UC San Diego UC San Diego Electronic Theses and Dissertations

Total Page:16

File Type:pdf, Size:1020Kb

UC San Diego UC San Diego Electronic Theses and Dissertations UC San Diego UC San Diego Electronic Theses and Dissertations Title Molecular diversity and adaptations of microorganisms from the deep ocean Permalink https://escholarship.org/uc/item/73g359mk Author Eloe, Emiley Ansley Publication Date 2011 Peer reviewed|Thesis/dissertation eScholarship.org Powered by the California Digital Library University of California UNIVERSITY OF CALIFORNIA, SAN DIEGO Molecular diversity and adaptations of microorganisms from the deep ocean A dissertation submitted in partial satisfaction of the Requirements for the degree Doctor of Philosophy in Marine Biology by Emiley Ansley Eloe Committee in charge: Professor Douglas H. Bartlett, Chair Professor Eric E. Allen Professor Lihini I. Aluwihare Professor Farooq Azam Professor Kit Pogliano 2011 Copyright Emiley Ansley Eloe, 2011 All rights reserved. ii The Dissertation of Emiley Ansley Eloe is approved, and it is acceptable in quality and form for publication on microfilm and electronically: ________________________________________________________________________ ________________________________________________________________________ ________________________________________________________________________ ________________________________________________________________________ ________________________________________________________________________ Chair University of California, San Diego 2011 iii DEDICATION For my family – Mama, Dad, Tommy And for my Doug With all my love, always. iv EPIGRAPH The reports of biologists are the measure, not of the science, but of the men themselves. John Steinbeck The Log from the Sea of Cortez v TABLE OF CONTENTS Signature Page…………………………………………………………………. iii Dedication………..……………………………………………………………. iv Epigraph……….………………………………………………………………. v Table of Contents……………………………………………………………… vi List of Abbreviations…………………………………………………..……… vii List of Figures………………………………………………………………… viii List of Tables……………………………………………………………….… xi Acknowledgements………………………………………………………..…. xii Vita…………………………………………………………………………… xv Abstract of the Dissertation.…………………………………………….…… xvi Chapter I Into the deep: An Introduction………………………………. 1 Chapter II Compositional differences in particle-associated and free-living microbial assemblages from an extreme deep-ocean environment…………………………………….. 15 Chapter III Going deeper: Metagenome of a hadopelagic microbial community…………………………………...…… 39 Chapter IV The elusive art of microbial cultivation……………………… 94 Chapter V Isolation and characterization of the first psychropiezophilic Alphaproteobacterium………………….. 124 Chapter VI The deep-sea bacterium Photobacterium profundum SS9 utilizes separate flagellar systems for swimming and swarming under high-pressure conditions…………………… 160 Chapter VII Deep perspectives: Concluding remarks…………………….. 172 vi LIST OF ABBREVIATIONS AABW Antarctic bottom water AT atmospheric pressure BLAST basic local alignment search tool Cm chloramphenicol COG cluster of orthologous groups DOC dissolved organic carbon DNA deoxyribonucleic acid EGS estimated genome size FACS Fluorescence-activated cell sorting HP high pressure HSP high-scoring pair HV high viscosity KEGG Kyoto Encyclopedia of Genes and Genomes Kn kanamycin MDA Multiple Displacement Amplification MPa Megapascal (0.101 MPa = 1 atmosphere) NADW North Atlantic deep water ORF open reading frame OTU operational taxonomic unit PCR polymerase chain reaction POM particulate organic matter Rif rifampicin RNA ribonucleic acid rRNA ribosomal RNA RT-PCR reverse transcription PCR tRNA transfer RNA vii LIST OF FIGURES Chapter II Figure 1 Rarefaction analysis for bacterial and archaeal ribosomal small-subunit rRNA libraries………………………………… 18 Figure 2 Heatmap of classified bacterial orders from the free-living and particle-associated libraries……………………………… 19 Figure 3 UPGMA hierarchical clustering based on (A) phylum-level and (B) OTU-level groupings………………………………… 22 Figure S1 Coverage plots for the bacterial and archaeal libraries……… 26 Figure S2 Bacterial phylogenetic trees depicting the relationship of the particle-associated and free-living sequences from the Puerto Rico Trench……………………………………… 27 Figure S3 Archaeal phylogenetic tree depicting the relationship of the particle-associated and free-living sequences from the Puerto Rico Trench……………………………………… 31 Figure S4 Eukaryal phylogenetic trees depicting the relationship of (A) Opisthokonta and (B) non-Opisthokonta sequences from the Puerto Rico Trench……………………. 