高山蚱蜢和蟋蟀肠道和内共生细菌群落的宿主特异性对比

IF 5.1 Q1 ECOLOGY ISME communications Pub Date : 2024-01-10 DOI:10.1093/ismeco/ycad013
Mazel Florent, Pitteloud Camille, Guisan Antoine, Pellissier Loïc
{"title":"高山蚱蜢和蟋蟀肠道和内共生细菌群落的宿主特异性对比","authors":"Mazel Florent, Pitteloud Camille, Guisan Antoine, Pellissier Loïc","doi":"10.1093/ismeco/ycad013","DOIUrl":null,"url":null,"abstract":"\n Bacteria colonize the body of macroorganisms to form associations ranging from parasitic to mutualistic. Endosymbiont and gut symbiont community are distinct microbiomes whose compositions are influenced by host ecology and evolution. Although the composition of horizontally acquired symbiont communities can correlate to host species identity (i.e., harbor host specificity) and host phylogeny (i.e., harbor phylosymbiosis), we hypothesize that the microbiota structure of vertically inherited symbionts (e.g., endosymbionts like Wolbachia) is more strongly associated with the host species identity and phylogeny than horizontally acquired symbionts (e.g., most gut symbionts). Here, using 16S metabarcoding on 336 guts from 24 orthopteran species (grasshoppers and crickets) in the Alps, we observed that microbiota correlated to host species identity, i.e., hosts from the same species had more similar microbiota than hosts from different species. This effect was ~5 times stronger for endosymbionts than for putative gut symbionts. While elevation correlated with microbiome composition, we did not detect phylosymbiosis for endosymbionts and putative gut symbionts: closely related host species did not harbor more similar microbiota than distantly related species. Our findings indicate that gut microbiota of studied orthopteran species is more correlated to host identity and habitat than to the host phylogeny. The higher specificity in endosymbionts corroborates the idea that -everything else being equal- vertically transmitted microbes harbor stronger specificity signal, but the absence of phylosymbiosis suggests that specificity changes quickly on evolutionary time scales.","PeriodicalId":73516,"journal":{"name":"ISME communications","volume":"2 3","pages":""},"PeriodicalIF":5.1000,"publicationDate":"2024-01-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Contrasted host specificity of gut and endosymbiont bacterial communities in alpine grasshoppers and crickets\",\"authors\":\"Mazel Florent, Pitteloud Camille, Guisan Antoine, Pellissier Loïc\",\"doi\":\"10.1093/ismeco/ycad013\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"\\n Bacteria colonize the body of macroorganisms to form associations ranging from parasitic to mutualistic. Endosymbiont and gut symbiont community are distinct microbiomes whose compositions are influenced by host ecology and evolution. Although the composition of horizontally acquired symbiont communities can correlate to host species identity (i.e., harbor host specificity) and host phylogeny (i.e., harbor phylosymbiosis), we hypothesize that the microbiota structure of vertically inherited symbionts (e.g., endosymbionts like Wolbachia) is more strongly associated with the host species identity and phylogeny than horizontally acquired symbionts (e.g., most gut symbionts). Here, using 16S metabarcoding on 336 guts from 24 orthopteran species (grasshoppers and crickets) in the Alps, we observed that microbiota correlated to host species identity, i.e., hosts from the same species had more similar microbiota than hosts from different species. This effect was ~5 times stronger for endosymbionts than for putative gut symbionts. While elevation correlated with microbiome composition, we did not detect phylosymbiosis for endosymbionts and putative gut symbionts: closely related host species did not harbor more similar microbiota than distantly related species. Our findings indicate that gut microbiota of studied orthopteran species is more correlated to host identity and habitat than to the host phylogeny. The higher specificity in endosymbionts corroborates the idea that -everything else being equal- vertically transmitted microbes harbor stronger specificity signal, but the absence of phylosymbiosis suggests that specificity changes quickly on evolutionary time scales.\",\"PeriodicalId\":73516,\"journal\":{\"name\":\"ISME communications\",\"volume\":\"2 3\",\"pages\":\"\"},\"PeriodicalIF\":5.1000,\"publicationDate\":\"2024-01-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ISME communications\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1093/ismeco/ycad013\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"ECOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ISME communications","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1093/ismeco/ycad013","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ECOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

细菌在大型生物体内定植,形成从寄生到互生的各种关系。内共生菌和肠道共生菌群落是不同的微生物群落,其组成受宿主生态学和进化的影响。虽然水平获得的共生体群落的组成与宿主的物种特征(即宿主特异性)和宿主的系统发育(即宿主系统共生)相关,但我们假设垂直遗传的共生体(如 Wolbachia 等内共生体)的微生物群结构与宿主的物种特征和系统发育的关系比水平获得的共生体(如大多数肠道共生体)更密切。在这里,我们对阿尔卑斯山的 24 种直翅目昆虫(蚱蜢和蟋蟀)的 336 个内脏进行了 16S 代谢编码,观察到微生物群与宿主的物种特征相关,即同一物种的宿主比不同物种的宿主具有更相似的微生物群。内共生菌的这种效应比假定的肠道共生菌强5倍。虽然海拔高度与微生物群组成相关,但我们并没有检测到内共生菌和假定肠道共生菌的系统共生现象:亲缘关系近的宿主物种并没有比亲缘关系远的物种拥有更相似的微生物群。我们的研究结果表明,所研究的直翅目物种的肠道微生物群与宿主身份和栖息地的相关性比与宿主系统发育的相关性更大。内共生微生物具有更高的特异性,这证实了在其他条件相同的情况下,垂直传播的微生物具有更强的特异性信号的观点,但不存在系统共生现象表明,特异性在进化时间尺度上变化很快。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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
Contrasted host specificity of gut and endosymbiont bacterial communities in alpine grasshoppers and crickets
Bacteria colonize the body of macroorganisms to form associations ranging from parasitic to mutualistic. Endosymbiont and gut symbiont community are distinct microbiomes whose compositions are influenced by host ecology and evolution. Although the composition of horizontally acquired symbiont communities can correlate to host species identity (i.e., harbor host specificity) and host phylogeny (i.e., harbor phylosymbiosis), we hypothesize that the microbiota structure of vertically inherited symbionts (e.g., endosymbionts like Wolbachia) is more strongly associated with the host species identity and phylogeny than horizontally acquired symbionts (e.g., most gut symbionts). Here, using 16S metabarcoding on 336 guts from 24 orthopteran species (grasshoppers and crickets) in the Alps, we observed that microbiota correlated to host species identity, i.e., hosts from the same species had more similar microbiota than hosts from different species. This effect was ~5 times stronger for endosymbionts than for putative gut symbionts. While elevation correlated with microbiome composition, we did not detect phylosymbiosis for endosymbionts and putative gut symbionts: closely related host species did not harbor more similar microbiota than distantly related species. Our findings indicate that gut microbiota of studied orthopteran species is more correlated to host identity and habitat than to the host phylogeny. The higher specificity in endosymbionts corroborates the idea that -everything else being equal- vertically transmitted microbes harbor stronger specificity signal, but the absence of phylosymbiosis suggests that specificity changes quickly on evolutionary time scales.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Recurrent association between Trichodesmium colonies and calcifying amoebae. Taxon-specific contributions of microeukaryotes to biological carbon pump in the Oyashio region. Significant role of symbiotic bacteria in the blood digestion and reproduction of Dermanyssus gallinae mites. Cover crop monocultures and mixtures enhance bacterial abundance and functionality in the maize root zone. Genomic dissection of Escherichia marmotae provides insights into diversity and pathogenic potential.
×
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