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首页> 外文期刊>Experimental parasitology >Opisthorchis viverrini and Haplorchis taichui: development of a multiplex PCR assay for their detection and differentiation using specific primers derived from HAT-RAPD.
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Opisthorchis viverrini and Haplorchis taichui: development of a multiplex PCR assay for their detection and differentiation using specific primers derived from HAT-RAPD.

机译:Viistrchis viverrini和Haplorchis taichui:使用从HAT-RAPD衍生的特异性引物开发多重PCR检测和分化检测方法。

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摘要

Specific primers for the detection of Opisthorchis viverrini and Haplorchis taichui were investigated by using the HAT-RAPD PCR method. Fourteen arbitrary primers (Operon Technologies) were performed for the generation of polymorphic DNA profiles. The results showed that a 319 bp fragment generated from the OPA-04 primer was expected to be O. viverrini-specific while a 256 bp fragment generated from the OPP-11 primer was considered to be H. taichui-specific. Based on each sequence data, two pairs of specific primers were designed and sequences of each primer were as follows; H. taichui; Hapt_F5'-GGCCAACGCAATCGTCATCC-3' and Hapt_R1 5'-CTCTCGACCTCCTCTAGAAT-3' which yielded a 170 bp PCR product. For O. viverrini, OpV-1F: 5'-AATCGGGCTGCATATTGACCGAT-3' and OpV-1R: 5'-CGGTGTTGCTTATTTTGCAGACAA-3' which generated a 319 bp PCR product. These specific primers were tested for efficacy and specific detection for all parasites DNA samples. The results showed that 170 and 319 bp specific PCR products were generated as equivalent to positive result in H. taichui and O. viverrini, respectively by having no cross-reaction with any parasites tested. PCR conditions are recommended at 68 degrees C annealing temperature and with 0.5 mM magnesium chloride (Mg Cl2). Additionally, specific primers developed in this study were effective to determine the presence of both parasites in fish and snail intermediate hosts, which the DNA of O. viverrini was artificially spiked since it is rarely found in northern Thailand. The H. taichui and O. viverrini-specific primers successfully developed in this study can be use for epidemiological monitoring, preventing management and control programs.
机译:采用HAT-RAPD PCR方法研究了用于检测Visperrini viverrini和Haplorchis taichui的特异性引物。进行了十四种任意引物(Operon Technologies)用于生成多态性DNA图谱。结果表明,从OPA-04引物产生的319bp片段被认为是维氏弧菌特异性的,而从OPP-11引物产生的256bp片段被认为是太杆志贺菌的特异性。根据各序列数据,设计了两对特异性引物,各引物的序列如下。太翠Hapt_F5'-GGCCAACGCAATCGTCATCC-3'和Hapt_R1 5'-CTCTCGACCTCCTCTAGAAT-3'产生170 bp PCR产物。对于维氏弧菌,OpV-1F:5'-AATCGGGCTGCATATTGACCGAT-3'和OpV-1R:5'-CGGTGTTGCTTATTTTGCAGACAA-3',产生了319 bp PCR产物。测试了这些特异性引物对所有寄生虫DNA样品的功效和特异性检测。结果表明,通过与被测寄生虫没有交叉反应,分别产生了170 bp和319 bp的特异性PCR产物,分别相当于taichui和O. viverrini中的阳性结果。建议在68℃退火温度和0.5 mM氯化镁(Mg Cl 2 )上进行PCR条件。此外,在这项研究中开发的特异性引物可有效地确定鱼类和蜗牛中间宿主中两种寄生虫的存在,由于泰国北部很少见到这种虫,所以人为地掺入了维维立尼虫的DNA。在这项研究中成功开发的太白杆菌和维氏弧菌特异性引物可用于流行病学监测,预防管理和控制程序。

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