Single Cell Analyses Reveal Contrasting Life Strategies of the Two Main Nitrifiers in the Ocean
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Differential Depth Distribution of Microbial Function and Putative Symbionts Through Sediment-Hosted Aquifers in the Deep Terrestrial Subsurface
ARTICLES https://doi.org/10.1038/s41564-017-0098-y Differential depth distribution of microbial function and putative symbionts through sediment-hosted aquifers in the deep terrestrial subsurface Alexander J. Probst1,5,7, Bethany Ladd2,7, Jessica K. Jarett3, David E. Geller-McGrath1, Christian M. K. Sieber1,3, Joanne B. Emerson1,6, Karthik Anantharaman1, Brian C. Thomas1, Rex R. Malmstrom3, Michaela Stieglmeier4, Andreas Klingl4, Tanja Woyke 3, M. Cathryn Ryan 2* and Jillian F. Banfield 1* An enormous diversity of previously unknown bacteria and archaea has been discovered recently, yet their functional capacities and distributions in the terrestrial subsurface remain uncertain. Here, we continually sampled a CO2-driven geyser (Colorado Plateau, Utah, USA) over its 5-day eruption cycle to test the hypothesis that stratified, sandstone-hosted aquifers sampled over three phases of the eruption cycle have microbial communities that differ both in membership and function. Genome- resolved metagenomics, single-cell genomics and geochemical analyses confirmed this hypothesis and linked microorganisms to groundwater compositions from different depths. Autotrophic Candidatus “Altiarchaeum sp.” and phylogenetically deep- branching nanoarchaea dominate the deepest groundwater. A nanoarchaeon with limited metabolic capacity is inferred to be a potential symbiont of the Ca. “Altiarchaeum”. Candidate Phyla Radiation bacteria are also present in the deepest groundwater and they are relatively abundant in water from intermediate depths. During the recovery phase of the geyser, microaerophilic Fe- and S-oxidizers have high in situ genome replication rates. Autotrophic Sulfurimonas sustained by aerobic sulfide oxidation and with the capacity for N2 fixation dominate the shallow aquifer. Overall, 104 different phylum-level lineages are present in water from these subsurface environments, with uncultivated archaea and bacteria partitioned to the deeper subsurface. -
Revealing the Full Biosphere Structure and Versatile Metabolic Functions In
Chen et al. Genome Biology (2021) 22:207 https://doi.org/10.1186/s13059-021-02408-w RESEARCH Open Access Revealing the full biosphere structure and versatile metabolic functions in the deepest ocean sediment of the Challenger Deep Ping Chen1†, Hui Zhou1,2†, Yanyan Huang3,4†, Zhe Xie5†, Mengjie Zhang1,2†, Yuli Wei5, Jia Li1,2, Yuewei Ma3, Min Luo5, Wenmian Ding3, Junwei Cao5, Tao Jiang1,2, Peng Nan3*, Jiasong Fang5* and Xuan Li1,2* * Correspondence: nanpeng@fudan. edu.cn; [email protected]; lixuan@ Abstract sippe.ac.cn †Ping Chen, Hui Zhou, Yanyan Background: The full biosphere structure and functional exploration of the microbial Huang, Zhe Xie and Mengjie Zhang communities of the Challenger Deep of the Mariana Trench, the deepest known contributed equally to this work. hadal zone on Earth, lag far behind that of other marine realms. 3Ministry of Education Key Laboratory for Biodiversity Science Results: We adopt a deep metagenomics approach to investigate the microbiome and Ecological Engineering, School in the sediment of Challenger Deep, Mariana Trench. We construct 178 of Life Sciences, Fudan University, Shanghai, China metagenome-assembled genomes (MAGs) representing 26 phyla, 16 of which are 5Shanghai Engineering Research reported from hadal sediment for the first time. Based on the MAGs, we find the Center of Hadal Science and microbial community functions are marked by enrichment and prevalence of Technology, College of Marine Sciences, Shanghai Ocean mixotrophy and facultative anaerobic metabolism. The microeukaryotic community is University, Shanghai, China found to be dominated by six fungal groups that are characterized for the first time 1CAS-Key Laboratory of Synthetic in hadal sediment to possess the assimilatory and dissimilatory nitrate/sulfate Biology, CAS Center for Excellence in Molecular Plant Sciences, Institute reduction, and hydrogen sulfide oxidation pathways. -
