首页> 外文期刊>Transboundary and emerging diseases >Molecular demonstration of Trypanosoma evansi and Trypanosoma lewisi DNA in wild rodents from Cambodia, Lao PDR and Thailand.
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Molecular demonstration of Trypanosoma evansi and Trypanosoma lewisi DNA in wild rodents from Cambodia, Lao PDR and Thailand.

机译:在柬埔寨,老挝和泰国的野生啮齿动物中,伊万氏锥虫和路易斯氏锥虫DNA的分子展示。

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In this study, we investigated the molecular evidence of Trypanosoma evansi in wild rodents from Cambodia, Lao PDR and Thailand. Between November 2007 and June 2009, 1664 rodents were trapped at eight sites representative of various ecological habitats. Of those animals, 94 were tested by direct microscopic blood examination, 633 using the Card Agglutination Test for Trypanosomes (CATT/T. evansi) and 145 by Polymerase Chain Reaction (PCR) with two sets of primers: TRYP1 (amplifying ITS1 of ribosomal DNA of all trypanosomes) and TBR (amplifying satellite genomic DNA of Trypanozoon parasites). Using TRYP1, based on the size of the PCR products, 15 samples from the three countries were positive for Trypanosoma lewisi (two were confirmed by sequencing), and three were positive for Trypanozoon (one was confirmed by sequencing and three by TBR primers); the specificity of the primers failed as rodent DNA was amplified in some cases. Using TBR, six samples were positive for Trypanozoon (one was confirmed by sequencing); as T. evansi is the only species of the Trypanozoon sub-genus possibly present in Asian rodents, these results confirmed its presence in rodents from Thailand (Rattus tanezumi) and Cambodia (R. tanezumi, Niviventer fulvescens & Maxomys surifer). Further investigations are necessary to establish the situation in Lao PDR. None of the 16 samples most strongly positive to the CATT proved to be positive for Trypanozoon by PCR. The merits of the CATT for such studies were not confirmed. Studying the urban and rural circulation of these parasites in rodents will enable an evaluation of human exposure and infection risk, as human infections by T. evansi were recently described in India and by T. lewisi in India and Thailand. As sequencing PCR products is expensive, the development of new molecular and serological tools for rodents would be very useful.
机译:在这项研究中,我们调查了来自柬埔寨,老挝和泰国的野生啮齿类动物埃文氏锥虫的分子证据。在2007年11月至2009年6月之间,有1664只啮齿动物被困在八个代表各种生态栖息地的地点。在这些动物中,通过直接显微血液检查检测了94只动物,使用锥虫的卡凝集试验(CATT / T。evansi)检测了633只,通过聚合酶链反应(PCR)使用两组引物检测了145只:TRYP1(扩增核糖体DNA的ITS1)所有锥虫体和TBR(锥虫寄生虫的卫星基因组DNA扩增)。使用TRYP1,基于PCR产物的大小,来自三个国家的15个样品对路易斯氏锥虫呈阳性(两个通过测序确认),三个样品对锥虫呈阳性(一个通过测序确认,三个通过TBR引物证实);在某些情况下,由于啮齿动物DNA被扩增,引物的特异性失败。使用TBR,六种锥虫阳性呈阳性(通过测序确认其中一种);由于埃文斯氏锥虫是亚洲啮齿动物中可能存在的锥虫亚属的唯一物种,这些结果证实了它存在于泰国(Rattus tanezumi)和柬埔寨(R. tanezumi,Niviventer fulvescens和Maxomys surifer)的啮齿动物中。为了确定老挝的局势,有必要进行进一步调查。通过PCR检测,对CATT最强阳性的16个样品中没有一个对锥虫病呈阳性。 CATT在此类研究中的优点尚未得到证实。研究啮齿动物中这些寄生虫在城市和农村的流通状况,将有助于评估人类接触和感染的风险,因为最近在印度描述了埃文氏螺旋体对人类的感染,在印度和泰国也描述了T. lewisi对人体的感染。由于测序PCR产品的价格昂贵,因此开发用于啮齿动物的新分子和血清学工具将非常有用。

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