Multiple stressors affect function rather than taxonomic structure of freshwater microbial communities.

IF 7.8 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Rose Fuggle, Miguel G Matias, Mariana Mayer-Pinto, Ezequiel M Marzinelli
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引用次数: 0

Abstract

Microbial community responses to environmental stressors are often characterised by assessing changes in taxonomic structure, but such changes, or lack thereof, may not reflect functional changes that are critical to ecosystem processes. We investigated the individual and combined effects of nutrient enrichment ( + 10 mg/L N, + 1 mg/L P) and salinisation ( + 15 g/L NaCl)-key stressors in freshwater systems-on the taxonomic structure and metabolic function of benthic microbial communities using 1000 L open freshwater ponds established >10 years ago in the field. Combined stressors drove strong decreases in maximum and mean total carbon metabolic rates and shifted carbon metabolic profiles compared to either stressor individually and compared to ambient conditions. These metabolic functional changes did not recover through time and occurred without significant alterations in bacterial community taxonomic structure. These results imply that critical functions, including organic carbon release, are likely to be impaired under multiple stressors, even when taxonomic structure remains stable.

多重压力源影响淡水微生物群落的功能而非分类结构。
微生物群落对环境压力的响应通常通过评估分类结构的变化来表征,但这种变化或缺乏这种变化可能无法反映对生态系统过程至关重要的功能变化。利用10年前在野外建立的1000 L开放淡水池塘,研究了淡水系统中主要应激源营养物富集(+ 10 mg/L N, + 1 mg/L P)和盐碱化(+ 15 g/L NaCl)对底栖微生物群落分类结构和代谢功能的单独和联合影响。与单独的应激源和环境条件相比,联合应激源导致最大和平均总碳代谢率的大幅下降,并改变了碳代谢谱。这些代谢功能的变化不会随着时间的推移而恢复,并且在细菌群落分类结构中没有明显的变化。这些结果表明,即使在分类结构保持稳定的情况下,包括有机碳释放在内的关键功能也可能在多重胁迫下受到损害。
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来源期刊
npj Biofilms and Microbiomes
npj Biofilms and Microbiomes Immunology and Microbiology-Microbiology
CiteScore
12.10
自引率
3.30%
发文量
91
审稿时长
9 weeks
期刊介绍: npj Biofilms and Microbiomes is a comprehensive platform that promotes research on biofilms and microbiomes across various scientific disciplines. The journal facilitates cross-disciplinary discussions to enhance our understanding of the biology, ecology, and communal functions of biofilms, populations, and communities. It also focuses on applications in the medical, environmental, and engineering domains. The scope of the journal encompasses all aspects of the field, ranging from cell-cell communication and single cell interactions to the microbiomes of humans, animals, plants, and natural and built environments. The journal also welcomes research on the virome, phageome, mycome, and fungome. It publishes both applied science and theoretical work. As an open access and interdisciplinary journal, its primary goal is to publish significant scientific advancements in microbial biofilms and microbiomes. The journal enables discussions that span multiple disciplines and contributes to our understanding of the social behavior of microbial biofilm populations and communities, and their impact on life, human health, and the environment.
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