Large Filamentous Bacteria Isolated From Sulphidic Sediments Reveal Novel Species and Distinct Energy and Defence Mechanisms for Survival

IF 4 2区 生物学 Q2 MICROBIOLOGY Environmental microbiology Pub Date : 2025-03-18 DOI:10.1111/1462-2920.70083
Alexis Fonseca, Thomas Ishoey, Carola Espinoza, Ian P. G. Marshall, Lars Peter Nielsen, Victor Ariel Gallardo
{"title":"Large Filamentous Bacteria Isolated From Sulphidic Sediments Reveal Novel Species and Distinct Energy and Defence Mechanisms for Survival","authors":"Alexis Fonseca,&nbsp;Thomas Ishoey,&nbsp;Carola Espinoza,&nbsp;Ian P. G. Marshall,&nbsp;Lars Peter Nielsen,&nbsp;Victor Ariel Gallardo","doi":"10.1111/1462-2920.70083","DOIUrl":null,"url":null,"abstract":"<p>Various morphotypes of large filamentous bacteria were isolated through micromanipulation from sulphidic sediment mats in the Bay of Concepción, central Chile. This study employed DNA amplification, whole-genome sequencing and bioinformatics analyses to unveil the taxonomic and genomic features of previously unidentified bacteria. The results revealed several novel genera, families and species, including three specimens belonging to Beggiatoales (Beggiatoaceae family), five to Desulfobacterales (Desulfobacteraceae family), two to the Chloroflexi phylum and one to the phylum Firmicutes. Metabolically, Beggiatoaceae bacteria exhibit a flexible and versatile genomic repertoire, enabling them to adapt to variable conditions at the sediment–water interface. All the bacteria demonstrated a mixotrophic mode, gaining energy from both inorganic and organic carbon sources. Except for the Firmicutes bacterium, all others displayed the ability to grow chemolithoautotrophically using H<sub>2</sub> and CO<sub>2</sub>. Remarkably, the reverse tricarboxylic acid (rTCA) and Calvin–Benson–Bassham (CBB) pathways coexisted in one Beggiatoaceae bacterium. Additionally, various defence systems, such as CRISPR-Cas, along with evidence of viral interactions, have been identified. These defence mechanisms suggest that large filamentous bacteria inhabiting sulphidic sediments frequently encounter bacteriophages. Thus, robust defence mechanisms coupled with multicellularity may determine the survival or death of these large bacteria.</p>","PeriodicalId":11898,"journal":{"name":"Environmental microbiology","volume":"27 3","pages":""},"PeriodicalIF":4.0000,"publicationDate":"2025-03-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/1462-2920.70083","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Environmental microbiology","FirstCategoryId":"99","ListUrlMain":"https://enviromicro-journals.onlinelibrary.wiley.com/doi/10.1111/1462-2920.70083","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

Abstract

Various morphotypes of large filamentous bacteria were isolated through micromanipulation from sulphidic sediment mats in the Bay of Concepción, central Chile. This study employed DNA amplification, whole-genome sequencing and bioinformatics analyses to unveil the taxonomic and genomic features of previously unidentified bacteria. The results revealed several novel genera, families and species, including three specimens belonging to Beggiatoales (Beggiatoaceae family), five to Desulfobacterales (Desulfobacteraceae family), two to the Chloroflexi phylum and one to the phylum Firmicutes. Metabolically, Beggiatoaceae bacteria exhibit a flexible and versatile genomic repertoire, enabling them to adapt to variable conditions at the sediment–water interface. All the bacteria demonstrated a mixotrophic mode, gaining energy from both inorganic and organic carbon sources. Except for the Firmicutes bacterium, all others displayed the ability to grow chemolithoautotrophically using H2 and CO2. Remarkably, the reverse tricarboxylic acid (rTCA) and Calvin–Benson–Bassham (CBB) pathways coexisted in one Beggiatoaceae bacterium. Additionally, various defence systems, such as CRISPR-Cas, along with evidence of viral interactions, have been identified. These defence mechanisms suggest that large filamentous bacteria inhabiting sulphidic sediments frequently encounter bacteriophages. Thus, robust defence mechanisms coupled with multicellularity may determine the survival or death of these large bacteria.

Abstract Image

Abstract Image

Abstract Image

Abstract Image

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
从硫化物沉积物中分离出的大型丝状细菌揭示了新的物种和独特的生存能量和防御机制
通过显微操作从智利中部Concepción湾的硫化物沉积物席中分离出各种形态的大型丝状细菌。本研究采用DNA扩增、全基因组测序和生物信息学分析揭示了以前未识别的细菌的分类和基因组特征。结果发现了几个新属、新科和新种,包括3个属Beggiatoales (Beggiatoaceae), 5个属Desulfobacterales (Desulfobacteraceae), 2个属Chloroflexi门,1个属厚壁菌门。在代谢方面,Beggiatoaceae细菌表现出灵活多样的基因组库,使它们能够适应沉积物-水界面的可变条件。所有细菌都表现出混合营养模式,从无机和有机碳源中获取能量。除了厚壁菌门细菌外,所有其他细菌都显示出利用H2和CO2进行化石化自养生长的能力。值得注意的是,在一个Beggiatoaceae细菌中,逆转录三羧酸(rTCA)和Calvin-Benson-Bassham (CBB)途径共存。此外,各种防御系统,如CRISPR-Cas,以及病毒相互作用的证据,已经被确定。这些防御机制表明,居住在硫化物沉积物中的大型丝状细菌经常遇到噬菌体。因此,强大的防御机制加上多细胞性可能决定这些大型细菌的生存或死亡。
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 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
Soil Functionality Undermined by Symbiotic Fungal Decline Following Forest Conversion Comparative Physiology and Genomics of Thermincola and Carboxydocella Strains and Description of Two Novel Isolates Distribution and Feeding of Hexatilemonas jangsaensis , a Novel Cosmopolitan Member of the Uncultured Marine Apusomonad Clade Organic Fertiliser Additions Promote Transformation of Extracellular Antibiotic Resistance Genes to Soil Bacteria Activity and Abundance of Nitrous Oxide Reducing Bacteria in Platismatia glauca : An Epiphytic Lichen in the Boreal Spruce Forest
×
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:604180095
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