首页> 外文期刊>Journal of Clinical Microbiology >Multilocus Variable-Number Tandem Repeat Analysis Distinguishes Outbreak and Sporadic Escherichia coli O157:H7 Isolates
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Multilocus Variable-Number Tandem Repeat Analysis Distinguishes Outbreak and Sporadic Escherichia coli O157:H7 Isolates

机译:多基因座可变数串联重复分析可区分暴发和散发性大肠杆菌O157:H7分离株

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Escherichia coli O157:H7 is a major cause of food-borne illness in the United States. Outbreak detection involves traditional epidemiological methods and routine molecular subtyping by pulsed-field gel electrophoresis (PFGE). PFGE is labor-intensive, and the results are difficult to analyze and not easily transferable between laboratories. Multilocus variable-number tandem repeat (VNTR) analysis (MLVA) is a fast, portable method that analyzes multiple VNTR loci, which are areas of the bacterial genome that evolve quickly. Eighty isolates, including 21 isolates from five epidemiologically well-characterized outbreaks from Pennsylvania and Minnesota, were analyzed by PFGE and MLVA. Strains in PFGE clusters were defined as strains that differed by less than or equal to one band by using XbaI and the confirmatory enzyme SpeI. MLVA was performed by comparing the number of tandem repeats at seven loci. From 6 to 30 alleles were found at the seven loci, resulting in 64 MLVA types among the 80 isolates. MLVA correctly identified the isolates from all five outbreaks if only a single-locus variant was allowed. MLVA differentiated strains with unique PFGE types. Additionally, MLVA discriminated strains within PFGE-defined clusters that were not known to be part of an outbreak. In addition to being a simple and validated method for E. coli O157:H7 outbreak detection, MLVA appears to have a sensitivity equal to that of PFGE and a specificity superior to that of PFGE.
机译:O157:H7大肠杆菌是美国食源性疾病的主要原因。爆发检测涉及传统的流行病学方法和通过脉冲场凝胶电泳(PFGE)进行的常规分子亚型分析。 PFGE是劳动密集型的,其结果难以分析,而且在实验室之间不易转移。多基因座可变数目串联重复序列(VNTR)分析(MLVA)是一种快速,便携式的方法,可以分析多个VNTR基因座,这些基因座是细菌基因组中快速进化的区域。通过PFGE和MLVA分析了80个分离株,包括来自宾夕法尼亚州和明尼苏达州5个流行病学特征明确的暴发的21个分离株。通过使用 Xba I和确认酶 Spe I,将PFGE簇中的菌株定义为差异小于或等于一个条带的菌株。 MLVA通过比较七个位点的串联重复数进行。在七个基因座中发现了6至30个等位基因,在80个分离物中共有64种MLVA类型。如果只允许单基因座变异,MLVA会正确识别出所有五次爆发的分离株。具有独特PFGE类型的MLVA分化菌株。此外,MLVA可以区分PFGE定义的簇中的菌株,这些菌株不属于暴发。除了是 E的简单且经过验证的方法。在O157:H7大肠埃希氏菌暴发检测中,MLVA的敏感性似乎与PFGE相等,而且特异性也优于PFGE。

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