32 Figure S5 Heatmap of relative abundances of bacterial phyla for deep ocean datasets……………………………………... 34 Chapter III Figure 1 Phylogenetic distribution of partial SSU ribosomal genes…. 77 Figure 2 Phylogenetic distribution of PRT protein sequences based on APIS classifications……………………………..... 78 Figure 3 Cluster analysis of (A) COG categories and (B) KEGG pathways within each metagenome………………………… 79 Figure 4 Metagenomic profile comparisons of COG families for the PRT and Sargasso Sea metagenomes……………….. 80 Figure 5 Transporter family distribution……………………………… 81 viii Figure 6 Fragment recruitment for the PRT metagenome compared to the GS00d metagenome………………………. 82 Figure S1 Metagenomic profile comparison of COG families for the PRT and HOT4000 metagenomes…….…………….. 83 Figure S2 Abundance of the functional OG category Signal Transduction (T)……………………….…………….. 84 Figure S3 Abundance of the functional OG category Transcription (K)……………………….…….…………….. 85 Figure S4 Abundance of the functional OG category Inorganic ion transport and metabolism (P)………………….…………….. 86 Figure S5 Relative abundance of COG categories and distribution within phylum-level groupings based on APIS…….……….. 87 Chapter IV Figure 1 Phylogenetic novelty: The case for ‘Candidate’ divisions…. 119 Figure 2 The ‘cultivation landscape’…….…………………………… 120 Chapter V Figure 1 Growth of PRT in natural seawater medium……………….. 151 Figure 2 Morphological features of PRT1…………………………… 152 Figure 3 Phylogenetic placement of PRT1 within the Roseobacter clade…………………………………………… 153 Figure 4 Interpolated contour diagram of the temperature-pressure dependence of the exponential growth rate constant (k)……. 154 Figure S1 Phylogenetic placement of the PRT1 g5 GTA protein……... 158 Chapter VI Figure 1 Polar (A) and lateral (B) flagellar gene clusters in P. profundum SS9……………………………………….. 162 Figure 2 Growth-based 0.3% agar bulb assay to qualitatively assess motility for P. profundum strain 3TCK and SS9…………… 164 ix Figure 3 Growth-based agar bulb assay to qualitatively assess motility at high hydrostatic pressure and high viscosity……. 164 Figure 4 Flagella visualized with NanoOrange staining for P. profundum SS9 and deletion mutants……………………. 165 Figure 5 Flagellin B increases under conditions of high pressure and increased viscosity……………………………………… 166 Figure 6 Swimming velocity as a function of increasing hydrostatic pressure for three strains……………………………………. 166 x LIST OF TABLES Chapter II Table 1 Chemical and biological constituents of unfiltered surface (1 m) and hadal (6,000 m) seawater………………… 17 Table 2 Similarity-based OTUs and species richness estimates……... 18 Table 3 Eukaryal classifications for partial 18S ribosomal gene sequences……………………………………………… 20 Chapter III Table 1 General features of the metagenomic dataset from the Puerto Rico Trench……………………………………… 73 Table 2 Functional annotations for non-redundant proteins for the PRT metagenome and comparison metagenomes………. 74 Table 3 Single cell sequencing, assembly, and annotation statistics… 75 Table 4 Comparison of single cell phylogeny to closest sequenced isolate genome…………………………………… 76 Table S1 Detailed assembly and putative contaminant statistics for single-cell genomes……………………………………… 88 Chapter IV Table 1 Single-cell technologies implemented for cultivation……….. 121 Chapter V Table 1 Growth properties of piezotolerant and piezophilic isolates… 155 Chapter VI Table 1 Bacterial strains and plasmids used in this study…………… 163 Table S1 Primer sequences used in this study………………………… 169 Table S2 Swimming velocity as a function of increasing hydrostatic pressure………………………………………… 170 xi ACKNOWLEDGEMENTS I am indebted to countless individuals with whom I have shared this adventure over the past few years. I have been exceedingly fortunate to work alongside superb scientists as well as dear friends. I would first like to sincerely thank Doug Bartlett for giving me the independence to develop as a critical thinker, the guidance and financial security when I needed support, and a true sense of what it means to be a scientist. His uncanny optimism and dedication have helped to inspire and inform my research. I would also like to sincerely thank my committee members, Eric Allen, Lihini Aluwihare, Farooq Azam, and Kit Pogliano. They have all welcomed me into their labs and provided invaluable insight in the construction of this body