实验研究

云南省中华按蚊种群mtDNA-COⅠ基因序列的遗传结构分析

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  • 云南省寄生虫病防治所应急办公室, 云南省疟疾研究中心, 云南省虫媒传染病防控研究重点实验室, 云南省寄生虫病防治所虫媒传染病防控关键技术省创新团队(培育), 面向南亚东南亚热带病国际科技人员交流与教育培训基地, 云南 普洱 665000
曾旭灿,男,副主任医师,从事寄生虫病防控研究工作,E-mail:531044248@qq.com

收稿日期: 2020-12-30

  网络出版日期: 2021-06-20

基金资助

国家自然科学基金(81960374);云南省医疗卫生单位内设研究机构科研项目(2017NS120)

A genetic structure analysis of mtDNA COⅠ gene sequence of Anopheles sinensis populations in Yunnan province, China

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  • Emergency Office, Yunnan Institute of Parasitic Diseases, Yunnan Provincial Center of Malaria Research, Yunnan Provincial Key Laboratory of Vector-borne Diseases Control and Research, Yunnan Institute of Parasitic Diseases Innovative Team of Key Techniques for Vector Borne Disease Control and Prevention(Developing), Training Base of International Scientific Exchange and Education in Tropical Diseases for South and Southeast Asia, Pu'er, Yunnan 665000, China

Received date: 2020-12-30

  Online published: 2021-06-20

Supported by

Supported by the National Natural Science Foundation of China (No. 81960374) and the Scientific Research Projects of Internal Research Institutes of Health Units in Yunnan Province (No. 2017NS120)

摘要

目的 通过对云南省中华按蚊线粒体DNA细胞色素C氧化酶亚基Ⅰ(mtDNA-COⅠ)基因进行分析,探讨当地中华按蚊种群间的遗传变异和种群结构特征。方法 2018-2019年,在绥江、勐腊、腾冲、罗平、元江、富宁县(市)6个采样点使用功夫小帅诱蚊灯采集蚊虫。经过形态学和分子生物学鉴定为中华按蚊后,对线粒体COⅠ基因扩增后测序。测序结果用MEGA 6软件对比分析,用DnaSP 5软件计算各地中华按蚊种群的多态性相关指数和错配分析。Arlequin 3.5.2.2软件进行分子变异分析(AMOVA)和中性检验,以及计算遗传分化FST值和基因交流值(Nm值)。结果 6个中华按蚊种群共成功扩增210个样本,有96种单倍型,单倍型多样性为0.97,核苷酸多样性为0.011。种群内变异率为90.80%,种群间变异率为9.20%,绥江和罗平县FST值最高为0.21,基因流最低为0.96,除腾冲市外,其余地区Tajima’s D的值均为负值,且均P>0.05,错配分析时曲线呈双峰。结论 云南省内中华按蚊种群有丰富的遗传多样性,种群内变异大于种群间变异,绥江和罗平县存在遗传分化,其他地区无遗传分化。云南省中华按蚊种群近期未出现种群扩张。

本文引用格式

曾旭灿, 许翔, 杨锐, 魏春, 吴林波, 罗春海, 孙晓东 . 云南省中华按蚊种群mtDNA-COⅠ基因序列的遗传结构分析[J]. 中国媒介生物学及控制杂志, 2021 , 32(3) : 265 -270 . DOI: 10.11853/j.issn.1003.8280.2021.03.002

Abstract

Objective To explore the genetic variation and population structure of Anopheles sinensis by analyzing the mitochondrial cytochrome c oxidase subunitⅠ(mtDNA COⅠ) gene of An. sinensis in Yunnan province, China. Methods From 2018 to 2019, mosquito trap lamps (Gongfu Xiaoshuai) were used to collect mosquitoes in six sampling sites, namely, Suijiang, Mengla, Tengchong, Luoping, Yuanjiang, and Funing. After the mosquitoes were identified as An. sinensis via morphology and molecular biology, the mitochondrial COⅠ gene was amplified and sequenced. MEGA 6 software was used to analyze the sequencing results, and DnaSP5 software was used to calculate the polymorphism-related indices and perform the mismatch analysis of An. sinensis populations from various areas. Arlequin 3.5.2.2 software was used to perform the analysis of molecular variance and neutrality tests and calculate the genetic differentiation (FST values) and the number of migrants (Nm values). Results In this study, 210 samples were successfully amplified from 6 An. sinensis populations (from six sampling sites) and there were 96 haplotypes. The haplotype diversity was 0.97 and nucleotide diversity was 0.011; the intra-population variation rate was 90.80% and the inter-population variation rate was 9.20%. Suijiang and Luoping had the highest FST value (0.21) and the lowest Nm (0.96). Apart from Tengchong, the Tajima's D values in other places were negative, and the P values were all greater than 0.05. The mismatch analysis showed that the curve had two peaks. Conclusion There is abundant genetic diversity among An. sinensis populations in Yunnan province and the rate of intra-population variation is greater than that of inter-population variation. Genetic differentiation is observed in Suijiang and Luoping, with no genetic differentiation observed in other areas. There is no population expansion of An. sinensis in Yunnan province recently.

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