Thanchomnang Tongjit, Tantrawatpan Chairat, Intapan Pewpan M, Sanpool Oranuch, Janwan Penchom, Lulitanond Viraphong, Tourtip Somjintana, Yamasaki Hiroshi, Maleewong Wanchai
Research and Diagnostic Center for Emerging Infectious Diseases, Khon Kaen University, Khon Kaen, Thailand; Faculty of Medicine, Mahasarakham University, Mahasarakham, Thailand.
Research and Diagnostic Center for Emerging Infectious Diseases, Khon Kaen University, Khon Kaen, Thailand; Division of Cell Biology, Department of Preclinical Sciences, Faculty of Medicine, Thammasat University, Rangsit Campus, Pathum Thani, Thailand.
PLoS One. 2014 Jun 19;9(6):e100611. doi: 10.1371/journal.pone.0100611. eCollection 2014.
Taenia saginata, T. solium, and T. asiatica are causative agents of taeniasis in humans. The difficulty of morphological identification of human taeniids can lead to misdiagnosis or confusion. To overcome this problem, several molecular methods have been developed, but use of these tends to be time-consuming. Here, a rapid and high-throughput pyrosequencing approach was developed for the identification of three human taeniids originating from various countries. Primers targeting the mitochondrial cytochrome c oxidase subunit 1 (cox1) gene of the three Taenia species were designed. Variations in a 26-nucleotide target region were used for identification. The reproducibility and accuracy of the pyrosequencing technology was confirmed by Sanger sequencing. This technique will be a valuable tool to distinguish between sympatric human taeniids that occur in Thailand, Asia and Pacific countries. This method could potentially be used for the molecular identification of the taeniid species that might be associated with suspicious cysts and lesions, or cyst residues in humans or livestock at the slaughterhouse.
牛带绦虫、猪带绦虫和亚洲带绦虫是人类绦虫病的病原体。人体绦虫形态鉴定困难可能导致误诊或混淆。为克服这一问题,已开发出多种分子方法,但使用这些方法往往耗时。在此,开发了一种快速且高通量的焦磷酸测序方法,用于鉴定来自不同国家的三种人体绦虫。设计了靶向这三种绦虫线粒体细胞色素c氧化酶亚基1(cox1)基因的引物。利用一个26个核苷酸靶区域的变异进行鉴定。通过桑格测序证实了焦磷酸测序技术的可重复性和准确性。该技术将成为区分在泰国、亚洲和太平洋国家出现的同域人体绦虫的有价值工具。该方法有可能用于分子鉴定可能与可疑囊肿和病变相关的绦虫物种,或用于鉴定人类或屠宰场牲畜身上的囊肿残留物中的绦虫物种。