红海沿岸盐藻菌群的微生物多样性及功能潜力。

IF 5.4 2区 环境科学与生态学 Q1 GENETICS & HEREDITY
Juan David Escobar-Prieto, Marc W Van Goethem, Bob Vernooij, Chakkiath Paul Antony, Lanna Cheng, Himanshu Mishra, Ramona Marasco, Daniele Daffonchio
{"title":"红海沿岸盐藻菌群的微生物多样性及功能潜力。","authors":"Juan David Escobar-Prieto, Marc W Van Goethem, Bob Vernooij, Chakkiath Paul Antony, Lanna Cheng, Himanshu Mishra, Ramona Marasco, Daniele Daffonchio","doi":"10.1186/s40793-025-00761-y","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Halobates, commonly known as sea skaters, are predatory Hemipterans uniquely adapted to tropical marine environments. Their ability to thrive in oligotrophic and environmentally extreme habitats, such as the open ocean surface and marine coastal areas, suggests the evolution of specialised adaptations, possibly including symbiotic associations with microorganisms that can support nutrition, niche adaptation, and stress resilience. To explore this hypothesis, we analysed the bacterial communities associated with Halobates melleus, a species inhabiting the Red Sea coastal mangroves in Saudi Arabia.</p><p><strong>Results: </strong>Amplicon sequencing of the 16S rRNA gene and metagenomic analyses of composite body and gut samples from adult H. melleus revealed a population-level bacterial community dominated by Wolbachia and Spiroplasma, consistent with patterns observed in several terrestrial predatory insects. Members of Providencia and Swaminathania were also detected, along with other minor taxa that may represent transient environmental commensals. The identified bacteria encoded genes for the biosynthesis of essential vitamins and prosthetic groups, such as riboflavin and heme-compounds typically not synthesised de novo by insects-as well as amino acids, likely contributing to the host's nutritional requirements. Notably, the Wolbachia metagenome-assembled genome from H. melleus clustered within the supergroup B, showing high genetic similarity to strains from phylogenetically distant Dipteran and Lepidopteran hosts that nonetheless inhabit common ecological niches, i.e., mangrove and tropical environments. This extends the known ecological breadth of Wolbachia symbioses to marine insects, underscoring their evolutionary and environmental versatility.</p><p><strong>Conclusion: </strong>Our findings highlight the potential nutritional and metabolic roles of the Halobates-associated bacterial microbiome, particularly members of the Wolbachia genus. This emphasises the importance of microbial symbionts in the ecological success and adaptation of marine insects, offering a perspective complementary to previously studied terrestrial insect microbiomes.</p>","PeriodicalId":48553,"journal":{"name":"Environmental Microbiome","volume":"20 1","pages":"103"},"PeriodicalIF":5.4000,"publicationDate":"2025-08-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12335105/pdf/","citationCount":"0","resultStr":"{\"title\":\"Microbial diversity and functional potential of the Halobates melleus (Heteroptera: Gerridae) microbiome from the Red Sea coastline.\",\"authors\":\"Juan David Escobar-Prieto, Marc W Van Goethem, Bob Vernooij, Chakkiath Paul Antony, Lanna Cheng, Himanshu Mishra, Ramona Marasco, Daniele Daffonchio\",\"doi\":\"10.1186/s40793-025-00761-y\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Halobates, commonly known as sea skaters, are predatory Hemipterans uniquely adapted to tropical marine environments. Their ability to thrive in oligotrophic and environmentally extreme habitats, such as the open ocean surface and marine coastal areas, suggests the evolution of specialised adaptations, possibly including symbiotic associations with microorganisms that can support nutrition, niche adaptation, and stress resilience. To explore this hypothesis, we analysed the bacterial communities associated with Halobates melleus, a species inhabiting the Red Sea coastal mangroves in Saudi Arabia.</p><p><strong>Results: </strong>Amplicon sequencing of the 16S rRNA gene and metagenomic analyses of composite body and gut samples from adult H. melleus revealed a population-level bacterial community dominated by Wolbachia and Spiroplasma, consistent with patterns observed in several terrestrial predatory insects. Members of Providencia and Swaminathania were also detected, along with other minor taxa that may represent transient environmental commensals. The identified bacteria encoded genes for the biosynthesis of essential vitamins and prosthetic groups, such as riboflavin and heme-compounds typically not synthesised de novo by insects-as well as amino acids, likely contributing to the host's nutritional requirements. Notably, the Wolbachia metagenome-assembled genome from H. melleus clustered within the supergroup B, showing high genetic similarity to strains from phylogenetically distant Dipteran and Lepidopteran hosts that nonetheless inhabit common ecological niches, i.e., mangrove and tropical environments. This extends the known ecological breadth of Wolbachia symbioses to marine insects, underscoring their evolutionary and environmental versatility.</p><p><strong>Conclusion: </strong>Our findings highlight the potential nutritional and metabolic roles of the Halobates-associated bacterial microbiome, particularly members of the Wolbachia genus. This emphasises the importance of microbial symbionts in the ecological success and adaptation of marine insects, offering a perspective complementary to previously studied terrestrial insect microbiomes.</p>\",\"PeriodicalId\":48553,\"journal\":{\"name\":\"Environmental Microbiome\",\"volume\":\"20 1\",\"pages\":\"103\"},\"PeriodicalIF\":5.4000,\"publicationDate\":\"2025-08-08\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12335105/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Environmental Microbiome\",\"FirstCategoryId\":\"93\",\"ListUrlMain\":\"https://doi.org/10.1186/s40793-025-00761-y\",\"RegionNum\":2,\"RegionCategory\":\"环境科学与生态学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"GENETICS & HEREDITY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Environmental Microbiome","FirstCategoryId":"93","ListUrlMain":"https://doi.org/10.1186/s40793-025-00761-y","RegionNum":2,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
引用次数: 0

