| 基于DNA条形码技术的湖南省柑橘主产区实蝇幼虫分子鉴定 |
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| 引用本文：张岳,张佳峰,秦誉嘉,曾译影,李志红.基于DNA条形码技术的湖南省柑橘主产区实蝇幼虫分子鉴定.植物保护学报,2019,46(1):71-81 |
| DOI：10.13802/j.cnki.zwbhxb.2019.2019909 |
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| 中文摘要:为明确湖南省柑橘主产区的实蝇入侵为害现状，从该省7个市（自治州）22个地点收集柑橘蛆果中的幼虫，利用DNA条形码技术对其进行分子鉴定，并以DNA条形码序列作为分子标记探究橘大实蝇Bactrocera minax的20个中国地理种群（湖南省6个组群共16个种群、其它3省市4个种群）以及1个印度地理种群间的亲缘地理关系，分析橘大实蝇在我国的遗传进化关系。结果表明，仅采集自邵阳市城步苗族自治县柑橘蛆果中的5头幼虫被鉴定为蜜柑大实蝇B.tsuneonis，其余21个地点采集的595头幼虫均被鉴定为橘大实蝇。21个橘大实蝇地理种群的平均单倍型多样性为0.75，核苷酸多样性为0.0032，核苷酸差异数为2.13，中国所有地理种群均具有较高的遗传多样性；单倍型网络进化图显示湖南、重庆、贵州种群共享的单倍型H3为原始单倍型，表明其为比较原始的种群；AMOVA分析结果显示种群内个体间遗传变异占总体变异的59.04%，是遗传变异的主要来源；遗传分化结果表明湖南省6个组群间均出现了中度至高度的遗传分化，FST在0.0521~0.7795之间。表明DNA条形码技术可用于蜜柑大实蝇和橘大实蝇幼虫的分子鉴定及其种群遗传进化分析。 |
| 中文关键词:蜜柑大实蝇 橘大实蝇 DNA条形码技术 种群遗传结构 |
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| Molecular identification of the fruit fly larvae in major citrus production areas in Hunan Province based on DNA barcoding |
| Author Name | Affiliation | E-mail | | Zhang Yue | Department of Entomology, College of Plant Protection, China Agricultural University, Beijing 100193, China | | | Zhang Jiafeng | Hunan Plant Protection and Plant Quarantine Station, Changsha 410006, Hunan Province, China | | | Qin Yujia | Department of Entomology, College of Plant Protection, China Agricultural University, Beijing 100193, China | | | Zeng Yiying | Department of Entomology, College of Plant Protection, China Agricultural University, Beijing 100193, China | | | Li Zhihong | Department of Entomology, College of Plant Protection, China Agricultural University, Beijing 100193, China | lizh@cau.edu.cn |
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| Abstract:To investigate the invasion and damage of fruit flies in major citrus main production areas in Hunan Province, the larvae from 22 sites of seven cities or autonomic prefectures in Hunan were collected and identified with DNA barcoding. The DNA barcoding sequences were used as molecular markers to explore the phylogeography of Bactrocera minax, including 20 geographical populations from China (16 geographical populations in six groups of Hunan Province and four geographical populations of other three provinces or cities) and one geographical population from India, and analyze the population genetic structure. The results showed that five individuals collected from Chengbu Miao Autonomous County of Shaoyang City were identified as B. tsuneonis, and 595 individuals collected from the other 21 sites were identified as B. minax. The average haplotype diversity, nucleotide diversity and numbers of nucleotide differences of the 21 geographical populations were 0.75, 0.0032 and 2.13, respectively. All the populations from China had high genetic diversity. Haplotype network revealed that H3 shared by Hunan, Chongqing, Guizhou populations was the original haplotype, which implied that the above three provinces or city might share the same origin. AMOVA analysis showed that the variation within populations was the main source of variation, contributing 59.04% of total genetic variation. Genetic differentiation analysis indicted that the six groups in Hunan had moderate to high genetic differentiation, with the FST values between 0.0521 and 0.7795. The results indicated that DNA barcodes could be an effective method for the molecular identification and population genetic structure analysis of B. minax and B. tsuneonis. |
| keywords:Bactrocera tsuneonis Bactrocera minax DNA barcode population genetic structure |
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