文献类型：期刊文献

中文题名：弓首蛔虫和狮弓蛔虫线粒体nad1基因部分序列多态性研究

英文题名：DNA Polymorphism in Mitochondrial NADH Dehydrogenase Subunit-1 Within and Among Toxocara and Toxascaris Species

作者：李明伟[1,2];林瑞庆[3];邹丰才[3];何芳[3];邓艳[3];宋慧群[3];朱兴全[3]

机构：[1]广东海洋大学农学院动物医学系;[2]华南农业大学兽医学院寄生虫学研究室,广州510642;[3]华南农业大学兽医学院寄生虫学研究室

年份：2006

卷号：39

期号：9

起止页码：1915

中文期刊名：中国农业科学

外文期刊名：Scientia Agricultura Sinica

收录：CSTPCD、、北大核心2004、Scopus、CSCD2011_2012、北大核心、CSCD

基金：国家杰出青年科学基金(No.30225033);教育部留学回国人员科研启动基金[教外司留(2003)406号];教育部高等学校博士点专项科研基金(No.20040564008)资助

语种：中文

中文关键词：弓首蛔虫;狮弓蛔虫;线粒体DNA;nad1基因;PCR;单链构象多态性分析;序列分析

外文关键词：Toxocara; Toxascaris; Mitochondrial DNA; nadl ; PCR; SSCP; Sequence analysis

中文摘要：【目的】对弓首属犬弓首蛔虫、猫弓首蛔虫、马来西亚弓首蛔虫、牛弓首蛔虫和狮弓属狮弓蛔虫线粒体DNA(mtDNA)中烟酰胺脱氢酶亚基I(nad1)基因部分序列(pnad1)进行比较研究,分析它们之间的序列差异和种群遗传关系。【方法】先用同位素(γ33P)标记上下游引物,通过PCR方法扩增出单个虫体线粒体pnad1片段,然后采用单链构象多态性(SSCP)分析技术对pnad1片段进行多态性研究,最后挑选出代表性样品进行测序,并利用基因分析软件DNAStar(版本5.01)对序列进行分析比较。【结果】犬弓首蛔虫种内pnad1基因序列差异为0.3%～1.9%,与猫弓首蛔虫、马来亚弓首蛔虫、牛弓首蛔虫和狮弓蛔虫的种间序列差异分别为11.0%～14.1%、10.7%～12.4%、12.6%～13.7%和17.5%～18.2%。猫弓首蛔虫种内pnad1基因序列差异为2.8%,与马来西亚弓首蛔虫、牛弓首蛔虫和狮弓蛔虫的种间序列差异分别是12.0%～13.0%、15.1%和18.6%～21.2%。马来西亚弓首蛔虫种内pnad1基因序列差异为0～0.3%,与牛弓首蛔虫和狮弓蛔虫的种间序列差异分别是12.4%～12.8%和18.6%～19.0%。【结论】犬弓首蛔虫、猫弓首蛔虫和马来西亚弓首蛔虫不同地方虫株的pnad1序列都有一定差异(0～2.8%)。但种间pnad1的序列差异(10.7%～21.2%)明显高于种内的序列差异,说明nad1基因可以作为弓首蛔虫和狮弓蛔虫分子分类及种群遗传关系研究的遗传标记。

外文摘要：[ Objective ] The objectives of the present study were to examine sequence variation in a portion of the mitochondrial NADH dehydrogenase subunit 1 gene （pnadl ） within and among Toxocara canis, T. cati, T. malaysiensis, T. vitulorum and Toxascaris leonina, and to study their systematic and population genetics. [Method] Total genomic DNA was extracted from individuals of Toxocara and Toxascaris species from different geographical locations. The pnadl of each sample was amplified by a polymerase chain reaction （PCR） using primers end-labelled with γ^33P-ATP. Sequence variation in the pnad1 was examined and compared among these nematodes using single-strand conformation polymorphism （SSCP） analysis, followed by DNA sequencing. [ Result] While the average intraspecific variations in the pnadl sequences were 0.3% -1.9% for T. canis, 2.8% for T. cati, 0-0.3% for 77 malaysiensis from different geographical origins, the interspecific differences were 1 1.0%-14.1% between T. canis and T. cati, 10.7%-12.4% between T. canis and T. malaysiensis, 12.6%-13.7% between T. canis and T. vitulorum, 17.5%-18.2% between T. canis and T. leonina, 12.0%-13.0% between T. cati and T. malaysiensis, 15.1% between T. cati and T. vitulorum, 18.6%-21.2% between T. cati and T. leonina, 12.4%-12.8% between T. malaysiensis and T. vitulorum, and 18.6%-19.0% between T. rnalaysiensis and T. leonina. [Conclusion] The findings of this study showed that the intras-pecific variations in pnadl within these ascaridoid species were subtle, and significantly lower than interspecific differences, indicating that the pnadl provides genetic markers for the identification of these ascaridoid nematodes, and should have an important implication for studying systematic, population genetic structures and the molecular ecology of Toxocara and Toxascaris species.