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太氏半尾吸虫,维滕贝格,1930年:用于检测微小肠道吸虫感染的HAT-RAPD标记的开发。

Haplorchis taichui, Witenberg, 1930: Development of a HAT-RAPD marker for the detection of minute intestinal fluke infection.

作者信息

Wongsawad Chalobol, Wongsawad Pheravut, Chai Jong Yil, Anuntalabhochai Somboon

机构信息

Department of Biology, Chiang Mai University, Chiang Mai Province, Thailand.

出版信息

Exp Parasitol. 2009 Oct;123(2):158-61. doi: 10.1016/j.exppara.2009.06.016. Epub 2009 Jun 27.

Abstract

Specific primers to determine the presence of an intestinal fluke, Haplorchis taichui, were investigated using the high annealing temperature random amplified polymorphic DNA (HAT-RAPD) PCR, and 18 arbitrary primers (Operon Technologies), to generate different polymorphic DNA profiles. Thirteen kinds of parasites were used to compare fingerprints. A 256bp HAT-RAPD marker, generated from the OPP-11 primer, was found to be H. taichui-specific, and this marker was cloned, transformed, and sequenced. From the sequence data, a pair of primers were designed with Genetyx-MAC ver.11 and indicated as: Hap-t F 5'-GGC CAA CGC AAT CGT CAT CC-3' and Hap-t R 5'-GCG TCG GGT TTC AGA CAT GG-3'. These specific primers were tested for efficacy and specificity by amplifying them with all 13 parasites DNAs in PCR reaction. A 256bp amplicon was generated, which was shown to have a positive result, only for H. taichui DNA. It revealed no cross-reaction with any of the other tested parasite species. The minimum DNA template, needed for detection by PCR, was 0.1picogram (pg). The successful development of H. taichui-specific primers is expected to be beneficial for epidemiological studies and for prevention and control of these parasitic infections.

摘要

使用高退火温度随机扩增多态性DNA(HAT-RAPD)PCR和18种任意引物(Operon Technologies公司)研究了用于确定肠道吸虫——泰国棘口吸虫存在的特异性引物,以产生不同的多态性DNA图谱。使用13种寄生虫来比较指纹图谱。发现由OPP-11引物产生的一个256bp的HAT-RAPD标记是泰国棘口吸虫特异性的,对该标记进行了克隆、转化和测序。根据序列数据,使用Genetyx-MAC ver.11设计了一对引物,序列如下:Hap-t F 5'-GGC CAA CGC AAT CGT CAT CC-3'和Hap-t R 5'-GCG TCG GGT TTC AGA CAT GG-3'。通过在PCR反应中用所有13种寄生虫的DNA扩增这些特异性引物,测试了其有效性和特异性。产生了一个256bp的扩增子,结果显示仅对泰国棘口吸虫的DNA呈阳性。它与任何其他测试的寄生虫物种均未显示交叉反应。PCR检测所需的最小DNA模板量为0.1皮克(pg)。泰国棘口吸虫特异性引物的成功开发有望对流行病学研究以及这些寄生虫感染的预防和控制有益。

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