共栖的蚂蚁和银鱼显示出一种趋同的觅食生态。

IF 4.4 1区 生物学 Q1 BIOLOGY BMC Biology Pub Date : 2024-05-29 DOI:10.1186/s12915-024-01914-0
Thomas Parmentier, Rafael Molero-Baltanás, Catalina Valdivia, Miquel Gaju-Ricart, Pascal Boeckx, Piotr Łukasik, Nicky Wybouw
{"title":"共栖的蚂蚁和银鱼显示出一种趋同的觅食生态。","authors":"Thomas Parmentier, Rafael Molero-Baltanás, Catalina Valdivia, Miquel Gaju-Ricart, Pascal Boeckx, Piotr Łukasik, Nicky Wybouw","doi":"10.1186/s12915-024-01914-0","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Various animal taxa have specialized to living with social hosts. Depending on their level of specialization, these symbiotic animals are characterized by distinct behavioural, chemical, and morphological traits that enable close heterospecific interactions. Despite its functional importance, our understanding of the feeding ecology of animals living with social hosts remains limited. We examined how host specialization of silverfish co-habiting with ants affects several components of their feeding ecology. We combined stable isotope profiling, feeding assays, phylogenetic reconstruction, and microbial community characterization of the Neoasterolepisma silverfish genus and a wider nicoletiid and lepismatid silverfish panel where divergent myrmecophilous lifestyles are observed.</p><p><strong>Results: </strong>Stable isotope profiling (δ<sup>13</sup>C and δ<sup>15</sup>N) showed that the isotopic niches of granivorous Messor ants and Messor-specialized Neoasterolepisma exhibit a remarkable overlap within an ant nest. Trophic experiments and gut dissections further supported that these specialized Neoasterolepisma silverfish transitioned to a diet that includes plant seeds. In contrast, the isotopic niches of generalist Neoasterolepisma silverfish and generalist nicoletiid silverfish were clearly different from their ant hosts within the shared nest environment. The impact of the myrmecophilous lifestyle on feeding ecology was also evident in the internal silverfish microbiome. Compared to generalists, Messor-specialists exhibited a higher bacterial density and a higher proportion of heterofermentative lactic acid bacteria. Moreover, the nest environment explained the infection profile (or the 16S rRNA genotypes) of Weissella bacteria in Messor-specialized silverfish and the ant hosts.</p><p><strong>Conclusions: </strong>Together, we show that social hosts are important determinants for the feeding ecology of symbiotic animals and can induce diet convergence.</p>","PeriodicalId":9339,"journal":{"name":"BMC Biology","volume":null,"pages":null},"PeriodicalIF":4.4000,"publicationDate":"2024-05-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11134936/pdf/","citationCount":"0","resultStr":"{\"title\":\"Co-habiting ants and silverfish display a converging feeding ecology.\",\"authors\":\"Thomas Parmentier, Rafael Molero-Baltanás, Catalina Valdivia, Miquel Gaju-Ricart, Pascal Boeckx, Piotr Łukasik, Nicky Wybouw\",\"doi\":\"10.1186/s12915-024-01914-0\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Various animal taxa have specialized to living with social hosts. Depending on their level of specialization, these symbiotic animals are characterized by distinct behavioural, chemical, and morphological traits that enable close heterospecific interactions. Despite its functional importance, our understanding of the feeding ecology of animals living with social hosts remains limited. We examined how host specialization of silverfish co-habiting with ants affects several components of their feeding ecology. We combined stable isotope profiling, feeding assays, phylogenetic reconstruction, and microbial community characterization of the Neoasterolepisma silverfish genus and a wider nicoletiid and lepismatid silverfish panel where divergent myrmecophilous lifestyles are observed.</p><p><strong>Results: </strong>Stable isotope profiling (δ<sup>13</sup>C and δ<sup>15</sup>N) showed that the isotopic niches of granivorous Messor ants and Messor-specialized Neoasterolepisma exhibit a remarkable overlap within an ant nest. Trophic experiments and gut dissections further supported that these specialized Neoasterolepisma silverfish transitioned to a diet that includes plant seeds. In contrast, the isotopic niches of generalist Neoasterolepisma silverfish and generalist nicoletiid silverfish were clearly different from their ant hosts within the shared nest environment. The impact of the myrmecophilous lifestyle on feeding ecology was also evident in the internal silverfish microbiome. Compared to generalists, Messor-specialists exhibited a higher bacterial density and a higher proportion of heterofermentative lactic acid bacteria. Moreover, the nest environment explained the infection profile (or the 16S rRNA genotypes) of Weissella bacteria in Messor-specialized silverfish and the ant hosts.</p><p><strong>Conclusions: </strong>Together, we show that social hosts are important determinants for the feeding ecology of symbiotic animals and can induce diet convergence.</p>\",\"PeriodicalId\":9339,\"journal\":{\"name\":\"BMC Biology\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":4.4000,\"publicationDate\":\"2024-05-29\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11134936/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"BMC Biology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1186/s12915-024-01914-0\",\"RegionNum\":1,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"BMC Biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1186/s12915-024-01914-0","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

