Diversity and Activity of Roseobacters and Roseophage

Total Page:16

File Type:pdf, Size:1020Kb

Diversity and Activity of Roseobacters and Roseophage University of Tennessee, Knoxville TRACE: Tennessee Research and Creative Exchange Doctoral Dissertations Graduate School 5-2012 Diversity and Activity of Roseobacters and Roseophage Charles Ryan Budinoff [email protected] Follow this and additional works at: https://trace.tennessee.edu/utk_graddiss Part of the Bacteriology Commons, Biodiversity Commons, Bioinformatics Commons, Ecology and Evolutionary Biology Commons, Environmental Microbiology and Microbial Ecology Commons, and the Marine Biology Commons Recommended Citation Budinoff, Charles Ryan, "Diversity and Activity of Roseobacters and Roseophage. " PhD diss., University of Tennessee, 2012. https://trace.tennessee.edu/utk_graddiss/1276 This Dissertation is brought to you for free and open access by the Graduate School at TRACE: Tennessee Research and Creative Exchange. It has been accepted for inclusion in Doctoral Dissertations by an authorized administrator of TRACE: Tennessee Research and Creative Exchange. For more information, please contact [email protected]. To the Graduate Council: I am submitting herewith a dissertation written by Charles Ryan Budinoff entitled "Diversity and Activity of Roseobacters and Roseophage." I have examined the final electronic copy of this dissertation for form and content and recommend that it be accepted in partial fulfillment of the requirements for the degree of Doctor of Philosophy, with a major in Microbiology. Alison Buchan, Major Professor We have read this dissertation and recommend its acceptance: Steven W. Wilhelm, Erik Zinser, Mark Radosevich Accepted for the Council: Carolyn R. Hodges Vice Provost and Dean of the Graduate School (Original signatures are on file with official studentecor r ds.) Diversity and Activity of Roseobacters and Roseophage A Dissertation Presented for the Doctor of Philosophy Degree The University of Tennessee, Knoxville Charles Ryan Budinoff May 2012 Copyright © 2011 by Charles Ryan Budinoff All rights reserved. ii DEDICATION I dedicate my dissertation to my maternal grandmother, for her unwavering love and support. iii ACKNOWLEDGEMENTS Dr. Alison Buchan, your mentorship was essential for the completion of this dissertation and of my doctoral degree. I have learned many things from you over the past four years. Your expertise in bacterial diversity and your knowledge of molecular biology were of great value. But the most important lesson I learned was how to be a good mentor and leader. Your extraordinary interpersonal skills and astounding work ethic allow you to effectively lead a large university laboratory. In my opinion, these are two of the most important traits of a supervisor. Through leading by example, you undoubtedly earn the respect of fellow faculty and staff, but also of every student in the department. I am honored to have been in your lab and know that the examples you have set will guide me for the rest of my life. Dr. Gary LeCleir, your friendship over the past decade cannot be summed in a few sentences. I will never be able to repay you for the help, advice, and laughter you gave to me, nor will I ever forget it. You are a person who never says ‘no’ to his friends. No matter how difficult the favor, I know you will be there with a big heart and a big smile. I hope to pay this forward by providing such guidance and friendship to others whenever I can. Kellina Morris, thanks for being by my side this past year. You listened to all my griping, all my lapses in confidence, and never let me think about giving up. Knowing that my graduation would bring us one step closer to each other was the extra motivation I needed. Your support has allowed us to close our first chapter and will be the springboard for our future together. Mary Hadden, thanks for keeping the lab in tip-top shape. I could not of had so many successful experiments without your hard work and devotion. iv ABSTRACT Bacteria of the Roseobacter lineage are dominant bacterioplankton in coastal systems and contribute significantly to secondary production in oceanic environments. Generalities of Roseobacter ecology, diversity, and distributions are known, but the intraspecific differences between species and their dynamics over short temporal periods is not well understood. Bacteriophage that infect Roseobacters (‘roseophage’) have the potential to shunt secondary production into the dissolved carbon pool and through the process of infection alter Roseobacter physiology. Despite their significance, little effort was made prior to the onset of this study to characterize roseophage. Using culture dependent and independent approaches, I describe the diversity and activity of Roseobacters and roseophage from two distinct coastal environments. Chapter 2 describes the development of an alternative method to enumerate viruses using epifluorescence microscopy that not only reduces sample processing costs, but also the total volume of sample required. A novel species of the Roseobacter lineage (Marivita roseacus) is proposed in Chapter 3. M. roseacus is unique in its needle-like morphology, forming long, relatively inflexible chains of cells. The Marivita genus is characterized by a distinct ecology, being closely associated with algae, resistant to grazing, and present in numerous marine and saline environments. Chapter 4 details the use of deep-amplicon sequencing (16S rDNA) to describe bacterial succession patterns during a mesocosm algal bloom, revealing the temporal dynamics of ~100 distinct phylotypes. A multivariate analysis showed that temporal portioning amongst the bacterial community was occurring at both high and low taxonomic levels. Chapter 5 