of research. It was an honor to learn from such a phenomenal group of scientists. Thanks to past and present members of the illustrious Bartlett lab, particularly Federico Lauro, Taylor Stratton, Ian Kerman, Lauren Franco, and Angeliki Marietou. I would like to thank Kevin Hardy for constructing and allowing me to use his ‘pick-up truck’ to the deep sea. I would also like to thank Roger Chastain, the guardian of all pressure equipment. Many thanks as well to past and present members of the Azam and Allen labs for technical assistance, helpful advice, and riveting discussions. I am grateful for the many collaborators I have had the pleasure to work with, particularly Shannon Williamson, Rudi Vogel, Shibu Yooseph, and Roger
Recommended publications
  • Download Full Article As
    Article Genomic Signature Analysis for the Strategic Bioremediation of Polycyclic Aromatic Hydrocarbons in Mangrove Ecosystems in the Gulf of Tonkin Nam H. Dao1, Quan M. Le2, Thang X. Dao3 1The Hill School, USA 2The Loomis Chaffee School, USA 3Unaffiliated SUMMARY processes. Once oil has entered the roots and rhizosphere Current oil spill cleanup methods can be inefficient, (the soil directly influenced by plant roots) of mangrove costly, and have many more downsides. In an effort to trees, they fail to participate in regular salt management and create an efficient, cost-effective, and environmentally- respiration (3). As mangrove trees are responsible for various friendly solution to cleaning oil spills, there has been important functions in this habitat such as protection of soil a flurry of advancements in microbiological vectors. These plasmids confer oil-degrading genes that can be from erosion, improving water quality or helping provide implemented into the native microbial population. For nutrients for microbial communities, the death or failure of this strategy to work, it is critical that an appropriate these trees to function can pose heavy consequences for naturally-found plasmid be picked as a base to local organisms (3). Upon direct contamination by an oil spill, ensure long-term plasmid survival and activation of mangrove trees usually face death within several months, and its genes. To help realize this goal, this study relies other organisms living in the area that depend on a host of on emerging computational technologies to measure benefits provided by mangrove trees are subsequently either genetic similarity between the host chromosome and impacted directly by the influx of oil or indirectly through the the potential plasmid vector, utilizing an algorithm for loss of mangrove trees (3).
    [Show full text]
  • Draft Genome Sequence of Thalassobius Mediterraneus CECT 5383T, a Poly-Beta-Hydroxybutyrate Producer
    Genomics Data 7 (2016) 237–239 Contents lists available at ScienceDirect Genomics Data journal homepage: www.elsevier.com/locate/gdata Data in Brief Draft genome sequence of Thalassobius mediterraneus CECT 5383T, a poly-beta-hydroxybutyrate producer Lidia Rodrigo-Torres, María J. Pujalte, David R. Arahal ⁎ Departamento de Microbiología y Ecología and Colección Española de Cultivos Tipo (CECT), Universidad de Valencia, Valencia, Spain article info abstract Article history: Thalassobius mediterraneus is the type species of the genus Thalassobius and a member of the Roseobacter clade, an Received 23 December 2015 abundant representative of marine bacteria. T. mediterraneus XSM19T (=CECT 5383T) was isolated from the Received in revised form 8 January 2016 Western Mediterranean coast near Valencia (Spain) in 1989. We present here the draft genome sequence and Accepted 14 January 2016 annotation of this strain (ENA/DDBJ/NCBI accession number CYSF00000000), which is comprised of Available online 15 January 2016 3,431,658 bp distributed in 19 contigs and encodes 10 rRNA genes, 51 tRNA genes and 3276 protein coding fi Keywords: genes. Relevant ndings are commented, including the complete set of genes required for poly-beta- Rhodobacteraceae hydroxybutyrate (PHB) synthesis and genes related to degradation of aromatic compounds. Roseobacter clade © 2016 The Authors. Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license PHB (http://creativecommons.org/licenses/by-nc-nd/4.0/). Aromatic compounds 1. Direct link to deposited data has not been yet validated, and even more recently T. abysii has been Specifications also proposed [6]. Organism/cell line/tissue Thalassobius mediterraneus Strain CECT 5383T Sequencer or array type Illumina MiSeq 2.