背景:各种动物类群专门与社会宿主共生。根据其特化程度,这些共生动物具有不同的行为、化学和形态特征,从而能够进行密切的异种相互作用。尽管与社会性宿主共生的动物具有重要的功能,但我们对其摄食生态学的了解仍然有限。我们研究了与蚂蚁共栖的银鱼的宿主特化如何影响其摄食生态的几个组成部分。我们将稳定同位素分析、摄食试验、系统发育重建和微生物群落特征描述结合起来,研究了Neoasterolepisma银鱼属以及更广泛的nicoletiid和lepismatid银鱼类群,在这些类群中观察到了不同的嗜蚁生活方式:结果:稳定同位素分析(δ13C和δ15N)显示,食粒的梅氏蚁和梅氏特化的Neoasterolepisma的同位素壁龛在蚁巢内有明显的重叠。营养实验和肠道解剖进一步证明,这些专化的Neoasterolepisma银鱼过渡到以植物种子为食。与此相反,在共同的巢穴环境中,通食Neoasterolepisma银鱼和通食nicoletiid银鱼的同位素龛位明显不同于它们的蚂蚁宿主。嗜肉生活方式对摄食生态的影响在银鱼内部微生物组中也很明显。与普通银鱼相比,梅索尔特化银鱼表现出更高的细菌密度和更高比例的异发酵乳酸菌。此外,巢穴环境也解释了Messor专精银鱼和蚂蚁宿主中魏氏菌的感染概况(或16S rRNA基因型):总之,我们的研究表明,社会宿主是共生动物摄食生态学的重要决定因素,并能诱导食谱趋同。
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
Co-habiting ants and silverfish display a converging feeding ecology.

Background: Various animal taxa have specialized to living with social hosts. Depending on their level of specialization, these symbiotic animals are characterized by distinct behavioural, chemical, and morphological traits that enable close heterospecific interactions. Despite its functional importance, our understanding of the feeding ecology of animals living with social hosts remains limited. We examined how host specialization of silverfish co-habiting with ants affects several components of their feeding ecology. We combined stable isotope profiling, feeding assays, phylogenetic reconstruction, and microbial community characterization of the Neoasterolepisma silverfish genus and a wider nicoletiid and lepismatid silverfish panel where divergent myrmecophilous lifestyles are observed.

Results: Stable isotope profiling (δ13C and δ15N) showed that the isotopic niches of granivorous Messor ants and Messor-specialized Neoasterolepisma exhibit a remarkable overlap within an ant nest. Trophic experiments and gut dissections further supported that these specialized Neoasterolepisma silverfish transitioned to a diet that includes plant seeds. In contrast, the isotopic niches of generalist Neoasterolepisma silverfish and generalist nicoletiid silverfish were clearly different from their ant hosts within the shared nest environment. The impact of the myrmecophilous lifestyle on feeding ecology was also evident in the internal silverfish microbiome. Compared to generalists, Messor-specialists exhibited a higher bacterial density and a higher proportion of heterofermentative lactic acid bacteria. Moreover, the nest environment explained the infection profile (or the 16S rRNA genotypes) of Weissella bacteria in Messor-specialized silverfish and the ant hosts.

Conclusions: Together, we show that social hosts are important determinants for the feeding ecology of symbiotic animals and can induce diet convergence.

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
BMC Biology
BMC Biology 生物-生物学
CiteScore
7.80
自引率
1.90%
发文量
260
审稿时长
3 months
期刊介绍: BMC Biology is a broad scope journal covering all areas of biology. Our content includes research articles, new methods and tools. BMC Biology also publishes reviews, Q&A, and commentaries.
期刊最新文献
Novel function of single-target regulator NorR involved in swarming motility and biofilm formation revealed in Vibrio alginolyticus. Hibernation reduces GABA signaling in the brainstem to enhance motor activity of breathing at cool temperatures. A powerful and versatile new fixation protocol for immunostaining and in situ hybridization that preserves delicate tissues. Bridging chemical structure and conceptual knowledge enables accurate prediction of compound-protein interaction. Evolutionary divergent clusters of transcribed extinct truncated retroposons drive low mRNA expression and developmental regulation in the protozoan Leishmania.
×
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