Extensive data mining uncovers novel diversity among members of the rare biosphere within the Thermoplasmatota.

IF 13.8 1区 生物学 Q1 MICROBIOLOGY
Mara D Maeke, Xiuran Yin, Lea C Wunder, Chiara Vanni, Tim Richter-Heitmann, Samuel Miravet-Verde, Hans-Joachim Ruscheweyh, Shinichi Sunagawa, Jenny Fabian, Judith Piontek, Michael W Friedrich, Christiane Hassenrück
{"title":"Extensive data mining uncovers novel diversity among members of the rare biosphere within the Thermoplasmatota.","authors":"Mara D Maeke, Xiuran Yin, Lea C Wunder, Chiara Vanni, Tim Richter-Heitmann, Samuel Miravet-Verde, Hans-Joachim Ruscheweyh, Shinichi Sunagawa, Jenny Fabian, Judith Piontek, Michael W Friedrich, Christiane Hassenrück","doi":"10.1186/s40168-025-02140-8","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Rare species, especially of the marine sedimentary biosphere, have long been overlooked owing to the complexity of sediment microbial communities, their sporadic temporal and patchy spatial abundance, and challenges in cultivating environmental microorganisms. In this study, we combined enrichments, targeted metagenomic sequencing, and extensive data mining to uncover uncultivated members of the archaeal rare biosphere in marine sediments.</p><p><strong>Results: </strong>In protein-amended enrichments, we detected the ecologically and metabolically uncharacterized class Candidatus Penumbrarchaeia within the phylum Thermoplasmatota. By screening more than 8000 metagenomic runs and 11,479 published genome assemblies, we expanded the phylogeny of Ca. Penumbrarchaeia by 3 novel orders. All six identified families of this class show low abundance in environmental samples characteristic of rare biosphere members. Members of the class Ca. Penumbrarchaeia were predicted to be involved in organic matter degradation in anoxic, carbon-rich habitats. All Ca. Penumbrarchaeia families contain high numbers of taxon-specific orthologous genes, highlighting their environmental adaptations and habitat specificity. Besides, members of this group exhibit the highest proportion of unknown genes within the entire phylum Thermoplasmatota, suggesting a high degree of functional novelty in this class.</p><p><strong>Conclusions: </strong>In this study, we emphasize the necessity of targeted, data-integrative approaches to deepen our understanding of the rare biosphere and uncover the functions and metabolic potential hidden within these understudied taxa. Video Abstract.</p>","PeriodicalId":18447,"journal":{"name":"Microbiome","volume":"13 1","pages":"155"},"PeriodicalIF":13.8000,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12220078/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Microbiome","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1186/s40168-025-02140-8","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Rare species, especially of the marine sedimentary biosphere, have long been overlooked owing to the complexity of sediment microbial communities, their sporadic temporal and patchy spatial abundance, and challenges in cultivating environmental microorganisms. In this study, we combined enrichments, targeted metagenomic sequencing, and extensive data mining to uncover uncultivated members of the archaeal rare biosphere in marine sediments.

Results: In protein-amended enrichments, we detected the ecologically and metabolically uncharacterized class Candidatus Penumbrarchaeia within the phylum Thermoplasmatota. By screening more than 8000 metagenomic runs and 11,479 published genome assemblies, we expanded the phylogeny of Ca. Penumbrarchaeia by 3 novel orders. All six identified families of this class show low abundance in environmental samples characteristic of rare biosphere members. Members of the class Ca. Penumbrarchaeia were predicted to be involved in organic matter degradation in anoxic, carbon-rich habitats. All Ca. Penumbrarchaeia families contain high numbers of taxon-specific orthologous genes, highlighting their environmental adaptations and habitat specificity. Besides, members of this group exhibit the highest proportion of unknown genes within the entire phylum Thermoplasmatota, suggesting a high degree of functional novelty in this class.

Conclusions: In this study, we emphasize the necessity of targeted, data-integrative approaches to deepen our understanding of the rare biosphere and uncover the functions and metabolic potential hidden within these understudied taxa. Video Abstract.

广泛的数据挖掘揭示了热原胞内稀有生物圈成员之间的新多样性。
背景:由于沉积物微生物群落的复杂性、时间上的散发性和空间上的斑块性,以及环境微生物的培养面临的挑战,长期以来,海洋沉积生物圈的珍稀物种一直被忽视。在这项研究中,我们将富集、定向宏基因组测序和广泛的数据挖掘相结合,揭示了海洋沉积物中未开垦的古细菌稀有生物圈成员。结果:在蛋白质修饰的富集中,我们检测到了热原门中生态和代谢特征不明显的准原生Candidatus Penumbrarchaeia。通过对8000多个宏基因组序列和11479个已发表基因组序列的筛选,我们将半卷古菌的系统发育扩展了3个新目。所有已鉴定的6个科在稀有生物圈成员的环境样品中都显示出低丰度。据预测,在缺氧、富碳的栖息地中,半原生细菌类的成员参与了有机物的降解。所有半原生Ca. Penumbrarchaeia科都含有大量的分类群特异性同源基因,突出了它们的环境适应性和栖息地特异性。此外,这一类群的成员在整个热原动物门中显示出最高比例的未知基因,这表明这一类动物具有高度的功能新颖性。结论:在本研究中,我们强调有针对性的数据整合方法的必要性,以加深我们对稀有生物圈的理解,揭示隐藏在这些未被研究的分类群中的功能和代谢潜力。视频摘要。
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
Microbiome
Microbiome MICROBIOLOGY-
CiteScore
21.90
自引率
2.60%
发文量
198
审稿时长
4 weeks
期刊介绍: Microbiome is a journal that focuses on studies of microbiomes in humans, animals, plants, and the environment. It covers both natural and manipulated microbiomes, such as those in agriculture. The journal is interested in research that uses meta-omics approaches or novel bioinformatics tools and emphasizes the community/host interaction and structure-function relationship within the microbiome. Studies that go beyond descriptive omics surveys and include experimental or theoretical approaches will be considered for publication. The journal also encourages research that establishes cause and effect relationships and supports proposed microbiome functions. However, studies of individual microbial isolates/species without exploring their impact on the host or the complex microbiome structures and functions will not be considered for publication. Microbiome is indexed in BIOSIS, Current Contents, DOAJ, Embase, MEDLINE, PubMed, PubMed Central, and Science Citations Index Expanded.
×
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