Jeon Hyeong-Kyu, Yong Tai-Soon, Sohn Woon-Mok, Chai Jong-Yil, Hong Sung-Jong, Han Eun-Taek, Jeong Hoo-Gn, Chhakda Tep, Sinuon Muth, Socheat Duong, Eom Keeseon S
Department of Parasitology and Medical Research Institute, Chungbuk National University School of Medicine, Cheongju 361-711, Korea.
Korean J Parasitol. 2011 Jun;49(2):195-7. doi: 10.3347/kjp.2011.49.2.195. Epub 2011 Jun 14.
We collected fecal samples from 21 individuals infected with Taenia tapeworms in Koh Kong Province, Cambodia, and performed nucleotide sequencing of the cox1 gene and multiplex PCR on the eggs for DNA differential diagnosis of human Taenia tapeworms. Genomic DNA was extracted from the eggs of a minimum number of 10 isolated from fecal samples. Using oligonucleotide primers Ta7126F, Ts7313F, Tso7466F, and Rev7915, the multiplex PCR assay proved useful for differentially diagnosing Taenia solium, Taenia saginata, and Taenia asiatica based on 706, 629, and 474 bp bands, respectively. All of the Taenia specimens from Kho Kong, Cambodia, were identified as either T. saginata (n=19) or T. solium (n=2) by cox1 sequencing and multiplex PCR.
我们从柬埔寨国公省21名感染绦虫的个体中采集了粪便样本,并对cox1基因进行了核苷酸测序,同时对虫卵进行多重PCR,以对人体绦虫进行DNA鉴别诊断。从粪便样本中分离出的至少10个虫卵中提取基因组DNA。使用寡核苷酸引物Ta7126F、Ts7313F、Tso7466F和Rev7915,多重PCR检测法分别基于706、629和474 bp的条带,可有效鉴别诊断猪带绦虫、牛带绦虫和亚洲带绦虫。通过cox1测序和多重PCR,柬埔寨国公省的所有绦虫标本均被鉴定为牛带绦虫(n = 19)或猪带绦虫(n = 2)。