Organic matter degradation in the deep, sulfidic waters of the Black Sea: insights into the ecophysiology of novel anaerobic bacteria.

IF 13.8 1区 生物学 Q1 MICROBIOLOGY
Subhash Yadav, Michel Koenen, Nicole J Bale, Wietse Reitsma, Julia C Engelmann, Kremena Stefanova, Jaap S Sinninghe Damsté, Laura Villanueva
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引用次数: 0

Abstract

Background: Recent studies have reported the identity and functions of key anaerobes involved in the degradation of organic matter (OM) in deep (> 1000 m) sulfidic marine habitats. However, due to the lack of available isolates, detailed investigation of their physiology has been precluded. In this study, we cultivated and characterized the ecophysiology of a wide range of novel anaerobes potentially involved in OM degradation in deep (2000 m depth) sulfidic waters of the Black Sea.

Results: We have successfully cultivated a diverse group of novel anaerobes belonging to various phyla, including Fusobacteriota (strain S5), Bacillota (strains A1T and A2), Spirochaetota (strains M1T, M2, and S2), Bacteroidota (strains B1T, B2, S6, L6, SYP, and M2P), Cloacimonadota (Cloa-SY6), Planctomycetota (Plnct-SY6), Mycoplasmatota (Izemo-BS), Chloroflexota (Chflx-SY6), and Desulfobacterota (strains S3T and S3-i). These microorganisms were able to grow at an elevated hydrostatic pressure of up to 50 MPa. Moreover, this study revealed that different anaerobes were specialized in degrading specific types of OM. Strains affiliated with the phyla Fusobacteriota, Bacillota, Planctomycetota, and Mycoplasmatota were found to be specialized in the degradation of cellulose, cellobiose, chitin, and DNA, respectively, while strains affiliated with Spirochaetota, Bacteroidota, Cloacimonadota, and Chloroflexota preferred to ferment less complex forms of OM. We also identified members of the phylum Desulfobacterota as terminal oxidizers, potentially involved in the consumption of hydrogen produced during fermentation. These results were supported by the identification of genes in the (meta)genomes of the cultivated microbial taxa which encode proteins of specific metabolic pathways. Additionally, we analyzed the composition of membrane lipids of selected taxa, which could be critical for their survival in the harsh environment of the deep sulfidic waters and could potentially be used as biosignatures for these strains in the sulfidic waters of the Black Sea.

Conclusions: This is the first report that demonstrates the cultivation and ecophysiology of such a diverse group of microorganisms from any sulfidic marine habitat. Collectively, this study provides a step forward in our understanding of the microbes thriving in the extreme conditions of the deep sulfidic waters of the Black Sea. Video Abstract.

黑海深层硫化水域的有机物降解:新型厌氧细菌生态生理学研究。
背景:最近的研究报道了参与深海(> 1000 米)硫化海洋栖息地有机物(OM)降解的关键厌氧菌的特性和功能。然而,由于缺乏可用的分离物,无法对它们的生理机能进行详细研究。在这项研究中,我们培养并鉴定了可能参与黑海深层(2000 米深)硫酸盐水域有机物降解的多种新型厌氧菌的生态生理学:结果:我们成功培养了属于不同门类的多种新型厌氧菌,包括镰刀菌门(菌株 S5)、芽孢杆菌门(菌株 A1T 和 A2)、螺菌门(菌株 M1T、M2 和 S2)、类杆菌门(菌株 B1T、B2T 和 B3T)、细菌群(菌株 B1T、B2、S6、L6、SYP 和 M2P)、球菌群(菌株 Cloa-SY6)、 Planctomycetota(菌株 Plnct-SY6)、霉菌群(菌株 Izemo-BS)、绿僵菌群(菌株 Chflx-SY6)和脱硫菌群(菌株 S3T 和 S3-i)。这些微生物能够在高达 50 兆帕的高压下生长。此外,这项研究还发现,不同的厌氧菌专门降解特定类型的有机物。研究发现,隶属于镰刀菌门、芽孢杆菌门、扁孢菌门和支原体门的菌株分别擅长降解纤维素、纤维生物糖、几丁质和 DNA,而隶属于螺菌门、类杆菌门、球菌门和绿僵菌门的菌株则更喜欢发酵复杂程度较低的 OM。我们还发现脱硫菌门(Desulfobacterota)的成员是末端氧化剂,可能参与消耗发酵过程中产生的氢气。在培养微生物类群的(元)基因组中发现了编码特定代谢途径蛋白质的基因,这为上述结果提供了支持。此外,我们还分析了所选分类群的膜脂组成,这可能是它们在深硫酸盐水域的恶劣环境中生存的关键,并有可能被用作这些菌株在黑海硫酸盐水域的生物特征:这是第一份关于硫化海洋栖息地中如此多样的微生物群的培养和生态生理学的报告。总之,这项研究使我们对在黑海深层硫化水域极端条件下生长的微生物的了解向前迈进了一步。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。
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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.
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