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dc.contributor.authorMcKay, Luke J.
dc.contributor.authorNigro, Olivia D.
dc.contributor.authorDlakić, Mensur
dc.contributor.authorLuttrell, Karen M.
dc.contributor.authorRusch, Douglas B.
dc.contributor.authorFields, Matthew W.
dc.contributor.authorInskeep, William P.
dc.date.accessioned2022-12-30T16:30:57Z
dc.date.available2022-12-30T16:30:57Z
dc.date.issued2021-10
dc.identifier.citationMcKay, L.J., Nigro, O.D., Dlakić, M. et al. Sulfur cycling and host-virus interactions in Aquificales-dominated biofilms from Yellowstone’s hottest ecosystems. ISME J 16, 842–855 (2022). https://doi.org/10.1038/s41396-021-01132-4en_US
dc.identifier.issn1751-7370
dc.identifier.urihttps://scholarworks.montana.edu/xmlui/handle/1/17552
dc.description© The Author(s), under exclusive licence to International Society for Microbial Ecology 2021en_US
dc.description.abstractModern linkages among magmatic, geochemical, and geobiological processes provide clues about the importance of thermophiles in the origin of biogeochemical cycles. The aim of this study was to identify the primary chemoautotrophs and host–virus interactions involved in microbial colonization and biogeochemical cycling at sublacustrine, vapor-dominated vents that represent the hottest measured ecosystems in Yellowstone National Park (~140 °C). Filamentous microbial communities exposed to extreme thermal and geochemical gradients were sampled using a remotely operated vehicle and subjected to random metagenome sequencing and microscopic analyses. Sulfurihydrogenibium (phylum Aquificae) was the predominant lineage (up to 84% relative abundance) detected at vents that discharged high levels of dissolved H2, H2S, and CO2. Metabolic analyses indicated carbon fixation by Sulfurihydrogenibium spp. was powered by the oxidation of reduced sulfur and H2, which provides organic carbon for heterotrophic community members. Highly variable Sulfurihydrogenibium genomes suggested the importance of intra-population diversity under extreme environmental and viral pressures. Numerous lytic viruses (primarily unclassified taxa) were associated with diverse archaea and bacteria in the vent community. Five circular dsDNA uncultivated virus genomes (UViGs) of ~40 kbp length were linked to the Sulfurihydrogenibium metagenome-assembled genome (MAG) by CRISPR spacer matches. Four UViGs contained consistent genome architecture and formed a monophyletic cluster with the recently proposed Pyrovirus genus within the Caudovirales. Sulfurihydrogenibium spp. also contained CRISPR arrays linked to plasmid DNA with genes for a novel type IV filament system and a highly expressed β-barrel porin. A diverse suite of transcribed secretion systems was consistent with direct microscopic analyses, which revealed an extensive extracellular matrix likely critical to community structure and function. We hypothesize these attributes are fundamental to the establishment and survival of microbial communities in highly turbulent, extreme-gradient environments.en_US
dc.language.isoen_USen_US
dc.publisherSpringer Natureen_US
dc.rightscopyright springer nature 2022en_US
dc.rights.urihttps://www.nature.com/nature-portfolio/reprints-and-permissionsen_US
dc.subjectsulfer cyclingen_US
dc.subjectbiofilmsen_US
dc.subjectYellowstoneen_US
dc.subjectYellowstone ecosystemen_US
dc.titleSulfur cycling and host-virus interactions in Aquificales-dominated biofilms from Yellowstone’s hottest ecosystemsen_US
dc.typeArticleen_US
mus.citation.extentfirstpage1en_US
mus.citation.extentlastpage14en_US
mus.citation.journaltitleISMEen_US
mus.identifier.doi10.1038/s41396-021-01132-4en_US
mus.relation.collegeCollege of Agricultureen_US
mus.relation.departmentLand Resources & Environmental Sciences.en_US
mus.relation.universityMontana State University - Bozemanen_US


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