硫酸盐还原脱硫菌和芽孢杆菌在 50%空气-氧气饱和度的周期性氧胁迫下的生长。

IF 13.8 1区 生物学 Q1 MICROBIOLOGY Microbiome Pub Date : 2024-10-04 DOI:10.1186/s40168-024-01909-7
Stefan Dyksma, Michael Pester
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引用次数: 0

摘要

背景:硫酸盐还原菌(SRB)经常出现在缺氧到缺氧的过渡带,它们会经常短暂地暴露在微氧甚至缺氧条件下。这可能是海洋潮汐沉积物、微生物垫和泥炭地等淡水湿地。在后者中,一个隐秘但高度活跃的硫循环支持着它们的厌氧活动。在这里,我们旨在更好地了解 SRB 如何对周期性波动的氧化还原机制做出反应:结果:为了模拟这些波动的氧化还原条件,我们在一个生物反应器中接种了支持隐性硫循环的泥炭土,并在超过 200 天的时间内连续暴露于缺氧(一周)和缺氧(四周)阶段。尽管每周暴露于 133 µM(50% 空气饱和度)的氧气中,但隶属于脱硫孢子菌属(芽孢杆菌科)和合成杆菌科、脱硫单胞菌科、脱硫帽菌科和脱硫荚膜菌科(脱硫杆菌科)的 SRB 仍相继建立了不断增长的种群(相对丰度高达 2.9%)。以基因组为中心的元转录组学分析了适应机制。尽管在缺氧阶段基因表达量全面下降,但所有 SRB 的能量代谢基因表达量均保持不变。不同SRB的耐氧转录反应模式各不相同,这表明它们采取了不同的适应策略。大多数 SRB 转录了不同的氧消耗、活性氧解毒和氧化蛋白质修复基因集,以应对从缺氧到缺氧条件的周期性氧化还原转换。值得注意的是,即使在缺氧条件下,Desulfosporosinus、Desulfovibrionaceaea 和 Desulfocapsaceaea 代表的编码氧防御蛋白的基因仍能保持较高的转录水平,同时在生物反应器运行半年后代表了优势 SRB 种群:在原位相关泥炭地SRB建立了大量种群,尽管周期性一周的氧气水平比已知SRB纯培养物所能耐受的氧气水平高出一个数量级。观察到的基因表达调控下降可能是这些原本严格厌氧的微生物承受周期性发生的氧化还原机制变化的关键。我们的研究为SRB的应激反应提供了重要见解,SRB的应激反应推动了硫在缺氧-缺氧间期的循环。视频摘要。
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Growth of sulfate-reducing Desulfobacterota and Bacillota at periodic oxygen stress of 50% air-O2 saturation.

Background: Sulfate-reducing bacteria (SRB) are frequently encountered in anoxic-to-oxic transition zones, where they are transiently exposed to microoxic or even oxic conditions on a regular basis. This can be marine tidal sediments, microbial mats, and freshwater wetlands like peatlands. In the latter, a cryptic but highly active sulfur cycle supports their anaerobic activity. Here, we aimed for a better understanding of how SRB responds to periodically fluctuating redox regimes.

Results: To mimic these fluctuating redox conditions, a bioreactor was inoculated with peat soil supporting cryptic sulfur cycling and consecutively exposed to oxic (one week) and anoxic (four weeks) phases over a period of > 200 days. SRB affiliated to the genus Desulfosporosinus (Bacillota) and the families Syntrophobacteraceae, Desulfomonilaceae, Desulfocapsaceae, and Desulfovibrionaceae (Desulfobacterota) successively established growing populations (up to 2.9% relative abundance) despite weekly periods of oxygen exposures at 133 µM (50% air saturation). Adaptation mechanisms were analyzed by genome-centric metatranscriptomics. Despite a global drop in gene expression during oxic phases, the perpetuation of gene expression for energy metabolism was observed for all SRBs. The transcriptional response pattern for oxygen resistance was differentiated across individual SRBs, indicating different adaptation strategies. Most SRB transcribed differing sets of genes for oxygen consumption, reactive oxygen species detoxification, and repair of oxidized proteins as a response to the periodical redox switch from anoxic to oxic conditions. Noteworthy, a Desulfosporosinus, a Desulfovibrionaceaea, and a Desulfocapsaceaea representative maintained high transcript levels of genes encoding oxygen defense proteins even under anoxic conditions, while representing dominant SRB populations after half a year of bioreactor operation.

Conclusions: In situ-relevant peatland SRB established large populations despite periodic one-week oxygen levels that are one order of magnitude higher than known to be tolerated by pure cultures of SRB. The observed decrease in gene expression regulation may be key to withstand periodically occurring changes in redox regimes in these otherwise strictly anaerobic microorganisms. Our study provides important insights into the stress response of SRB that drives sulfur cycling at oxic-anoxic interphases. Video Abstract.

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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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