Metabolic Versatility of the Nitrite-Oxidizing Bacterium Nitrospira
bioRxiv preprint doi: https://doi.org/10.1101/2020.07.02.185504; this version posted July 4, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC 4.0 International license. 1 Metabolic versatility of the nitrite-oxidizing bacterium Nitrospira 2 marina and its proteomic response to oxygen-limited conditions 3 Barbara Bayer1*, Mak A. Saito2, Matthew R. McIlvin2, Sebastian Lücker3, Dawn M. Moran2, 4 Thomas S. Lankiewicz1, Christopher L. Dupont4, and Alyson E. Santoro1* 5 6 1 Department of Ecology, Evolution and Marine Biology, University of California, Santa Barbara, 7 CA, USA 8 2 Marine Chemistry and Geochemistry Department, Woods Hole Oceanographic Institution, 9 Woods Hole, MA, USA 10 3 Department of Microbiology, IWWR, Radboud University, Nijmegen, The Netherlands 11 4 J. Craig Venter Institute, La Jolla, CA, USA 12 13 *Correspondence: 14 Barbara Bayer, Department of Ecology, Evolution and Marine Biology, University of California, 15 Santa Barbara, CA, USA. E-mail: [email protected] 16 Alyson E. Santoro, Department of Ecology, Evolution and Marine Biology, University of 17 California, Santa Barbara, CA, USA. E-mail: [email protected] 18 19 Running title: Genome and proteome of Nitrospira marina 20 21 Competing Interests: The authors declare that they have no conflict of interest. 22 1 bioRxiv preprint doi: https://doi.org/10.1101/2020.07.02.185504; this version posted July 4, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. -
(Antarctica) Glacial, Basal, and Accretion Ice
CHARACTERIZATION OF ORGANISMS IN VOSTOK (ANTARCTICA) GLACIAL, BASAL, AND ACCRETION ICE Colby J. Gura A Thesis Submitted to the Graduate College of Bowling Green State University in partial fulfillment of the requirements for the degree of MASTER OF SCIENCE December 2019 Committee: Scott O. Rogers, Advisor Helen Michaels Paul Morris © 2019 Colby Gura All Rights Reserved iii ABSTRACT Scott O. Rogers, Advisor Chapter 1: Lake Vostok is named for the nearby Vostok Station located at 78°28’S, 106°48’E and at an elevation of 3,488 m. The lake is covered by a glacier that is approximately 4 km thick and comprised of 4 different types of ice: meteoric, basal, type 1 accretion ice, and type 2 accretion ice. Six samples were derived from the glacial, basal, and accretion ice of the 5G ice core (depths of 2,149 m; 3,501 m; 3,520 m; 3,540 m; 3,569 m; and 3,585 m) and prepared through several processes. The RNA and DNA were extracted from ultracentrifugally concentrated meltwater samples. From the extracted RNA, cDNA was synthesized so the samples could be further manipulated. Both the cDNA and the DNA were amplified through polymerase chain reaction. Ion Torrent primers were attached to the DNA and cDNA and then prepared to be sequenced. Following sequencing the sequences were analyzed using BLAST. Python and Biopython were then used to collect more data and organize the data for manual curation and analysis. Chapter 2: As a result of the glacier and its geographic location, Lake Vostok is an extreme and unique environment that is often compared to Jupiter’s ice-covered moon, Europa. -
The Bacterial Sulfur Cycle in Expanding Dysoxic and Euxinic Marine Waters