    [Show full text]
  • Bismis-2016 Abstract Book
    BISMiS-2016 Abstract Book Third Meeting of Bergey's International Society for Microbial Systematics on Microbial Systematics and Metagenomics September 12-15, 2016 | Pune, INDIA PUNE UNIT Abstracts - Opening Address - Keynotes Abstract Book | BISMiS-2016 | Pune, India Opening Address TAXONOMY OF PROKARYOTES - NEW CHALLENGES IN A GLOBAL WORLD Peter Kämpfer* Justus-Liebig-University Giessen, HESSEN, Germany Email: [email protected] Systematics can be considered as a comprehensive science, because in science it is an essential aspect in comparing any two or more elements, whether they are genes or genomes, proteins or proteomes, biochemical pathways or metabolomes (just to list a few examples), or whole organisms. The development of high throughput sequencing techniques has led to an enormous amount of data (genomic and other “omic” data) and has also revealed an extensive diversity behind these data. These data are more and more used also in systematics and there is a strong trend to classify and name the taxonomic units in prokaryotic systematics preferably on the basis of sequence data. Unfortunately, the knowledge of the meaning behind the sequence data does not keep up with the tremendous increase of generated sequences. The extent of the accessory genome in any given cell, and perhaps the infinite extent of the pan-genome (as an aggregate of all the accessory genomes) is fascinating but it is an open question if and how these data should be used in systematics. Traditionally the polyphasic approach in bacterial systematics considers methods including both phenotype and genotype. And it is the phenotype that is (also) playing an essential role in driving the evolution.
    [Show full text]
  • Metaproteomics Characterization of the Alphaproteobacteria
    Avian Pathology ISSN: 0307-9457 (Print) 1465-3338 (Online) Journal homepage: https://www.tandfonline.com/loi/cavp20 Metaproteomics characterization of the alphaproteobacteria microbiome in different developmental and feeding stages of the poultry red mite Dermanyssus gallinae (De Geer, 1778) José Francisco Lima-Barbero, Sandra Díaz-Sanchez, Olivier Sparagano, Robert D. Finn, José de la Fuente & Margarita Villar To cite this article: José Francisco Lima-Barbero, Sandra Díaz-Sanchez, Olivier Sparagano, Robert D. Finn, José de la Fuente & Margarita Villar (2019) Metaproteomics characterization of the alphaproteobacteria microbiome in different developmental and feeding stages of the poultry red mite Dermanyssusgallinae (De Geer, 1778), Avian Pathology, 48:sup1, S52-S59, DOI: 10.1080/03079457.2019.1635679 To link to this article: https://doi.org/10.1080/03079457.2019.1635679 © 2019 The Author(s). Published by Informa View supplementary material UK Limited, trading as Taylor & Francis Group Accepted author version posted online: 03 Submit your article to this journal Jul 2019. Published online: 02 Aug 2019. Article views: 694 View related articles View Crossmark data Citing articles: 3 View citing articles Full Terms & Conditions of access and use can be found at https://www.tandfonline.com/action/journalInformation?journalCode=cavp20 AVIAN PATHOLOGY 2019, VOL. 48, NO. S1, S52–S59 https://doi.org/10.1080/03079457.2019.1635679 ORIGINAL ARTICLE Metaproteomics characterization of the alphaproteobacteria microbiome in different developmental and feeding stages of the poultry red mite Dermanyssus gallinae (De Geer, 1778) José Francisco Lima-Barbero a,b, Sandra Díaz-Sanchez a, Olivier Sparagano c, Robert D. Finn d, José de la Fuente a,e and Margarita Villar a aSaBio.
