K1的内膜和外膜中分泌的。为了研究大肠杆菌K1中CNF1分泌的遗传决定因素,我们通过应用β-内酰胺酶作为报告基因来监测CNF1的分泌,进行了Tn5诱变筛选。我们确定了一个Tn5突变体,在培养上清液中没有β-内酰胺酶活性,并且其中突变的基因编码铁氧还蛋白基因(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。与CNF1突变体观察到的相似,fdx突变体显示出对HBMEC的入侵显着降低。通过与fdx互补,将fdx突变体的分泌CNF1和入侵HBMEC的失败恢复到亲本菌株的水平。这些发现首次证明了铁氧还蛋白与引起脑膜炎的大肠杆菌K1中内膜中CNF1的分泌有关。

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