首页> 外文期刊>Molecular and Cellular Probes: The Location, Diagnosis and Monitoring of Disease by Specific Molecules and Cell Lines >Specific real-time PCR assays for the detection and quantification of Mycoplasma mycoides subsp. mycoides SC and Mycoplasma capricolum subsp. capripneumoniae.
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Specific real-time PCR assays for the detection and quantification of Mycoplasma mycoides subsp. mycoides SC and Mycoplasma capricolum subsp. capripneumoniae.

机译:用于检测和定量支原体亚种的实时荧光定量PCR检测方法。杀真菌剂SC和支原体亚种。肺炎克雷伯氏菌。

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摘要

Contagious bovine pleuropneumonia and contagious caprine pleuropneumonia are two severe respiratory infections of ruminants due to infection by Mycoplasma mycoides subsp. mycoides SC (MmmSC) and Mycoplasma capricolum subsp. capripneumoniae (Mccp), respectively. They are included in the OIE list of notifiable diseases. Here we describe the development of rapid, sensitive, and specific real-time PCR assays for the detection and quantification of MmmSC and Mccp DNA. MmmSC PCR primers were designed after whole genome comparisons between the published sequence of MmmSC strain type PG1(T) and the sequence of an M. mycoides subsp. mycoides large colony strain. For Mccp, previously published conventional PCR primers were applied. SYBR green was used as a detection agent for both assays. The assays specifically detected the targeted species in both cultures and clinical samples, and no cross-amplifications were obtained from either heterologous mycoplasma strain cultures or European field samples. The sensitivity of these new assays was estimated at 3-80 colony forming units per reaction and 4-80fg of DNA, representing a 2-3log increase in sensitivity compared to established conventional PCR tests. These new real-time PCR assays will be invaluable for application in various fields such as direct detection in diagnostic laboratories.
机译:牛传染性胸膜肺炎和犬传染性胸膜肺炎是由于支原体支原体感染引起的两种反刍动物的严重呼吸道感染。 Mycoides SC(MmmSC)和支原体亚种Capripneumoniae(Mccp)分别。它们被包括在世界动物卫生组织的法定疾病清单中。在这里,我们描述了用于检测和定量MmmSC和Mccp DNA的快速,灵敏和特异的实时PCR分析方法的发展。 MmmSC PCR引物是在比较已发表的PG1型MM1SC菌株序列和分支霉菌亚种的序列之间进行全基因组比较后设计的。霉菌大菌落菌株。对于Mccp,使用以前发布的常规PCR引物。 SYBR green用作两种测定的检测剂。该测定法特异性地检测了培养物和临床样品中的目标物种,并且从异源支原体菌株培养物或欧洲野外样品中均未获得交叉扩增。这些新方法的灵敏度估计为每个反应3-80个菌落形成单位和4-80fg DNA,与已建立的常规PCR测试相比,灵敏度提高了2-3log。这些新的实时PCR分析方法可用于各种领域,例如在诊断实验室中直接检测。

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