details the isolation and genomic characterization of roseophage and describes their ecology using publically available metagenomic databases collected from throughout the world. Four distinct phage were isolated and sequenced including an N4-like strain, a novel Siphoviridae, and two temperate Podoviridae. The two temperate phage were practically identical at the nucleotide level, except for a 3000 bp putative replication module, which showed no homology between the two. Overall, this dissertation suggests that ecological partitioning within the Roseobacter lineage is occurring at and arguably below traditional species level taxonomic classifications and microdiversity amongst closely related marine bacteria is likely the norm rather than the exception. v TABLE OF CONTENTS Chapter 1 - Introduction ...................................................................................................... 1! References ....................................................................................................................... 5! Chapter 2 - A protocol for enumeration of aquatic viruses by epifluorescence microscopy using Anodisc™ 13 membranes ......................................................................................... 6! Abstract ........................................................................................................................... 7! Background ................................................................................................................. 7! Results ......................................................................................................................... 7! Conclusions ................................................................................................................. 8! Background ..................................................................................................................... 8! Results and Discussion ................................................................................................... 9! Construction of custom filter holders for 13 mm Anodisc membranes ...................... 9! Enumeration of VLP using 13mm Anodisc membranes .......................................... 10! Comparison of VLP counts using Anodisc membranes and evaluation of staining methods ..................................................................................................................... 11! Analysis of Nuclepore membranes ........................................................................... 12! Conclusions ................................................................................................................... 13! Methods......................................................................................................................... 13! Sample collection and preparation ............................................................................ 13! Enumeration of viruses using 25 mm Anodisc membranes ...................................... 13! Enumeration of viruses using Nuclepore membranes .............................................. 14! SEM imaging of Nuclepore membranes ................................................................... 15! Statistical comparison of virus counts from the Anodisc membranes ...................... 15! Acknowledgements ....................................................................................................... 15! References ..................................................................................................................... 16! Appendix ....................................................................................................................... 18! Tables ........................................................................................................................ 18! vi Chapter 3 - Marivita roseacus sp. nov., of the family Rhodobacteraceae, isolated from a temperate estuary
Recommended publications
  • Phylogenetic Analysis Reveals an Ancient Gene Duplication As The
    1 Phylogenetic analysis reveals an ancient gene duplication as 2 the origin of the MdtABC efflux pump. 3 4 Kamil Górecki1, Megan M. McEvoy1,2,3 5 1Institute for Society & Genetics, 2Department of MicroBiology, Immunology & Molecular 6 Genetics, and 3Molecular Biology Institute, University of California, Los Angeles, CA 90095, 7 United States of America 8 Corresponding author: [email protected] (M.M.M.) 9 1 10 Abstract 11 The efflux pumps from the Resistance-Nodulation-Division family, RND, are main 12 contributors to intrinsic antibiotic resistance in Gram-negative bacteria. Among this family, the 13 MdtABC pump is unusual by having two inner membrane components. The two components, 14 MdtB and MdtC are homologs, therefore it is evident that the two components arose by gene 15 duplication. In this paper, we describe the results obtained from a phylogenetic analysis of the 16 MdtBC pumps in the context of other RNDs. We show that the individual inner membrane 17 components (MdtB and MdtC) are conserved throughout the Proteobacterial species and that their 18 existence is a result of a single gene duplication. We argue that this gene duplication was an ancient 19 event which occurred before the split of Proteobacteria into Alpha-, Beta- and Gamma- classes. 20 Moreover, we find that the MdtABC pumps and the MexMN pump from Pseudomonas aeruginosa 21 share a close common ancestor, suggesting the MexMN pump arose by another gene duplication 22 event of the original Mdt ancestor. Taken together, these results shed light on the evolution of the 23 RND efflux pumps and demonstrate the ancient origin of the Mdt pumps and suggest that the core 24 bacterial efflux pump repertoires have been generally stable throughout the course of evolution.
