土壤微食物网中细菌和古细菌的演替改变了土壤呼吸动力学

IF 4.3 2区 生物学 Q2 MICROBIOLOGY Environmental microbiology Pub Date : 2024-11-21 DOI:10.1111/1462-2920.70007
Mandip Tamang, Johannes Sikorski, Miriam van Bommel, Marc Piecha, Tim Urich, Liliane Ruess, Katharina Huber, Meina Neumann-Schaal, Michael Pester
{"title":"土壤微食物网中细菌和古细菌的演替改变了土壤呼吸动力学","authors":"Mandip Tamang,&nbsp;Johannes Sikorski,&nbsp;Miriam van Bommel,&nbsp;Marc Piecha,&nbsp;Tim Urich,&nbsp;Liliane Ruess,&nbsp;Katharina Huber,&nbsp;Meina Neumann-Schaal,&nbsp;Michael Pester","doi":"10.1111/1462-2920.70007","DOIUrl":null,"url":null,"abstract":"<p>Bacterivorous nematodes are important grazers in the soil micro-food web. Their trophic regulation shapes the composition and ecosystem services of the soil microbiome, but the underlying population dynamics of bacteria and archaea are poorly understood. We followed soil respiration and 221 dominant bacterial and archaeal 16S rRNA gene amplicon sequencing variants (ASVs) in response to top-down control by a common bacterivorous soil nematode, <i>Acrobeloides buetschlii</i>, bottom-up control by maize litter amendment and their combination over 32 days. Maize litter amendment significantly increased soil respiration, while <i>A. buetschlii</i> addition caused an earlier peak in soil respiration. Underlying bacterial and archaeal population dynamics separated into five major response types, differentiating in their temporal abundance maxima and minima. In-depth analysis of these population dynamics identified a broad imprint of <i>A. buetschlii</i> grazing on dominant bacterial (<i>Acidobacteriota, Bacteroidota, Gemmatimonadota, Pseudomonadota</i>) and archaeal (<i>Nitrososphaerota</i>) ASVs. Combined bottom-up control by maize litter and top-down control by <i>A. buetschlii</i> grazing caused a succession of soil microbiota, driven by population changes first in the <i>Bacteroidota</i>, then in the <i>Pseudomonadota</i> and finally in the <i>Acidobacteriota</i> and <i>Nitrososphaerota</i>. Our results are an essential step forward in understanding trophic modulation of soil microbiota and its feedback on soil respiration.</p>","PeriodicalId":11898,"journal":{"name":"Environmental microbiology","volume":"26 11","pages":""},"PeriodicalIF":4.3000,"publicationDate":"2024-11-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/1462-2920.70007","citationCount":"0","resultStr":"{\"title\":\"Succession of Bacteria and Archaea Within the Soil Micro-Food Web Shifts Soil Respiration Dynamics\",\"authors\":\"Mandip Tamang,&nbsp;Johannes Sikorski,&nbsp;Miriam van Bommel,&nbsp;Marc Piecha,&nbsp;Tim Urich,&nbsp;Liliane Ruess,&nbsp;Katharina Huber,&nbsp;Meina Neumann-Schaal,&nbsp;Michael Pester\",\"doi\":\"10.1111/1462-2920.70007\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Bacterivorous nematodes are important grazers in the soil micro-food web. Their trophic regulation shapes the composition and ecosystem services of the soil microbiome, but the underlying population dynamics of bacteria and archaea are poorly understood. We followed soil respiration and 221 dominant bacterial and archaeal 16S rRNA gene amplicon sequencing variants (ASVs) in response to top-down control by a common bacterivorous soil nematode, <i>Acrobeloides buetschlii</i>, bottom-up control by maize litter amendment and their combination over 32 days. Maize litter amendment significantly increased soil respiration, while <i>A. buetschlii</i> addition caused an earlier peak in soil respiration. Underlying bacterial and archaeal population dynamics separated into five major response types, differentiating in their temporal abundance maxima and minima. In-depth analysis of these population dynamics identified a broad imprint of <i>A. buetschlii</i> grazing on dominant bacterial (<i>Acidobacteriota, Bacteroidota, Gemmatimonadota, Pseudomonadota</i>) and archaeal (<i>Nitrososphaerota</i>) ASVs. Combined bottom-up control by maize litter and top-down control by <i>A. buetschlii</i> grazing caused a succession of soil microbiota, driven by population changes first in the <i>Bacteroidota</i>, then in the <i>Pseudomonadota</i> and finally in the <i>Acidobacteriota</i> and <i>Nitrososphaerota</i>. Our results are an essential step forward in understanding trophic modulation of soil microbiota and its feedback on soil respiration.</p>\",\"PeriodicalId\":11898,\"journal\":{\"name\":\"Environmental microbiology\",\"volume\":\"26 11\",\"pages\":\"\"},\"PeriodicalIF\":4.3000,\"publicationDate\":\"2024-11-21\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1111/1462-2920.70007\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Environmental microbiology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1111/1462-2920.70007\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Environmental microbiology","FirstCategoryId":"99","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/1462-2920.70007","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

