{"title":"Genetic differences between Chabertia ovina and C. erschowi revealed by sequence analysis of four mitochondrial genes.","authors":"Lei Zhao, Guo-Hua Liu, Guang-Hui Zhao, Jin-Zhong Cai, Xing-Quan Zhu, Ai-Dong Qian","doi":"10.3109/19401736.2013.843089","DOIUrl":null,"url":null,"abstract":"<p><p>This study examined sequence differences in mitochondrial cytochrome c oxidase subunit 1 (cox1), large subunit ribosomal RNA (rrnL) and NADH dehydrogenase subunits 1 and 4 (nad1 and nad4) between Chabertia ovina and C. erschowi from yaks in Qinghai and goats in Shaanxi provinces, China. A part of the cox1 (pcox1), rrnL (prrnL), nad1 and nad4 genes (pnad1 and pnad4) were amplified separately from individual nematodes by PCR and sequenced. The length of the sequences of pcox1, prrnL, pnad1 and pnad4 was 441 bp, 450 bp, 526 bp and 914 bp for C. ovina, and 441 bp, 451 bp, 517 bp and 810 bp for C. erschowi, respectively. The intra-specific sequence variations within C. ovina were 0.2-2.9% for pcox1, 0-0.9% for prrnL, 0.6-2.3% for pnad1, and 0.4-2.0% for pnad4, and were 0.5-1.6% for pcox1, 0-1.1% for prrnL, 0.2-1.7% for pnad1, and 0.4-1.1% for pnad4 within C. erschowi. Whereas, the inter-specific sequence differences between the two species were obviously higher, being 11.6-12.9% for pcox1, 9.8-11.1% for prrnL, 14.4-15.9% for pnad1, and 16.4-17.7% for pnad4. Phylogenetic analyses using Bayesian inference (BI), based on combined sequences of four genes, indicated that the C. ovina and C. erschowi represent distinct species. These results demonstrate that these mt gene sequences provide novel genetic markers for the identificaiton and differentiation C. ovina and C. erschowi, and have implications for studying the population genetics and molecular epidemiology of Chabertia spp.</p>","PeriodicalId":49805,"journal":{"name":"Mitochondrial Dna","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2015-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.3109/19401736.2013.843089","citationCount":"6","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Mitochondrial Dna","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3109/19401736.2013.843089","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2013/12/11 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 6
Abstract
This study examined sequence differences in mitochondrial cytochrome c oxidase subunit 1 (cox1), large subunit ribosomal RNA (rrnL) and NADH dehydrogenase subunits 1 and 4 (nad1 and nad4) between Chabertia ovina and C. erschowi from yaks in Qinghai and goats in Shaanxi provinces, China. A part of the cox1 (pcox1), rrnL (prrnL), nad1 and nad4 genes (pnad1 and pnad4) were amplified separately from individual nematodes by PCR and sequenced. The length of the sequences of pcox1, prrnL, pnad1 and pnad4 was 441 bp, 450 bp, 526 bp and 914 bp for C. ovina, and 441 bp, 451 bp, 517 bp and 810 bp for C. erschowi, respectively. The intra-specific sequence variations within C. ovina were 0.2-2.9% for pcox1, 0-0.9% for prrnL, 0.6-2.3% for pnad1, and 0.4-2.0% for pnad4, and were 0.5-1.6% for pcox1, 0-1.1% for prrnL, 0.2-1.7% for pnad1, and 0.4-1.1% for pnad4 within C. erschowi. Whereas, the inter-specific sequence differences between the two species were obviously higher, being 11.6-12.9% for pcox1, 9.8-11.1% for prrnL, 14.4-15.9% for pnad1, and 16.4-17.7% for pnad4. Phylogenetic analyses using Bayesian inference (BI), based on combined sequences of four genes, indicated that the C. ovina and C. erschowi represent distinct species. These results demonstrate that these mt gene sequences provide novel genetic markers for the identificaiton and differentiation C. ovina and C. erschowi, and have implications for studying the population genetics and molecular epidemiology of Chabertia spp.
期刊介绍:
Previously published under the title DNA Sequence (Vols 1-19.3), Mitochondrial DNA accepts original high-quality reports based on mapping, sequencing and analysis of mitochondrial DNA and RNA. Descriptive papers on DNA sequences from mitochondrial genomes, and also analytical papers in the areas of population genetics, medical genetics, phylogenetics and human evolution that use mitochondrial DNA as a source of evidence for studies will be considered for publication. The editorial board will also consider manuscripts that examine population genetic and systematic theory that specifically address the use of mitochondrial DNA sequences.