    [Show full text]
  • Download As A
    Pseudaestuariivita rosea sp. nov., a novel species of genus Pseudaestuariivita, isolated from Acmaea, a kind of marine mollusea Shuai-Ting Yun Shandong University Zhuo Chen Shandong University Yan-Jun Yi Shandong University Ming-Jing Zhang Shandong University Shu-Kun Gao Shandong University Yan-Xia Zhou ( [email protected] ) Shandong University https://orcid.org/0000-0003-0393-8136 Research Article Keywords: Genome, Marine creature, Polyphasic analysis, Pseudaestuariivita, 16S rRNA Posted Date: July 8th, 2021 DOI: https://doi.org/10.21203/rs.3.rs-612446/v1 License: This work is licensed under a Creative Commons Attribution 4.0 International License. Read Full License 1 Pseudaestuariivita rosea sp. nov., a novel species of genus Pseudaestuariivita, 2 isolated from Acmaea, a kind of marine mollusea. 3 Shuai-Ting Yun · Zhuo Chen · Yan-Jun Yi · Ming-Jing Zhang · Shu-Kun 4 Gao · Yan-Xia Zhou * 5 Marine College, Shandong University, Weihai 264209, China 6 *Correspondence: Yan-Xia Zhou; Email: [email protected] 7 Abbreviations: 8 AAI, Average Amino Acid identity 9 ANI, Average Nucleotide Identity 10 cAAI, core-gene average amino acid identity 11 COG, Cluster of Orthologous Group 12 dDDH, digital DNA-DNA Hybridisation; 13 GGDC, Genome-to-Genome Distance Calculator 14 HPLC, High Performance Liquid Chromatography 15 KCTC, Korean Collection for Type Cultures 16 KEGG, Kyoto Encyclopedia of Genes and Genomes 17 LPS, lipopolysaccharide 18 MA, Marine agar 2216 19 MB, Marine broth 2216 20 MCCC, Marine Culture Collection of China 21 MEGA, Molecular Evolutionary Genetics Analysis 22 NCBI, National Center for Biotechnology Information 1 23 PC, phosphatidylcholine 24 PE, phosphatidylethanolamine 25 PG, phosphatidylglycerol 26 POCP, percent of conserved proteins 27 TLC, Two-dimensional thin-layer chromatogram 28 VFDB, Virulence Factors of Pathogenic Bacteria.
    [Show full text]
  • Taxonomic Hierarchy of the Phylum Proteobacteria and Korean Indigenous Novel Proteobacteria Species
    Journal of Species Research 8(2):197-214, 2019 Taxonomic hierarchy of the phylum Proteobacteria and Korean indigenous novel Proteobacteria species Chi Nam Seong1,*, Mi Sun Kim1, Joo Won Kang1 and Hee-Moon Park2 1Department of Biology, College of Life Science and Natural Resources, Sunchon National University, Suncheon 57922, Republic of Korea 2Department of Microbiology & Molecular Biology, College of Bioscience and Biotechnology, Chungnam National University, Daejeon 34134, Republic of Korea *Correspondent: [email protected] The taxonomic hierarchy of the phylum Proteobacteria was assessed, after which the isolation and classification state of Proteobacteria species with valid names for Korean indigenous isolates were studied. The hierarchical taxonomic system of the phylum Proteobacteria began in 1809 when the genus Polyangium was first reported and has been generally adopted from 2001 based on the road map of Bergey’s Manual of Systematic Bacteriology. Until February 2018, the phylum Proteobacteria consisted of eight classes, 44 orders, 120 families, and more than 1,000 genera. Proteobacteria species isolated from various environments in Korea have been reported since 1999, and 644 species have been approved as of February 2018. In this study, all novel Proteobacteria species from Korean environments were affiliated with four classes, 25 orders, 65 families, and 261 genera. A total of 304 species belonged to the class Alphaproteobacteria, 257 species to the class Gammaproteobacteria, 82 species to the class Betaproteobacteria, and one species to the class Epsilonproteobacteria. The predominant orders were Rhodobacterales, Sphingomonadales, Burkholderiales, Lysobacterales and Alteromonadales. The most diverse and greatest number of novel Proteobacteria species were isolated from marine environments. Proteobacteria species were isolated from the whole territory of Korea, with especially large numbers from the regions of Chungnam/Daejeon, Gyeonggi/Seoul/Incheon, and Jeonnam/Gwangju.
