...
首页> 外文期刊>Journal of Clinical Microbiology >Genotypic Analyses of Vibrio parahaemolyticus and Development of a Pandemic Group-Specific Multiplex PCR Assay
【24h】

Genotypic Analyses of Vibrio parahaemolyticus and Development of a Pandemic Group-Specific Multiplex PCR Assay

机译:副溶血弧菌的基因型分析和大流行群特异性多重PCR检测的发展

获取原文
           

摘要

A total of 54 Vibrio parahaemolyticus strains including pandemic O3:K6 strains and newly emerged O4:K68, O1:K25, O1:K26, and O1:K untypeable strains (collectively referred to as the “pandemic group”) were examined for their pulsed-field gel electrophoresis (PFGE) and arbitrarily primed PCR (AP-PCR) profiles and for the presence or absence of genetic marker DNA sequences, toxRS/new or orf8, that had been reported elsewhere to be specific for the pandemic group. Both PFGE and AP-PCR analyses indicated that all strains of the pandemic group formed a distinct genotypic cluster, suggesting that they originated from the same clone. In addition to the pandemic group, four O3:K6 strains that did not possess the thermostable direct hemolysin (tdh) gene also belonged to this cluster and possessed the toxRS/new sequence. However, three O3:K6 strains that clearly belonged to the pandemic group by PFGE and AP-PCR did not possess the orf8 sequence. The evidence suggests that neither the toxRS/new nor the orf8 sequence is a reliable gene marker for definite identification of the pandemic group. We therefore developed a novel multiplex PCR assay specific for the pandemic group. The assay successfully distinguished pandemic group strains from other V. parahaemolyticus strains by yielding two distinct PCR products for tdh (263 bp) and the toxRS/new sequence (651 bp).
机译:共有54株副溶血性弧菌菌株,包括大流行的O3:K6菌株和新出现的O4:K68,O1:K25,O1:K26和O1:K无法分型的菌株(统称为“大流行病组” ”)检查其脉冲场凝胶电泳(PFGE)和任意引物PCR(AP-PCR)谱以及是否存在遗传标记DNA序列, toxRS / new < / em>或 orf8 ,据报道在其他地方专门针对大流行人群。 PFGE和AP-PCR分析均表明,大流行人群的所有菌株均形成了独特的基因型簇,表明它们源自同一克隆。除大流行病组外,还有四个不具有热稳定直接溶血素( tdh )基因的O3:K6菌株也属于该簇,并具有 toxRS / new 序列。但是,通过PFGE和AP-PCR明确属于大流行人群的三株O3:K6菌株不具有 orf8 序列。有证据表明, toxRS / new orf8 序列都不是可靠地确定大流行人群的基因标记。因此,我们开发了针对大流行人群的新型多重PCR检测方法。该测定法成功地将大流行群株与其他 V区分开。通过为 tdh (263 bp)和 toxRS / new 序列(651 bp)产生两个不同的PCR产物,对副溶血性菌株进行了分析。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

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