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采用核糖体 DNA ITS1 区 PCR-RFLP 和巢式 PCR 检测和鉴别罗阿罗阿丝虫、曼氏裂头蚴和班氏丝虫。

Detection and discrimination of Loa loa, Mansonella perstans and Wuchereria bancrofti by PCR-RFLP and nested-PCR of ribosomal DNA ITS1 region.

机构信息

Servicio de Parasitología, Centro Nacional de Microbiología, Instituto de Salud Carlos III, 28220 Majadahonda, Madrid, Spain.

出版信息

Exp Parasitol. 2011 Jan;127(1):282-6. doi: 10.1016/j.exppara.2010.06.019. Epub 2010 Jun 19.

Abstract

The ribosomal deoxyribonucleic acid (DNA) internal transcribed spacer region (ITS1) of two filarial nematodes, Loa loa and Mansonella perstans, was amplified and further sequenced to develop an species-specific polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) protocol for the differentiation of both species from Wuchereria bancrofti, three filarial nematodes with blood circulating microfilariae. The ITS1-PCR product digested with the restriction endonuclease Ase I generated an specific diagnostic pattern for each of the three species. Moreover, three new specific nested-PCRs, targeting the ITS1 region, for differential detection of L. loa, M. perstans and W. bancrofti were developed and used when the ITS1-PCR products were insufficient for the Ase I enzymatic digestion. These filarial species-specific molecular protocols were evaluated in forty blood samples from African adult immigrants attending in the Hospital Insular of Gran Canaria, Canarias, Spain.

摘要

两种丝虫(罗阿丝虫和曼森氏丝虫)核糖体脱氧核糖核酸(DNA)内转录间隔区(ITS1)被扩增并进一步测序,以开发一种用于区分三种具有循环微丝蚴血液丝虫(班氏吴策线虫、罗阿丝虫和曼森氏丝虫)的种特异性聚合酶链反应-限制性片段长度多态性(PCR-RFLP)方案。ITS1-PCR 产物用限制性内切酶 Ase I 消化后,为三种物种中的每一种生成了一个特异性诊断模式。此外,还开发了三种针对 ITS1 区域的新的特异性巢式-PCR,用于检测罗阿丝虫、曼森氏丝虫和班氏吴策线虫的差异,当 ITS1-PCR 产物不足以进行 Ase I 酶切时,使用这些特异性分子方案。这些丝虫种特异性分子方案在西班牙加那利群岛大加那利岛的 Insular 医院就诊的 40 份非洲成年移民的血液样本中进行了评估。

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