Ohari Yuma, Matsuo Kayoko, Yoshida Ayako, Nonaka Nariaki, Sato Hiroshi, Itagaki Tadashi
Laboratory of Veterinary Parasitology, Faculty of Agriculture, Iwate University, 3-18-8 Ueda, Morioka, 020-8550, Japan.
Department of Pathogenetic Veterinary Science, United Graduate School of Veterinary Sciences, Gifu University, 1-1 Yanagido, Gifu, 501-1193, Japan.
Parasitol Res. 2021 Apr;120(4):1341-1350. doi: 10.1007/s00436-021-07061-7. Epub 2021 Feb 8.
Understanding the population structure of Fasciola flukes in domestic and wild animals is important for determining the extent of cross-infection between them. Although the parthenogenetic Fasciola flukes in Japan have been shown to comprise five genetic types based on the ribosomal internal transcribed spacer 1 (ITS1) and mitochondrial NADH dehydrogenase subunit 1 (nad1) regions, these genetic regions are not suitable for analyzing their population structure. In the present study, the genetic diversity and population structure of the parthenogenetic Fasciola flukes in Japan were studied using microsatellite DNA, ITS1, and nad1 regions. A total of 144 parthenogenetic Fasciola flukes, obtained from cattle and sika deer in 16 localities, were individually analyzed using PCR-RFLP for ITS1, PCR-direct sequence analysis for nad1, and post-labeling PCR and capillary electrophoresis for microsatellite DNA regions. The flukes showed higher genetic diversity in the microsatellite DNA regions than ITS1 and nad1. The population structures of parthenogenetic Fasciola flukes were unclear, however, it was suggested that the flukes are more diverse populations. We hypothesized that their distribution throughout Japan is closely related to livestock movement dependent on human activity. Moreover, it is considered that cross-infection of the flukes between cattle and sika deer possibly has occurred in the past.
了解家畜和野生动物体内肝片吸虫的种群结构对于确定它们之间交叉感染的程度很重要。尽管日本孤雌生殖的肝片吸虫已被证明根据核糖体内部转录间隔区1(ITS1)和线粒体烟酰胺腺嘌呤二核苷酸脱氢酶亚基1(nad1)区域可分为五种遗传类型,但这些遗传区域并不适合分析它们的种群结构。在本研究中,利用微卫星DNA、ITS1和nad1区域对日本孤雌生殖肝片吸虫的遗传多样性和种群结构进行了研究。从16个地区的牛和梅花鹿身上采集了总共144条孤雌生殖肝片吸虫,分别采用PCR-RFLP分析ITS1、PCR直接测序分析nad1以及微卫星DNA区域的标记后PCR和毛细管电泳进行分析。肝片吸虫在微卫星DNA区域显示出比ITS1和nad1更高的遗传多样性。然而,孤雌生殖肝片吸虫的种群结构尚不清楚,不过提示这些吸虫是更为多样的种群。我们推测它们在日本的分布与依赖人类活动的家畜移动密切相关。此外,认为过去可能已发生过牛和梅花鹿之间肝片吸虫的交叉感染。