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首页> 外文期刊>Parasitology Research >Simultaneous detection and differentiation of Theileria and Babesia parasites infecting small ruminants by reverse line blotting.
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Simultaneous detection and differentiation of Theileria and Babesia parasites infecting small ruminants by reverse line blotting.

机译:反向线印迹法同时检测和区分感染小反刍动物的泰勒虫和巴贝斯虫。

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摘要

Characteristic sequence signatures were identified within the hypervariable region 4 (V4 region) of the small ribosomal RNA gene of ovine/caprine piroplasm species including Theileria lestoquardi, T. ovis, T. separata, Babesia ovis, B. motasi, B. crassa [comprising strains B. crassa (Iran) and B. crassa (Turkey)] and several novel species: Theileria sp. 1 (China), Theileria sp. 2 (China) and Babesia sp. (China), [comprising strain Babesia sp. (Lintan), and Babesia sp. (Ningxian)] as defined previously. Based on the ascertained gene variations a reverse line blotting (RLB) assay was developed enabling direct, concurrent, highly specific and sensitive identification of virtually all presently known ovine/caprine piroplasm species. All probes bound to their respective target sequence only, therefore, no cross-reaction was observed resulting in clear recognition of either individual strains, species or groups. No signal was observed when ovine and caprine genomic DNA was used as the control, demonstrating that the signals are due to the presence of parasite DNA in investigated samples. Furthermore, the sensitivity of RLB could be considerably enhanced to detect a parasitemia level of at least 10(-12)% by reamplification of PCR products (nested PCR) thereby substantially increasing the possibility of identifying carrier animals.
机译:在绵羊/山羊螺质的小核糖体RNA基因的高变区4(V4区域)中鉴定了特征序列特征,包括Theileria lestoquardi,T。ovis,T。separata,Babesia ovis,B。motasi,B。crassa [包括菌株B. crassa(伊朗)和B. crassa(土耳其)]和几个新种:Theileria sp。 1(中国),Theileria sp。 2(中国)和巴贝斯虫sp。 (中国),[由菌株Babesia sp。 (Lintan)和Babesia sp。 (宁县)]。基于确定的基因变异,开发了一种反向线印迹(RLB)分析方法,可以直接,同时,高度特异性和灵敏地鉴定几乎所有目前已知的绵羊/山羊圈螺物种。所有探针仅结合其各自的靶序列,因此,未观察到交叉反应,导致对单个菌株,物种或组的清楚识别。当使用绵羊和山羊基因组DNA作为对照时,未观察到任何信号,表明该信号是由于研究样品中存在寄生虫DNA而引起的。此外,通过重新扩增PCR产物(嵌套PCR),可以显着提高RLB的敏感性,以检测至少10(-12)%的寄生虫病水平,从而大大增加了鉴定携带动物的可能性。

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