Ichikawa-Seki Madoka, Hayashi Kei, Tashiro Michiyo, Khadijah S
Laboratory of Veterinary Parasitology, Faculty of Agriculture, Iwate University, 3-18-8 Ueda, Morioka 020-8550, Japan.
Laboratory of Parasitology, Faculty of Veterinary Medicine, Okayama University of Science, 1-3 Ikoinooka, Imabari 794-8555, Japan.
Infect Genet Evol. 2022 Nov;105:105373. doi: 10.1016/j.meegid.2022.105373. Epub 2022 Oct 4.
Fasciola gigantica and hybrid Fasciola flukes, responsible for the disease fasciolosis, are found in Southeast Asian countries. In the present study, we performed molecular species identification of Fasciola flukes distributed in Terengganu, Malaysia using multiplex PCR for phosphoenolpyruvate carboxykinase (pepck) and PCR-restriction fragment length polymorphism (RFLP) for DNA polymerase delta (pold). Simultaneously, phylogenetic analysis based on mitochondrial NADH dehydrogenase subunit 1 (nad1) was performed for the first time on Malaysian Fasciola flukes to infer the dispersal direction among neighboring countries. A total of 40 flukes used in this study were identified as F. gigantica. Eight nad1 haplotypes were identified in the F. gigantica population of Terengganu. Median-joining network analysis revealed that the Malaysian population was related to those obtained from bordering countries such as Thailand and Indonesia. However, genetic differentiation was detected using population genetics analyses. Nevertheless, the nucleotide diversity (π) value suggested that F. gigantica with the predominant haplotypes was introduced into Malaysia from Thailand and Indonesia. The dispersal direction suggested by population genetics in the present study may not be fully reliable since Fasciola flukes were collected from a single location in one state of Malaysia. Further studies analyzing more samples from many locations are required to validate the dispersal direction proposed herein.
导致肝片吸虫病的巨片吸虫和杂交肝片吸虫在东南亚国家被发现。在本研究中,我们使用磷酸烯醇式丙酮酸羧激酶(pepck)的多重PCR和DNA聚合酶δ(pold)的PCR-限制性片段长度多态性(RFLP)对马来西亚丁加奴州分布的肝片吸虫进行分子物种鉴定。同时,首次对马来西亚肝片吸虫基于线粒体烟酰胺腺嘌呤二核苷酸脱氢酶亚基1(nad1)进行系统发育分析,以推断其在邻国之间的传播方向。本研究中使用的总共40条吸虫被鉴定为巨片吸虫。在丁加奴州的巨片吸虫种群中鉴定出8种nad1单倍型。中位数连接网络分析表明,马来西亚种群与从泰国和印度尼西亚等邻国获得的种群有关。然而,通过群体遗传学分析检测到了遗传分化。尽管如此,核苷酸多样性(π)值表明,具有主要单倍型的巨片吸虫是从泰国和印度尼西亚引入马来西亚的。由于本研究中的肝片吸虫是从马来西亚一个州的单一地点收集的,群体遗传学所表明的传播方向可能不完全可靠。需要进一步分析来自多个地点的更多样本的研究来验证本文提出的传播方向。