非产毒性O1与产毒性O1霍乱弧菌的基因组比较分析。

Munmun Mukherjee, Prathusha Kakarla, Sanath Kumar, Esmeralda Gonzalez, Jared T Floyd, Madhuri Inupakutika, Amith Reddy Devireddy, Selena R Tirrell, Merissa Bruns, Guixin He, Ingrid E Lindquist, Anitha Sundararajan, Faye D Schilkey, Joann Mudge, Manuel F Varela
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引用次数: 10

摘要

霍乱弧菌的致病菌株是霍乱流行病和大流行暴发的原因。弧菌菌株毒力的完整产毒机制尚不清楚。这项工作的假设是,霍乱弧菌的毒力菌株与非毒力菌株具有编码毒力的独特基因组元素。本研究的目的是阐明O1血清型和非O1霍乱弧菌PS15(一种非产毒菌株)之间的基因组差异,以确定可能负责毒力的新基因。在本研究中,我们在系统发育水平上比较了非o1型PS15菌株的全基因组与产毒血清型的全基因组,发现PS15基因组与产毒霍乱弧菌的基因组有远亲关系。因此,我们将重点放在PS15与近亲O1霍乱弧菌N16961之间的详细基因比较上。基于序列比对,我们初步将1号染色体和2号染色体分配给非o1型霍乱弧菌PS15基因组中的元件。此外,我们发现PS15和O1霍乱弧菌N16961有98%的同源性,共有766个基因,但在N16961中存在的非O1霍乱弧菌PS15基因组中缺失的基因中,有56个基因不仅编码与毒力相关的基因(定植、抗菌素耐药性和持久性细胞的调控),还编码涉及脂质、核苷和硫化合物代谢生物合成的基因。此外,我们发现了113个PS15特有的基因,这些基因被预测编码与毒力、疾病、防御、膜运输和DNA代谢相关的其他特性。在这里,我们确定了O1型和非O1型霍乱弧菌基因组之间独特的新基因组元件,作为潜在的毒力因子,因此是未来治疗的靶点。调节这些新目标可能最终加强在受影响国家消灭地方性和大流行性霍乱的努力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Comparative genome analysis of non-toxigenic non-O1 versus toxigenic O1 <i>Vibrio cholerae.</i>

Comparative genome analysis of non-toxigenic non-O1 versus toxigenic O1 <i>Vibrio cholerae.</i>

Comparative genome analysis of non-toxigenic non-O1 versus toxigenic O1 <i>Vibrio cholerae.</i>

Comparative genome analysis of non-toxigenic non-O1 versus toxigenic O1 Vibrio cholerae.

Pathogenic strains of Vibrio cholerae are responsible for endemic and pandemic outbreaks of the disease cholera. The complete toxigenic mechanisms underlying virulence in Vibrio strains are poorly understood. The hypothesis of this work was that virulent versus non-virulent strains of V. cholerae harbor distinctive genomic elements that encode virulence. The purpose of this study was to elucidate genomic differences between the O1 serotypes and non-O1 V. cholerae PS15, a non-toxigenic strain, in order to identify novel genes potentially responsible for virulence. In this study, we compared the whole genome of the non-O1 PS15 strain to the whole genomes of toxigenic serotypes at the phylogenetic level, and found that the PS15 genome was distantly related to those of toxigenic V. cholerae. Thus we focused on a detailed gene comparison between PS15 and the distantly related O1 V. cholerae N16961. Based on sequence alignment we tentatively assigned chromosome numbers 1 and 2 to elements within the genome of non-O1 V. cholerae PS15. Further, we found that PS15 and O1 V. cholerae N16961 shared 98% identity and 766 genes, but of the genes present in N16961 that were missing in the non-O1 V. cholerae PS15 genome, 56 were predicted to encode not only for virulence-related genes (colonization, antimicrobial resistance, and regulation of persister cells) but also genes involved in the metabolic biosynthesis of lipids, nucleosides and sulfur compounds. Additionally, we found 113 genes unique to PS15 that were predicted to encode other properties related to virulence, disease, defense, membrane transport, and DNA metabolism. Here, we identified distinctive and novel genomic elements between O1 and non-O1 V. cholerae genomes as potential virulence factors and, thus, targets for future therapeutics. Modulation of such novel targets may eventually enhance eradication efforts of endemic and pandemic disease cholera in afflicted nations.

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