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产碱普罗威登斯菌致腹泻分离株细胞致死膨胀毒素的分子特征。

Molecular characterizations of cytolethal distending toxin produced by Providencia alcalifaciens strains isolated from patients with diarrhea.

机构信息

Graduate School of Life and Environmental Sciences, Osaka Prefecture University, Osaka, Japan.

出版信息

Infect Immun. 2012 Apr;80(4):1323-32. doi: 10.1128/IAI.05831-11. Epub 2012 Jan 17.

Abstract

Cytolethal distending toxins (CDTs), which block eukaryotic cell proliferation by acting as inhibitory cyclomodulins, are produced by diverse groups of Gram-negative bacteria. Active CDT is composed of three polypeptides--CdtA, CdtB, and CdtC--encoded by the genes cdtA, cdtB, and cdtC, respectively. We developed a PCR-restriction fragment length polymorphism assay for the detection and differentiation of five alleles of cdtB (Cdt-I through Cdt-V) in Escherichia coli and used the assay to investigate the prevalence and characteristic of CDT-producing E. coli in children with diarrhea (A. Hinenoya et al., Microbiol. Immunol. 53:206-215, 2009). In these assays, two untypable cdtB genes were detected and the organisms harboring the cdtB gene were identified as Providencia alcalifaciens (strains AH-31 and AS-1). Nucleotide sequence analysis of the cdt gene cluster revealed that the cdtA, cdtB, and cdtC genes of P. alcalifaciens are of 750, 810, and 549 bp, respectively. To understand the possible horizontal transfer of the cdt genes among closely related species, the presence of cdt genes was screened in various Providencia spp. by colony hybridization assay, and the cdt gene cluster was found in only limited strains of P. alcalifaciens. Genome walking revealed that the cdt gene cluster of P. alcalifaciens is located adjacent to a putative transposase gene, suggesting the locus might be horizontally transferable. Interestingly, the CDT of P. alcalifaciens (PaCDT) showed some homology with the CDT of Shigella boydii. Whereas filter-sterilized lysates of strains AH-31 and AS-1 showed distention of CHO but not of HeLa cells, E. coli CDT-I exhibited distention of both cells. This activity of PaCDT was confirmed by generating recombinant PaCDT protein, which could also be neutralized by rabbit anti-PaCdtB antibody. Furthermore, recombinant PaCDT was found to induce G(2)/M cell cycle arrest and phosphorylation of host histone H2AX, a sensitive marker of DNA double-strand breaks. To our knowledge, this is the first report showing that certain clinical P. alcalifaciens strains could produce variants of the CDTs compared.

摘要

细胞致死膨胀毒素(CDT)通过作为抑制性环调制素作用而阻断真核细胞增殖,由多种革兰氏阴性菌产生。活性 CDT 由三个多肽组成-CdtA、CdtB 和 CdtC-分别由基因 cdtA、cdtB 和 cdtC 编码。我们开发了一种用于检测和区分大肠杆菌中五个 cdtB 等位基因(Cdt-I 至 Cdt-V)的 PCR-限制性片段长度多态性检测方法,并使用该方法调查了腹泻儿童中产生 CDT 的大肠杆菌的流行情况和特征(A. Hinenoya 等人,Microbiol。Immunol. 53:206-215, 2009)。在这些检测中,检测到两个无法分型的 cdtB 基因,并且携带 cdtB 基因的生物体被鉴定为产碱普罗威登斯菌(菌株 AH-31 和 AS-1)。cdt 基因簇的核苷酸序列分析表明,产碱普罗威登斯菌的 cdtA、cdtB 和 cdtC 基因分别为 750、810 和 549bp。为了了解 cdt 基因在密切相关的物种之间可能发生的水平转移,通过菌落杂交检测筛选了各种普罗威登斯菌属中的 cdt 基因,仅在有限的产碱普罗威登斯菌菌株中发现了 cdt 基因簇。基因组步移显示,产碱普罗威登斯菌的 cdt 基因簇位于一个推定的转座酶基因附近,表明该基因座可能是可水平转移的。有趣的是,产碱普罗威登斯菌的 CDT(PaCDT)与志贺氏菌的 CDT 具有一定的同源性。虽然菌株 AH-31 和 AS-1 的过滤除菌上清液显示 CHO 膨胀但 HeLa 细胞不膨胀,但大肠杆菌 CDT-I 显示两种细胞都膨胀。通过生成重组 PaCDT 蛋白证实了 PaCDT 的这种活性,兔抗 PaCdtB 抗体也可以中和该活性。此外,发现重组 PaCDT 可诱导细胞周期 G(2)/M 期阻滞和宿主组蛋白 H2AX 的磷酸化,H2AX 是 DNA 双链断裂的敏感标志物。据我们所知,这是首次报道某些临床产碱普罗威登斯菌株能够产生 CDT 变体的报告。

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