Distribution and genomic variation of ammonia-oxidizing archaea in abyssal and hadal surface sediments

IF 5.1 Q1 ECOLOGY
Blandine Trouche, Clemens Schauberger, Feriel Bouderka, Jean-Christophe Auguet, Caroline Belser, Julie Poulain, Bo Thamdrup, Patrick Wincker, Sophie Arnaud-Haond, Ronnie N. Glud, Loïs Maignien
{"title":"Distribution and genomic variation of ammonia-oxidizing archaea in abyssal and hadal surface sediments","authors":"Blandine Trouche, Clemens Schauberger, Feriel Bouderka, Jean-Christophe Auguet, Caroline Belser, Julie Poulain, Bo Thamdrup, Patrick Wincker, Sophie Arnaud-Haond, Ronnie N. Glud, Loïs Maignien","doi":"10.1038/s43705-023-00341-6","DOIUrl":null,"url":null,"abstract":"Ammonia-oxidizing archaea of the phylum Thaumarchaeota play a central role in the biogeochemical cycling of nitrogen in benthic sediments, at the interface between pelagic and subsurface ecosystems. However, our understanding of their niche separation and of the processes controlling their population structure in hadal and abyssal surface sediments is still limited. Here, we reconstructed 47 AOA metagenome-assembled genomes (MAGs) from surface sediments of the Atacama and Kermadec trench systems. They formed deep-sea-specific groups within the family Nitrosopumilaceae and were assigned to six amoA gene-based clades. MAGs from different clades had distinct distribution patterns along oxygen-ammonium counter gradients in surface sediments. At the species level, MAGs thus seemed to form different ecotypes and follow deterministic niche-based distributions. In contrast, intraspecific population structure, defined by patterns of Single Nucleotide Variants (SNV), seemed to reflect more complex contributions of both deterministic and stochastic processes. Firstly, the bathymetric range had a strong effect on population structure, with distinct populations in abyssal plains and hadal trenches. Then, hadal populations were clearly separated by trench system, suggesting a strong isolation-by-topography effect, whereas abyssal populations were rather controlled by sediment depth or geographic distances, depending on the clade considered. Interestingly, genetic variability between samples was lowest in sediment layers where the mean MAG coverage was highest, highlighting the importance of selective pressure linked with each AOA clade’s ecological niche. Overall, our results show that deep-sea AOA genome distributions seem to follow both deterministic and stochastic processes, depending on the genomic variability scale considered.","PeriodicalId":73516,"journal":{"name":"ISME communications","volume":" ","pages":"1-12"},"PeriodicalIF":5.1000,"publicationDate":"2023-12-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10746724/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ISME communications","FirstCategoryId":"1085","ListUrlMain":"https://www.nature.com/articles/s43705-023-00341-6","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

Abstract

Ammonia-oxidizing archaea of the phylum Thaumarchaeota play a central role in the biogeochemical cycling of nitrogen in benthic sediments, at the interface between pelagic and subsurface ecosystems. However, our understanding of their niche separation and of the processes controlling their population structure in hadal and abyssal surface sediments is still limited. Here, we reconstructed 47 AOA metagenome-assembled genomes (MAGs) from surface sediments of the Atacama and Kermadec trench systems. They formed deep-sea-specific groups within the family Nitrosopumilaceae and were assigned to six amoA gene-based clades. MAGs from different clades had distinct distribution patterns along oxygen-ammonium counter gradients in surface sediments. At the species level, MAGs thus seemed to form different ecotypes and follow deterministic niche-based distributions. In contrast, intraspecific population structure, defined by patterns of Single Nucleotide Variants (SNV), seemed to reflect more complex contributions of both deterministic and stochastic processes. Firstly, the bathymetric range had a strong effect on population structure, with distinct populations in abyssal plains and hadal trenches. Then, hadal populations were clearly separated by trench system, suggesting a strong isolation-by-topography effect, whereas abyssal populations were rather controlled by sediment depth or geographic distances, depending on the clade considered. Interestingly, genetic variability between samples was lowest in sediment layers where the mean MAG coverage was highest, highlighting the importance of selective pressure linked with each AOA clade’s ecological niche. Overall, our results show that deep-sea AOA genome distributions seem to follow both deterministic and stochastic processes, depending on the genomic variability scale considered.

Abstract Image

深海和浅海表层沉积物中氨氧化古细菌的分布和基因组变异。
氨氧化古细菌门(Thaumarchaeota)的氨氧化古细菌在底栖沉积物氮的生物地球化学循环中发挥着核心作用,它们处于浮游生态系统和地表下生态系统的交界处。然而,我们对它们在海底和深海表层沉积物中的生态位分离及其种群结构控制过程的了解仍然有限。在这里,我们从阿塔卡马和凯尔马代克海沟系统的表层沉积物中重建了 47 个 AOA 元基因组(MAGs)。它们在亚硝基藻科(Nitrosopumilaceae)中形成了特定的深海群,并被归入六个基于amoA基因的支系。不同支系的 MAGs 在表层沉积物中沿氧-铵反梯度具有不同的分布模式。因此,在物种水平上,MAGs 似乎形成了不同的生态型,并遵循基于生态位的确定性分布。相比之下,由单核苷酸变异(SNV)模式定义的种群内结构似乎反映了更为复杂的决定性和随机过程。首先,水深范围对种群结构有很大影响,在深海平原和海沟有不同的种群。然后,海沟系统明显地将黑线鳕种群分开,这表明地形具有很强的隔离效应,而深海种群则受沉积深度或地理距离的控制,这取决于所考虑的支系。有趣的是,在 MAG 平均覆盖率最高的沉积层中,样本间的遗传变异性最低,这凸显了与每个 AOA 支系生态位相关的选择压力的重要性。总之,我们的研究结果表明,根据所考虑的基因组变异规模,深海 AOA 基因组分布似乎既遵循确定性过程,也遵循随机过程。
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
自引率
0.00%
发文量
0
×
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:481959085
Book学术官方微信