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采用单链构象多态性方法区分具齿食道口线虫和四刺食道口线虫的发育阶段。

Distinguishing Oesophagostomum dentatum from Oesophagostomum quadrispinulatum developmental stages by a single-strand conformation polymorphism method.

作者信息

Gasser R B, Woods W G, Bjørn H

机构信息

Department of Veterinary Science, The University of Melbourne, Werribee, Victoria, Australia.

出版信息

Int J Parasitol. 1998 Dec;28(12):1903-9. doi: 10.1016/s0020-7519(98)00133-7.

DOI:10.1016/s0020-7519(98)00133-7
PMID:9925271
Abstract

At some life-cycle stages, it is impossible to distinguish between the two species of porcine nodular worm, Oesophagostomum dentatum and Oesophagostomum quadrispinulatum, using morphological features. A PCR-based single-strand conformation polymorphism technique was established to overcome this limitation. The rDNA region spanning the second internal transcribed spacer was amplified by PCR from genomic DNA from morphologically well-defined adult worms. The PCR products were then denatured and subjected to electrophoresis in a non-denaturing gel matrix. Single-strand conformation polymorphism analysis of the products generated characteristic and reproducible patterns for each of the two species and allowed their unequivocal delineation. The single-strand conformation polymorphism was also applied effectively to assess the purity of nine laboratory-maintained cultures of infective third-stage larvae believed to be monospecific for O. dentatum or O. quadrispinulatum. The analysis showed that all six O. dentatum cultures were indeed monospecific, whereas the three cultures believed to be monospecific for O. quadrispinulatum were either a mixture of O. dentatum and O. quadrispinulatum larvae or pure O. dentatum larvae. These findings demonstrated the usefulness of the single-strand conformation polymorphism approach for the routine monitoring of the purity of parasite "lines" and indicated its value for studies on the population biology of porcine nodular worms.

摘要

在某些生命周期阶段,利用形态学特征无法区分猪结节虫的两种物种——有齿食道口线虫和四棘食道口线虫。为克服这一局限性,建立了一种基于聚合酶链反应(PCR)的单链构象多态性技术。从形态明确的成虫基因组DNA中通过PCR扩增跨越第二个内部转录间隔区的核糖体DNA(rDNA)区域。然后将PCR产物变性,并在非变性凝胶基质中进行电泳。产物的单链构象多态性分析为这两个物种各自产生了特征性且可重复的图谱,从而能够明确区分它们。单链构象多态性还被有效地用于评估九种实验室保存的感染性三期幼虫培养物的纯度,这些培养物被认为是有齿食道口线虫或四棘食道口线虫的单物种培养物。分析表明,所有六种有齿食道口线虫培养物确实是单物种的,而三种被认为是四棘食道口线虫单物种培养物的培养物,要么是有齿食道口线虫和四棘食道口线虫幼虫的混合物,要么是纯的有齿食道口线虫幼虫。这些发现证明了单链构象多态性方法在常规监测寄生虫“品系”纯度方面的有用性,并表明了其在猪结节虫种群生物学研究中的价值。

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引用本文的文献

1
A multiplex PCR tool for the specific identification of Oesophagostomum spp. from pigs.一种用于从猪中特异性鉴定食道口线虫属物种的多重PCR工具。
Parasitol Res. 2008 Sep;103(4):993-7. doi: 10.1007/s00436-008-1070-9. Epub 2008 Jun 26.
2
Characterization of Oesophagostomum spp. from pigs in China by PCR-based approaches using genetic markers in the internal transcribed spacers of ribosomal DNA.利用核糖体DNA内转录间隔区的遗传标记,通过基于聚合酶链式反应(PCR)的方法对中国猪源食道口线虫进行鉴定
Parasitol Res. 2007 Jul;101(2):351-6. doi: 10.1007/s00436-007-0498-7. Epub 2007 Feb 22.