    [Show full text]
  • Supplementary Information
    doi: 10.1038/nature06269 SUPPLEMENTARY INFORMATION METAGENOMIC AND FUNCTIONAL ANALYSIS OF HINDGUT MICROBIOTA OF A WOOD FEEDING HIGHER TERMITE TABLE OF CONTENTS MATERIALS AND METHODS 2 • Glycoside hydrolase catalytic domains and carbohydrate binding modules used in searches that are not represented by Pfam HMMs 5 SUPPLEMENTARY TABLES • Table S1. Non-parametric diversity estimators 8 • Table S2. Estimates of gross community structure based on sequence composition binning, and conserved single copy gene phylogenies 8 • Table S3. Summary of numbers glycosyl hydrolases (GHs) and carbon-binding modules (CBMs) discovered in the P3 luminal microbiota 9 • Table S4. Summary of glycosyl hydrolases, their binning information, and activity screening results 13 • Table S5. Comparison of abundance of glycosyl hydrolases in different single organism genomes and metagenome datasets 17 • Table S6. Comparison of abundance of glycosyl hydrolases in different single organism genomes (continued) 20 • Table S7. Phylogenetic characterization of the termite gut metagenome sequence dataset, based on compositional phylogenetic analysis 23 • Table S8. Counts of genes classified to COGs corresponding to different hydrogenase families 24 • Table S9. Fe-only hydrogenases (COG4624, large subunit, C-terminal domain) identified in the P3 luminal microbiota. 25 • Table S10. Gene clusters overrepresented in termite P3 luminal microbiota versus soil, ocean and human gut metagenome datasets. 29 • Table S11. Operational taxonomic unit (OTU) representatives of 16S rRNA sequences obtained from the P3 luminal fluid of Nasutitermes spp. 30 SUPPLEMENTARY FIGURES • Fig. S1. Phylogenetic identification of termite host species 38 • Fig. S2. Accumulation curves of 16S rRNA genes obtained from the P3 luminal microbiota 39 • Fig. S3. Phylogenetic diversity of P3 luminal microbiota within the phylum Spirocheates 40 • Fig.
    [Show full text]
  • Review Article Yersinia Enterocolitica: Mode of Transmission, Molecular Insights of Virulence, and Pathogenesis of Infection
    SAGE-Hindawi Access to Research Journal of Pathogens Volume 2011, Article ID 429069, 10 pages doi:10.4061/2011/429069 Review Article Yersinia enterocolitica: Mode of Transmission, Molecular Insights of Virulence, and Pathogenesis of Infection Yeasmin Sabina,1 Atiqur Rahman,2 Ramesh Chandra Ray,3 and Didier Montet4 1 Department of Genetic Engineering and Biotechnology, University of Dhaka, Dhaka 1000, Bangladesh 2 Department of Microbiology, University of Dhaka, Dhaka 1000, Bangladesh 3 Central Tuber Crops Research Institute, Bhubaneswar, India 4 Centre International de Recherche en Agronomie pour le Developpement (CIRAD), Montpellier, France Correspondence should be addressed to Yeasmin Sabina, y [email protected] Received 19 April 2011; Revised 28 May 2011; Accepted 5 June 2011 Academic Editor: Latiful Bari Copyright © 2011 Yeasmin Sabina et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Although Yersinia enterocolitica is usually transmitted through contaminated food and untreated water, occasional transmission such as human-to-human, animal-to-human and blood transfusion associated transmission have also identified in human disease. Of the six Y. enterocolitica biotypes, the virulence of the pathogenic biotypes, namely, 1B and 2–5 is attributed to the presence of a highly conserved 70-kb virulence plasmid, termed pYV/pCD and certain chromosomal genes. Some biotype 1A strains, despite lacking virulence plasmid (pYV) and traditional chromosomal virulence genes, are isolated frequently from humans with gastrointestinal diseases similar to that produced by isolates belonging known pathogenic biotypes. Y. enterocolitica pathogenic biotypes have evolved two major properties: the ability to penetrate the intestinal wall, which is thought to be controlled by plasmid genes, and the production of heat-stable enterotoxin, which is controlled by chromosomal genes.
