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利用三重聚合酶链反应快速鉴定啮齿动物中的肺炎克雷伯菌、科氏棒状杆菌和肺炎链球菌。

Rapid identification of Klebsiella pneumoniae, Corynebacterium kutscheri, and Streptococcus pneumoniae using triplex polymerase chain reaction in rodents.

机构信息

Department of Laboratory Animal Medicine, College of Veterinary Medicine, Konkuk University, 1 Hwayang-dong, Gwangjin-gu, Seoul 143-701, Republic of Korea.

出版信息

Exp Anim. 2013;62(1):35-40. doi: 10.1538/expanim.62.35.

Abstract

Klebsiella pneumoniae, Corynebacterium kutscheri, and Streptococcus pneumoniae are important pathogens that cause respiratory infections in laboratory rodents. In this study, we used species-specific triplex PCR analysis to directly detect three common bacterial pathogens associated with respiratory diseases. Specific targets were amplified with conventional PCR using the tyrB gene from K. pneumoniae, gyrB gene from C. kutscheri, and ply gene from S. pneumoniae. Our primers were tested against purified DNA from another eleven murine bacteria to determine primer specificity. Under optimal PCR conditions, the triplex assay simultaneously yielded a 931 bp product from K. pneumoniae, a 540 bp product from C. kutscheri, and a 354 bp product from S. pneumoniae. The triplex assay detection thresholds for pure cultures were 10 pg for K. pneumoniae and S. pneumoniae, and 100 pg for C. kutscheri. All three bacteria were successfully identified in the trachea and lung of experimentally infected mice at the same time. Our triplex PCR method can be used as a useful method for detecting pathogenic bacterial infections in laboratory rodents.

摘要

肺炎克雷伯菌、库氏棒状杆菌和肺炎链球菌是引起实验动物呼吸道感染的重要病原体。在本研究中,我们使用种特异性三重 PCR 分析直接检测与呼吸道疾病相关的三种常见细菌病原体。使用来自肺炎克雷伯菌的 tyrB 基因、来自库氏棒状杆菌的 gyrB 基因和来自肺炎链球菌的 ply 基因进行常规 PCR 扩增特异性靶标。我们的引物针对从另外 11 种鼠源细菌中提取的 DNA 进行了测试,以确定引物的特异性。在最佳 PCR 条件下,三重 PCR 分析同时从肺炎克雷伯菌中产生 931 bp 的产物,从库氏棒状杆菌中产生 540 bp 的产物,从肺炎链球菌中产生 354 bp 的产物。纯培养物的三重 PCR 检测阈值为肺炎克雷伯菌和肺炎链球菌 10 pg,库氏棒状杆菌 100 pg。三种细菌均能在实验感染小鼠的气管和肺部同时成功鉴定。我们的三重 PCR 方法可作为检测实验动物致病性细菌感染的有用方法。

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