Environmental Microbiology (2020) 00(00), 00–00 doi:10.1111/1462-2920.15265 Special Issue Article The bacterial sulfur cycle in expanding dysoxic and euxinic marine waters Daan M. van Vliet ,1 F.A. Bastiaan von Meijenfeldt,2 bacteria, and discuss the probable involvement of Bas E. Dutilh,2 Laura Villanueva,3 uncultivated SAR324 and BS-GSO2 bacteria in sulfur Jaap S. Sinninghe Damsté,3,4 Alfons J.M. Stams1,5 oxidation. Uncultivated Marinimicrobia bacteria with and Irene Sánchez-Andrea 1* a presumed organoheterotrophic metabolism are 1Laboratory of Microbiology, Wageningen University and abundant in DMW. Like SRB, they may use specific Research, Stippeneng 4, 6708WE, Wageningen, molybdoenzymes to conserve energy from the oxida- Netherlands. tion, reduction or disproportionation of sulfur cycle 2Theoretical Biology and Bioinformatics, Science for intermediates such as S0 and thiosulfate, produced Life, Utrecht University, Padualaan 8, 3584 CH, Utrecht, from the oxidation of sulfide. We expect that tailored Netherlands. sampling methods and a renewed focus on cultiva- 3Department of Marine Microbiology and tion will yield deeper insight into sulfur-cycling bacte- Biogeochemistry, Royal Netherlands Institute for Sea ria in DMW. Research (NIOZ), Utrecht University, Landsdiep 4, 1797 SZ, ’t Horntje (Texel), Netherlands. Introduction 4Department of Earth Sciences, Faculty of Geosciences, Oxygen deficiency is a rather common phenomenon in Utrecht University, Princetonlaan 8A, 3584 CB, Utrecht, marine waters caused by microbial aerobic respiration Netherlands. coupled to the degradation of organic matter, combined 5Centre of Biological Engineering, University of Minho, with insufficient supply of oxygen through water circulation Campus de Gualtar, 4710-057 Braga, Portugal. or diffusion (Canfield et al., 2005). -
Diversification and Niche Adaptations of Nitrospina-Like Bacteria in The
The ISME Journal (2016) 10, 1383–1399 OPEN © 2016 International Society for Microbial Ecology All rights reserved 1751-7362/16 www.nature.com/ismej ORIGINAL ARTICLE Diversification and niche adaptations of Nitrospina- like bacteria in the polyextreme interfaces of Red Sea brines David Kamanda Ngugi1, Jochen Blom2, Ramunas Stepanauskas3 and Ulrich Stingl1 1Red Sea Research Centre, King Abdullah University of Science and Technology, Thuwal, Saudi Arabia; 2Bioinformatics and Systems Biology, Justus Liebig University Giessen, Germany and 3Bigelow Laboratories for Ocean Sciences, East Boothbay, ME 04544-0380, USA Nitrite-oxidizing bacteria (NOB) of the genus Nitrospina have exclusively been found in marine environments. In the brine–seawater interface layer of Atlantis II Deep (Red Sea), Nitrospina-like bacteria constitute up to one-third of the bacterial 16S ribosomal RNA (rRNA) gene sequences. This is much higher compared with that reported in other marine habitats (~10% of all bacteria), and was unexpected because no NOB culture has been observed to grow above 4.0% salinity, presumably due to the low net energy gained from their metabolism that is insufficient for both growth and osmoregulation. Using phylogenetics, single-cell genomics and metagenomic fragment recruitment approaches, we document here that these Nitrospina-like bacteria, designated as Candidatus Nitromaritima RS, are not only highly diverged from the type species Nitrospina gracilis (pairwise genome identity of 69%) but are also ubiquitous in the deeper, highly saline interface layers (up to 11.2% salinity) with temperatures of up to 52 °C. Comparative pan-genome analyses revealed that less than half of the predicted proteome of Ca. Nitromaritima RS is shared with N. -
(Halichoerus Grypus) to Harbour Porpoises Research