食菌线虫是土壤微食物网中的重要食草动物。它们的营养调控决定了土壤微生物组的组成和生态系统服务,但人们对细菌和古细菌的潜在种群动态却知之甚少。在 32 天的时间里,我们跟踪了土壤呼吸和 221 个优势细菌和古细菌 16S rRNA 基因扩增子测序变体(ASVs)对常见食菌性土壤线虫 Acrobeloides buetschlii 自上而下控制、玉米秸秆改良剂自下而上控制以及两者结合控制的反应。玉米凋落物的添加大大提高了土壤的呼吸作用,而 A. buetschlii 的添加则使土壤呼吸作用的峰值提前。基本的细菌和古细菌种群动态分为五种主要反应类型,它们在时间上的丰度最大值和最小值各不相同。对这些种群动态的深入分析发现,布氏酵母菌对优势细菌(酸性杆菌群、类杆菌群、革兰氏菌群、假单胞菌群)和古细菌(亚硝化细菌群)的ASV具有广泛的影响。玉米秸秆自下而上的控制和布氏矢车菊自上而下的控制相结合,导致了土壤微生物群的演替,首先是类杆菌群,然后是假单胞菌群,最后是酸性杆菌群和亚硝基磷脂菌群。我们的研究结果为了解土壤微生物区系的营养调节及其对土壤呼吸的反馈作用迈出了重要一步。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

摘要图片

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
Succession of Bacteria and Archaea Within the Soil Micro-Food Web Shifts Soil Respiration Dynamics

Bacterivorous nematodes are important grazers in the soil micro-food web. Their trophic regulation shapes the composition and ecosystem services of the soil microbiome, but the underlying population dynamics of bacteria and archaea are poorly understood. We followed soil respiration and 221 dominant bacterial and archaeal 16S rRNA gene amplicon sequencing variants (ASVs) in response to top-down control by a common bacterivorous soil nematode, Acrobeloides buetschlii, bottom-up control by maize litter amendment and their combination over 32 days. Maize litter amendment significantly increased soil respiration, while A. buetschlii addition caused an earlier peak in soil respiration. Underlying bacterial and archaeal population dynamics separated into five major response types, differentiating in their temporal abundance maxima and minima. In-depth analysis of these population dynamics identified a broad imprint of A. buetschlii grazing on dominant bacterial (Acidobacteriota, Bacteroidota, Gemmatimonadota, Pseudomonadota) and archaeal (Nitrososphaerota) ASVs. Combined bottom-up control by maize litter and top-down control by A. buetschlii grazing caused a succession of soil microbiota, driven by population changes first in the Bacteroidota, then in the Pseudomonadota and finally in the Acidobacteriota and Nitrososphaerota. Our results are an essential step forward in understanding trophic modulation of soil microbiota and its feedback on soil respiration.

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 microbiology
Environmental microbiology 环境科学-微生物学
CiteScore
9.90
自引率
3.90%
发文量
427
审稿时长
2.3 months
期刊介绍: Environmental Microbiology provides a high profile vehicle for publication of the most innovative, original and rigorous research in the field. The scope of the Journal encompasses the diversity of current research on microbial processes in the environment, microbial communities, interactions and evolution and includes, but is not limited to, the following: the structure, activities and communal behaviour of microbial communities microbial community genetics and evolutionary processes microbial symbioses, microbial interactions and interactions with plants, animals and abiotic factors microbes in the tree of life, microbial diversification and evolution population biology and clonal structure microbial metabolic and structural diversity microbial physiology, growth and survival microbes and surfaces, adhesion and biofouling responses to environmental signals and stress factors modelling and theory development pollution microbiology extremophiles and life in extreme and unusual little-explored habitats element cycles and biogeochemical processes, primary and secondary production microbes in a changing world, microbially-influenced global changes evolution and diversity of archaeal and bacterial viruses new technological developments in microbial ecology and evolution, in particular for the study of activities of microbial communities, non-culturable microorganisms and emerging pathogens
期刊最新文献
Contrasting Methane, Sulfide and Nitrogen-Loading Regimes in Bioreactors Shape Microbial Communities Originating From Methane-Rich Coastal Sediment of the Stockholm Archipelago Thermodynamics Underpinning the Microbial Community-Level Nitrogen Energy Metabolism Phylogenetic and Functional Diversity of Soluble Di-Iron Monooxygenases Highly Dynamic Archaeal and Bacterial Communities From the Surface to the Deep in the Atlantic Ocean Insects as Natural Hosts, Vectors and Reservoirs of Botulinum Neurotoxin-Producing Clostridia and Their Non-Toxinogenic Counterparts: Preliminary Evidence
×
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