Tominaga Tatsuya
Saitama Industrial Technology Center North Institute, 2-133, Suehiro, Kumagaya, Saitama 360-0031, Japan.
J Clin Microbiol. 2006 Jun;44(6):2199-206. doi: 10.1128/JCM.00344-06.
Microtemperature gradient gel electrophoresis (mu-TGGE) was examined for use for the rapid subtyping of Listeria monocytogenes strains. Comparison of genomes between L. monocytogenes strains F2365 and H7858 identified a sequence encoding a portion of the PRT/PTS system IIA 2 protein domain as appropriate for mu-TGGE analysis. Thirty-one strains belonging to 10 different serovar types were tested by PCR, and sequence analysis of the amplified products revealed that the strains comprise 11 groups. All 55 possible pairs within the 11 groups were examined by mu-TGGE analysis. Of these, 47 pairs could be successfully discriminated, with a total electrophoresis time of only 7 min. Moreover, Cy3/Cy5 labeling allowed rapid identification of the sequence type in unknown strains of L. monocytogenes isolated from meat. These findings collectively indicate that mu-TGGE can be used for the rapid analysis of L. monocytogenes strains, facilitating determination of routes of contamination when these bacteria are found in food products.
研究了微温度梯度凝胶电泳(mu-TGGE)用于单核细胞增生李斯特菌菌株快速分型的情况。单核细胞增生李斯特菌菌株F2365和H7858之间的基因组比较确定了一段编码PRT/PTS系统IIA 2蛋白结构域一部分的序列适用于mu-TGGE分析。通过PCR对属于10种不同血清型的31株菌株进行了检测,扩增产物的序列分析表明这些菌株分为11组。通过mu-TGGE分析检查了11组内的所有55种可能组合。其中,47种组合能够成功区分,总电泳时间仅为7分钟。此外,Cy3/Cy5标记能够快速鉴定从肉类中分离出的单核细胞增生李斯特菌未知菌株的序列类型。这些发现共同表明,mu-TGGE可用于单核细胞增生李斯特菌菌株的快速分析,有助于在食品中发现这些细菌时确定污染途径。