After the bite: bacterial transmission from grey royalsocietypublishing.org/journal/rsos seals (Halichoerus grypus) to harbour porpoises Research Cite this article: Gilbert MJ, IJsseldijk LL, (Phocoena phocoena) Rubio-García A, Gröne A, Duim B, Rossen J, Zomer AL, Wagenaar JA. 2020 After the bite: Maarten J. Gilbert1,3, Lonneke L. IJsseldijk2, bacterial transmission from grey seals (Halichoerus grypus) to harbour porpoises Ana Rubio-García1,4,5, Andrea Gröne2, Birgitta Duim1,6, (Phocoena phocoena). R. Soc. Open Sci. 7: 5 1,6 192079. John Rossen , Aldert L. Zomer http://dx.doi.org/10.1098/rsos.192079 and Jaap A. Wagenaar1,6,7 1Faculty of Veterinary Medicine, Department of Infectious Diseases and Immunology, and 2Faculty of Veterinary Medicine, Department of Biomolecular Health Sciences, Division of Received: 28 November 2019 Pathology, Utrecht University, Utrecht, The Netherlands Accepted: 24 March 2020 3Reptile, Amphibian and Fish Conservation Netherlands (RAVON), Nijmegen, The Netherlands 4Sealcentre, Pieterburen, The Netherlands 5Department of Medical Microbiology and Infection Prevention, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands 6WHO Collaborating Centre for Campylobacter/OIE Reference Laboratory for Subject Category: Campylobacteriosis, Utrecht, The Netherlands 7Wageningen Bioveterinary Research, Lelystad, The Netherlands Genetics and genomics MJG, 0000-0002-9967-2936; JR, 0000-0002-7167-8623 Subject Areas: microbiology Recent population growth of the harbour porpoise (Phocoena phocoena), grey seal (Halichoerus grypus) and common seal (Phoca vitulina) in the North Sea has increased potential Keywords: interaction between these species. Grey seals are known to harbour porpoise, grey seal, common seal, attack harbour porpoises. Some harbour porpoises survive microbiome, bacterial transmission initially, but succumb eventually, often showing severely infected skin lesions. -
Cluster 1 Cluster 3 Cluster 2
5 9 Luteibacter yeojuensis strain SU11 (Ga0078639_1004, 2640590121) 7 0 Luteibacter rhizovicinus DSM 16549 (Ga0078601_1039, 2631914223) 4 7 Luteibacter sp. UNCMF366Tsu5.1 (FG06DRAFT_scaffold00001.1, 2595447474) 5 5 Dyella japonica UNC79MFTsu3.2 (N515DRAFT_scaffold00003.3, 2558296041) 4 8 100 Rhodanobacter sp. Root179 (Ga0124815_151, 2699823700) 9 4 Rhodanobacter sp. OR87 (RhoOR87DRAFT_scaffold_21.22, 2510416040) Dyella japonica DSM 16301 (Ga0078600_1041, 2640844523) Dyella sp. OK004 (Ga0066746_17, 2609553531) 9 9 9 3 Xanthomonas fuscans (007972314) 100 Xanthomonas axonopodis (078563083) 4 9 Xanthomonas oryzae pv. oryzae KACC10331 (NC_006834, 637633170) 100 100 Xanthomonas albilineans USA048 (Ga0078502_15, 2651125062) 5 6 Xanthomonas translucens XT123 (Ga0113452_1085, 2663222128) 6 5 Lysobacter enzymogenes ATCC 29487 (Ga0111606_103, 2678972498) 100 Rhizobacter sp. Root1221 (056656680) Rhizobacter sp. Root1221 (Ga0102088_103, 2644243628) 100 Aquabacterium sp. NJ1 (052162038) Aquabacterium sp. NJ1 (Ga0077486_101, 2634019136) Uliginosibacterium gangwonense DSM 18521 (B145DRAFT_scaffold_15.16, 2515877853) 9 6 9 7 Derxia lacustris (085315679) 8 7 Derxia gummosa DSM 723 (H566DRAFT_scaffold00003.3, 2529306053) 7 2 Ideonella sp. B508-1 (I73DRAFT_BADL01000387_1.387, 2553574224) Zoogloea sp. LCSB751 (079432982) PHB-accumulating bacterium (PHBDraf_Contig14, 2502333272) Thiobacillus sp. 65-1059 (OJW46643.1) 8 4 Dechloromonas aromatica RCB (NC_007298, 637680051) 8 4 7 7 Dechloromonas sp. JJ (JJ_JJcontig4, 2506671179) Dechloromonas RCB 100 Azoarcus -
Geochemical Transition Zone Powering Microbial Growth in Subsurface Sediments
