首页> 美国卫生研究院文献>Journal of Clinical Microbiology >Selective Discrimination of Listeria monocytogenes Epidemic Strains by a Mixed-Genome DNA Microarray Compared to Discrimination by Pulsed-Field Gel Electrophoresis Ribotyping and Multilocus Sequence Typing
【2h】

Selective Discrimination of Listeria monocytogenes Epidemic Strains by a Mixed-Genome DNA Microarray Compared to Discrimination by Pulsed-Field Gel Electrophoresis Ribotyping and Multilocus Sequence Typing

机译:混合基因组DNA微阵列对李斯特菌李斯特菌流行株的选择性鉴别与脉冲场凝胶电泳核糖分型和多基因座序列分型的鉴别相比

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Listeria monocytogenes can cause serious illness in humans, and subsequent epidemiological investigation requires molecular characterization to allow the identification of specific isolates. L. monocytogenes is usually characterized by serotyping and is subtyped by using pulsed-field gel electrophoresis (PFGE) or ribotyping. DNA microarrays provide an alternative means to resolve genetic differences among isolates, and unlike PFGE and ribotyping, microarrays can be used to identify specific genes associated with strains of interest. Twenty strains of L. monocytogenes representing six serovars were used to generate a shotgun library, and subsequently a 629-probe microarray was constructed by using features that included only potentially polymorphic gene probe sequences. Fifty-two strains of L. monocytogenes were genotyped by using the condensed array, including strains associated with five major listeriosis epidemics. Cluster analysis of the microarray data grouped strains according to phylogenetic lineage and serotype. Most epidemiologically linked strains were grouped together, and subtyping resolution was the same as that with PFGE (using AscI and ApaI) and better than that with multilocus sequence typing (using six housekeeping genes) and ribotyping. Additionally, a majority of epidemic strains were grouped together within phylogenetic Division I. This epidemic cluster was clearly distinct from the two other Division I clusters, which encompassed primarily sporadic and environmental strains. Discriminant function analysis allowed identification of 22 probes from the mixed-genome array that distinguish serotypes and subtypes, including several potential markers that were distinct for the epidemic cluster. Many of the subtype-specific genes encode proteins that likely confer survival advantages in the environment and/or host.
机译:单核细胞增生李斯特菌可导致人类严重疾病,随后的流行病学研究要求分子鉴定以鉴定特定的分离株。单核细胞增生李斯特菌通常以血清分型为特征,并通过使用脉冲场凝胶电泳(PFGE)或核糖分型进行亚型化。 DNA微阵列提供了解决分离株之间遗传差异的另一种方法,与PFGE和核糖分型法不同,微阵列可用于鉴定与目标菌株相关的特定基因。用二十个代表六个血清型的单核细胞增生李斯特氏菌菌株生成a弹枪文库,随后使用仅包含潜在多态性基因探针序列的特征构建了629个探针的微阵列。使用浓缩阵列对52种单核细胞增生李斯特菌菌株进行基因分型,包括与5种主要李斯特菌病流行有关的菌株。根据系统发育谱系和血清型对菌株进行微阵列数据聚类分析。大多数与流行病学相关的菌株被归为一类,亚型分辨率与PFGE(使用AscI和ApaI)相同,并且优于多基因座序列分型(使用六个管家基因)和核糖分型。此外,大多数流行病菌株在系统发生I类中归为一类。该流行病群与其他两个I类群明显不同,后者主要包含零星和环境菌株。判别功能分析可以从混合基因组阵列中鉴定出22种探针,以区分血清型和亚型,包括针对该流行病群的几种潜在标记。许多亚型特异性基因编码可能赋予环境和/或宿主生存优势的蛋白质。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号