    [Show full text]
  • Spatiotemporal Dynamics of Marine Bacterial and Archaeal Communities in Surface Waters Off the Northern Antarctic Peninsula
    Spatiotemporal dynamics of marine bacterial and archaeal communities in surface waters off the northern Antarctic Peninsula Camila N. Signori, Vivian H. Pellizari, Alex Enrich Prast and Stefan M. Sievert The self-archived postprint version of this journal article is available at Linköping University Institutional Repository (DiVA): http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-149885 N.B.: When citing this work, cite the original publication. Signori, C. N., Pellizari, V. H., Enrich Prast, A., Sievert, S. M., (2018), Spatiotemporal dynamics of marine bacterial and archaeal communities in surface waters off the northern Antarctic Peninsula, Deep-sea research. Part II, Topical studies in oceanography, 149, 150-160. https://doi.org/10.1016/j.dsr2.2017.12.017 Original publication available at: https://doi.org/10.1016/j.dsr2.2017.12.017 Copyright: Elsevier http://www.elsevier.com/ Spatiotemporal dynamics of marine bacterial and archaeal communities in surface waters off the northern Antarctic Peninsula Camila N. Signori1*, Vivian H. Pellizari1, Alex Enrich-Prast2,3, Stefan M. Sievert4* 1 Departamento de Oceanografia Biológica, Instituto Oceanográfico, Universidade de São Paulo (USP). Praça do Oceanográfico, 191. CEP: 05508-900 São Paulo, SP, Brazil. 2 Department of Thematic Studies - Environmental Change, Linköping University. 581 83 Linköping, Sweden 3 Departamento de Botânica, Instituto de Biologia, Universidade Federal do Rio de Janeiro (UFRJ). Av. Carlos Chagas Filho, 373. CEP: 21941-902. Rio de Janeiro, Brazil 4 Biology Department, Woods Hole Oceanographic Institution (WHOI). 266 Woods Hole Road, Woods Hole, MA 02543, United States. *Corresponding authors: Camila Negrão Signori Address: Departamento de Oceanografia Biológica, Instituto Oceanográfico, Universidade de São Paulo, São Paulo, Brazil.
