Santana-Pereira Alinne L R, Moen Francesco S, Severance Beatrice, Liles Mark R
Department of Biological Sciences, Auburn University, Auburn, AL, United States.
Front Microbiol. 2023 Jul 27;14:1114548. doi: 10.3389/fmicb.2023.1114548. eCollection 2023.
Bacteria affiliated with the Candidate Phyla Radiation (CPR) are a hyper-diverse group of ultra-small bacteria with versatile yet sparse metabolisms. However, most insights into this group come from a surprisingly small number of environments, and recovery of CPR bacteria from soils has been hindered due to their extremely low abundance within complex microbial assemblages. In this study we enriched soil samples from 14 different soil fertility treatments for ultra-small (<0.45 μm) bacteria in order to study rare soil CPR. 42 samples were sequenced, enabling the reconstruction of 27 quality CPR metagenome-assembled genomes (MAGs) further classified as Parcubacteria/Paceibacteria, Saccharibacteria/Saccharimonadia and ABY1, in addition to representative genomes from Gemmatimonadetes, Dependentiae and Chlamydae phyla. These genomes were fully annotated and used to reconstruct the CPR community across all 14 plots. Additionally, for five of these plots, the entire microbiota was reconstructed using 16S amplification, showing that specific soil CPR may form symbiotic relationships with a varied and circumstantial range of hosts. Cullars CPR had a prevalence of enzymes predicted to degrade plant-derived carbohydrates, which suggests they have a role in plant biomass degradation. Parcubacteria appear to be more apt at microfauna necromass degradation. Cullars Saccharibacteria and a Parcubacteria group were shown to carry a possible aerotolerance mechanism coupled with potential for aerobic respiration, which appear to be a unique adaptation to the oxic soil environment. Reconstruction of CPR communities across treatment plots showed that they were not impacted by changes in nutrient levels or microbiota composition, being only impacted by extreme conditions, causing some CPR to dominate the community. These findings corroborate the understanding that soil-dwelling CPR bacteria have a very broad symbiont range and have metabolic capabilities associated to soil environments which allows them to scavenge resources and form resilient communities. The contributions of these microbial dark matter species to soil ecology and plant interactions will be of significant interest in future studies.
与候选门辐射类群(CPR)相关的细菌是一类超多样的超小细菌,其代谢功能多样但不丰富。然而,对这一类群的大多数认识来自数量惊人少的环境,并且由于CPR细菌在复杂微生物群落中的丰度极低,从土壤中回收它们一直受到阻碍。在本研究中,我们对来自14种不同土壤肥力处理的土壤样本进行富集,以研究超小(<0.45μm)细菌,从而研究土壤中罕见的CPR细菌。对42个样本进行了测序,除了来自芽单胞菌门、依赖菌门和衣原体门的代表性基因组外,还能够重建27个高质量的CPR宏基因组组装基因组(MAG),并进一步分类为 Parcubacteria/Paceibacteria、Saccharibacteria/Saccharimonadia 和 ABY1。这些基因组经过了全面注释,并用于重建所有14个样地中的CPR群落。此外,对于其中五个样地,使用16S扩增重建了整个微生物群,表明特定的土壤CPR可能与各种各样的宿主形成共生关系。Cullars CPR 中预测可降解植物衍生碳水化合物的酶普遍存在,这表明它们在植物生物量降解中发挥作用。Parcubacteria似乎更擅长降解小型动物的尸体。研究表明,Cullars Saccharibacteria和一个Parcubacteria 群体具有一种可能的耐氧机制以及有氧呼吸的潜力,这似乎是对有氧土壤环境的独特适应。跨处理样地重建CPR群落表明,它们不受养分水平或微生物群组成变化的影响,仅受极端条件的影响,导致一些CPR在群落中占主导地位。这些发现证实了这样的认识,即生活在土壤中的CPR细菌具有非常广泛的共生体范围,并且具有与土壤环境相关的代谢能力,这使它们能够获取资源并形成有弹性的群落。这些微生物暗物质物种对土壤生态和植物相互作用的贡献将是未来研究的重要关注点。