首页> 外文期刊>Applied Microbiology >Specific Real-Time PCR for Simultaneous Detection and Identification of Legionella pneumophila Serogroup 1 in Water and Clinical Samples
【24h】

Specific Real-Time PCR for Simultaneous Detection and Identification of Legionella pneumophila Serogroup 1 in Water and Clinical Samples

机译:用于实时检测和鉴定水和临床样品中嗜肺军团菌血清群1的特异性实时PCR

获取原文
           

摘要

Legionella pneumophila , a bacterium that replicates within aquatic amoebae and persists in the environment as a free-living microbe, is the causative agent of Legionnaires' disease. Among the many Legionella species described, L. pneumophila is associated with 90% of human disease, and within the 15 serogroups (Sg), L. pneumophila Sg1 causes more than 84% of Legionnaires' disease worldwide. Thus, rapid and specific identification of L. pneumophila Sg1 is of the utmost importance for evaluation of the contamination of collective water systems and the risk posed. Previously we had shown that about 20 kb of the 33-kb locus carrying the genes coding for the proteins involved in lipopolysaccharide biosynthesis (LPS gene cluster) by L. pneumophila was highly specific for Sg1 strains and that three genes ( lpp0831 , wzm , and wzt ) may serve as genetic markers. Here we report the sequencing and comparative analyses of this specific region of the LPS gene cluster in L. pneumophila Sg6, -10, -12, -13, and -14. Indeed, the wzm and wzt genes were present only in the Sg1 LPS gene cluster, which showed a very specific gene content with respect to the other five serogroups investigated. Based on this observation, we designed primers and developed a classical and a real-time PCR method for the detection and simultaneous identification of L. pneumophila Sg1 in clinical and environmental isolates. Evaluation of the selected primers with 454 Legionella and 38 non- Legionella strains demonstrated 100% specificity. Sensitivity, specificity, and predictive values were further evaluated with 209 DNA extracts from water samples of hospital water supply systems and with 96 respiratory specimens. The results showed that the newly developed quantitative Sg1-specific PCR method is a highly specific and efficient tool for the surveillance and rapid detection of high-risk L. pneumophila Sg1 in water and clinical samples.
机译:嗜肺军团菌是一种细菌,可在水生变形虫内复制并作为一种自由生存的微生物在环境中持续存在,是引起军团病的病原体。在描述的许多军团菌物种中,肺炎支原体与90%的人类疾病有关,在15个血清群(Sg)中,肺炎支原体Sg1引起全世界军团病的84%以上。因此,对于评估集体水系统的污染和所造成的风险,快速而特异性地鉴定肺炎链球菌Sg1至关重要。以前,我们已经证明,在33 kb的基因座中,约有20 kb携带着编码嗜肺乳杆菌的脂多糖生物合成(LPS基因簇)所涉及的蛋白质的基因,并且对Sg1菌株具有高度特异性,并且三个基因(lpp0831,wzm和wzt)可以作为遗传标记。在这里,我们报告了肺炎链球菌Sg6,-10,-12,-13和-14中LPS基因簇这一特定区域的测序和比较分析。的确,wzm和wzt基因仅存在于Sg1 LPS基因簇中,相对于其他五个血清群显示了非常特定的基因含量。基于此观察,我们设计了引物,并开发了一种经典的实时PCR方法,用于检测和同时鉴定临床和环境分离株中的嗜肺乳杆菌Sg1。用454个军团菌和38个非军团菌菌株对所选引物的评估显示出100%的特异性。用医院供水系统水样中的209种DNA提取物和96种呼吸道样品进一步评估了敏感性,特异性和预测值。结果表明,新开发的定量Sg1特异性PCR方法是监测和快速检测水和临床样品中高风险嗜肺乳杆菌Sg1的高度特异性和高效工具。

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