    [Show full text]
  • The Protein Import Machinery of Mitochondria-A Regulatory Hub In
    Cell Metabolism Perspective The Protein Import Machinery of Mitochondria—A Regulatory Hub in Metabolism, Stress, and Disease Angelika B. Harbauer,1,2,3,4 Rene´ P. Zahedi,5 Albert Sickmann,5,6 Nikolaus Pfanner,1,4,* and Chris Meisinger1,4,* 1Institut fu¨ r Biochemie und Molekularbiologie, ZBMZ 2Trinationales Graduiertenkolleg 1478 3Faculty of Biology 4BIOSS Centre for Biological Signalling Studies Universita¨ t Freiburg, 79104 Freiburg, Germany 5Leibniz-Institute for Analytical Sciences–ISAS–e.V., 44139 Dortmund, Germany 6Medizinisches Proteom-Center, Ruhr-Universita¨ t Bochum, 44801 Bochum, Germany *Correspondence: [email protected] (N.P.), [email protected] (C.M.) http://dx.doi.org/10.1016/j.cmet.2014.01.010 Mitochondria fulfill central functions in bioenergetics, metabolism, and apoptosis. They import more than 1,000 different proteins from the cytosol. It had been assumed that the protein import machinery is constitu- tively active and not subject to detailed regulation. However, recent studies indicate that mitochondrial protein import is regulated at multiple levels connected to cellular metabolism, signaling, stress, and patho- genesis of diseases. Here, we discuss the molecular mechanisms of import regulation and their implications for mitochondrial homeostasis. The protein import activity can function as a sensor of mitochondrial fitness and provides a direct means of regulating biogenesis, composition, and turnover of the organelle. Introduction machinery is essential for the viability
    [Show full text]
  • Roseisalinus Antarcticus Gen. Nov., Sp. Nov., a Novel Aerobic Bacteriochlorophyll A-Producing A-Proteobacterium Isolated from Hypersaline Ekho Lake, Antarctica
    International Journal of Systematic and Evolutionary Microbiology (2005), 55, 41–47 DOI 10.1099/ijs.0.63230-0 Roseisalinus antarcticus gen. nov., sp. nov., a novel aerobic bacteriochlorophyll a-producing a-proteobacterium isolated from hypersaline Ekho Lake, Antarctica Matthias Labrenz,13 Paul A. Lawson,2 Brian J. Tindall,3 Matthew D. Collins2 and Peter Hirsch1 Correspondence 1Institut fu¨r Allgemeine Mikrobiologie, Christian-Albrechts-Universita¨t, Kiel, Germany Matthias Labrenz 2School of Food Biosciences, University of Reading, PO Box 226, Reading RG6 6AP, UK matthias.labrenz@ 3DSMZ – Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH, Mascheroder io-warnemuende.de Weg 1b, D-38124 Braunschweig, Germany A Gram-negative, aerobic to microaerophilic rod was isolated from 10 m depths of the hypersaline, heliothermal and meromictic Ekho Lake (East Antarctica). The strain was oxidase- and catalase-positive, metabolized a variety of carboxylic acids and sugars and produced lipase. Cells had an absolute requirement for artificial sea water, which could not be replaced by NaCl. A large in vivo absorption band at 870 nm indicated production of bacteriochlorophyll a. The predominant fatty acids of this organism were 16 : 0 and 18 : 1v7c, with 3-OH 10 : 0, 16 : 1v7c and 18 : 0 in lower amounts. The main polar lipids were diphosphatidylglycerol, phosphatidylglycerol and phosphatidylcholine. Ubiquinone 10 was produced. The DNA G+C content was 67 mol%. 16S rRNA gene sequence comparisons indicated that the isolate represents a member of the Roseobacter clade within the a-Proteobacteria. The organism showed no particular relationship to any members of this clade but clustered on the periphery of the genera Jannaschia, Octadecabacter and ‘Marinosulfonomonas’ and the species Ruegeria gelatinovorans.
