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A quantitative TaqMan PCR assay for the detection of Mycoplasma suis

机译:TaqMan PCR定量检测猪支原体

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Aim: To develop a TaqMan probe-based, highly sensitive and specific quantitative PCR (qPCR) assay for the detection and quantification of Mycoplasma suis in the blood of pigs.Methods and Results: Primers and probes specific to Myc. suis 16S rRNA gene were designed. The qPCR assay's specificity, detection limit, intra- and inter-assay variability were evaluated and its performance was compared with a Myc. suis conventional PCR assay (cPCR). Blood of two experimentally infected pigs, 40 Indiana pigs, 40 Brazilian sows and 28 peccaries were tested. The assay detected as few as ten copies of Myc. suis plasmids and was 100-fold more sensitive than the cPCR. No cross-reactivity with nontarget pig mycoplasmas was observed. An average of 1.62 x 10(11) and 2.75 x 10(8) target copies ml(-1) of blood were detected in the acutely and chronically infected pigs, respectively. Three (7.5%) pigs and 32 (80.0%) sows were positive while all peccaries were negative for Myc. suis.Conclusion: The developed qPCR assay is highly sensitive and specific for Myc. suis detection and quantification.Significance and Impact of the Study: TaqMan qPCR is an accurate and quick test for detection of Myc. suis infected pigs, which can be used on varied instrumentation platforms.
机译:目的:开发一种基于TaqMan探针的高灵敏度和特异性定量PCR(qPCR)分析方法,用于检测和定量猪血中的猪支原体。方法与结果:Myc特异的引物和探针。设计了suis 16S rRNA基因。评估了qPCR测定的特异性,检测限,测定内和测定间变异性,并将其性能与Myc进行了比较。可以使用常规PCR分析(cPCR)。测试了两只实验感染猪,40头印第安纳猪,40头巴西母猪和28头猪的血液。该测定法检测到只有十个Myc拷贝。 suis质粒,比cPCR敏感100倍。没有观察到与非目标猪支原体的交叉反应。在急性和慢性感染的猪中分别平均检测到1.62 x 10(11)和2.75 x 10(8)个目标拷贝ml(-1)的血液。三只(7.5%)猪和32头(80.0%)母猪均为阳性,而所有猪瘟的Myc均为阴性。结论:所开发的qPCR测定法对Myc具有高度的敏感性和特异性。 suis检测和定量。研究的意义和影响:TaqMan qPCR是检测Myc的准确而快速的测试。猪感染的猪,可以在各种仪器平台上使用。

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