Geochemical transition zone powering microbial growth in subsurface sediments Rui Zhaoa,b,1, José M. Mogollónc, Sophie S. Abbyd,2, Christa Schleperd, Jennifer F. Biddleb, Desiree L. Roerdinka, Ingunn H. Thorsetha, and Steffen L. Jørgensena,1 aK.G. Jebsen Centre for Deep Sea Research, University of Bergen, 5007 Bergen, Norway; bSchool of Marine Science and Policy, University of Delaware, Lewes, DE 19958; cInstitute of Environmental Sciences (CML), Leiden University, 2333 CC Leiden, The Netherlands; and dDivision of Archaea Biology and Ecogenomics, Department of Functional and Evolutionary Ecology, University of Vienna, A-1090 Vienna, Austria Edited by Dianne K. Newman, California Institute of Technology, Pasadena, CA, and approved October 30, 2020 (received for review March 30, 2020) No other environment hosts as many microbial cells as the marine depth (13) is typically explained by reduction in energy avail- sedimentary biosphere. While the majority of these cells are expected ability over time, leading to a net decay of biomass (14). While it tobealive,theyarespeculatedtobepersistinginastateof stands to reason that the deep sedimentary realm generally can maintenance without net growth due to extreme starvation. Here, be viewed as an energetic desert with diminishing energy fol- we report evidence for in situ growth of anaerobic ammonium- lowing increasing sediment depth/age, a number of geochemical oxidizing (anammox) bacteria in ∼80,000-y-old subsurface sediments transition zones (GTZs) with higher energy density exist. Typical from the Arctic Mid-Ocean Ridge. The growth is confined to the GTZs include the sulfate–methane transition zones (15) and the nitrate–ammonium transition zone (NATZ), a widespread geochemi- oxic–anoxic transition zones (16), which both represent oases for cal transition zone where most of the upward ammonium flux from microbial cells where energy from redox reactions can be har- deep anoxic sediments is being consumed. -
Expanded Diversity of Microbial Groups That Shape the Dissimilatory Sulfur Cycle
The ISME Journal (2018) 12:1715–1728 https://doi.org/10.1038/s41396-018-0078-0 ARTICLE Expanded diversity of microbial groups that shape the dissimilatory sulfur cycle 1,2 3 4,11 5 1 Karthik Anantharaman ● Bela Hausmann ● Sean P. Jungbluth ● Rose S. Kantor ● Adi Lavy ● 6 7 8 3 1 Lesley A. Warren ● Michael S. Rappé ● Michael Pester ● Alexander Loy ● Brian C. Thomas ● Jillian F. Banfield 1,9,10 Received: 11 October 2017 / Revised: 10 January 2018 / Accepted: 13 January 2018 / Published online: 21 February 2018 © The Author(s) 2018. This article is published with open access Abstract A critical step in the biogeochemical cycle of sulfur on Earth is microbial sulfate reduction, yet organisms from relatively few lineages have been implicated in this process. Previous studies using functional marker genes have detected abundant, novel dissimilatory sulfite reductases (DsrAB) that could confer the capacity for microbial sulfite/sulfate reduction but were not affiliated with known organisms. Thus, the identity of a significant fraction of sulfate/sulfite-reducing microbes has remained elusive. Here we report the discovery of the capacity for sulfate/sulfite reduction in the genomes of organisms from 1234567890();,: 13 bacterial and archaeal phyla, thereby more than doubling the number of microbial phyla associated with this process. Eight of the 13 newly identified groups are candidate phyla that lack isolated representatives, a finding only possible given genomes from metagenomes. Organisms from Verrucomicrobia and two candidate phyla, Candidatus Rokubacteria and Candidatus Hydrothermarchaeota, contain some of the earliest evolved dsrAB genes. The capacity for sulfite reduction has been laterally transferred in multiple events within some phyla, and a key gene potentially capable of modulating sulfur metabolism in associated cells has been acquired by putatively symbiotic bacteria. -
Chapter 6 | Synthesis and Outlook