摘要

背景:盐藻,通常被称为海洋滑冰者,是一种适应热带海洋环境的掠食性半翅类动物。它们能够在贫营养和环境极端的栖息地茁壮成长,如开阔的海洋表面和海洋沿海地区,这表明了专门适应的进化,可能包括与微生物的共生关系,这些微生物可以支持营养、生态位适应和压力恢复能力。为了探索这一假设,我们分析了与居住在沙特阿拉伯红海沿岸红树林的盐藻(Halobates melleus)相关的细菌群落。结果:16S rRNA基因扩增子测序和对成年鼠体和肠道样本的宏基因组分析显示,该种群水平的细菌群落以沃尔巴克氏体和螺旋体为主,这与在几种陆生掠食性昆虫中观察到的模式一致。还发现了Providencia和Swaminathania的成员,以及其他可能代表短暂环境共生的小分类群。鉴定出的细菌编码了必要维生素和辅助基团的生物合成基因,如核黄素和血红素——这些化合物通常不是昆虫从头合成的——以及氨基酸,可能有助于宿主的营养需求。值得注意的是,沃尔巴克氏体宏基因组组装的基因组聚集在超群B中,与来自系统发育上遥远的双翅目和鳞翅目宿主的菌株显示出高度的遗传相似性,尽管这些菌株生活在共同的生态位,即红树林和热带环境中。这将沃尔巴克氏体共生体已知的生态广度扩展到海洋昆虫,强调了它们的进化和环境多样性。结论:我们的研究结果强调了与盐酸盐相关的细菌微生物群,特别是沃尔巴克氏菌属成员的潜在营养和代谢作用。这强调了微生物共生体在海洋昆虫生态成功和适应中的重要性,为先前研究的陆地昆虫微生物组提供了一个补充的视角。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Microbial diversity and functional potential of the Halobates melleus (Heteroptera: Gerridae) microbiome from the Red Sea coastline.

Background: Halobates, commonly known as sea skaters, are predatory Hemipterans uniquely adapted to tropical marine environments. Their ability to thrive in oligotrophic and environmentally extreme habitats, such as the open ocean surface and marine coastal areas, suggests the evolution of specialised adaptations, possibly including symbiotic associations with microorganisms that can support nutrition, niche adaptation, and stress resilience. To explore this hypothesis, we analysed the bacterial communities associated with Halobates melleus, a species inhabiting the Red Sea coastal mangroves in Saudi Arabia.

Results: Amplicon sequencing of the 16S rRNA gene and metagenomic analyses of composite body and gut samples from adult H. melleus revealed a population-level bacterial community dominated by Wolbachia and Spiroplasma, consistent with patterns observed in several terrestrial predatory insects. Members of Providencia and Swaminathania were also detected, along with other minor taxa that may represent transient environmental commensals. The identified bacteria encoded genes for the biosynthesis of essential vitamins and prosthetic groups, such as riboflavin and heme-compounds typically not synthesised de novo by insects-as well as amino acids, likely contributing to the host's nutritional requirements. Notably, the Wolbachia metagenome-assembled genome from H. melleus clustered within the supergroup B, showing high genetic similarity to strains from phylogenetically distant Dipteran and Lepidopteran hosts that nonetheless inhabit common ecological niches, i.e., mangrove and tropical environments. This extends the known ecological breadth of Wolbachia symbioses to marine insects, underscoring their evolutionary and environmental versatility.

Conclusion: Our findings highlight the potential nutritional and metabolic roles of the Halobates-associated bacterial microbiome, particularly members of the Wolbachia genus. This emphasises the importance of microbial symbionts in the ecological success and adaptation of marine insects, offering a perspective complementary to previously studied terrestrial insect microbiomes.

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
Environmental Microbiome
Environmental Microbiome Immunology and Microbiology-Microbiology
CiteScore
7.40
自引率
2.50%
发文量
55
审稿时长
13 weeks
期刊介绍: Microorganisms, omnipresent across Earth's diverse environments, play a crucial role in adapting to external changes, influencing Earth's systems and cycles, and contributing significantly to agricultural practices. Through applied microbiology, they offer solutions to various everyday needs. Environmental Microbiome recognizes the universal presence and significance of microorganisms, inviting submissions that explore the diverse facets of environmental and applied microbiological research.
×
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:604180095
Book学术官方微信