    [Show full text]
  • Article-Associated Bac- Teria and Colony Isolation in Soft Agar Medium for Bacteria Unable to Grow at the Air-Water Interface
    Biogeosciences, 8, 1955–1970, 2011 www.biogeosciences.net/8/1955/2011/ Biogeosciences doi:10.5194/bg-8-1955-2011 © Author(s) 2011. CC Attribution 3.0 License. Diversity of cultivated and metabolically active aerobic anoxygenic phototrophic bacteria along an oligotrophic gradient in the Mediterranean Sea C. Jeanthon1,2, D. Boeuf1,2, O. Dahan1,2, F. Le Gall1,2, L. Garczarek1,2, E. M. Bendif1,2, and A.-C. Lehours3 1Observatoire Oceanologique´ de Roscoff, UMR7144, INSU-CNRS – Groupe Plancton Oceanique,´ 29680 Roscoff, France 2UPMC Univ Paris 06, UMR7144, Adaptation et Diversite´ en Milieu Marin, Station Biologique de Roscoff, 29680 Roscoff, France 3CNRS, UMR6023, Microorganismes: Genome´ et Environnement, Universite´ Blaise Pascal, 63177 Aubiere` Cedex, France Received: 21 April 2011 – Published in Biogeosciences Discuss.: 5 May 2011 Revised: 7 July 2011 – Accepted: 8 July 2011 – Published: 20 July 2011 Abstract. Aerobic anoxygenic phototrophic (AAP) bac- detected in the eastern basin, reflecting the highest diver- teria play significant roles in the bacterioplankton produc- sity of pufM transcripts observed in this ultra-oligotrophic tivity and biogeochemical cycles of the surface ocean. In region. To our knowledge, this is the first study to document this study, we applied both cultivation and mRNA-based extensively the diversity of AAP isolates and to unveil the ac- molecular methods to explore the diversity of AAP bacte- tive AAP community in an oligotrophic marine environment. ria along an oligotrophic gradient in the Mediterranean Sea By pointing out the discrepancies between culture-based and in early summer 2008. Colony-forming units obtained on molecular methods, this study highlights the existing gaps in three different agar media were screened for the production the understanding of the AAP bacteria ecology, especially in of bacteriochlorophyll-a (BChl-a), the light-harvesting pig- the Mediterranean Sea and likely globally.
    [Show full text]
  • Recurring Patterns in Bacterioplankton Dynamics During Coastal Spring
    RESEARCH ARTICLE Recurring patterns in bacterioplankton dynamics during coastal spring algae blooms Hanno Teeling1*†, Bernhard M Fuchs1*†, Christin M Bennke1‡, Karen Kru¨ ger1, Meghan Chafee1, Lennart Kappelmann1, Greta Reintjes1, Jost Waldmann1, Christian Quast1, Frank Oliver Glo¨ ckner1, Judith Lucas2, Antje Wichels2, Gunnar Gerdts2, Karen H Wiltshire3, Rudolf I Amann1* 1Max Planck Institute for Marine Microbiology, Bremen, Germany; 2Biologische Anstalt Helgoland, Alfred Wegener Institute for Polar and Marine Research, Helgoland, Germany; 3Alfred Wegener Institute for Polar and Marine Research, List auf Sylt, Germany Abstract A process of global importance in carbon cycling is the remineralization of algae biomass by heterotrophic bacteria, most notably during massive marine algae blooms. Such blooms can trigger secondary blooms of planktonic bacteria that consist of swift successions of distinct *For correspondence: hteeling@ mpi-bremen.de (HT); bfuchs@mpi- bacterial clades, most prominently members of the Flavobacteriia, Gammaproteobacteria and the bremen.de (BMF); ramann@mpi- alphaproteobacterial Roseobacter clade. We investigated such successions during spring bremen.de (RIA) phytoplankton blooms in the southern North Sea (German Bight) for four consecutive years. Dense sampling and high-resolution taxonomic analyses allowed the detection of recurring patterns down † These authors contributed to the genus level. Metagenome analyses also revealed recurrent patterns at the functional level, in equally to this work particular with respect to algal polysaccharide degradation genes. We, therefore, hypothesize that Present address: ‡Section even though there is substantial inter-annual variation between spring phytoplankton blooms, the Biology, Leibniz Institute for accompanying succession of bacterial clades is largely governed by deterministic principles such as Baltic Sea Research, substrate-induced forcing.
