Tolumonas Auensis Type Strain (TA 4T)
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CUED Phd and Mphil Thesis Classes
High-throughput Experimental and Computational Studies of Bacterial Evolution Lars Barquist Queens' College University of Cambridge A thesis submitted for the degree of Doctor of Philosophy 23 August 2013 Arrakis teaches the attitude of the knife { chopping off what's incomplete and saying: \Now it's complete because it's ended here." Collected Sayings of Muad'dib Declaration High-throughput Experimental and Computational Studies of Bacterial Evolution The work presented in this dissertation was carried out at the Wellcome Trust Sanger Institute between October 2009 and August 2013. This dissertation is the result of my own work and includes nothing which is the outcome of work done in collaboration except where specifically indicated in the text. This dissertation does not exceed the limit of 60,000 words as specified by the Faculty of Biology Degree Committee. This dissertation has been typeset in 12pt Computer Modern font using LATEX according to the specifications set by the Board of Graduate Studies and the Faculty of Biology Degree Committee. No part of this dissertation or anything substantially similar has been or is being submitted for any other qualification at any other university. Acknowledgements I have been tremendously fortunate to spend the past four years on the Wellcome Trust Genome Campus at the Sanger Institute and the European Bioinformatics Institute. I would like to thank foremost my main collaborators on the studies described in this thesis: Paul Gardner and Gemma Langridge. Their contributions and support have been invaluable. I would also like to thank my supervisor, Alex Bateman, for giving me the freedom to pursue a wide range of projects during my time in his group and for advice. -
An Update on the Genus Aeromonas: Taxonomy, Epidemiology, and Pathogenicity
microorganisms Review An Update on the Genus Aeromonas: Taxonomy, Epidemiology, and Pathogenicity Ana Fernández-Bravo and Maria José Figueras * Unit of Microbiology, Department of Basic Health Sciences, Faculty of Medicine and Health Sciences, IISPV, University Rovira i Virgili, 43201 Reus, Spain; [email protected] * Correspondence: mariajose.fi[email protected]; Tel.: +34-97-775-9321; Fax: +34-97-775-9322 Received: 31 October 2019; Accepted: 14 January 2020; Published: 17 January 2020 Abstract: The genus Aeromonas belongs to the Aeromonadaceae family and comprises a group of Gram-negative bacteria widely distributed in aquatic environments, with some species able to cause disease in humans, fish, and other aquatic animals. However, bacteria of this genus are isolated from many other habitats, environments, and food products. The taxonomy of this genus is complex when phenotypic identification methods are used because such methods might not correctly identify all the species. On the other hand, molecular methods have proven very reliable, such as using the sequences of concatenated housekeeping genes like gyrB and rpoD or comparing the genomes with the type strains using a genomic index, such as the average nucleotide identity (ANI) or in silico DNA–DNA hybridization (isDDH). So far, 36 species have been described in the genus Aeromonas of which at least 19 are considered emerging pathogens to humans, causing a broad spectrum of infections. Having said that, when classifying 1852 strains that have been reported in various recent clinical cases, 95.4% were identified as only four species: Aeromonas caviae (37.26%), Aeromonas dhakensis (23.49%), Aeromonas veronii (21.54%), and Aeromonas hydrophila (13.07%). -
Comparative Pathogenomics of Aeromonas Veronii from Pigs in South Africa: Dominance of the Novel ST657 Clone
microorganisms Article Comparative Pathogenomics of Aeromonas veronii from Pigs in South Africa: Dominance of the Novel ST657 Clone Yogandree Ramsamy 1,2,3,* , Koleka P. Mlisana 2, Daniel G. Amoako 3 , Akebe Luther King Abia 3 , Mushal Allam 4 , Arshad Ismail 4 , Ravesh Singh 1,2 and Sabiha Y. Essack 3 1 Medical Microbiology, College of Health Sciences, University of KwaZulu-Natal, Durban 4000, South Africa; [email protected] 2 National Health Laboratory Service, Durban 4001, South Africa; [email protected] 3 Antimicrobial Research Unit, College of Health Sciences, University of KwaZulu-Natal, Durban 4000, South Africa; [email protected] (D.G.A.); [email protected] (A.L.K.A.); [email protected] (S.Y.E.) 