Wu Shan G, Wang Gui T, Xi Bing W, Xiong Fan, Liu Tao, Nie Pin
Key Laboratory of Genetic Breeding and Aquaculture Biology of Freshwater Fishes, Ministry of Agriculture, Freshwater Fisheries Research Center, Chinese Academy of Fishery Sciences, Wuxi 214081, PR China.
Vet Parasitol. 2009 Oct 14;164(2-4):248-56. doi: 10.1016/j.vetpar.2009.04.030. Epub 2009 May 4.
The population genetic structure of fish parasitic nematode, Camallanus cotti, collected from the Yangtze River, Pearl River and Minjiang River in China was investigated. From these parasites, the approximately 730 bp of the first internal transcribed spacer of ribosomal DNA (ITS1 rDNA) and the 428bp of mitochondrial cytochrome c oxidase subunit I (COI) gene were sequenced. For the ITS1 rDNA data set, highly significant Fst values and low rates of migration were detected between the Pearl River group and both the Yangtze River (Fst=0.70, P<0.00001; Nm=0.21) and Minjiang River (Fst=0.73, P<0.00001; Nm=0.18) groups, while low Fst value (Fst=0.018, P>0.05) and high rate of migration (Nm=28.42) were found between the Minjiang and the Yangtze rivers. When different host/locality populations (subpopulations) within each river were considered, subpopulations between the Yangtze River and Minjiang River had low Fst values (<or=0.12) and high Nm values (>3.72), while Pearl River subpopulations were significantly different from the Yangtze River and Minjiang River subpopulations (Fst>or=0.59; Nm<1). The COI gene data set revealed a similar genetic structure. Both phylogenetic analyses and a statistical parsimony network grouped the Pearl River haplotypes into one phylogroup, while the Yangtze River and Minjiang River haplotypes formed a second group. These results suggested that the Yangtze River and Minjiang River subpopulations constituted a single reproductive pool that was distinct from the Pearl River subpopulations. In addition, the present study did not find host-related genetic differentiation occurring in the same drainage.
对采自中国长江、珠江和闽江的鱼类寄生线虫——柯氏锥体线虫(Camallanus cotti)的群体遗传结构进行了研究。从这些寄生虫中,对核糖体DNA的第一个内部转录间隔区(ITS1 rDNA)约730bp和线粒体细胞色素c氧化酶亚基I(COI)基因的428bp进行了测序。对于ITS1 rDNA数据集,在珠江群体与长江群体(Fst = 0.70,P < 0.00001;Nm = 0.21)和闽江群体(Fst = 0.73,P < 0.00001;Nm = 0.18)之间检测到高度显著的Fst值和低迁移率,而在闽江和长江之间发现低Fst值(Fst = 0.018,P > 0.05)和高迁移率(Nm = 28.42)。当考虑每条河流内不同的宿主/地点群体(亚群体)时,长江和闽江之间的亚群体具有低Fst值(≤0.12)和高Nm值(> 3.72),而珠江亚群体与长江和闽江亚群体有显著差异(Fst≥0.59;Nm < 1)。COI基因数据集揭示了类似的遗传结构。系统发育分析和统计简约网络都将珠江单倍型归为一个系统发育组,而长江和闽江单倍型形成了第二个组。这些结果表明,长江和闽江亚群体构成了一个与珠江亚群体不同的单一繁殖库。此外,本研究未发现在同一流域内存在宿主相关的遗传分化。