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Tlaskal, V.

Publications and source records attributed to Tlaskal, V..

5 recordsLinked to original sources

Adaptation of the freshwater anaerobic methanotroph 'Ca. Methanoperedens vercellensis' to low pH levels reveals membrane lipid remodelling

Anaerobic methanotrophic archaea are key members of the biological methane filter, thereby preventing emissions of this strong greenhouse gas into the atmosphere. Previous studies on freshwater anaerobic methanotrophs targeted the activity of these microorganisms at circumneutral pH whereas molecular ecology studies identified this phylotype also in acidic environments such as peatlands; it is currently unknown whether they can adapt to low pH and remain effective in the biological methane filter in low pH environments. Here we show that a granular enrichment culture of the freshwater methanotroph Ca. M. vercellensis loses activity when experiencing pH stress but remains metabolically active down to pH 5.65 with appropriate adaptation time, indicating that adaptive changes are necessary to accommodate anaerobic methane oxidation at lower pH. Analyses of archaeal lipids revealed an increase in zwitterionic intact polar lipids over anionic lipids as an adaptation. This coincided with a change in granule structure while methane oxidation rate and enrichment state of Ca. M. vercellensis remained stable. We show that Ca. M. vercellensis remains metabolically active at lower pH values, despite increased maintenance energy demands and the need for cytoplasmic pH homeostasis. Our study demonstrates that adaptations to stress by slow-growing microorganisms may require long-term observation and is thereby instrumental for a better understanding of methane cycling in acidic ecosystems.

microbiology↗

Soil trace gas oxidizers divergently respond to short- and long-term warming

The upland soil microbiome is dominated by aerobic bacteria that oxidize atmospheric trace gases, including CO, H2, and CH4. As a result, soils are the largest biological sink for these climate-active gases. Whether global warming will enhance or suppress these processes remains unclear. Here, we studied the warming responses of soil trace gas oxidizers by profiling natural geothermal gradients in a subarctic grassland with over 60 years of field warming at +6{degrees}C. We integrate field flux measurements, ex situ biogeochemical assays, metagenomics, and metatranscriptomics to determine ecosystem and cellular-level responses. Our results show that the oxidation of atmospheric CO and H2, but not CH4, increased with long-term warming due to higher cell numbers. However, at the cellular level, trace gas oxidizers, especially methanotrophs, tended to reduce gas consumption and transcription of gas-metabolizing enzymes in response to long-term warming. Our findings suggest that soils may remain a robust sink for trace gases despite lower per-cell activity. This work establishes a framework for interpreting the relationships between temperature and microbial trace gas oxidation on timescales relevant to Earths climate system.

microbiology↗

Uncovering hidden phylo- and ecogenomic diversity of the widespread methanotrophic genus Methylobacter

The globally distributed genus Methylobacter plays a crucial role in mitigating methane emissions from diverse ecosystems, including freshwater and marine habitats, wetlands, soils, sediments, groundwater, and landfills. Despite their frequent presence and abundance in these systems, we still know little about the genomic adaptations that they exhibit. Here, we used a collection of 97 genomes and metagenome-assembled genomes to ecogenomically characterise the genus. Our analyses suggest that the genus Methylobacter may contain more species than previously thought, with >30 putative species clusters. Some species clusters shared >98.65% sequence identity of the full-length 16S rRNA gene, demonstrating the need for genome-resolved species delineation. The ecogenomic differences between Methylobacter spp. include various combinations of methane monooxygenases, multigene loci for alternative dissimilatory metabolisms related to hydrogen, sulphur cycling, and denitrification, as well as other lifestyle-associated functions. Additionally, we describe and tentatively name the two new Methylobacter species, which we recently cultured from sediment of a temperate eutrophic fishpond, as Methylobacter methanoversatilis, sp. nov. and Methylobacter spei, sp. nov. Overall, our study highlights previously unrecognised species diversity within the Methylobacter genus, their diverse metabolic potential, versatility, as well as the presence of distinct genomic adaptations for thriving in various environments.

microbiology↗

Short- and mid-term temporal variability of the human urinary microbiota: an observational cohort study

Understanding the temporal variability of the microbiome is critical for translating associations of the microbiome with health and disease into clinical practice. The aim of this study is to assess the extent of temporal variability of the human urinary microbiota. A pair of catheterized or mid-stream urine samples were collected from study participants at 3-40-month interval. DNA was extracted and the bacterial V4 hypervariable region of the 16S rRNA gene was sequenced on the Illumina MiSeq platform. The alpha and beta diversity of paired samples was analyzed using Chao1 and Shannon indices and PERMANOVA. A total of 63 participants (43 men and 20 women with a mean age of 63.0 and 57.1 years, respectively) were included in the final analysis. An average of 152 {+/-} 128 bacterial operational taxonomic units (OTUs) were identified in each urine sample from the entire cohort. There was an average of 41 {+/-} 32 overlapping OTUs in each sample pair, accounting for 66.3 {+/-} 29.4% of the relative abundance. There was a clear correlation between the number of overlapping OTUs and the relative abundance covered. The difference in Chao1 index between paired samples was statistically significant; the difference in Shannon index was not. Beta diversity did not differ significantly within the paired samples. Neither age nor sex of the participants influenced the variation in community composition. With a longer interval between the collections, the relative abundance covered by the overlapping OTUs changed significantly but not the number of OTUs. The abundance of bacterial taxa present in both collections fluctuated, but the proportion of these taxa in the community was about two-thirds of the total bacterial community. No significant intraindividual differences in beta diversity were observed between the two urine samples. Data SummaryThe raw DNA sequences together with anonymized sample metadata have been deposited at the NCBI SRA under the accession number PRJNA1093489. Processing scripts are deposited at a public repository https://doi.org/10.5281/zenodo.12556460. Processed sequencing files and tables including full taxonomic assignment are deposited at https://doi.org/10.6084/m9.figshare.26046355. ImportanceThis study represents a comprehensive investigation dedicated specifically to the subject of urinary microbiome (UM) temporal stability. Our dataset (n = 63) consists of a relatively large group of patients of one ethnic origin but varying ages and both sexes. Additionally, samples from individual participants are separated by different lengths of time. This approach allows us to assess the effects of three variables on the stability of human UM. Our findings demonstrate that, while the relative abundance of dominant bacteria varies, repeated collections generally share more than 60% of the bacterial community. Furthermore, we observe little variation in the alpha and beta diversity of the microbial community in human urine. These results help to understand the dynamics of human UM and enable interpretation of future studies.

microbiology↗

GlobalFungi: Global database of fungal records from high-throughput-sequencing metabarcoding studies

Fungi are key players in vital ecosystem services, spanning carbon cycling, decomposition, symbiotic associations with cultural and wild plants and pathogenicity. The high importance of fungi in the ecosystem processes contrasts with the incompleteness of understanding of the patterns of fungal biogeography and the environmental factors that drive it. To close this gap of knowledge, we have here collected and validated data published on the composition of soil fungal communities in terrestrial environments including soil and plant-associated habitats and made them publicly accessible through a user interface at http://globalfungi.com. The GlobalFungi database contains over 650 million observations of fungal sequences across >20 000 samples with geographical locations and additional metadata contained in 207 original studies with millions of unique sequence variants of the fungal internal transcribed spacers (ITS) 1 and 2 representing fungal species and genera. As it is, the study represents the most comprehensive atlas of fungal distribution on the global scale open to further additions.

ecology↗