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首页> 外文期刊>Journal of Clinical Microbiology >Development of a Multilocus Sequence Typing Method for Analysis of Listeria monocytogenes Clones
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Development of a Multilocus Sequence Typing Method for Analysis of Listeria monocytogenes Clones

机译:用于分析李斯特菌李斯特菌的多基因座序列分型方法的建立

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This study is a first step in the development of multilocus sequence typing (MLST) method for Listeria monocytogenes. Nine housekeeping genes were analyzed in a set of 62 strains isolated from different sources and geographic locations in Spain. These strains were previously characterized by pulsed-field gel electrophoresis (PFGE). Because of low diversity, two loci were discarded from the study. The sequence analysis of the seven remaining genes showed 29 different allelic combinations, with 22 of them represented by only one strain. The results of this sequence analysis were generally consistent with those of PFGE. Because MLST allows the easy comparison and exchange of results obtained in different laboratories, the future application of this new molecular method could be a useful tool for the listeriosis surveillance systems that will allow the identification and distribution of analysis of L. monocytogenes clones in the environment.
机译:这项研究是开发单核细胞增生李斯特菌的多基因座序列分型(MLST)方法的第一步。在从西班牙不同来源和地理位置分离的62株菌株中分析了9个管家基因。这些菌株以前通过脉冲场凝胶电泳(PFGE)表征。由于多样性低,从该研究中丢弃了两个基因座。其余七个基因的序列分析显示了29种不同的等位基因组合,其中22种仅由一种菌株代表。该序列分析的结果通常与PFGE一致。因为MLST可以轻松比较和交换在不同实验室中获得的结果,所以这种新的分子方法的未来应用可能是李斯特菌病监测系统的有用工具,从而可以识别和分布Lem。单核细胞增生克隆

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