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SYBR Green 实时 HRM PCR 技术在区分波兰东部地区分离的犬巴贝斯虫原虫中的应用。

Application of the SYBR Green real-time HRM PCR technique in the differentiation of the Babesia canis canis protozoa isolated in the areas of eastern Poland.

机构信息

Department of Epizootiology and Infectious Diseases, Faculty of Veterinary Medicine, University of Life Sciences Lublin, 30 Głeboka St, 20-612, Lublin, Poland.

出版信息

Parasitol Res. 2010 Apr;106(5):1253-6. doi: 10.1007/s00436-010-1784-3. Epub 2010 Feb 13.

Abstract

The aim of this study was to determine the usefulness of the real-time polymerised chain reaction (PCR) high-resolution melting (HRM) method in the differentiation of the Babesia canis canis protozoa isolated from dogs in the areas of eastern Poland. The studies involved 20 isolates of B. canis canis qualified depending on the analysis of the 18S RNA gene sequence to group A (EU 622792) and 20 isolates qualified to group B (EU 622793). It was proven with the real-time PCR technique that the melting temperature (Tm) of the obtained products of amplification was 78 degrees C for the representatives of group A and 81 degrees C for the representatives of group B, which proves that the real-time SYBR Green HRM PCR method is a technique allowing for the differentiation of the B. canis isolates which are slightly different with respect to the genetic structure, without the necessity to carry out time-consuming studies, i.e., sequencing and restriction fragment length polymorphism.

摘要

本研究旨在确定实时聚合酶链反应(PCR)高分辨率熔解(HRM)方法在区分波兰东部地区犬巴贝斯虫分离株中的有用性。研究涉及 20 株 B. canis canis 分离株,根据 18S RNA 基因序列分析,将其分为 A 组(EU 622792)和 20 株 B 组(EU 622793)。实时 PCR 技术证明,A 组代表物扩增产物的熔点(Tm)为 78°C,B 组代表物为 81°C,这证明实时 SYBR Green HRM PCR 方法是一种能够区分遗传结构略有不同的犬巴贝斯虫分离株的技术,而无需进行耗时的研究,即测序和限制性片段长度多态性。

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