Ichikawa-Seki Madoka, Tokashiki Minami, Opara Maxwell Nwachukwu, Iroh Gabriel, Hayashi Kei, Kumar Uday Mohanta, Itagaki Tadashi
Laboratory of Veterinary Parasitology, Faculty of Agriculture, Iwate University, 3-18-8 Ueda, Morioka, Japan.
Department of Veterinary Parasitology and Entomology, Faculty of Veterinary Medicine, University of Abuja, PMB 117, Abuja, Nigeria.
Parasitol Int. 2017 Feb;66(1):893-897. doi: 10.1016/j.parint.2016.10.010. Epub 2016 Oct 19.
Fasciola gigantica is considered the major pathogen causing fasciolosis in Africa; however, molecular characterization of this fluke has not been adequately elucidated. It is important to scientifically elucidate the dispersal history of F. gigantica by analyzing its genetic diversity. Fasciola flukes from Nigeria were analyzed using nuclear and mitochondrial DNA markers. A total of 172 Fasciola flukes collected from cattle were identified as F. gigantica because they displayed the F. gigantica fragment pattern in multiplex PCR for the nuclear marker, phosphoenolpyruvate carboxykinase (pepck). In total, 70 haplotypes were detected from Nigerian F. gigantica on the basis of the concatenated sequence of mitochondrial NADH dehydrogenase subunit 1 (nad1) and cytochrome c oxidase 1 (cox1). The index of neutrality (Fu's Fs) suggests rapid expansion of the Nigerian F. gigantica population. Although four haplogroups, Nigeria 1A, 1B, 2A, and 2B, were detected from Nigerian F. gigantica, a climate-specific genetic structure was not observed among F. gigantica populations from three agro-climatic regions (Sahel, Savannah, and Forest). This is probably because of the frequent transportation of livestock from one part of the country to the other. Nigeria 1A and 1B had close relationships with the Egyptian population of F. gigantica, whereas Nigeria 2A and 2B were comparatively related to the Zambian population. No haplotype was shared among the three countries, and it therefore is difficult to estimate the dispersal route of F. gigantica within the African continent.
巨片形吸虫被认为是非洲导致片形吸虫病的主要病原体;然而,这种吸虫的分子特征尚未得到充分阐明。通过分析其遗传多样性来科学地阐明巨片形吸虫的传播历史很重要。使用核DNA和线粒体DNA标记对来自尼日利亚的片形吸虫进行了分析。从牛身上采集的总共172条片形吸虫被鉴定为巨片形吸虫,因为它们在用于核标记磷酸烯醇丙酮酸羧激酶(pepck)的多重PCR中显示出巨片形吸虫的片段模式。基于线粒体烟酰胺腺嘌呤二核苷酸脱氢酶亚基1(nad1)和细胞色素c氧化酶1(cox1)的串联序列,从尼日利亚巨片形吸虫中总共检测到70个单倍型。中性指数(Fu's Fs)表明尼日利亚巨片形吸虫种群迅速扩张。尽管从尼日利亚巨片形吸虫中检测到四个单倍群,即尼日利亚1A、1B、2A和2B,但在来自三个农业气候区域(萨赫勒、萨凡纳和森林)的巨片形吸虫种群中未观察到特定气候的遗传结构。这可能是因为牲畜经常从该国的一个地区运输到另一个地区。尼日利亚1A和1B与埃及的巨片形吸虫种群关系密切,而尼日利亚2A和2B与赞比亚的种群相对相关。这三个国家之间没有共享单倍型,因此很难估计巨片形吸虫在非洲大陆内的传播途径。