Diversity of the Obligate Gut Bacteria Indicates Host–Symbiont Coevolution at the Population Level in the Plataspid Stinkbug Megacopta cribraria

IF 2.3 2区 生物学 Q2 ECOLOGY Ecology and Evolution Pub Date : 2024-11-25 DOI:10.1002/ece3.70611
Yuan Wang, Xiu-Xiu Zhu, Bo-Ren Xiao, Xin-Rui Hou, Yu-Xin Liu, Jia-Yue Zhou, Yi-Peng Ren, Wen-Jun Bu, Huai-Jun Xue
{"title":"Diversity of the Obligate Gut Bacteria Indicates Host–Symbiont Coevolution at the Population Level in the Plataspid Stinkbug Megacopta cribraria","authors":"Yuan Wang,&nbsp;Xiu-Xiu Zhu,&nbsp;Bo-Ren Xiao,&nbsp;Xin-Rui Hou,&nbsp;Yu-Xin Liu,&nbsp;Jia-Yue Zhou,&nbsp;Yi-Peng Ren,&nbsp;Wen-Jun Bu,&nbsp;Huai-Jun Xue","doi":"10.1002/ece3.70611","DOIUrl":null,"url":null,"abstract":"<p><i>Ishikawaella</i> is an obligate gut bacterium in stinkbugs that belong to Plataspidae family (Hemiptera: Heteroptera). It is vertically transmitted to newborn nymphs through capsules laid on eggs by maternal stinkbugs. Previous research has established a pattern of strict cospeciation between Plataspidae stinkbugs and <i>Ishikawaella</i>. However, the possibility of host–symbiont coevolution at the population level within Plataspidae stinkbugs has not been thoroughly explored. This study analyzed the samples of <i>Megacopta cribraria</i> from three phylogenetic clades to investigate host–symbiont coevolution in this insect species. We compared data from third-generation sequencing (PacBio), next-generation sequencing (Illumina), and first-generation sequencing (Sanger), and the results indicated that Illumina sequencing most accurately represents the composition of gut bacterial communities. All stinkbug individuals shared a dominant amplicon sequence variant (ASV), which accounted for an average of 65.99% of <i>Ishikawaella</i> sequences (ranging from 58.68% to 87.01%). The top five ASVs (ASV0–ASV4) represented 99.82% of all <i>Ishikawaella</i> sequences. Among these, the number of base substitutions between any two ASVs ranged from 1 to 3, significantly lower than the number of substitutions between the main and minor ASVs. This finding suggests that closely related strains are likely to coexist in the same host. Beta diversity analyses revealed significant differences in <i>Ishikawaella</i> composition among the three phylogenetic clades, providing evidence for host–symbiont coevolution at the population level in Plataspidae stinkbugs.</p>","PeriodicalId":11467,"journal":{"name":"Ecology and Evolution","volume":"14 11","pages":""},"PeriodicalIF":2.3000,"publicationDate":"2024-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/ece3.70611","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Ecology and Evolution","FirstCategoryId":"99","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/ece3.70611","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ECOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Ishikawaella is an obligate gut bacterium in stinkbugs that belong to Plataspidae family (Hemiptera: Heteroptera). It is vertically transmitted to newborn nymphs through capsules laid on eggs by maternal stinkbugs. Previous research has established a pattern of strict cospeciation between Plataspidae stinkbugs and Ishikawaella. However, the possibility of host–symbiont coevolution at the population level within Plataspidae stinkbugs has not been thoroughly explored. This study analyzed the samples of Megacopta cribraria from three phylogenetic clades to investigate host–symbiont coevolution in this insect species. We compared data from third-generation sequencing (PacBio), next-generation sequencing (Illumina), and first-generation sequencing (Sanger), and the results indicated that Illumina sequencing most accurately represents the composition of gut bacterial communities. All stinkbug individuals shared a dominant amplicon sequence variant (ASV), which accounted for an average of 65.99% of Ishikawaella sequences (ranging from 58.68% to 87.01%). The top five ASVs (ASV0–ASV4) represented 99.82% of all Ishikawaella sequences. Among these, the number of base substitutions between any two ASVs ranged from 1 to 3, significantly lower than the number of substitutions between the main and minor ASVs. This finding suggests that closely related strains are likely to coexist in the same host. Beta diversity analyses revealed significant differences in Ishikawaella composition among the three phylogenetic clades, providing evidence for host–symbiont coevolution at the population level in Plataspidae stinkbugs.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
板蝽Megacopta cribraria的宿主与共生体在种群水平上的共同进化表明了宿主肠道细菌的多样性
石川氏菌(Ishikawaella)是蝽科(半翅目:异翅目)蝽体内的一种固有肠道细菌。它通过母体蝽产在卵上的蒴果垂直传播给新生若虫。先前的研究已经确定了蝽类与石川蝽之间严格的共生模式。然而,对于石川蝽体内宿主与共生体在种群水平上共同进化的可能性尚未进行深入探讨。本研究分析了来自三个系统发育支系的 Megacopta cribraria 样本,以研究该昆虫物种中宿主-共生体共同进化的情况。我们比较了第三代测序(PacBio)、新一代测序(Illumina)和第一代测序(Sanger)的数据,结果表明,Illumina测序最准确地代表了肠道细菌群落的组成。所有臭虫个体都有一个显性扩增片段序列变异(ASV),平均占石川氏菌序列的65.99%(从58.68%到87.01%不等)。排在前五位的 ASV(ASV0-ASV4)占所有石川氏菌序列的 99.82%。其中,任意两个 ASV 之间的碱基置换数在 1 到 3 之间,明显低于主 ASV 和次 ASV 之间的置换数。这一发现表明,密切相关的菌株很可能共存于同一宿主中。贝塔多样性分析表明,三个系统发育支系中的石川氏菌组成存在显著差异,为蝽类宿主与共生体在种群水平上的共同进化提供了证据。
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 去求助
来源期刊
CiteScore
4.40
自引率
3.80%
发文量
1027
审稿时长
3-6 weeks
期刊介绍: Ecology and Evolution is the peer reviewed journal for rapid dissemination of research in all areas of ecology, evolution and conservation science. The journal gives priority to quality research reports, theoretical or empirical, that develop our understanding of organisms and their diversity, interactions between them, and the natural environment. Ecology and Evolution gives prompt and equal consideration to papers reporting theoretical, experimental, applied and descriptive work in terrestrial and aquatic environments. The journal will consider submissions across taxa in areas including but not limited to micro and macro ecological and evolutionary processes, characteristics of and interactions between individuals, populations, communities and the environment, physiological responses to environmental change, population genetics and phylogenetics, relatedness and kin selection, life histories, systematics and taxonomy, conservation genetics, extinction, speciation, adaption, behaviour, biodiversity, species abundance, macroecology, population and ecosystem dynamics, and conservation policy.
期刊最新文献
Assessment of Climate Change Impacts on the Distribution of Endangered and Endemic Changnienia amoena (Orchidaceae) Using Ensemble Modeling and Gap Analysis in China Temporal Dynamics of Species Richness and Composition in a Peri-Urban Tropical Frog Community in Central Brazil Diversity of the Obligate Gut Bacteria Indicates Host–Symbiont Coevolution at the Population Level in the Plataspid Stinkbug Megacopta cribraria Competition and Facilitation Influence Central Place Foraging Ecology in a Colonial Marine Predator Parent-Specific Transgenerational Immune Priming Enhances Offspring Defense—Unless Heat Stress Negates It All
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1