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The chromosomal nature of LT-II enterotoxins solved: a lambdoid prophage encodes both LT-II and one of two novel pertussis-toxin-like toxin family members in type II enterotoxigenic Escherichia coli

机译:解决了LT-II肠毒素的染色体性质:lambdoid噬菌体同时编码LT-II和II型肠毒素性大肠杆菌中两个新颖的百日咳毒素样毒素家族成员之一

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摘要

Heat-labile enterotoxins (LT) of enterotoxigenic Escherichia coli (ETEC) are structurally and functionally related to cholera toxin (CT). LT-I toxins are plasmid-encoded and flanked by IS elements, while LT-II toxins of type II ETEC are chromosomally encoded with flanking genes that appear phage related. Here, I determined the complete genomic sequence of the locus for the LT-IIa type strain SA53, and show that the LT-IIa genes are encoded by a 51 239 bp lambdoid prophage integrated at the rac locus, the site of a defective prophage in E. coli K12 strains. Of 50 LT-IIa and LT-IIc, 46 prophages also encode one member of two novel two-gene ADP-ribosyltransferase toxin families that are both related to pertussis toxin, which I named eplBA or ealAB, respectively. The eplBA and ealAB genes are syntenic with the Shiga toxin loci in their lambdoid prophages of the enteric pathogen enterohemorrhagic E. coli. These novel AB5 toxins show pertussis-toxin-like activity on tissue culture cells, and like pertussis toxin bind to sialic acid containing glycoprotein ligands. Type II ETEC are the first mucosal pathogens known to simultaneously produce two ADP-ribosylating toxins predicted to act on and modulate activity of both stimulatory and inhibitory alpha subunits of host cell heterotrimeric G-proteins.
机译:产肠毒素大肠杆菌(ETEC)的不耐热肠毒素(LT)在结构和功能上与霍乱毒素(CT)有关。 LT-1毒素是质粒编码的,并带有IS元件侧翼,而II型ETEC的LT-II毒素是用与噬菌体相关的侧翼基因进行染色体编码的。在这里,我确定了LT-IIa型菌株SA53的基因座的完整基因组序列,并显示LT-IIa基因由在rac基因座上整合的51 239 bp lambdoid噬菌体编码,该基因座是有缺陷的Prohage的位点。大肠杆菌K12菌株在50个LT-IIa和LT-IIc中,有46个噬菌体还编码两个与百日咳毒素相关的新颖的两基因ADP-核糖基转移酶毒素家族的一个成员,我分别将其命名为eplBA或ealAB。 eplBA和ealAB基因在它们的肠病原体肠出血性大肠杆菌的lambdoid噬菌体中与志贺毒素基因座同同。这些新颖的AB5毒素在组织培养细胞上显示出百日咳毒素样活性,并且像百日咳毒素一样与含有唾液酸的糖蛋白配体结合。 II型ETEC是已知同时产生两种ADP-核糖基化毒素的第一个粘膜病原体,这些毒素预计会作用于并调节宿主细胞异源三聚体G蛋白的刺激性和抑制性α亚基的活性。

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