4 Sequencing Core Facility, National Institute for Communicable Diseases, National Health Laboratory Service, Johannesburg 2131, South Africa; [email protected] (M.A.); [email protected] (A.I.) * Correspondence: [email protected] Received: 9 November 2020; Accepted: 15 December 2020; Published: 16 December 2020 Abstract: The pathogenomics of carbapenem-resistant Aeromonas veronii (A. veronii) isolates recovered from pigs in KwaZulu-Natal, South Africa, was explored by whole genome sequencing on the Illumina MiSeq platform. Genomic functional annotation revealed a vast array of similar central networks (metabolic, cellular, and biochemical). The pan-genome analysis showed that the isolates formed a total of 4349 orthologous gene clusters, 4296 of which were shared; no unique clusters were observed. All the isolates had similar resistance phenotypes, which corroborated their chromosomally mediated resistome (blaCPHA3 and blaOXA-12) and belonged to a novel sequence type, ST657 (a satellite clone). -
Anaerobic Consumers of Monosaccharides in a Moderately Acidic Fenᰔ† Alexandra Hamberger,1 Marcus A
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, May 2008, p. 3112–3120 Vol. 74, No. 10 0099-2240/08/$08.00ϩ0 doi:10.1128/AEM.00193-08 Copyright © 2008, American Society for Microbiology. All Rights Reserved. Anaerobic Consumers of Monosaccharides in a Moderately Acidic Fenᰔ† Alexandra Hamberger,1 Marcus A. Horn,1* Marc G. Dumont,2 J. Colin Murrell,2 and Harold L. Drake1 Department of Ecological Microbiology, University of Bayreuth, 95445 Bayreuth, Germany,1 and Department of Biological Sciences, University of Warwick, Coventry CV4 7AL, United Kingdom2 Received 22 January 2008/Accepted 20 March 2008 16S rRNA-based stable isotope probing identified active xylose- and glucose-fermenting Bacteria and active Archaea, including methanogens, in anoxic slurries of material obtained from a moderately acidic, CH4- emitting fen. Xylose and glucose were converted to fatty acids, CO2,H2, and CH4 under moderately acidic, anoxic conditions, indicating that the fen harbors moderately acid-tolerant xylose- and glucose-using fermen- ters, as well as moderately acid-tolerant methanogens. Organisms of the families Acidaminococcaceae, Aero- monadaceae, Clostridiaceae, Enterobacteriaceae, and Pseudomonadaceae and the order Actinomycetales, including hitherto unknown organisms, utilized xylose- or glucose-derived carbon, suggesting that highly diverse facul- tative aerobes and obligate anaerobes contribute to the flow of carbon in the fen under anoxic conditions. Uncultured Euryarchaeota (i.e., Methanosarcinaceae and Methanobacteriaceae) and Crenarchaeota species were -
Genome Sequence and Description of the Anaerobic Lignin-Degrading Bacterium Tolumonas Lignolytica Sp
Lawrence Berkeley National Laboratory Recent Work Title Genome sequence and description of the anaerobic lignin-degrading bacterium Tolumonas lignolytica sp. nov. Permalink https://escholarship.org/uc/item/03j0f0k8 Journal Standards in genomic sciences, 10(1) ISSN 1944-3277 Authors Billings, Andrew F Fortney, Julian L Hazen, Terry C et al. Publication Date 2015 DOI 10.1186/s40793-015-0100-3 Peer reviewed eScholarship.org Powered by the California Digital Library University of California Billings et al. Standards in Genomic Sciences (2015) 10:106 DOI 10.1186/s40793-015-0100-3 EXTENDED GENOME REPORT Open Access Genome sequence and description of the anaerobic lignin-degrading bacterium Tolumonas lignolytica sp. nov. Andrew F. Billings1, Julian L. Fortney2,3, Terry C. Hazen3,4,5, Blake Simmons2,6, Karen W. Davenport7, Lynne Goodwin7, Natalia Ivanova8, Nikos C. Kyrpides8, Konstantinos Mavromatis8, Tanja Woyke8 and Kristen M. DeAngelis1* Abstract Tolumonas lignolytica BRL6-1T sp. nov. is the type strain of T. lignolytica sp. nov., a proposed novel species of the Tolumonas genus. This strain was isolated from tropical rainforest soils based on its ability to utilize lignin as a sole carbon source. Cells of Tolumonas lignolytica BRL6-1T are mesophilic, non-spore forming, Gram-negative rods that are oxidase and catalase negative. The genome for this isolate was sequenced and returned in seven unique contigs totaling 3.6Mbp, enabling the characterization of several putative pathways for lignin breakdown. Particularly, we found an extracellular peroxidase involved in lignin depolymerization, as well as several enzymes involved in β-aryl ether bond cleavage, which is the most abundant linkage between lignin monomers. -
