Novel and unusual genes for nitrogen and metal cycling in Planctomycetota- and KSB1-affiliated metagenome-assembled genomes reconstructed from a marine subsea tunnel.

IF 2.2 4区 生物学 Q3 MICROBIOLOGY
Carolina Suarez, Thomas Hackl, Britt-Marie Wilen, Frank Persson, Per Hagelia, Mike S M Jetten, Paula Dalcin Martins
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引用次数: 1

Abstract

The Oslofjord subsea road tunnel is a unique environment in which the typically anoxic marine deep subsurface is exposed to oxygen. Concrete biodeterioration and steel corrosion in the tunnel have been linked to the growth of iron- and manganese-oxidizing biofilms in areas of saline water seepage. Surprisingly, previous 16S rRNA gene surveys of biofilm samples revealed microbial communities dominated by sequences affiliated with nitrogen-cycling microorganisms. This study aimed to identify microbial genomes with metabolic potential for novel nitrogen- and metal-cycling reactions, representing biofilm microorganisms that could link these cycles and play a role in concrete biodeterioration. We reconstructed 33 abundant, novel metagenome-assembled genomes (MAGs) affiliated with the phylum Planctomycetota and the candidate phylum KSB1. We identified novel and unusual genes and gene clusters in these MAGs related to anaerobic ammonium oxidation, nitrite oxidation, and other nitrogen-cycling reactions. Additionally, 26 of 33 MAGs also had the potential for iron, manganese, and arsenite cycling, suggesting that bacteria represented by these genomes might couple these reactions. Our results expand the diversity of microorganisms putatively involved in nitrogen and metal cycling, and contribute to our understanding of potential biofilm impacts on built infrastructure.

从海洋海底隧道中重建的 Planctomycetota 和 KSB1 相关元基因组中氮和金属循环的新颖和不寻常基因。
奥斯陆峡湾海底公路隧道是一个独特的环境,在这里,通常缺氧的海洋深层地表暴露在氧气中。隧道中的混凝土生物劣化和钢材腐蚀与盐水渗出区域铁和锰氧化生物膜的生长有关。令人惊讶的是,之前对生物膜样本进行的 16S rRNA 基因调查显示,微生物群落以氮循环微生物序列为主。本研究旨在鉴定具有新型氮和金属循环反应代谢潜力的微生物基因组,这些基因组代表了可能连接这些循环并在混凝土生物劣化中发挥作用的生物膜微生物。我们重建了 33 个丰富、新颖的元基因组组装基因组(MAGs),它们隶属于 Planctomycetota 门和候选门 KSB1。我们在这些基因组中发现了与厌氧氨氧化、亚硝酸盐氧化和其他氮循环反应有关的新颖和不寻常基因及基因簇。此外,33 个 MAG 中的 26 个还具有铁、锰和亚砷酸盐循环的潜力,这表明这些基因组所代表的细菌可能会将这些反应结合起来。我们的研究结果扩大了可能参与氮和金属循环的微生物的多样性,有助于我们了解生物膜对已建基础设施的潜在影响。
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来源期刊
Fems Microbiology Letters
Fems Microbiology Letters 生物-微生物学
CiteScore
4.30
自引率
0.00%
发文量
112
审稿时长
1.9 months
期刊介绍: FEMS Microbiology Letters gives priority to concise papers that merit rapid publication by virtue of their originality, general interest and contribution to new developments in microbiology. All aspects of microbiology, including virology, are covered. 2019 Impact Factor: 1.987, Journal Citation Reports (Source Clarivate, 2020) Ranking: 98/135 (Microbiology) The journal is divided into eight Sections: Physiology and Biochemistry (including genetics, molecular biology and ‘omic’ studies) Food Microbiology (from food production and biotechnology to spoilage and food borne pathogens) Biotechnology and Synthetic Biology Pathogens and Pathogenicity (including medical, veterinary, plant and insect pathogens – particularly those relating to food security – with the exception of viruses) Environmental Microbiology (including ecophysiology, ecogenomics and meta-omic studies) Virology (viruses infecting any organism, including Bacteria and Archaea) Taxonomy and Systematics (for publication of novel taxa, taxonomic reclassifications and reviews of a taxonomic nature) Professional Development (including education, training, CPD, research assessment frameworks, research and publication metrics, best-practice, careers and history of microbiology) If you are unsure which Section is most appropriate for your manuscript, for example in the case of transdisciplinary studies, we recommend that you contact the Editor-In-Chief by email prior to submission. Our scope includes any type of microorganism - all members of the Bacteria and the Archaea and microbial members of the Eukarya (yeasts, filamentous fungi, microbial algae, protozoa, oomycetes, myxomycetes, etc.) as well as all viruses.
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