Rokni Mohammad Bagher, Bashiri Homayoon, Raeghi Saber, Teimouri Aref, Shojaeimotlagh Vahid, Shiee Mohammad Reza, Bozorgomid Arezoo
Department of Medical Parasitology and Mycology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.
Infectious Diseases Research Center, Health Institute, Kermanshah University of Medical Sciences, Kermanshah, Iran.
Vet Res Forum. 2020 Summer;11(3):265-271. doi: 10.30466/vrf.2019.98547.2350. Epub 2020 Sep 15.
Over the last decade, diagnostic tools to detect and differentiate species have improved, but our understanding of the distribution of haplotypes and population structure of this parasite is less clear. This study was designed to survey this gap in the epidemiology in Kermanshah province, western Iran from 2015 to 2017. Sixty-eight isolates were collected from slaughterhouses from this province. We evaluated the PCR-RFLP assay of the ITS1 genes for the identification of species using the RsaI enzyme. After species identification, the partial sequence of mitochondrial NADH dehydrogenase subunit 1 (ND1) gene of was used for subsequent construction of the phylogenetic tree and network analysis. Based on the PCR-PRFLP profile, one (6.25%) of sheep isolates and 19 (39.60%) of cattle isolates were detected as , whereas 93.75% of sheep isolates, 60.40% of cattle isolates and all of the goat isolates were . In the 20 analyzed flukes, five ND1 haplotypes were detected. Statistically significant genetic differentiation was demonstrated between the Iran population and all the other populations. Evidence is presented for the existence of two well-separated populations: African and West Asian flukes and East Asian flukes. Genetic relationships among haplotypes were associated with geographical divisions. Also, our results have heightened our knowledge about the genetic diversity of , providing the first evidence for the existence of two well-separated populations of this parasite.
在过去十年中,用于检测和区分物种的诊断工具有所改进,但我们对这种寄生虫的单倍型分布和种群结构的了解仍不够清晰。本研究旨在调查2015年至2017年伊朗西部克尔曼沙阿省该寄生虫流行病学方面的这一差距。从该省的屠宰场收集了68个分离株。我们使用RsaI酶评估了ITS1基因的PCR-RFLP分析以鉴定物种。在物种鉴定后,该寄生虫线粒体NADH脱氢酶亚基1(ND1)基因的部分序列用于后续的系统发育树构建和网络分析。基于PCR-PRFLP图谱,1个(6.25%)绵羊分离株和19个(39.60%)牛分离株被检测为某种吸虫,而93.75%的绵羊分离株、60.40%的牛分离株和所有山羊分离株为另一种吸虫。在分析的20个吸虫中,检测到5种ND1单倍型。伊朗种群与所有其他种群之间存在统计学上显著的遗传分化。有证据表明存在两个明显分开的种群:非洲和西亚吸虫以及东亚吸虫。单倍型之间的遗传关系与地理划分相关。此外,我们的结果增进了我们对该吸虫遗传多样性的了解,为这种寄生虫存在两个明显分开的种群提供了首个证据。