Sulaiman Irshad M, Torres Patricia, Simpson Steven, Kerdahi Khalil, Ortega Ynes
Microbiological Sciences Branch, Southeast Regional Laboratory, Food and Drug Administration, 60, Eighth Street NE, Atlanta, Georgia 30309, USA.
J Parasitol. 2013 Apr;99(2):379-82. doi: 10.1645/GE-3114.1. Epub 2012 Aug 27.
We have described the development of a 2-step nested PCR protocol based on the characterization of the 70-kDa heat shock protein (HSP70) gene for rapid detection of the human-pathogenic Cyclospora cayetanensis parasite. We tested and validated these newly designed primer sets by PCR amplification followed by nucleotide sequencing of PCR-amplified HSP70 fragments belonging to 16 human C. cayetanensis isolates from 3 different endemic regions that include Nepal, Mexico, and Peru. No genetic polymorphism was observed among the isolates at the characterized regions of the HSP70 locus. This newly developed HSP70 gene-based nested PCR protocol provides another useful genetic marker for the rapid detection of C. cayetanensis in the future.
我们基于对70 kDa热休克蛋白(HSP70)基因的特性描述,开发了一种两步巢式PCR方案,用于快速检测人类致病的卡耶塔环孢子虫寄生虫。我们通过PCR扩增,随后对来自尼泊尔、墨西哥和秘鲁这3个不同流行地区的16株人类卡耶塔环孢子虫分离株的PCR扩增HSP70片段进行核苷酸测序,对这些新设计的引物组进行了测试和验证。在HSP70基因座的特征区域,分离株之间未观察到基因多态性。这种新开发的基于HSP70基因的巢式PCR方案为未来快速检测卡耶塔环孢子虫提供了另一个有用的遗传标记。