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首页> 外文期刊>Experimental parasitology >Development of duplex PCR for simultaneous detection of Theileria spp. and Anaplasma spp. in sheep and goats
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Development of duplex PCR for simultaneous detection of Theileria spp. and Anaplasma spp. in sheep and goats

机译:双相PCR的开发同时检测Theileria SPP。 和anaplasma spp。 在羊和山羊

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摘要

Theileria spp. and Anaplasma spp., which are important tick-borne pathogens (TBP5), impact the health of humans and animals in tropical and subtropical areas. Theileria and Anaplasma co-infections are common in sheep and goats. Following alignment of the relevant DNA sequences, two primer sets were designed to specifically target the Theileria spp. 18S rRNA and Anaplasma spp. 16S rRNA gene sequences. Genomic DNA from the two genera was serially diluted tenfold for testing the sensitivities of detection of the primer sets. The specificities of the primer sets were confirmed when DNA from Anaplasma and Theileria (positive controls), other related hematoparasites (negative controls) and ddH2O were used as templates. Fifty field samples were also used to evaluate the utility of single PCR and duplex PCR assays, and the detection results were compared with those of the PCR methods previously published. An optimized duplex PCR assay was established from the two primer sets based on the relevant genes from the two TBPs, and this assay generated products of 298-bp (Theileria spp.) and 139-bp (Anaplasma spp.). The detection limit of the assay was 29.4 x 10(-3) ng per I, and there was no cross-reaction with the DNA from other hematoparasites. The results showed that the newly developed duplex PCR assay had an efficiency of detection (P > 0.05) similar to other published PCR methods. In this study, a duplex PCR assay was developed that can simultaneously identify Theileria spp. and Anaplasma spp. in sheep and goats. This duplex PCR is a potentially valuable assay for epidemiological studies of TBP5 in that it can detect cases of mixed infections of the pathogens. (C) 2017 Elsevier Inc. All rights reserved.
机译:Theileria SPP。和Anaplasma SPP。,这是重要的蜱传播病原体(TBP5),影响热带和亚热带地区的人类和动物的健康。 Theileria和Anaplasma的共感染是绵羊和山羊的常见。在对相关的DNA序列进行对准之后,设计了两组底漆,以特异性靶向Theileria SPP。 18s rRNA和Anaplasma SPP。 16S RRNA基因序列。来自两个属的基因组DNA是连续稀释的十倍,用于测试底漆的检测敏感性。当使用来自环胰管和Theileria(阳性对照)的DNA(阳性对照),其他相关的血催化(阴性对照)和DDH2O时,确认了引物组的特异性。还用于评估单PCR和双链PCR测定的效用,并将检测结果与先前公布的PCR方法进行比较。基于来自两种Tbps的相关基因的两个引物组建立了优化的双链PCR测定,并且该测定产生了298-BP(Theileria SPP)和139-BP(Anaplasma SPP)的产物。测定的检出限为29.4×10(-3)Ng,并且没有与其他血催化的DNA交叉反应。结果表明,新开发的双相PCR测定具有类似于其他公开的PCR方法的检测效率(P> 0.05)。在本研究中,开发了双链PCR测定,其可以同时鉴定TheLeria SPP。和anaplasma spp。在羊和山羊。这种双链PCR是TBP5的流行病学研究的潜在有价值的测定,因为它可以检测病原体的混合感染病例。 (c)2017年Elsevier Inc.保留所有权利。

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