    [Show full text]
  • Roseibacterium Beibuensis Sp. Nov., a Novel Member of Roseobacter Clade Isolated from Beibu Gulf in the South China Sea
    Curr Microbiol (2012) 65:568–574 DOI 10.1007/s00284-012-0192-6 Roseibacterium beibuensis sp. nov., a Novel Member of Roseobacter Clade Isolated from Beibu Gulf in the South China Sea Yujiao Mao • Jingjing Wei • Qiang Zheng • Na Xiao • Qipei Li • Yingnan Fu • Yanan Wang • Nianzhi Jiao Received: 6 April 2012 / Accepted: 25 June 2012 / Published online: 31 July 2012 Ó Springer Science+Business Media, LLC 2012 Abstract A novel aerobic, bacteriochlorophyll-contain- similarity), followed by Dinoroseobacter shibae DFL 12T ing bacteria strain JLT1202rT was isolated from Beibu Gulf (95.4 % similarity). The phylogenetic distance of pufM genes in the South China Sea. Cells were gram-negative, non- between strain JLT1202rT and R. elongatum OCh 323T was motile, and short-ovoid to rod-shaped with two narrower 9.4 %, suggesting that strain JLT1202rT was distinct from the poles. Strain JLT1202rT formed circular, opaque, wine-red only strain of the genus Roseibacterium. Based on the vari- colonies, and grew optimally at 3–4 % NaCl, pH 7.5–8.0 abilities of phylogenetic and phenotypic characteristics, strain and 28–30 °C. The strain was catalase, oxidase, ONPG, JLT1202rT stands for a novel species of the genus Roseibac- gelatin, and Voges–Proskauer test positive. In vivo terium and the name R. beibuensis sp. nov. is proposed with absorption spectrum of bacteriochlorophyll a presented two JLT1202rT as the type strain (=JCM 18015T = CGMCC peaks at 800 and 877 nm. The predominant cellular fatty 1.10994T). acid was C18:1 x7c and significant amounts of C16:0,C18:0, C10:0 3-OH, C16:0 2-OH, and 11-methyl C18:1 x7c were present.
    [Show full text]
  • Genomic Analysis of the Recent Viral Isolate Vb Bthp-Goe4 Reveals Increased Diversity of Φ29-Like Phages
    viruses Article Genomic Analysis of the Recent Viral Isolate vB_BthP-Goe4 Reveals Increased Diversity of φ29-Like Phages Tobias Schilling 1, Michael Hoppert 2 and Robert Hertel 1,* 1 Department of Genomic and Applied Microbiology & Göttingen Genomics Laboratory, Institute of Microbiology and Genetics, Georg-August-University Göttingen, 37077 Göttingen, Germany; [email protected] 2 Department of General Microbiology, Institute of Microbiology and Genetics, Georg-August-University Göttingen, 37077 Göttingen, Germany; [email protected] * Correspondence: [email protected]; Tel.: +49-551-39-91120 Received: 19 October 2018; Accepted: 8 November 2018; Published: 13 November 2018 Abstract: We present the recently isolated virus vB_BthP-Goe4 infecting Bacillus thuringiensis HD1. Morphological investigation via transmission electron microscopy revealed key characteristics of the genus Phi29virus, but with an elongated head resulting in larger virion particles of approximately 50 nm width and 120 nm height. Genome sequencing and analysis resulted in a linear phage chromosome of approximately 26 kb, harbouring 40 protein-encoding genes and a packaging RNA. Sequence comparison confirmed the relation to the Phi29virus genus and genomes of other related strains. A global average nucleotide identity analysis of all identified φ29-like viruses revealed the formation of several new groups previously not observed. The largest group includes Goe4 and may significantly expand the genus Phi29virus (Salasvirus) or the Picovirinae subfamily. Keywords: Bacillus; thuringiensis; vB_BthP-Goe4; Goe4; Picovirinae; Phi29virus; Salasvirus; Luci; bacteriophage; phage; pRNA 1. Introduction Bacteriophages or phages are viruses of bacteria and probably the most common biological entities on earth. Phage species outnumber their hosts by 10 times [1] and thus, represent the largest unexplored genetic reservoir.
