Department of Medical Microbiology, College of Health Sciences, University of Zimbabwe, Avondale, P. O. Box A178, Harare, Zimbabwe.
Ministry of Health and Child Care, National Institute of Health Research, Causeway, P.O. Box CY573, Harare, Zimbabwe.
Mol Biol Rep. 2020 Jul;47(7):4975-4987. doi: 10.1007/s11033-020-05541-0. Epub 2020 Jun 12.
The fresh water snail Biomphalaria pfeifferi is the intermediate host for Schistosoma mansoni, which causes human intestinal schistosomiasis in Zimbabwe. Despite the medical importance of this intermediate host, there are no current data on its molecular characterization in Zimbabwe. In 2016, human water contact sites were identified in four communities in Madziwa area, Shamva district, Zimbabwe. The survey sites were recorded and mapped using a global positioning system. A 655 bp region of the mitochondrial cytochrome oxidase subunit I gene was amplified in 70 B. pfeifferi snails. The sequence data were analysed to determine the relationships between the individual snails, their inter, intra population diversity and structure. Overall, four unique cox1 haplotypes, with a haplotype diversity of 0.608, were identified in the snails. One haplotype spanned across most of the sites. There was no clear geographical clustering of haplotypes. The mean diversity among the haplotypes was very low (0.009), while the net divergence among the collection sites ranged from 0.000 to 0.026. The diversity within and between the sites was 0.017 and 0.012 respectively. This data advances our knowledge of the understanding of the population structure of B. pfeifferi in Madziwa area, Zimbabwe, with the high occurrence of one haplotype indicating the possibility of a recent bottleneck followed by population expansion. The population genetic structure of B. pfeifferi snails described here has provided an opportunity to investigate the contribution of snail genetics to variation in disease burden; and development of control strategies that exploit genetic differences in susceptibility to parasites.
淡水蜗牛玻氏巴蜗牛是曼氏血吸虫的中间宿主,这种血吸虫会导致津巴布韦的人类肠道血吸虫病。尽管这种中间宿主具有重要的医学意义,但目前津巴布韦还没有关于其分子特征的相关数据。2016 年,在津巴布韦 Shamva 区 Madziwa 地区的四个社区确定了人类接触水的地点。使用全球定位系统记录和绘制了调查地点。在 70 只玻氏巴蜗牛中扩增了线粒体细胞色素氧化酶亚基 I 基因的 655bp 区域。对序列数据进行了分析,以确定个体蜗牛之间的关系、它们的种群内和种群间的多样性和结构。总体而言,在蜗牛中发现了四个独特的 cox1 单倍型,单倍型多样性为 0.608。一个单倍型跨越了大部分地点。没有明显的地理聚类。各单倍型之间的平均多样性非常低(0.009),而各采集地点之间的净分歧范围从 0.000 到 0.026。地点内和地点间的多样性分别为 0.017 和 0.012。该数据增进了我们对津巴布韦 Madziwa 地区玻氏巴蜗牛种群结构的理解,一个单倍型的高发生率表明可能存在近期瓶颈效应,随后是种群扩张。这里描述的玻氏巴蜗牛的种群遗传结构为研究蜗牛遗传对疾病负担变化的贡献提供了机会;并制定利用寄生虫易感性遗传差异的控制策略。