Al-Qassab S, Reichel M P, Ivens A, Ellis J T
Department of Medical and Molecular Biosciences, University of Technology, Sydney, P.O. Box 123, Broadway, New South Wales 2007, Australia.
Mol Cell Probes. 2009 Jun-Aug;23(3-4):132-9. doi: 10.1016/j.mcp.2009.01.006.
Infection with Neospora caninum is regarded as a significant cause of abortion in cattle. Despite the economic impact of this infection, relatively little is known about the biology of this parasite. In this study, mini and microsatellite DNAs were detected in the genome of N. caninum and eight loci were identified that each contained repetitive DNA which was polymorphic among different isolates of this parasite. A multiplex PCR assay was developed for the detection of genetic variation within N. caninum based on length polymorphism associated with three different repetitive markers. The utility of the multiplex PCR was demonstrated in that it was able to distinguish amongst strains of N. caninum used as either vaccine or challenge strains in animal vaccination experiments and that it could genotype N. caninum associated with naturally acquired infections of animals. The multiplex PCR is simple, rapid, informative and sensitive and should provide a valuable tool for further studies on the epidemiology of N. caninum in different host species.
犬新孢子虫感染被认为是牛流产的一个重要原因。尽管这种感染具有经济影响,但对这种寄生虫的生物学特性了解相对较少。在本研究中,在犬新孢子虫基因组中检测到小卫星和微卫星DNA,并鉴定出8个位点,每个位点都含有重复DNA,这些重复DNA在该寄生虫的不同分离株之间具有多态性。基于与三种不同重复标记相关的长度多态性,开发了一种多重PCR检测方法,用于检测犬新孢子虫内的遗传变异。多重PCR的实用性体现在它能够区分动物疫苗接种实验中用作疫苗或攻击株的犬新孢子虫菌株,并且能够对与动物自然感染相关的犬新孢子虫进行基因分型。该多重PCR方法简单、快速、信息丰富且灵敏,应为进一步研究犬新孢子虫在不同宿主物种中的流行病学提供有价值的工具。