首页> 美国卫生研究院文献>Journal of Clinical Microbiology >Multiplex Touchdown PCR for Rapid Typing of the Opportunistic Pathogen Propionibacterium acnes
【2h】

Multiplex Touchdown PCR for Rapid Typing of the Opportunistic Pathogen Propionibacterium acnes

机译:多重触地PCR快速键入机会性病原痤疮丙酸杆菌

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

The opportunistic human pathogen Propionibacterium acnes is composed of a number of distinct phylogroups, designated types IA1, IA2, IB, IC, II, and III, which vary in their production of putative virulence factors, their inflammatory potential, and their biochemical, aggregative, and morphological characteristics. Although multilocus sequence typing (MLST) currently represents the gold standard for unambiguous phylogroup classification and individual strain identification, it is a labor-intensive and time-consuming technique. As a consequence, we developed a multiplex touchdown PCR assay that in a single reaction can confirm the species identity and phylogeny of an isolate based on its pattern of reaction with six primer sets that target the 16S rRNA gene (all isolates), ATPase (types IA1, IA2, and IC), sodA (types IA2 and IB), atpD (type II), and recA (type III) housekeeping genes, as well as a Fic family toxin gene (type IC). When applied to 312 P. acnes isolates previously characterized by MLST and representing types IA1 (n = 145), IA2 (n = 20), IB (n = 65), IC (n = 7), II (n = 45), and III (n = 30), the multiplex displayed 100% sensitivity and 100% specificity for detecting isolates within each targeted phylogroup. No cross-reactivity with isolates from other bacterial species was observed. This multiplex assay will provide researchers with a rapid, high-throughput, and technically undemanding typing method for epidemiological and phylogenetic investigations. It will facilitate studies investigating the association of lineages with various infections and clinical conditions, and it will serve as a prescreening tool to maximize the number of genetically diverse isolates selected for downstream higher-resolution sequence-based analyses.
机译:机会性人类病原体痤疮丙酸杆菌由许多不同的类群组成,分别指定为IA1,IA2,IB,IC,II和III型,其推定毒力因子的产生,炎性潜力以及它们的生化,聚集,和形态特征。尽管多基因座序列分型(MLST)当前代表明确的系统分类和单个菌株鉴定的金标准,但这是一项劳动密集型且耗时的技术。因此,我们开发了一种多重着陆PCR检测方法,该方法可在一个反应​​中基于与六种针对16S rRNA基因的引物组(所有分离物),ATPase(类型)的反应模式,确定分离物的物种同一性和系统发育。 IA1,IA2和IC),sodA(IA2和IB型),atpD(II型)和recA(III型)管家基因,以及Fic家族毒素基因(IC型)。当应用于312个痤疮丙酸杆菌之前曾以MLST表征且代表IA1(n = 145),IA2(n = 20),IB(n = 65),IC(n = 7),II(n = 45)的分离株时,和III(n = 30),多重检测显示出100%的敏感性和100%的特异性,可用于检测每个目标菌群内的分离株。没有观察到与来自其他细菌物种的分离物的交叉反应。这种多重测定法将为研究人员提供一种快速,高通量,技术上不需要的打字方法,用于流行病学和系统发育研究。这将有助于研究谱系与各种感染和临床状况之间的关系,并将作为一种预筛选工具,以最大化用于下游高分辨率序列分析的遗传多样性分离株的数量。

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