    [Show full text]
  • CGM-18-001 Perseus Report Update Bacterial Taxonomy Final Errata
    report Update of the bacterial taxonomy in the classification lists of COGEM July 2018 COGEM Report CGM 2018-04 Patrick L.J. RÜDELSHEIM & Pascale VAN ROOIJ PERSEUS BVBA Ordering information COGEM report No CGM 2018-04 E-mail: [email protected] Phone: +31-30-274 2777 Postal address: Netherlands Commission on Genetic Modification (COGEM), P.O. Box 578, 3720 AN Bilthoven, The Netherlands Internet Download as pdf-file: http://www.cogem.net → publications → research reports When ordering this report (free of charge), please mention title and number. Advisory Committee The authors gratefully acknowledge the members of the Advisory Committee for the valuable discussions and patience. Chair: Prof. dr. J.P.M. van Putten (Chair of the Medical Veterinary subcommittee of COGEM, Utrecht University) Members: Prof. dr. J.E. Degener (Member of the Medical Veterinary subcommittee of COGEM, University Medical Centre Groningen) Prof. dr. ir. J.D. van Elsas (Member of the Agriculture subcommittee of COGEM, University of Groningen) Dr. Lisette van der Knaap (COGEM-secretariat) Astrid Schulting (COGEM-secretariat) Disclaimer This report was commissioned by COGEM. The contents of this publication are the sole responsibility of the authors and may in no way be taken to represent the views of COGEM. Dit rapport is samengesteld in opdracht van de COGEM. De meningen die in het rapport worden weergegeven, zijn die van de auteurs en weerspiegelen niet noodzakelijkerwijs de mening van de COGEM. 2 | 24 Foreword COGEM advises the Dutch government on classifications of bacteria, and publishes listings of pathogenic and non-pathogenic bacteria that are updated regularly. These lists of bacteria originate from 2011, when COGEM petitioned a research project to evaluate the classifications of bacteria in the former GMO regulation and to supplement this list with bacteria that have been classified by other governmental organizations.
    [Show full text]
  • Appendix 1. Validly Published Names, Conserved and Rejected Names, And
    Appendix 1. Validly published names, conserved and rejected names, and taxonomic opinions cited in the International Journal of Systematic and Evolutionary Microbiology since publication of Volume 2 of the Second Edition of the Systematics* JEAN P. EUZÉBY New phyla Alteromonadales Bowman and McMeekin 2005, 2235VP – Valid publication: Validation List no. 106 – Effective publication: Names above the rank of class are not covered by the Rules of Bowman and McMeekin (2005) the Bacteriological Code (1990 Revision), and the names of phyla are not to be regarded as having been validly published. These Anaerolineales Yamada et al. 2006, 1338VP names are listed for completeness. Bdellovibrionales Garrity et al. 2006, 1VP – Valid publication: Lentisphaerae Cho et al. 2004 – Valid publication: Validation List Validation List no. 107 – Effective publication: Garrity et al. no. 98 – Effective publication: J.C. Cho et al. (2004) (2005xxxvi) Proteobacteria Garrity et al. 2005 – Valid publication: Validation Burkholderiales Garrity et al. 2006, 1VP – Valid publication: Vali- List no. 106 – Effective publication: Garrity et al. (2005i) dation List no. 107 – Effective publication: Garrity et al. (2005xxiii) New classes Caldilineales Yamada et al. 2006, 1339VP VP Alphaproteobacteria Garrity et al. 2006, 1 – Valid publication: Campylobacterales Garrity et al. 2006, 1VP – Valid publication: Validation List no. 107 – Effective publication: Garrity et al. Validation List no. 107 – Effective publication: Garrity et al. (2005xv) (2005xxxixi) VP Anaerolineae Yamada et al. 2006, 1336 Cardiobacteriales Garrity et al. 2005, 2235VP – Valid publica- Betaproteobacteria Garrity et al. 2006, 1VP – Valid publication: tion: Validation List no. 106 – Effective publication: Garrity Validation List no. 107 – Effective publication: Garrity et al.
