通过元基因组组装的基因组发现脊椎动物宿主中具有孢子繁殖潜力的真菌新物种。

IF 3.7 2区 生物学 Q2 MICROBIOLOGY
Microbiology spectrum Pub Date : 2024-11-05 Epub Date: 2024-09-16 DOI:10.1128/spectrum.02113-24
Douglas Terra Machado, Beatriz do Carmo Dias, Rodrigo Cayô, Ana Cristina Gales, Fabíola Marques de Carvalho, Ana Tereza Ribeiro Vasconcelos
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引用次数: 0

摘要

元基因组组装基因组(MAGs)有助于识别不可培养的微生物并了解其生态功能。MAGs 在研究孢子化相关基因方面具有优势,尤其是考虑到很难分离居住在多个宿主肠道微生物群中的许多物种。细菌孢子化是一种关键的生存机制,对致病性和生物技术都有影响。在此,我们对脊椎动物宿主中的 MAGs 进行了研究,重点是分类鉴定和确定真菌门中潜在新物种的孢子相关基因。通过系统发育和功能通路分析,我们确定了梭菌(Borkfalkiaceae、Lachnospiraceae、Monoglobaceae 和 Oscillospiraceae 家族)和芽孢杆菌(Bacillaceae 和 Erysipelotrichaceae 家族)中的潜在新物种,并强调了它们的孢子潜能。我们的研究涵盖了 146 个 MAG,其中 124 个没有在科一级进行细化分类。我们发现,梭菌和芽孢杆菌在牛类、猪类、家禽类和人类宿主的细化科 MAGs 中具有独特的孢子传播基因谱。在 MAGs 中存在与 Spo0A 调节子、吞噬和孢子皮层有关的基因,这凸显了在目前尚未定性的物种中,孢子产生过程的基本机制,这些物种具有从元基因组暗物质中产生孢子的潜力。此外,基因组分析还可根据基因的存在、基因组大小以及参与孢子形成的代谢途径来预测孢子形成的潜力。我们强调的 MAGs 涵盖了尚未通过系统发育分析确定特征的科,以及梭状芽孢杆菌、芽孢杆菌、UBA4882 和 UBA994 类中具有广泛孢子形成潜力的细菌。这些发现有助于探索孢子形成细菌,为多种宿主中的新物种多样性、其适应策略以及在生物技术和宿主健康中的潜在应用提供了证据。探索来自不同宿主的元基因组组装基因组(MAGs)中的孢子相关基因有助于临床和生物技术领域的研究。我们的研究调查了来自家禽、猪、牛和人类的元基因组中与细菌孢子相关基因的范围,揭示了未培养细菌中的这些基因。通过系统发育和功能分析,我们发现了潜在的具有芽孢能力的新型真菌。值得注意的是,属于梭状芽孢杆菌、芽孢杆菌和未知类别的 MAGs(即 UBA4882 和 UBA994)在家族水平上仍未定性,这提出了这些基因组中也可能存在孢子化的假设。这些发现有助于我们了解微生物的适应性,对微生物生态学也有影响,强调了芽孢在不同宿主的真菌中的重要性。对新物种及其孢子能力的进一步研究有助于了解细菌在各种生物体内的维持机制及其在生物技术研究中的应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Uncovering new Firmicutes species in vertebrate hosts through metagenome-assembled genomes with potential for sporulation.

Metagenome-assembled genomes (MAGs) have contributed to identifying non-culturable microorganisms and understanding their ecological functions. MAGs offer an advantage in investigating sporulation-associated genes, especially given the difficulty of isolating many species residing in the gut microbiota of multiple hosts. Bacterial sporulation is a key survival mechanism with implications for pathogenicity and biotechnology. Here, we investigate MAGs from vertebrate hosts, emphasizing taxonomic identification and identifying sporulation-associated genes in potential novel species within the Firmicutes phylum. We identified potential new species in the classes Clostridia (Borkfalkiaceae, Lachnospiraceae, Monoglobaceae, and Oscillospiraceae families) and Bacilli (Bacillaceae and Erysipelotrichaceae families) through phylogenetic and functional pathway analyses, highlighting their sporulation potential. Our study covers 146 MAGs, 124 of them without refined taxonomic assignments at the family level. We found that Clostridia and Bacilli have unique sporulation gene profiles in the refined family MAGs for cattle, swine, poultry, and human hosts. The presence of genes related to Spo0A regulon, engulfment, and spore cortex in MAGs underscores fundamental mechanisms in sporulation processes in currently uncharacterized species with sporulation potential from metagenomic dark matter. Furthermore, genomic analyses predict sporulation potential based on gene presence, genome size, and metabolic pathways involved in spore formation. We emphasize MAGs covering families not yet characterized through the phylogenetic analysis, and with extensive potential for spore-forming bacteria within Clostridia, Bacilli, UBA4882, and UBA994 classes. These findings contribute to exploring spore-forming bacteria, which provides evidence for novel species diversity in multiple hosts, their adaptive strategies, and potential applications in biotechnology and host health.IMPORTANCESpores are essential for bacterial survival in harsh environments, facilitating their persistence and adaptation. Exploring sporulation-associated genes in metagenome-assembled genomes (MAGs) from different hosts contributes to clinical and biotechnological domains. Our study investigated the extent of genes associated with bacterial sporulation in MAGs from poultry, swine, cattle, and humans, revealing these genes in uncultivated bacteria. We identified potential novel Firmicutes species with sporulation capabilities through phylogenetic and functional analyses. Notably, MAGs belonging to Clostridia, Bacilli, and unknown classes, namely UBA4882 and UBA994, remained uncharacterized at the family level, which raises the hypothesis that sporulation would also be present in these genomes. These findings contribute to our understanding of microbial adaptation and have implications for microbial ecology, underlining the importance of sporulation in Firmicutes across different hosts. Further studies into novel species and their sporulation capability can contribute to bacterial maintenance mechanisms in various organisms and their applications in biotechnology studies.

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来源期刊
Microbiology spectrum
Microbiology spectrum Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.20
自引率
5.40%
发文量
1800
期刊介绍: Microbiology Spectrum publishes commissioned review articles on topics in microbiology representing ten content areas: Archaea; Food Microbiology; Bacterial Genetics, Cell Biology, and Physiology; Clinical Microbiology; Environmental Microbiology and Ecology; Eukaryotic Microbes; Genomics, Computational, and Synthetic Microbiology; Immunology; Pathogenesis; and Virology. Reviews are interrelated, with each review linking to other related content. A large board of Microbiology Spectrum editors aids in the development of topics for potential reviews and in the identification of an editor, or editors, who shepherd each collection.
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