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大肠杆菌O91:H21菌株B2F1中可激活的2d型志贺毒素基因的两个拷贝之一与一种可诱导噬菌体相关。

One of two copies of the gene for the activatable shiga toxin type 2d in Escherichia coli O91:H21 strain B2F1 is associated with an inducible bacteriophage.

作者信息

Teel Louise D, Melton-Celsa Angela R, Schmitt Clare K, O'Brien Alison D

机构信息

Department of Microbiology and Immunology, Uniformed Services University of the Health Sciences, Bethesda, Maryland 20814, USA.

出版信息

Infect Immun. 2002 Aug;70(8):4282-91. doi: 10.1128/IAI.70.8.4282-4291.2002.

Abstract

Shiga toxin (Stx) types 1 and 2 are encoded within intact or defective temperate bacteriophages in Stx-producing Escherichia coli (STEC), and expression of these toxins is linked to bacteriophage induction. Among Stx2 variants, only stx(2e) from one human STEC isolate has been reported to be carried within a toxin-converting phage. In this study, we examined the O91:H21 STEC isolate B2F1, which carries two functional alleles for the potent activatable Stx2 variant toxin, Stx2d, for the presence of Stx2d-converting bacteriophages. We first constructed mutants of B2F1 that produced one or the other Stx2d toxin and found that the mutant that produced only Stx2d1 made less toxin than the Stx2d2-producing mutant. Consistent with that result, the Stx2d1-producing mutant was attenuated in a streptomycin-treated mouse model of STEC infection. When the mutants were treated with mitomycin C to promote bacteriophage induction, Vero cell cytotoxicity was elevated only in extracts of the Stx2d1-producing mutant. Additionally, when mice were treated with ciprofloxacin, an antibiotic that induces the O157:H7 Stx2-converting phage, the animals were more susceptible to the Stx2d1-producing mutant. Moreover, an stx(2d1)-containing lysogen was isolated from plaques on strain DH5alpha that had been exposed to lysates of the mutant that produced Stx2d1 only, and supernatants from that lysogen transformed with a plasmid encoding RecA were cytotoxic when the lysogen was induced with mitomycin C. Finally, electron-microscopic examination of extracts from the Stx2d1-producing mutant showed hexagonal particles that resemble the prototypic Stx2-converting phage 933W. Together these observations provide strong evidence that expression of Stx2d1 is bacteriophage associated. We conclude that despite the sequence similarity of the stx(2d1)- and stx(2d2)-flanking regions in B2F1, Stx2d1 expression is repressed within the context of its toxin-converting phage while Stx2d2 expression is independent of phage induction.

摘要

1型和2型志贺毒素(Stx)由产志贺毒素大肠杆菌(STEC)中完整或有缺陷的温和噬菌体编码,这些毒素的表达与噬菌体诱导有关。在Stx2变体中,据报道,只有来自一株人类STEC分离株的stx(2e)携带在毒素转化噬菌体中。在本研究中,我们检测了携带两种功能性等位基因的O91:H21 STEC分离株B2F1,该等位基因编码强效可激活的Stx2变体毒素Stx2d,以检测是否存在Stx2d转化噬菌体。我们首先构建了产生一种或另一种Stx2d毒素的B2F1突变体,发现仅产生Stx2d1的突变体产生的毒素比产生Stx2d2的突变体少。与该结果一致,在链霉素处理的STEC感染小鼠模型中,产生Stx2d1的突变体毒力减弱。当用丝裂霉素C处理突变体以促进噬菌体诱导时,仅在产生Stx2d1的突变体提取物中,Vero细胞的细胞毒性升高。此外,当用环丙沙星(一种诱导O157:H7 Stx2转化噬菌体的抗生素)处理小鼠时,动物对产生Stx2d1的突变体更易感。此外,从仅暴露于产生Stx2d1的突变体裂解物的DH5α菌株上的噬菌斑中分离出一个含有stx(2d1)的溶原菌,当用丝裂霉素C诱导该溶原菌时,用编码RecA的质粒转化后的该溶原菌的上清液具有细胞毒性。最后,对产生Stx2d1的突变体提取物进行电子显微镜检查,发现了类似于原型Stx2转化噬菌体933W的六边形颗粒。这些观察结果共同提供了强有力的证据,证明Stx2d1的表达与噬菌体有关。我们得出结论,尽管B2F1中stx(2d1)和stx(2d2)侧翼区域的序列相似,但Stx2d1的表达在其毒素转化噬菌体的背景下受到抑制,而Stx2d2的表达与噬菌体诱导无关。

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