Genetic structure and symbiotic profile of worldwide natural populations of the Mediterranean fruit fly, Ceratitis capitata.

IF 2.9 Q2 Biochemistry, Genetics and Molecular Biology
Katerina Nikolouli, Antonios A Augustinos, Panagiota Stathopoulou, Elias Asimakis, Anastasios Mintzas, Kostas Bourtzis, George Tsiamis
{"title":"Genetic structure and symbiotic profile of worldwide natural populations of the Mediterranean fruit fly, Ceratitis capitata.","authors":"Katerina Nikolouli, Antonios A Augustinos, Panagiota Stathopoulou, Elias Asimakis, Anastasios Mintzas, Kostas Bourtzis, George Tsiamis","doi":"10.1186/s12863-020-00946-z","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>The Mediterranean fruit fly, Ceratitis capitata, is a cosmopolitan agricultural pest of worldwide economic importance and a model for the development of the Sterile Insect Technique (SIT) for fruit flies of the Tephritidae family (Diptera). SIT relies on the effective mating of laboratory-reared strains and natural populations, and therefore requires an efficient mass-rearing system that will allow for the production of high-quality males. Adaptation of wild flies to an artificial laboratory environment can be accompanied by negative effects on several life history traits through changes in their genetic diversity and symbiotic communities. Such changes may lead to reduced biological quality and mating competitiveness in respect to the wild populations. Profiling wild populations can help understand, and maybe reverse, deleterious effects accompanying laboratory domestication thus providing insects that can efficiently and effectively support SIT application.</p><p><strong>Results: </strong>In the present study, we analyzed both the genetic structure and gut symbiotic communities of natural medfly populations of worldwide distribution, including Europe, Africa, Australia, and the Americas. The genetic structure of 408 individuals from 15 distinct populations was analyzed with a set of commonly used microsatellite markers. The symbiotic communities of a subset of 265 individuals from 11 populations were analyzed using the 16S rRNA gene-based amplicon sequencing of single individuals (adults). Genetic differentiation was detected among geographically distant populations while adults originated from neighboring areas were genetically closer. Alpha and beta diversity of bacterial communities pointed to an overall reduced symbiotic diversity and the influence of the geographic location on the bacterial profile.</p><p><strong>Conclusions: </strong>Our analysis revealed differences both in the genetic profile and the structure of gut symbiotic communities of medfly natural populations. The genetic analysis expanded our knowledge to populations not analyzed before and our results were in accordance with the existing scenarios regarding this species expansion and colonization pathways. At the same time, the bacterial communities from different natural medfly populations have been characterized, thus broadening our knowledge on the microbiota of the species across its range. Genetic and symbiotic differences between natural and laboratory populations must be considered when designing AW-IPM approaches with a SIT component, since they may impact mating compatibility and mating competitiveness of the laboratory-reared males. In parallel, enrichment from wild populations and/or symbiotic supplementation could increase rearing productivity, biological quality, and mating competitiveness of SIT-important laboratory strains.</p>","PeriodicalId":9197,"journal":{"name":"BMC Genetics","volume":null,"pages":null},"PeriodicalIF":2.9000,"publicationDate":"2020-12-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7747371/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"BMC Genetics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1186/s12863-020-00946-z","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
引用次数: 0

Abstract

Background: The Mediterranean fruit fly, Ceratitis capitata, is a cosmopolitan agricultural pest of worldwide economic importance and a model for the development of the Sterile Insect Technique (SIT) for fruit flies of the Tephritidae family (Diptera). SIT relies on the effective mating of laboratory-reared strains and natural populations, and therefore requires an efficient mass-rearing system that will allow for the production of high-quality males. Adaptation of wild flies to an artificial laboratory environment can be accompanied by negative effects on several life history traits through changes in their genetic diversity and symbiotic communities. Such changes may lead to reduced biological quality and mating competitiveness in respect to the wild populations. Profiling wild populations can help understand, and maybe reverse, deleterious effects accompanying laboratory domestication thus providing insects that can efficiently and effectively support SIT application.