UvA-DARE (Digital Academic Repository) Interactions between microorganisms and oxic-anoxic transitions Diao, M. Publication date 2018 Document Version Other version License Other Link to publication Citation for published version (APA): Diao, M. (2018). Interactions between microorganisms and oxic-anoxic transitions. General rights It is not permitted to download or to forward/distribute the text or part of it without the consent of the author(s) and/or copyright holder(s), other than for strictly personal, individual use, unless the work is under an open content license (like Creative Commons). Disclaimer/Complaints regulations If you believe that digital publication of certain material infringes any of your rights or (privacy) interests, please let the Library know, stating your reasons. In case of a legitimate complaint, the Library will make the material inaccessible and/or remove it from the website. Please Ask the Library: https://uba.uva.nl/en/contact, or a letter to: Library of the University of Amsterdam, Secretariat, Singel 425, 1012 WP Amsterdam, The Netherlands. You will be contacted as soon as possible. UvA-DARE is a service provided by the library of the University of Amsterdam (https://dare.uva.nl) Download date:27 Sep 2021 Chapter 6 | Synthesis and Outlook 6 Synthesis and Outlook 145 Chapter 6 | Synthesis and Outlook Synthesis and Outlook This thesis described the diversity, dynamics, and community assembly of microorganisms in a seasonally stratified lake. Within the project, we have studied the spatio-temporal dynamics of bacterial communities and the interactions between microorganisms and oxic-anoxic transitions (Chapter 2). Combining microbial community dynamics, mathematical models, and biogeochemical processes, oxic- anoxic regime shifts and hysteresis were investigated in Chapter 3. -
The Role of a Porin-Cytochrome Fusion in Neutrophilic Fe Oxidation
THE ROLE OF A PORIN-CYTOCHROME FUSION IN NEUTROPHILIC FE OXIDATION: INSIGHTS FROM FUNCTIONAL CHARACTARIZATION AND METATRANSCRIPTOMICS by Arkadiy Garber A thesis submitted to the Faculty of the University of Delaware in partial fulfillment of the requirements for the degree of Master of Science in Geology Summer 2018 © 2018 Arkadiy Garber All Rights Reserved THE ROLE OF A PORIN-CYTOCHROME FUSION IN NEUTROPHILIC FE OXIDATION: INSIGHTS FROM FUNCTIONAL CHARACTARIZATION AND METATRANSCRIPTOMICS by Arkadiy Garber Approved: __________________________________________________________ Clara Chan, Ph.D. Professor in charge of thesis on behalf of the Advisory Committee Approved: __________________________________________________________ Neil Sturchio, Ph.D. Chair of the Department of Geological Sciences Approved: __________________________________________________________ Estella Atekwana, Ph.D. Dean of the College of Earth, Ocean, and Environment Approved: __________________________________________________________ Ann L. Ardis, Ph.D. Senior Vice Provost for the Office of Graduate and Professional Education ACKNOWLEDGMENTS I would like to thank my advisor, Clara Chan, for all the support and guidance over the last years. In addition to learning many valuable skills, my growth as a scientist would not have been possible without the direction and focus that Clara’s mentorship has instilled in me. Additionally, I would like to thank Sean McAllister for all the guidance and feedback; my understanding of bioinformatics and phylogenetics has benefited greatly from our many conversations. I would also like to thank other Chan lab members, past and present, for always being available and willing to help out and provide feedback, and for providing a great atmosphere to do science in. Thank you to my committee members, Dr. Thomas Hanson and Dr.