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Detection and differentiation of ovine Theileria and Babesia by reverse line blotting in China

机译:反向线印迹法在中国检测和鉴别绵羊纹状体和巴氏杆菌

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A reverse line blot (RLB) assay was developed for detection and specific identification of the different ovine Theileria and Babesia parasites. In a polymerase chain reaction (PCR), the hypervariable region 4 (V4 region) of the 18S ribosomal DNA gene was amplified with a set of general primers specific for members of the genera Theileria and Babesia. Meanwhile, specific oligonucleotide probes were designed and bound on membrane. After one single-PCR amplification, the amplified fragment was hybridized against different generic and species-specific probes. It was able to detect four species, i.e., Babesia motasi (Chengde, Lintan, Ningxian, Tianzhu), Babesia sp. (Kashi), Theileria luwenshuni (Lintan, Madang, Ningxian), Theileria uilenbergi (Longde, Zhangjiachuan) as defined previously. 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 in normal positive tests. Meanwhile, no signal was observed when ovine genomic DNA and water were used as a control, demonstrating that the signals are due to the presence of parasite DNA in the samples. Furthermore, the sensitivity of RLB could be considerably enhanced to detect a parasitemia level between10−3% and 10−8%. Finally, 117 samples from field were tested with RLB, PCR, and enzyme-linked immunosorbent assay (ELISA). The positive rate of RLB was higher than that of PCR and ELISA, and furthermore, RLB could determinate the species of piroplasms, the samples were infected with. Samples, 1,117, from five areas in Gannan Tibet Autonomous Region have been examined with RLB assay and compared with ELISA assay for corresponding samples. The results showed that the positive rate of RLB was higher than that of ELISA test obviously, and both T. luwenshuni and T. uilenbergi were widely distributed in these areas. RLB developed here could be used for differentiation of Babesia and Theileria infection and for epidemiological survey, which was difficult to achieve by classical methods. In conclusion, the RLB is a versatile technique for simultaneous detection and identification of all ovine piroplasms.
机译:开发了反向线印迹(RLB)测定法,用于检测和特异性鉴定不同的绵羊Theileria和Babesia寄生虫。在聚合酶链反应(PCR)中,用一组特异性针对Theileria和Babesia属的通用引物扩增18S核糖体DNA基因的高变区4(V4区)。同时,设计了特异性寡核苷酸探针并结合在膜上。单次PCR扩增后,将扩增的片段与不同的通用探针和物种特异性探针杂交。它能够检测出4个物种,即巴西巴贝斯虫(承德,临潭,宁县,天竺),巴贝斯虫。 (喀什),Theileria luwenshuni(临潭,马当,宁县),Theileria uilenbergi(隆德,张家川)。所有探针仅结合其各自的靶序列;因此,没有观察到交叉反应,从而在正常阳性试验中清楚地识别出各个菌株,物种或组。同时,当使用绵羊基因组DNA和水作为对照时未观察到信号,表明该信号是由于样品中存在寄生虫DNA引起的。此外,可以显着提高RLB的灵敏度,以检测10 -3 %和10 -8 %之间的寄生虫水平。最终,使用RLB,PCR和酶联免疫吸附测定(ELISA)对来自野外的117个样品进行了测试。 RLB的阳性率高于PCR和ELISA,并且RLB可以确定感染的标本的种类。西藏自治区甘南自治区五个地区的1117份样品已用RLB法进行了检测,并与ELISA法进行了比较。结果表明,RLB的阳性率明显高于ELISA检测,卢温氏杜氏杆菌和尤伦贝氏锥虫均分布在这些地区。此处开发的RLB可用于区分巴贝虫和泰勒虫感染以及进行流行病学调查,这是经典方法难以实现的。总而言之,RLB是一种用于同时检测和鉴定所有绵羊亚种质的通用技术。

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