ArticleFrontiers in microbiology2015
The transcriptional response of microbial communities in thawing Alaskan permafrost soils.
Article in Frontiers in microbiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.
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Who cites it
40 citing papers in PubMed.
- Predicting functions of uncharacterized gene products from microbial communities.Nature biotechnology · 2026Article
- Depth-resolved transcriptional activity of antibiotic resistance genes in deep permafrost of the Qinghai-Tibet Plateau.Communications biology · 2026Article
- Freeze-thaw strength regulates carbon density through microbial assembly processes and network clustering.mSystems · 2026Article
- Consistent microbial responses during the aerobic thaw of Alaskan permafrost soils.Frontiers in microbiology · 2025Article
- Microbial and chemical predictors of methane release from a stratified thermokarst permafrost hotspot.Frontiers in microbiology · 2025Article
- Comparative analysis of prokaryotic microbiomes in high-altitude active layer soils: insights from Ladakh and global analogues using In-Silico approaches.Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology] · 2024Article
- Opening Pandora's Box: Neglected Biochemical Potential of Permafrost-Associated Fungal Communities in a Warming Climate.Journal of fungi (Basel, Switzerland) · 2023Review
- Genomic evidence that microbial carbon degradation is dominated by iron redox metabolism in thawing permafrost.ISME communications · 2023Article
- Abrupt permafrost thaw triggers activity of copiotrophs and microbiome predators.FEMS microbiology ecology · 2023Article
- Permafrost microbial communities and functional genes are structured by latitudinal and soil geochemical gradients.The ISME journal · 2023Article
- Summer thaw duration is a strong predictor of the soil microbiome and its response to permafrost thaw in arctic tundra.Environmental microbiology · 2022Article
- Microbiome assembly in thawing permafrost and its feedbacks to climate.Global change biology · 2022Review
- AcetoBase Version 2: a database update and re-analysis of formyltetrahydrofolate synthetase amplicon sequencing data from anaerobic digesters.Database : the journal of biological databases and curation · 2022Article
- Reduced methane emissions in former permafrost soils driven by vegetation and microbial changes following drainage.Global change biology · 2022Article
- Unearthing Shifts in Microbial Communities Across a Soil Disturbance Gradient.Frontiers in microbiology · 2022Article
- Microbial Community Changes in 26,500-Year-Old Thawing Permafrost.Frontiers in microbiology · 2022Article
- Water is a preservative of microbes.Microbial biotechnology · 2022Article
- Impact of River Channel Lateral Migration on Microbial Communities across a Discontinuous Permafrost Floodplain.Applied and environmental microbiology · 2021Article
- Statistical approaches for differential expression analysis in metatranscriptomics.Bioinformatics (Oxford, England) · 2021Article
- Shotgun metagenomics reveals distinct functional diversity and metabolic capabilities between 12 000-year-old permafrost and active layers on Muot da Barba Peider (Swiss Alps).Microbial genomics · 2021Article
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2 authors.
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Abstract
Thawing of permafrost soils is expected to stimulate microbial decomposition and respiration of sequestered carbon. This could, in turn, increase atmospheric concentrations of greenhouse gasses, such as carbon dioxide and methane, and create a positive feedback to climate warming. Recent metagenomic studies suggest that permafrost has a large metabolic potential for carbon processing, including pathways for fermentation and methanogenesis. Here, we performed a pilot study using ultrahigh throughput Illumina HiSeq sequencing of reverse transcribed messenger RNA to obtain a detailed overview of active metabolic pathways and responsible organisms in up to 70 cm deep permafrost soils at a moist acidic tundra location in Arctic Alaska. The transcriptional response of the permafrost microbial community was compared before and after 11 days of thaw. In general, the transcriptional profile under frozen conditions suggests a dominance of stress responses, survival strategies, and maintenance processes, whereas upon thaw a rapid enzymatic response to decomposing soil organic matter (SOM) was observed. Bacteroidetes, Firmicutes, ascomycete fungi, and methanogens were responsible for largest transcriptional response upon thaw. Transcripts indicative of heterotrophic methanogenic pathways utilizing acetate, methanol, and methylamine were found predominantly in the permafrost table after thaw. Furthermore, transcripts involved in acetogenesis were expressed exclusively after thaw suggesting that acetogenic bacteria are a potential source of acetate for acetoclastic methanogenesis in freshly thawed permafrost. Metatranscriptomics is shown here to be a useful approach for inferring the activity of permafrost microbes that has potential to improve our understanding of permafrost SOM bioavailability and biogeochemical mechanisms contributing to greenhouse gas emissions as a result of permafrost thaw.
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