    [Show full text]
  • Supplement of Hidden Biosphere in an Oxygen-Deficient Atlantic Open
    Supplement of Biogeosciences, 12, 7467–7482, 2015 http://www.biogeosciences.net/12/7467/2015/ doi:10.5194/bg-12-7467-2015-supplement © Author(s) 2015. CC Attribution 3.0 License. Supplement of Hidden biosphere in an oxygen-deficient Atlantic open-ocean eddy: future implications of ocean deoxygenation on primary production in the eastern tropical North Atlantic C. R. Löscher et al. Correspondence to: C. R. Löscher ([email protected]) The copyright of individual parts of the supplement might differ from the CC-BY 3.0 licence. Supplemental material OTU counts/ sample 0 20000 40000 60000 0 100 200 300 depth depth [m] 400 eddy_1 CVOO 500 Figure S1: Vertical distribution of SUP05-related OTUs (counts per sample) in the eddy (eddy_1) and outside the eddy (at CVOO). A B C 0 0 0 Nitrosopumilales Nitrososphaerales 100 100 100 Halobacteriales Thermoplasmatales Methanomicrobiales 200 200 200 Methanobacteriales Methanosarcinales unclassified depth [m] depth [m] depth 300 [m] depth 300 300 oxygen vs depth 400 400 400 500 500 500 0 20 40 60 80 100 0 20 40 60 80 100 0 20 40 60 80 100 relative abundance [%] relative abundance [%] relative abundance [%] 0 50 100 150 200 250 0 50 100 150 200 250 0 50 100 150 200 250 -1 oxygen [µmol kg-1] oxygen [µmol kg ] oxygen [µmol kg-1] Figure S2: Distribution of archaeal phyla along vertical profiles from (A) CVOO, (B) eddy_1 and (C) eddy_2 based on 16S rDNA amplicon sequencing data. Oxygen profiles are shown in blue. Figure S3: Distribution of archaeal (A) and bacterial (B) phyla from 115 m water depth (33.9 -1 µmol O2 L ) at the presumed origin of the eddy on the Mauritanian shelf.
    [Show full text]
  • The Onset of Microbial Associations in the Coral Pocillopora Meandrina
    The ISME Journal (2009) 3, 685–699 & 2009 International Society for Microbial Ecology All rights reserved 1751-7362/09 $32.00 www.nature.com/ismej ORIGINAL ARTICLE The onset of microbial associations in the coral Pocillopora meandrina Amy Apprill1,2, Heather Q Marlow3, Mark Q Martindale3 and Michael S Rappe´1 1Hawaii Institute of Marine Biology, SOEST, University of Hawaii, Kaneohe, HI, USA; 2Department of Oceanography, SOEST, University of Hawaii, Honolulu, HI, USA and 3Kewalo Marine Laboratory, Pacific Biomedical Research Center, University of Hawaii, Honolulu, HI, USA Associations between healthy adult reef-building corals and bacteria and archaea have been observed in many coral species, but the initiation of their association is not understood. We investigated the onset of association between microorganisms and Pocillopora meandrina, a coral that vertically seeds its eggs with symbiotic dinoflagellates before spawning. We compared the bacterial communities associated with prespawned oocyte bundles, spawned eggs, and week old planulae using multivariate analyses of terminal restriction fragment length polymorphisms of SSU rRNA genes, which revealed that the composition of bacteria differed between these life stages. Additionally, planulae raised in ambient seawater and seawater filtered to reduce the microbial cell density harbored dissimilar bacterial communities, though SSU rRNA gene clone libraries showed that planulae raised in both treatments were primarily associated with different members of the Roseobacter clade of Alphaproteobacteria. Fluorescent in situ hybridization with an oligonucleotide probe suite targeting all bacteria and one oligonucleotide probe targeting members of the Roseobacter clade was used to localize the bacterial cells. Only planulae greater than 3 days old were observed to contain internalized bacterial cells, and members of the Roseobacter clade were detected in high abundance within planula tissues exposed to the ambient seawater treatment.
