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开发一种用于检测苏拉病病原体伊氏锥虫的TaqMan PCR检测方法。

Development of a TaqMan PCR assay for the detection of Trypanosoma evansi, the agent of surra.

作者信息

Taylor T K, Boyle D B, Bingham J

机构信息

CSIRO Livestock Industries, Australian Animal Health Laboratory, Private Bag 24, Geelong, Victoria 3220, Australia.

出版信息

Vet Parasitol. 2008 May 31;153(3-4):255-64. doi: 10.1016/j.vetpar.2008.01.045. Epub 2008 Feb 13.

Abstract

A TaqMan PCR assay was developed for the detection of Trypanosoma evansi. The assay targets the internal transcribed spacer 1 (ITS-1) region of rRNA. The ITS-1 region of eleven strains of T. evansi from widely separated geographical regions were sequenced and alignments compared. Primers and probe for the test were designed from these sequence data. The assay was tested using blood from infected rats and was found to be sensitive, detecting less than one genomic equivalent of T. evansi. The assay has been tested against 10 different species of trypanosomes found in native animals in Australia and did not detect any of these trypanosome species. Time course experiments using rats infected with T. evansi were performed to compare the TaqMan assay with the Haematocrit centrifugation test (HCT) and the mouse inoculation (MI) assay. The assay was more sensitive than the HCT but not as sensitive as the MI. The TaqMan assay has the ability to rapidly detect T. evansi and determine the number of organisms present in a blood sample from an infected animal. This is the first time a TaqMan assay has been developed for the detection of T. evansi.

摘要

开发了一种TaqMan PCR检测法用于检测伊氏锥虫。该检测法靶向rRNA的内部转录间隔区1(ITS-1)区域。对来自广泛分离地理区域的11株伊氏锥虫的ITS-1区域进行了测序,并比较了序列比对。根据这些序列数据设计了检测用的引物和探针。使用感染大鼠的血液对该检测法进行了测试,发现其具有敏感性,能检测到少于一个伊氏锥虫基因组当量的病原体。该检测法针对在澳大利亚本地动物中发现的10种不同锥虫物种进行了测试,未检测到任何这些锥虫物种。使用感染伊氏锥虫的大鼠进行了时间进程实验,以将TaqMan检测法与血细胞比容离心试验(HCT)和小鼠接种(MI)检测法进行比较。该检测法比HCT更敏感,但不如MI敏感。TaqMan检测法有能力快速检测伊氏锥虫,并确定感染动物血液样本中存在的病原体数量。这是首次开发用于检测伊氏锥虫的TaqMan检测法。

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