首页> 外文期刊>Molecular and Cellular Probes: The Location, Diagnosis and Monitoring of Disease by Specific Molecules and Cell Lines >Molecular detection of Mycoplasma haemomuris subspecies using dnaK-targeted real-time PCR with SYBR Green I and melting curve analysis
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Molecular detection of Mycoplasma haemomuris subspecies using dnaK-targeted real-time PCR with SYBR Green I and melting curve analysis

机译:使用SYBR Green I的dnaK靶向实时荧光定量PCR检测溶血支原体亚种并进行熔解曲线分析

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摘要

Hemoplasmas cause severe infections in mammals, but these pathogens are difficult to detect and identify at the species and subspecies level because of the need for time-consuming sequence based methods. Here, we used real-time PCR with SYBR Green I targeting of the dnaK gene followed by standard melting curve analysis to achieve rapid detection and differentiation of the Mycoplasma haemomuris subspecies 'Candidatus Mycoplasma haemomuris subsp. musculi' and 'Candidatus M. haemomuris subsp. ratti'. The melting temperatures of the PCR products, 84.63 +/- 0.14 degrees C for 'Candidatus M. haemomuris subsp. musculi', and 80.72 +/- 0.16 degrees C for 'Candidatus M. haemomuris subsp. ratti', provided clear differentiation between them. Murine hemoplasma DNA samples, which were used as references, were confirmed for species by an analysis of 16S rRNA sequences. The protocol described herein provides a new rapid detection and identification method suitable for use with two recognized subspecies of M. haemomuris. (C) 2016 Elsevier Ltd. All rights reserved.
机译:血肿在哺乳动物中引起严重的感染,但是由于需要耗时的基于序列的方法,这些病原体很难在物种和亚种水平上进行检测和鉴定。在这里,我们对dnaK基因使用SYBR Green I靶向进行实时PCR,然后进行标准熔解曲线分析,以快速检测和区分血统支原体亚种'Candidatus Mycoplasma haemomuris亚种。 musculi'和'Candidatus M. haemomuris subsp。批准”。 PCR产物的解链温度为'C.idad.M. haemomuris'subsp。的84.63 +/- 0.14℃。 musculi''和'Candidatus M. haemomuris subsp。的80.72 +/- 0.16摄氏度。比例”,从而明确区分它们。通过对16S rRNA序列的分析,确定了用作参考的鼠血质DNA样品的种类。本文所述的协议提供了一种新的快速检测和鉴定方法,适用于与血统分枝杆菌的两个公认的亚种一起使用。 (C)2016 Elsevier Ltd.保留所有权利。

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