Results: In the present study, we analyzed both the genetic structure and gut symbiotic communities of natural medfly populations of worldwide distribution, including Europe, Africa, Australia, and the Americas. The genetic structure of 408 individuals from 15 distinct populations was analyzed with a set of commonly used microsatellite markers. The symbiotic communities of a subset of 265 individuals from 11 populations were analyzed using the 16S rRNA gene-based amplicon sequencing of single individuals (adults). Genetic differentiation was detected among geographically distant populations while adults originated from neighboring areas were genetically closer. Alpha and beta diversity of bacterial communities pointed to an overall reduced symbiotic diversity and the influence of the geographic location on the bacterial profile.

Conclusions: Our analysis revealed differences both in the genetic profile and the structure of gut symbiotic communities of medfly natural populations. The genetic analysis expanded our knowledge to populations not analyzed before and our results were in accordance with the existing scenarios regarding this species expansion and colonization pathways. At the same time, the bacterial communities from different natural medfly populations have been characterized, thus broadening our knowledge on the microbiota of the species across its range. Genetic and symbiotic differences between natural and laboratory populations must be considered when designing AW-IPM approaches with a SIT component, since they may impact mating compatibility and mating competitiveness of the laboratory-reared males. In parallel, enrichment from wild populations and/or symbiotic supplementation could increase rearing productivity, biological quality, and mating competitiveness of SIT-important laboratory strains.

Abstract Image

Abstract Image

Abstract Image

地中海果蝇(Ceratitis capitata)全球自然种群的遗传结构和共生概况。
背景:地中海果蝇(Ceratitis capitata)是一种世界性农业害虫,在全球具有重要的经济意义,也是针对栉水母科(双翅目)果蝇开发昆虫不育技术(SIT)的典范。SIT 依赖于实验室饲养品系与自然种群的有效交配,因此需要一个高效的大规模饲养系统来生产高质量的雄蝇。野生苍蝇在适应人工实验室环境的同时,其遗传多样性和共生群落也会发生变化,从而对多种生活史特征产生负面影响。与野生种群相比,这些变化可能会导致生物质量和交配竞争力下降。对野生种群进行分析有助于了解并可能扭转实验室驯化带来的有害影响,从而为昆虫提供高效、有效的 SIT 应用支持:在本研究中,我们分析了分布于世界各地(包括欧洲、非洲、澳大利亚和美洲)的鳉鱼自然种群的遗传结构和肠道共生群落。我们使用一组常用的微卫星标记分析了来自 15 个不同种群的 408 个个体的遗传结构。利用基于 16S rRNA 基因的单个个体(成虫)扩增子测序分析了 11 个种群中 265 个个体的共生群落。在地理位置较远的种群之间发现了基因分化,而来自邻近地区的成体在基因上更为接近。细菌群落的阿尔法和贝塔多样性表明,共生多样性总体上有所降低,地理位置对细菌特征有影响:我们的分析揭示了褐飞虱自然种群肠道共生群落在遗传特征和结构上的差异。遗传分析将我们的知识扩展到了以前未分析过的种群,我们的结果符合现有的关于该物种扩张和定殖途径的设想。同时,我们还对不同褐飞虱自然种群的细菌群落进行了表征,从而拓宽了我们对该物种整个分布区微生物区系的了解。在设计具有 SIT 成分的 AW-IPM 方法时,必须考虑到自然种群和实验室种群之间的遗传和共生差异,因为它们可能会影响实验室饲养雄蝇的交配兼容性和交配竞争力。与此同时,从野生种群中增殖和/或补充共生生物可提高饲养生产力、生物质量和 SIT 重要实验室品系的交配竞争力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
BMC Genetics
BMC Genetics 生物-遗传学
CiteScore
4.30
自引率
0.00%
发文量
77
审稿时长
4-8 weeks
期刊介绍: BMC Genetics is an open access, peer-reviewed journal that considers articles on all aspects of inheritance and variation in individuals and among populations.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信