首页> 美国卫生研究院文献>Journal of Clinical Microbiology >Development and Evaluation of a Real-Time PCR Assay Targeting the Type III Secretion System of Burkholderia pseudomallei
【2h】

Development and Evaluation of a Real-Time PCR Assay Targeting the Type III Secretion System of Burkholderia pseudomallei

机译:针对假伯克霍尔德氏菌III型分泌系统的实时PCR分析方法的开发和评估

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。
获取外文期刊封面目录资料

摘要

Here we report on the development of a discriminatory real-time assay for the rapid identification of Burkholderia pseudomallei isolates and the evaluation of this assay for sensitivity against related species and detection in spiked human blood samples. The assay targets a 115-base-pair region within orf2 of the B. pseudomallei type III secretion system gene cluster and distinguishes B. pseudomallei from other microbial species. Assay performance was evaluated with 224 geographically, temporally, and clinically diverse B. pseudomallei isolates from the Centers for Disease Control and Prevention strain collection. This represents the first real-time PCR for rapid and sensitive identification of B. pseudomallei that has been tested for cross-reactivity with 23 Burkholderia mallei, 5 Burkholderia thailandensis, and 35 Burkholderia and 76 non-Burkholderia organisms which have historically presented diagnostic challenges. The assay performed with 100% specificity. The limit of detection was found to be 76 femtograms of DNA (equivalent to 5.2 × 103 genome equivalents per ml) in a single PCR. In spiked human blood, the assay could detect as few as 8.4 × 103 CFU per ml. This rapid assay is a valuable tool for identification of B. pseudomallei and may improve diagnosis in regions endemic for melioidosis.
机译:在这里,我们报告了一种鉴别性实时测定法的发展,该测定法可快速鉴定假苹果伯克霍尔德菌分离株,并对这种测定法对相关物种的敏感性和加标的人类血液样本中的检测进行评估。该测定法针对假疟原虫III型分泌系统基因簇orf2内的115个碱基对区域,并将假疟原虫与其他微生物区分开。用来自疾病控制和预防中心收集的224个地理,时间和临床上不同的假苹果芽孢杆菌分离株评估了测定性能。这代表了用于快速和灵敏鉴定假双歧芽孢杆菌的第一个实时PCR,已通过测试与23个伯克霍尔德菌,5个伯克霍尔德菌和35个伯克霍尔德菌和76个非伯克霍尔德菌进行了交叉反应,这些细菌在历史上一直存在诊断挑战。该测定以100%的特异性进行。在一次PCR中,检测限为76飞克DNA(相当于每毫升5.2×10 3 基因组当量)。在加标的人体血液中,该检测法每毫升可检测到8.4×10 3 CFU。这种快速的测定方法是鉴定假苹果芽孢杆菌的有价值的工具,并且可以改善类疟疾流行区的诊断。

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