    [Show full text]
  • 2—Impact of Environmental Changes on the Microbial Community
    Dynamics of a methanol-fed marine denitrifying biofilm: 2—impact of environmental changes on the microbial community Richard Villemur1, Geneviève Payette1, Valérie Geoffroy2, Florian Mauffrey3 and Christine Martineau4 1 INRS-Centre Armand-Frappier Santé et Biotechnologie, Laval, Québec, Canada 2 Lallemand, Montréal, Québec, Canada 3 Université de Genève, Geneva, Switzerland 4 Laurentian Forestry Centre, Québec, Canada ABSTRACT Background. The biofilm of a methanol-fed, marine denitrification system is composed of a multi-species microbial community, among which Hyphomicrobium nitrativorans and Methylophaga nitratireducenticrescens are the principal bacteria involved in the denitrifying activities. To assess its resilience to environmental changes, the biofilm was cultivated in artificial seawater (ASW) under anoxic conditions and exposed to a range of specific environmental conditions. We previously reported the impact of these changes on the denitrifying activities and the co-occurrence of H. nitrativorans strain NL23 and M. nitratireducenticrescens in the biofilm cultures. Here, we report the impact of these changes on the dynamics of the overall microbial community of the denitrifying biofilm. Methods. The original biofilm (OB) taken from the denitrification system was cultivated in ASW under anoxic conditions with a range of NaCl concentrations, and with four combinations of nitrate/methanol concentrations and temperatures. The OB was also cultivated in the commercial Instant Ocean seawater (IO). The bacterial Submitted 17 April 2019 diversity of the biofilm cultures and the OB was determined by 16S ribosomal RNA Accepted 12 July 2019 gene sequences. Culture approach was used to isolate other denitrifying bacteria from Published 13 August 2019 the biofilm cultures. The metatranscriptomes of selected biofilm cultures were derived, Corresponding author along with the transcriptomes of planktonic pure cultures of H.
    [Show full text]
  • Distinct Bacterial Communities Associated with the Coral Model Aiptasia in Aposymbiotic and Symbiotic States with Symbiodinium
    Distinct Bacterial Communities Associated with the Coral Model Aiptasia in Aposymbiotic and Symbiotic States with Symbiodinium Item Type Article Authors Röthig, Till; Martins Da Costa, Ruben; Simona, Fabia; Baumgarten, Sebastian; Torres, Ana F.; Radhakrishnan, Anand; Aranda, Manuel; Voolstra, Christian R. Citation Röthig T, Costa RM, Simona F, Baumgarten S, Torres AF, et al. (2016) Distinct Bacterial Communities Associated with the Coral Model Aiptasia in Aposymbiotic and Symbiotic States with Symbiodinium. Frontiers in Marine Science 3. Available: http:// dx.doi.org/10.3389/fmars.2016.00234. Eprint version Publisher's Version/PDF DOI 10.3389/fmars.2016.00234 Publisher Frontiers Media SA Journal Frontiers in Marine Science Rights This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. Download date 02/10/2021 17:11:02 Item License http://creativecommons.org/licenses/by/4.0/ Link to Item http://hdl.handle.net/10754/622707 ORIGINAL RESEARCH published: 18 November 2016 doi: 10.3389/fmars.2016.00234 Distinct Bacterial Communities Associated with the Coral Model Aiptasia in Aposymbiotic and Symbiotic States with Symbiodinium Till Röthig †, Rúben M. Costa †, Fabia Simona, Sebastian Baumgarten, Ana F. Torres, Anand Radhakrishnan, Manuel Aranda and Christian R. Voolstra * Division of Biological and Environmental Science and Engineering (BESE), Red Sea Research Center, King Abdullah University of Science and Technology (KAUST), Thuwal, Saudi Arabia Coral reefs are in decline.
    [Show full text]