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Multiple-locus variable-number tandem repeat analysis of Salmonella Enteritidis isolates from human and non-human sources using a single multiplex PCR

机译:使用单路多重PCR对人和非人来源肠炎沙门氏菌分离株进行多位点可变数目串联重复分析

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摘要

Simplified multiple-locus variable-number tandem repeat analysis (MLVA) was developed using one-shot multiplex PCR for seven variable-number tandem repeats (VNTR) markers with high diversity capacity. MLVA, phage typing, and PFGE methods were applied on 34 diverse Salmonella Enteritidis isolates from human and non-human sources. MLVA detected allelic variations that helped to classify the S. Enteritidis isolates into more evenly distributed subtypes than other methods. MLVA-based S. Enteritidis clonal groups were largely associated with sources of the isolates. Nei's diversity indices for polymorphism ranged from 0.25 to 0.70 for seven VNTR loci markers. Based on Simpson's and Shannon's diversity indices, MLVA had a higher discriminatory power than pulsed field gel electrophoresis (PFGE), phage typing, or multilocus enzyme electrophoresis. Therefore, MLVA may be used along with PFGE to enhance the effectiveness of the molecular epidemiologic investigation of S. Enteritidis infections.
机译:简化的多基因座可变数目串联重复重复分析(MLVA)是使用单次多重PCR技术开发的,具有七个具有高多样性能力的可变数目串联重复序列(VNTR)标记。 MLVA,噬菌体分型和PFGE方法应用于来自人类和非人类来源的34种不同的肠炎沙门氏菌分离株。 MLVA检测到的等位基因变异有助于将肠炎沙门氏菌分离株分为比其他方法更均匀分布的亚型。基于MLVA的肠炎沙门氏菌克隆群在很大程度上与分离株的来源有关。七个VNTR基因座标记的Nei多态性多样性指数范围从0.25到0.70。根据辛普森和香农的多样性指数,MLVA的鉴别能力比脉冲场凝胶电泳(PFGE),噬菌体分型或多位点酶电泳更高。因此,MLVA可以与PFGE一起使用,以增强肠炎沙门氏菌感染的分子流行病学调查的有效性。

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