Ito Akira, Yamasaki Hiroshi, Nakao Minoru, Sako Yasuhito, Okamoto Munehiro, Sato Marcello O, Nakaya Kazuhiro, Margono Sri S, Ikejima Takashi, Kassuku Ayub A, Afonso Sonia M S, Ortiz Washington Benitez, Plancarte Agustin, Zoli Andre, Geerts Stanny, Craig Philip S
Department of Parasitology, Asahikawa Medical College, Asahikawa 078-8510, Japan.
Acta Trop. 2003 Jun;87(1):95-101. doi: 10.1016/s0001-706x(03)00024-x.
Mitochondrial DNA sequences of Taenia solium have fully been analyzed. Analysis of the full length of cytochrome c oxidase subunit 1 (1620 bp) and cytochrome b (1068 bp) genes of T. solium, isolated from Asia (China, Thailand, Indonesia and India), from Latin America (Mexico, Ecuador, Bolivia, Peru and Brazil) and from Africa (Tanzania, Mozambique and Cameroon), has revealed that the two phylogenies obtained were similar to each other regardless of the genes examined. The isolates from Asia formed a single cluster, whereas those from Latin America combined with those from Africa to form an additional cluster. It was estimated that these two genotypes emerged approximately 4-8 x 10(5) years ago. These results together with recent study of the ancient of human taeniid cestodes emerged several MYA in Africa, historical data on swine domestication, distribution of pigs and colonization patterns suggest that T. solium was introduced recently into Latin America and Africa from different regions of Europe during the colonial age, which started 500 years ago, and that T. solium of another origin independently spread in Asian countries, perhaps from China. Why did not T. solium of European origin invade or spread into Asia during the colonial age? Analysis of T. solium distribution must include other Taenia species, especially T. saginata and T. asiatica, which can not be differentiated from each other morphologically. BESS T-base analysis for differentiation of all human Taenia species including the two genotypes of T. solium, and T. saginata and T. asiatica has also been characterized. BESS T-base analysis differentiates African isolates from Latin American isolates as well but more samples should be analyzed for obtaining conclusive evidence for the latter. Serological analysis of cyst fluid of T. solium cysticerci obtained in China and Indonesia and from Mozambique and Ecuador indicates geographical differences in their banding patterns. These differences are discussed in the light of possible differences in pathology of T. solium worldwide. As it has been speculated that the ancient T. solium emerged several million years ago in Africa, it is necessary to analyze more isolates from Africa. Such working hypothesis may be evaluated combined with symptomatology and serology when we get additional DNA data from such areas, since there are some varieties of manifestation of neurocysticercosis with or without subcutaneous cysticercosis and of antigens of cyst fluid of T. solium from Asia and from Africa and/or America. Transfer of techniques of molecular identification and sero- and immuno-diagnoses between researchers and technicians from endemic countries using their own materials should be promoted with the aim of better international cooperation for the control of cysticercosis.
猪带绦虫的线粒体DNA序列已得到充分分析。对从亚洲(中国、泰国、印度尼西亚和印度)、拉丁美洲(墨西哥、厄瓜多尔、玻利维亚、秘鲁和巴西)以及非洲(坦桑尼亚、莫桑比克和喀麦隆)分离出的猪带绦虫的细胞色素c氧化酶亚基1(1620 bp)和细胞色素b(1068 bp)基因全长进行分析后发现,无论检测的是哪个基因,所获得的两个系统发育树彼此相似。来自亚洲的分离株形成一个单一的聚类,而来自拉丁美洲的分离株与来自非洲的分离株合并形成另一个聚类。据估计,这两种基因型大约在4 - 8×10⁵年前出现。这些结果连同最近对几百万年前出现在非洲的人类带绦虫的古代研究、猪驯化的历史数据、猪的分布和殖民模式表明,猪带绦虫是在500年前开始的殖民时代从欧洲不同地区最近引入拉丁美洲和非洲的,并且另一个起源的猪带绦虫在亚洲国家独立传播,可能来自中国。为什么欧洲起源的猪带绦虫在殖民时代没有侵入或传播到亚洲?猪带绦虫分布的分析必须包括其他带绦虫物种,特别是牛带绦虫和亚洲带绦虫,它们在形态上无法相互区分。还对包括猪带绦虫的两种基因型以及牛带绦虫和亚洲带绦虫在内的所有人类带绦虫物种进行了用于区分的BESS T碱基分析。BESS T碱基分析也能区分非洲分离株和拉丁美洲分离株,但需要分析更多样本以获得后者的确凿证据。对在中国、印度尼西亚以及莫桑比克和厄瓜多尔获得的猪带绦虫囊尾蚴囊液进行的血清学分析表明,它们的条带模式存在地理差异。根据全球猪带绦虫病理学可能存在的差异对这些差异进行了讨论。由于据推测古代猪带绦虫几百万年前在非洲出现,因此有必要分析更多来自非洲的分离株。当我们从这些地区获得更多DNA数据时,这种工作假设可以结合症状学和血清学进行评估,因为亚洲、非洲和/或美洲的猪带绦虫囊液抗原存在一些伴有或不伴有皮下囊尾蚴病的神经囊尾蚴病表现形式。应促进来自流行国家的研究人员和技术人员之间使用他们自己的材料进行分子鉴定以及血清学和免疫诊断技术的转移,以更好地开展控制囊尾蚴病的国际合作。