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肠沙门氏菌的系统发育、毒力潜能与血清型之间的关系。

Association between phylogeny, virulence potential and serovars of Salmonella enterica.

机构信息

Statens Serum Institut, Artillerivej 5, DK-2300 Copenhagen S, Denmark.

出版信息

Infect Genet Evol. 2010 Oct;10(7):1132-9. doi: 10.1016/j.meegid.2010.07.015. Epub 2010 Jul 23.

Abstract

Salmonella enterica subsp. enterica is one of the leading causes of zoonotic food-borne disease worldwide. The consequence of these infections is a serious impact on economics of the society in the form of lost productivity and expenses for medical care. The objective of this study was to analyze the difference in genomic content between selected serovars, especially the content of pathogenicity genes and this was done with a DNA microarray. Furthermore, we investigated the phylogenetic relationship between serovars using multilocus sequence typing (MLST). We chose serovars Typhimurium and Enteritidis as they are responsible for 75% of human infections in Europe. Additionally, we included serovars Derby, Dublin, Saintpaul, 4,5,12:i:-, Java and 4,5,12:b:- which are suspected to have different degrees of virulence to humans. MLST analysis clustered strains according to serovar with the exception of Java and Derby. DNA microarray clustered strains according to serovar and serogroup except for serovar 4,5,12:b:-. Differences in content of pathogenicity related genes between serovars with various host preferences and virulence towards humans were not observed. However, our strains from the supposedly less virulent serovar Derby lacked a combination of genes important for virulence. It might be speculated that other serovars can sustain their pathogenicity lacking one or two of these genes, whereas lack of many virulence genes will result in reduced virulence. A partial lack of concordance between MLST and microarray was found and this can be explained by the underlying data. On one hand, microarray data include highly variable regions which are known to be involved in horizontal gene transfer. On the other hand, MLST data is restricted to seven sequences and disregards contribution of horizontally acquired genes when evaluating evolution. The DNA microarray and MLST analysis complement each other giving a clearer image of evolution of these serovars and, furthermore, a visualization of the horizontally acquired genes.

摘要

肠炎沙门氏菌亚种是世界范围内导致动物源性食源性疾病的主要原因之一。这些感染的后果是对社会经济造成严重影响,表现为生产力丧失和医疗费用增加。本研究的目的是分析选定血清型之间的基因组内容差异,特别是致病性基因的含量,并使用 DNA 微阵列进行分析。此外,我们使用多位点序列分型(MLST)研究血清型之间的系统发育关系。我们选择肠炎沙门氏菌和鼠伤寒沙门氏菌作为它们是欧洲人类感染的 75%的责任人。此外,我们还包括了都柏林沙门氏菌、圣-保尔沙门氏菌、4,5,12:i: -、4,5,12:b:-和雅加达沙门氏菌等血清型,这些血清型被怀疑对人类具有不同程度的毒力。MLST 分析根据血清型聚类菌株,除了雅加达和都柏林血清型。DNA 微阵列根据血清型和血清群聚类菌株,除了 4,5,12:b:-血清型。在宿主偏好和对人类的毒力不同的血清型之间,未观察到与致病性相关基因含量的差异。然而,我们来自所谓毒力较弱的都柏林血清型的菌株缺乏对毒力很重要的基因组合。可以推测,其他血清型可以在缺乏一个或两个这些基因的情况下维持其致病性,而缺乏许多毒力基因将导致毒力降低。发现 MLST 和微阵列之间存在部分不一致,这可以用基础数据来解释。一方面,微阵列数据包括高度可变区域,这些区域已知与水平基因转移有关。另一方面,MLST 数据限于七个序列,在评估进化时忽略了水平获得基因的贡献。DNA 微阵列和 MLST 分析相辅相成,更清晰地描绘了这些血清型的进化,并进一步可视化了水平获得的基因。

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