Pangenomes suggest ecological-evolutionary responses to experimental soil warming.

IF 3.7 2区 生物学 Q2 MICROBIOLOGY
mSphere Pub Date : 2025-04-29 Epub Date: 2025-03-19 DOI:10.1128/msphere.00059-25
Mallory J Choudoir, Achala Narayanan, Damayanti Rodriguez-Ramos, Rachel Simoes, Alon Efroni, Abigail Sondrini, Kristen M DeAngelis
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引用次数: 0

Abstract

Below-ground carbon transformations that contribute to healthy soils represent a natural climate change mitigation, but newly acquired traits adaptive to climate stress may alter microbial feedback mechanisms. To better define microbial evolutionary responses to long-term climate warming, we study microorganisms from an ongoing in situ soil warming experiment where, for over three decades, temperate forest soils are continuously heated at 5°C above ambient. We hypothesize that across generations of chronic warming, genomic signatures within diverse bacterial lineages reflect adaptations related to growth and carbon utilization. From our bacterial culture collection isolated from experimental heated and control plots, we sequenced genomes representing dominant taxa sensitive to warming, including lineages of Actinobacteria, Alphaproteobacteria, and Betaproteobacteria. We investigated genomic attributes and functional gene content to identify signatures of adaptation. Comparative pangenomics revealed accessory gene clusters related to central metabolism, competition, and carbon substrate degradation, with few functional annotations explicitly associated with long-term warming. Trends in functional gene patterns suggest genomes from heated plots were relatively enriched in central carbohydrate and nitrogen metabolism pathways, while genomes from control plots were relatively enriched in amino acid and fatty acid metabolism pathways. We observed that genomes from heated plots had less codon bias, suggesting potential adaptive traits related to growth or growth efficiency. Codon usage bias varied for organisms with similar 16S rrn operon copy number, suggesting that these organisms experience different selective pressures on growth efficiency. Our work suggests the emergence of lineage-specific trends as well as common ecological-evolutionary microbial responses to climate change.IMPORTANCEAnthropogenic climate change threatens soil ecosystem health in part by altering below-ground carbon cycling carried out by microbes. Microbial evolutionary responses are often overshadowed by community-level ecological responses, but adaptive responses represent potential changes in traits and functional potential that may alter ecosystem function. We predict that microbes are adapting to climate change stressors like soil warming. To test this, we analyzed the genomes of bacteria from a soil warming experiment where soil plots have been experimentally heated 5°C above ambient for over 30 years. While genomic attributes were unchanged by long-term warming, we observed trends in functional gene content related to carbon and nitrogen usage and genomic indicators of growth efficiency. These responses may represent new parameters in how soil ecosystems feedback to the climate system.

泛基因组显示了对实验性土壤变暖的生态进化反应。
有助于土壤健康的地下碳转化是一种自然的气候变化缓解,但适应气候压力的新获得的特征可能会改变微生物反馈机制。为了更好地定义微生物对长期气候变暖的进化反应,我们研究了一项正在进行的原位土壤变暖实验中的微生物,在该实验中,温带森林土壤在高于环境5°C的温度下连续加热30多年。我们假设,在长期变暖的世代中,不同细菌谱系中的基因组特征反映了与生长和碳利用相关的适应性。从实验加热区和对照区分离的细菌培养物中,我们对代表对变暖敏感的优势类群的基因组进行了测序,包括放线菌、α变形菌和β变形菌。我们研究了基因组属性和功能基因含量,以确定适应的特征。比较泛基因组学揭示了与中枢代谢、竞争和碳底物降解相关的辅助基因簇,很少有与长期变暖明确相关的功能注释。功能基因模式的趋势表明,加热小区的基因组在碳水化合物和氮代谢通路中相对富集,而对照小区的基因组在氨基酸和脂肪酸代谢通路中相对富集。我们观察到来自加热地块的基因组具有较少的密码子偏倚,这表明潜在的适应性状与生长或生长效率有关。具有相似16S rrn操纵子拷贝数的生物的密码子使用偏向性不同,表明这些生物在生长效率上经历了不同的选择压力。我们的工作表明,出现了特定谱系的趋势,以及共同的生态进化微生物对气候变化的反应。人为气候变化部分通过改变微生物进行的地下碳循环来威胁土壤生态系统的健康。微生物的进化反应常常被群落水平的生态反应所掩盖,但适应性反应代表了可能改变生态系统功能的性状和功能潜力的潜在变化。我们预测微生物正在适应气候变化的压力,比如土壤变暖。为了验证这一点,我们分析了土壤变暖实验中细菌的基因组,在该实验中,土壤地块已被实验加热超过环境温度5°C超过30年。虽然基因组属性不受长期变暖的影响,但我们观察到与碳氮利用和生长效率基因组指标相关的功能基因含量的趋势。这些响应可能代表土壤生态系统如何反馈给气候系统的新参数。
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来源期刊
mSphere
mSphere Immunology and Microbiology-Microbiology
CiteScore
8.50
自引率
2.10%
发文量
192
审稿时长
11 weeks
期刊介绍: mSphere™ is a multi-disciplinary open-access journal that will focus on rapid publication of fundamental contributions to our understanding of microbiology. Its scope will reflect the immense range of fields within the microbial sciences, creating new opportunities for researchers to share findings that are transforming our understanding of human health and disease, ecosystems, neuroscience, agriculture, energy production, climate change, evolution, biogeochemical cycling, and food and drug production. Submissions will be encouraged of all high-quality work that makes fundamental contributions to our understanding of microbiology. mSphere™ will provide streamlined decisions, while carrying on ASM''s tradition for rigorous peer review.
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