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uBio  Web  Results 1 - 10 of about 541 Broader Terms:    Proteobacteria     delta/epsilon subdivisions  More Specific:    Campylobacterales     Nautiliales     environmental samples     unclassified      Latest Articles on Epsilonproteobacteria from uBioRSS Genomes in turmoil: quantification of genome dynamics in prokaryote superge... - BMC Biology Non-contiguous finished genome sequence and description of Sulfurimonas hon... - PubMed: nov sp species External Resources: 1.  Biofilm development in a pilot-scale gravity sewer: Physical characteristics, microstructure, and microbial communities. Zan F, Guo G, Zheng T, Chen G Environmental research, 2021 http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0 2.  International Committee on Systematics of Prokaryotes Subcommittee on the Taxonomy of Campylobacter and related bacteria: Minutes of the meetings, 21st August and 10th September 2019. On SLW International journal of systematic and evolutionary microbiology, 2021 http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0 3.  Metal homeostasis in pathogenic Epsilonproteobacteria: mechanisms of acquisition, efflux, and regulation. Kelley BR, Lu J, Haley KP, Gaddy JA, Johnson JG Metallomics : integrated biometal science, 2021 http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0 4.  Hydrogenimonas urashimensis sp. nov., a hydrogen-oxidizing chemolithoautotroph isolated from a deep-sea hydrothermal vent in the Southern Mariana Trough. Mino S, Shiotani T, Nakagawa S, Takai K, Sawabe T Systematic and applied microbiology, 2021 http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0 5.  Time series metagenomic sampling of the Thermopyles, Greece, geothermal springs reveals stable microbial communities dominated by novel sulfur-oxidizing chemoautotrophs. Meziti A, Nikouli E, Hatt JK, Konstantinidis KT, Kormas KA Environmental microbiology Environ Microbiol Time series metagenomic sampling of the Thermopyles, Greece, geothermal springs reveals stable microbial communities dominated by novel sulfur-oxidizing chemoautotrophs. 10.1111/1462-2920.15373 Geothermal springs are essentially unaffected by environmental conditions aboveground as they are continuously supplied with subsurface water with little variability in chemistry. Therefore, changes in their microbial community composition and function, especially over a long period, are expected to be limited but this assumption has not yet been rigorously tested. Toward closing this knowledge gap, we applied whole metagenome sequencing to 17 water samples collected between 2010 and 2016 from the Thermopyles sulfur-rich geothermal springs in central Greece. As revealed by 16S rRNA gene fragments recovered in the metagenomes, Epsilonproteobacteria-related operational taxonomic units (OTUs) dominated most samples and grouping of samples based on OTU abundances exhibited no apparent seasonal pattern. Similarities between samples regarding functional gene content were high, with all samples sharing >70% similarity in functional pathways. These community-wide patterns were further confirmed by analysis of metagenome-assembled genomes (MAGs), which showed that novel species and genera of the chemoautotrophic Campylobacterales order dominated the springs. These MAGs carried different pathways for thiosulfate or sulfide oxidation coupled to carbon fixation pathways. Overall, our study showed that even in the long term, functions of microbial communities in a moderately hot terrestrial spring remain stable, presumably driving the corresponding stability in community structure. © 2020 Society for Applied Microbiology and John Wiley & Sons Ltd. Meziti A A https://orcid.org/0000-0001-5672-7653 Department of Ichthyology and Aquatic Environment, University of Thessaly, Volos, 38446, Greece. School of Civil and Environmental Engineering, Georgia Institute of Technology, Ford Environmental Science and Technology Building, 311 Ferst Drive, Atlanta, GA, 30332, USA. Nikouli E E Department of Ichthyology and Aquatic Environment, University of Thessaly, Volos, 38446, Greece. School of Civil and Environmental Engineering, Georgia Institute of Technology, Ford Environmental Science and Technology Building, 311 Ferst Drive, Atlanta, GA, 30332, USA. Hatt J K JK https://orcid.org/0000-0002-5666-0994 School of Civil and Environmental Engineering, Georgia Institute of Technology, Ford Environmental Science and Technology Building, 311 Ferst Drive, Atlanta, GA, 30332, USA. Konstantinidis K T KT School of Civil and Environmental Engineering, Georgia Institute of Technology, Ford Environmental Science and Technology Building, 311 Ferst Drive, Atlanta, GA, 30332, USA. School of Biological Sciences, Georgia Institute of Technology, Ford Environmental Sciences and Technology Building, 311 Ferst Drive, Atlanta, GA, 30332, USA. Kormas K A KA Department of Ichthyology and Aquatic Environment, University of Thessaly, Volos, 38446, Greece. eng Internal funds University of Thessaly 1831582 USA National Science Foundation Journal Article 2020 12 21 England Environ Microbiol 100883692 1462-2912 IM 2020 08 25 2020 12 19 2020 12 23 6 0 2020 12 23 6 0 2020 12 22 5 51 aheadofprint 33350070 10.1111/1462-2920.15373