地衣 Lobaria pulmonaria 的微生物组随亚大陆范围的气候而变化。

IF 3.6 4区 生物学 Q2 ENVIRONMENTAL SCIENCES
Anteneh Tamirat Bogale, Maria Braun, Jörg Bernhardt, Daniela Zühlke, Ulf Schiefelbein, Manuela Bog, Christoph Scheidegger, Veronika Zengerer, Dörte Becher, Martin Grube, Katharina Riedel, Mia M. Bengtsson
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引用次数: 0

摘要

Lobaria pulmonaria全生物群由藻类、真菌、蓝藻和细菌组成。我们研究了 L. pulmonaria 的细菌微生物组,以了解这一生态敏感的地衣物种对不同气候条件的适应情况。我们的核心假设是,微生物组的组成和功能与亚大陆尺度(绵延约 1100 公里)与温度和降水相关的气候参数相一致。我们还测试了短期天气动态、采样季节和藻类/真菌基因型对微生物组变化的影响。元蛋白组学深入揭示了微生物组的组成和功能变化。气候变量解释了微生物组变异的 41.64%,超过了当地天气和采样季节的综合影响(31.63%)。值得注意的是,年平均气温和气温季节性是重要的气候驱动因素。微生物组的组成与藻类基因型而非真菌基因型相关,这表明藻类伙伴和微生物组的环境招募相似。差异丰度分析表明,次大西洋低地和高山地区的蛋白质组成不同,这表明微生物组对截然不同的环境/气候条件做出了不同的反应。参与氧化和细胞压力的蛋白质明显不同。我们的研究结果突显了微生物组在适应稳定气候方面的可塑性,以及对短期波动的有限反应,为地衣共生中的气候适应提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The microbiome of the lichen Lobaria pulmonaria varies according to climate on a subcontinental scale

The microbiome of the lichen Lobaria pulmonaria varies according to climate on a subcontinental scale

The Lobaria pulmonaria holobiont comprises algal, fungal, cyanobacterial and bacterial components. We investigated L. pulmonaria's bacterial microbiome in the adaptation of this ecologically sensitive lichen species to diverse climatic conditions. Our central hypothesis posited that microbiome composition and functionality aligns with subcontinental-scale (a stretch of ~1100 km) climatic parameters related to temperature and precipitation. We also tested the impact of short-term weather dynamics, sampling season and algal/fungal genotypes on microbiome variation. Metaproteomics provided insights into compositional and functional changes within the microbiome. Climatic variables explained 41.64% of microbiome variation, surpassing the combined influence of local weather and sampling season at 31.63%. Notably, annual mean temperature and temperature seasonality emerged as significant climatic drivers. Microbiome composition correlated with algal, not fungal genotype, suggesting similar environmental recruitment for the algal partner and microbiome. Differential abundance analyses revealed distinct protein compositions in Sub-Atlantic Lowland and Alpine regions, indicating differential microbiome responses to contrasting environmental/climatic conditions. Proteins involved in oxidative and cellular stress were notably different. Our findings highlight microbiome plasticity in adapting to stable climates, with limited responsiveness to short-term fluctuations, offering new insights into climate adaptation in lichen symbiosis.

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来源期刊
Environmental Microbiology Reports
Environmental Microbiology Reports ENVIRONMENTAL SCIENCES-MICROBIOLOGY
CiteScore
6.00
自引率
3.00%
发文量
91
审稿时长
3.0 months
期刊介绍: The journal is identical in scope to Environmental Microbiology, shares the same editorial team and submission site, and will apply the same high level acceptance criteria. The two journals will be mutually supportive and evolve side-by-side. Environmental Microbiology Reports provides a high profile vehicle for publication of the most innovative, original and rigorous research in the field. The scope of the Journal encompasses the diversity of current research on microbial processes in the environment, microbial communities, interactions and evolution and includes, but is not limited to, the following: the structure, activities and communal behaviour of microbial communities microbial community genetics and evolutionary processes microbial symbioses, microbial interactions and interactions with plants, animals and abiotic factors microbes in the tree of life, microbial diversification and evolution population biology and clonal structure microbial metabolic and structural diversity microbial physiology, growth and survival microbes and surfaces, adhesion and biofouling responses to environmental signals and stress factors modelling and theory development pollution microbiology extremophiles and life in extreme and unusual little-explored habitats element cycles and biogeochemical processes, primary and secondary production microbes in a changing world, microbially-influenced global changes evolution and diversity of archaeal and bacterial viruses new technological developments in microbial ecology and evolution, in particular for the study of activities of microbial communities, non-culturable microorganisms and emerging pathogens.
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