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肠沙门氏菌亚种的多位点可变数目串联重复分析。

Multilocus variable number tandem repeat analysis for Salmonella enterica subspecies.

机构信息

Food Microbiology Laboratory, Institut Pasteur du Cambodge, 5 Bd. Monivong, Phnom Penh, Cambodia.

出版信息

Eur J Clin Microbiol Infect Dis. 2011 Apr;30(4):465-73. doi: 10.1007/s10096-010-1110-0. Epub 2010 Dec 11.

Abstract

Genomic analysis of Salmonella enterica revealed the existence of a variable number of tandem repeats (VNTR) at multiple loci. Some S. enterica strains are considered as references (Typhi Ty2, Typhi CT18, Typhimurium LT2, Enteritidis LK5, PT4, and Enteritidis 07-2642, and Newport). These allowed the selection of markers to develop the genotyping technique, multiple-locus VNTR analysis (MLVA). These markers were used to discriminate S. enterica isolated from humans, food, or the environment. In this report, the characteristics and specifications of 58 salmonella markers described from 2003 to 2009 are analyzed. Some VNTR loci were used as markers. The markers were used to discriminate S. enterica isolates from different sources and geographical localizations. Among the VNTR loci described in the published reports, eight presented with a high diversity index (DI) of polymorphism of more than 0.80. The selection of several markers within a single locus validated their polymorphism characteristic. Despite unequal DI values, the use of a panel of markers is a powerful discriminatory tool for the surveillance and identification of the source of salmonella outbreak. Depending on the markers selected, MLVA should be used either for macro- or microepidemiological purposes. The main challenge in the future for this technique is standardization.

摘要

对沙门氏菌的基因组分析显示,多个基因座存在可变数目的串联重复(VNTR)。一些沙门氏菌菌株被认为是参考菌株(伤寒 Ty2、伤寒 CT18、肠炎 Typhimurium LT2、肠炎 Enteritidis LK5、PT4 和肠炎 Enteritidis 07-2642、纽波特)。这些菌株允许选择标记物来开发基因分型技术,即多位点 VNTR 分析(MLVA)。这些标记物用于区分从人类、食物或环境中分离的沙门氏菌。在本报告中,分析了 2003 年至 2009 年描述的 58 个沙门氏菌标记物的特征和规格。一些 VNTR 基因座被用作标记物。这些标记物用于区分来自不同来源和地理位置的沙门氏菌分离株。在所描述的 VNTR 基因座中,有 8 个呈现出高于 0.80 的高多态性指数(DI)。在单个基因座内选择多个标记物验证了它们的多态性特征。尽管 DI 值不等,但使用一组标记物是监测和识别沙门氏菌暴发来源的有力鉴别工具。根据所选标记物,MLVA 可用于宏观或微观流行病学目的。该技术未来的主要挑战是标准化。

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