低营养建造环境中微生物多样化和特殊化的代谢能力。

IF 13.8 1区 生物学 Q1 MICROBIOLOGY Microbiome Pub Date : 2024-10-17 DOI:10.1186/s40168-024-01926-6
Xinzhao Tong, Danli Luo, Marcus H Y Leung, Justin Y Y Lee, Zhiyong Shen, Wengyao Jiang, Christopher E Mason, Patrick K H Lee
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引用次数: 0

摘要

背景:建筑环境(BE)通常被认为是微生物群落在正常、非潮湿条件下的低营养和恶劣环境。然而,人们对建筑环境中微生物群落的代谢功能仍然知之甚少。本研究旨在通过分析从全港 BE 和人类居住者皮肤表面采集的 738 个样本中重建的 860 个代表性元基因组(rMAGs),揭示 BE 中微生物的功能能力。研究特别关注了在系统发育上新颖或在 BE 中普遍存在的 rMAGs 的代谢功能:结果:BE 微生物组的多样性和组成主要受样本类型的影响,其中以黄体微球菌和痤疮杆菌最为普遍。rMAGs的代谢功能因分类而有很大差异,甚至在菌株水平上也是如此。与近亲相比,一种隶属于念珠菌门(Candidatus)Xenobia类的新型菌株和两种隶属于超细菌门(Patescibacteria)的新型菌株表现出独特的功能,这可能有助于它们在BE和人类皮肤上生存。Xenobia类中的新型菌株拥有转运硝酸盐和亚硝酸盐作为氮源的基因,以及在反硝化过程中由一氧化氮诱导的亚硝酸应激缓解基因。两株新型棒状杆菌都拥有一系列氨基酸和微量元素转运基因,其中一株携带类胡萝卜素和泛醌生物合成基因。在 BEs 中全球流行的黄体霉菌显示了一个庞大而开放的泛基因组,在单一地理区域的 BEs 中发现的 11 个同种菌株贡献了高度的种下基因组多样性。黄曲霉大型附属基因组所编码的多功能代谢功能可能是其在BEs中全球普遍存在和专业化的原因:这项研究表明,BEs 中的微生物居民具有新陈代谢潜能,能够耐受和对抗不同的生物和非生物条件。此外,这些微生物还能有效利用居住者活动产生的各种有限的残余资源,从而提高它们在 BEs 中的生存能力和持久性。更好地了解 BE 微生物的新陈代谢功能,最终将有助于制定创建健康室内微生物群的策略。视频摘要。
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Diverse and specialized metabolic capabilities of microbes in oligotrophic built environments.

Background: Built environments (BEs) are typically considered to be oligotrophic and harsh environments for microbial communities under normal, non-damp conditions. However, the metabolic functions of microbial inhabitants in BEs remain poorly understood. This study aimed to shed light on the functional capabilities of microbes in BEs by analyzing 860 representative metagenome-assembled genomes (rMAGs) reconstructed from 738 samples collected from BEs across the city of Hong Kong and from the skin surfaces of human occupants. The study specifically focused on the metabolic functions of rMAGs that are either phylogenetically novel or prevalent in BEs.

Results: The diversity and composition of BE microbiomes were primarily shaped by the sample type, with Micrococcus luteus and Cutibacterium acnes being prevalent. The metabolic functions of rMAGs varied significantly based on taxonomy, even at the strain level. A novel strain affiliated with the Candidatus class Xenobia in the Candidatus phylum Eremiobacterota and two novel strains affiliated with the superphylum Patescibacteria exhibited unique functions compared with their close relatives, potentially aiding their survival in BEs and on human skins. The novel strains in the class Xenobia possessed genes for transporting nitrate and nitrite as nitrogen sources and nitrosative stress mitigation induced by nitric oxide during denitrification. The two novel Patescibacteria strains both possessed a broad array of genes for amino acid and trace element transport, while one of them carried genes for carotenoid and ubiquinone biosynthesis. The globally prevalent M. luteus in BEs displayed a large and open pangenome, with high infraspecific genomic diversity contributed by 11 conspecific strains recovered from BEs in a single geographic region. The versatile metabolic functions encoded in the large accessory genomes of M. luteus may contribute to its global ubiquity and specialization in BEs.

Conclusions: This study illustrates that the microbial inhabitants of BEs possess metabolic potentials that enable them to tolerate and counter different biotic and abiotic conditions. Additionally, these microbes can efficiently utilize various limited residual resources from occupant activities, potentially enhancing their survival and persistence within BEs. A better understanding of the metabolic functions of BE microbes will ultimately facilitate the development of strategies to create a healthy indoor microbiome. 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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