    [Show full text]
  • Microbial Diversity Under Extreme Euxinia: Mahoney Lake, Canada V
    Geobiology (2012), 10, 223–235 DOI: 10.1111/j.1472-4669.2012.00317.x Microbial diversity under extreme euxinia: Mahoney Lake, Canada V. KLEPAC-CERAJ,1,2 C. A. HAYES,3 W. P. GILHOOLY,4 T. W. LYONS,5 R. KOLTER2 AND A. PEARSON3 1Department of Molecular Genetics, Forsyth Institute, Cambridge, MA, USA 2Department of Microbiology and Molecular Genetics, Harvard Medical School, Boston, MA, USA 3Department of Earth and Planetary Sciences, Harvard University, Cambridge, MA, USA 4Department of Earth and Planetary Sciences, Washington University, Saint Louis, MO, USA 5Department of Earth Sciences, University of California, Riverside, CA, USA ABSTRACT Mahoney Lake, British Columbia, Canada, is a stratified, 15-m deep saline lake with a euxinic (anoxic, sulfidic) hypolimnion. A dense plate of phototrophic purple sulfur bacteria is found at the chemocline, but to date the rest of the Mahoney Lake microbial ecosystem has been underexamined. In particular, the microbial community that resides in the aphotic hypolimnion and ⁄ or in the lake sediments is unknown, and it is unclear whether the sulfate reducers that supply sulfide for phototrophy live only within, or also below, the plate. Here we profiled distribu- tions of 16S rRNA genes using gene clone libraries and PhyloChip microarrays. Both approaches suggest that microbial diversity is greatest in the hypolimnion (8 m) and sediments. Diversity is lowest in the photosynthetic plate (7 m). Shallower depths (5 m, 7 m) are rich in Actinobacteria, Alphaproteobacteria, and Gammaproteo- bacteria, while deeper depths (8 m, sediments) are rich in Crenarchaeota, Natronoanaerobium, and Verrucomi- crobia. The heterogeneous distribution of Deltaproteobacteria and Epsilonproteobacteria between 7 and 8 m is consistent with metabolisms involving sulfur intermediates in the chemocline, but complete sulfate reduction in the hypolimnion.
    [Show full text]
  • Diversity of Cultivated and Metabolically Active Aerobic Anoxygenic Phototrophic Bacteria Along an Oligotrophic Gradientthe in Mediterranean Sea C
    Discussion Paper | Discussion Paper | Discussion Paper | Discussion Paper | Biogeosciences Discuss., 8, 4421–4457, 2011 Biogeosciences www.biogeosciences-discuss.net/8/4421/2011/ Discussions doi:10.5194/bgd-8-4421-2011 © Author(s) 2011. CC Attribution 3.0 License. This discussion paper is/has been under review for the journal Biogeosciences (BG). Please refer to the corresponding final paper in BG if available. Diversity of cultivated and metabolically active aerobic anoxygenic phototrophic bacteria along an oligotrophic gradient in the Mediterranean Sea C. Jeanthon1,2, D. Boeuf1,2, O. Dahan1,2, F. Le Gall1,2, L. Garczarek1,2, E. M. Bendif1,2, and A.-C. Lehours3 1INSU-CNRS, UMR 7144, Observatoire Oceanologique´ de Roscoff, Groupe Plancton Oceanique,´ 29680 Roscoff, France 2UPMC Univ Paris 06, UMR 7144, Adaptation et Diversite´ en Milieu Marin, Station Biologique de Roscoff, 29680 Roscoff, France 3CNRS, UMR 6023, Microorganismes: Genome´ et Environnement, Universite´ Blaise Pascal, 63177 Aubiere` Cedex, France Received: 21 April 2011 – Accepted: 29 April 2011 – Published: 5 May 2011 Correspondence to: C. Jeanthon (jeanthon@sb-roscoff.fr) Published by Copernicus Publications on behalf of the European Geosciences Union. 4421 Discussion Paper | Discussion Paper | Discussion Paper | Discussion Paper | Abstract Aerobic anoxygenic phototrophic (AAP) bacteria play significant roles in the bacterio- plankton productivity and biogeochemical cycles of the surface ocean. In this study, we applied both cultivation and mRNA-based molecular methods to explore the diversity of 5 AAP bacteria along an oligotrophic gradient in the Mediterranean Sea in early summer 2008. Colony-forming units obtained on three different agar media were screened for the production of bacteriochlorophyll-a (BChl-a), the light-harvesting pigment of AAP bacteria.
    [Show full text]