Microbial Communities Mediating Algal Detritus Turnover Under Anaerobic Conditions
Microbial communities mediating algal detritus turnover under anaerobic conditions Jessica M. Morrison1,*, Chelsea L. Murphy1,*, Kristina Baker1, Richard M. Zamor2, Steve J. Nikolai2, Shawn Wilder3, Mostafa S. Elshahed1 and Noha H. Youssef1 1 Department of Microbiology and Molecular Genetics, Oklahoma State University, Stillwater, OK, USA 2 Grand River Dam Authority, Vinita, OK, USA 3 Department of Integrative Biology, Oklahoma State University, Stillwater, OK, USA * These authors contributed equally to this work. ABSTRACT Background. Algae encompass a wide array of photosynthetic organisms that are ubiquitously distributed in aquatic and terrestrial habitats. Algal species often bloom in aquatic ecosystems, providing a significant autochthonous carbon input to the deeper anoxic layers in stratified water bodies. In addition, various algal species have been touted as promising candidates for anaerobic biogas production from biomass. Surprisingly, in spite of its ecological and economic relevance, the microbial community involved in algal detritus turnover under anaerobic conditions remains largely unexplored. Results. Here, we characterized the microbial communities mediating the degradation of Chlorella vulgaris (Chlorophyta), Chara sp. strain IWP1 (Charophyceae), and kelp Ascophyllum nodosum (phylum Phaeophyceae), using sediments from an anaerobic spring (Zodlteone spring, OK; ZDT), sludge from a secondary digester in a local wastewater treatment plant (Stillwater, OK; WWT), and deeper anoxic layers from a seasonally stratified lake -
Microbial Degradation of Organic Micropollutants in Hyporheic Zone Sediments
Microbial degradation of organic micropollutants in hyporheic zone sediments Dissertation To obtain the Academic Degree Doctor rerum naturalium (Dr. rer. nat.) Submitted to the Faculty of Biology, Chemistry, and Geosciences of the University of Bayreuth by Cyrus Rutere Bayreuth, May 2020 This doctoral thesis was prepared at the Department of Ecological Microbiology – University of Bayreuth and AG Horn – Institute of Microbiology, Leibniz University Hannover, from August 2015 until April 2020, and was supervised by Prof. Dr. Marcus. A. Horn. This is a full reprint of the dissertation submitted to obtain the academic degree of Doctor of Natural Sciences (Dr. rer. nat.) and approved by the Faculty of Biology, Chemistry, and Geosciences of the University of Bayreuth. Date of submission: 11. May 2020 Date of defense: 23. July 2020 Acting dean: Prof. Dr. Matthias Breuning Doctoral committee: Prof. Dr. Marcus. A. Horn (reviewer) Prof. Harold L. Drake, PhD (reviewer) Prof. Dr. Gerhard Rambold (chairman) Prof. Dr. Stefan Peiffer In the battle between the stream and the rock, the stream always wins, not through strength but by perseverance. Harriett Jackson Brown Jr. CONTENTS CONTENTS CONTENTS ............................................................................................................................ i FIGURES.............................................................................................................................. vi TABLES .............................................................................................................................. -
Caracterización De Bacterias Aeromonadales Móviles Aisladas De Peces Cultivados En Uruguay
UNIVERSIDAD DE LA REPÚBLICA FACULTAD DE VETERINARIA Programa de Posgrados CARACTERIZACIÓN DE BACTERIAS AEROMONADALES MÓVILES AISLADAS DE PECES CULTIVADOS EN URUGUAY Alejandro Perretta TESIS DE MAESTRÍA EN SALUD ANIMAL URUGUAY 2016 i ii iii UNIVERSIDAD DE LA REPÚBLICA FACULTAD DE VETERINARIA Programa de Posgrados CARACTERIZACIÓN DE BACTERIAS AEROMONADALES MÓVILES AISLADAS DE PECES CULTIVADOS EN URUGUAY Alejandro Perretta _________________________ _________________________ Dr. Pablo Zunino Dra. Karina Antúnez Director de Tesis Codirectora de Tesis 2016 iv INTEGRACIÓN DEL TRIBUNAL DE DEFENSA DE TESIS Claudia Piccini; MS, PhD Departamento de Microbiología Instituto de Investigaciones Biológicas "Clemente Estable"- Ministerio de Educación y Cultura - Uruguay Laura Bentancor; MS, PhD Departamento de Bacteriología y Virología Instituto de Higiene - Facultad de Medicina Universidad de la República - Uruguay Martín Fraga; MS, PhD Plataforma de Salud Animal Instituto de Investigaciones Agropecuarias - Uruguay 2016 v vi vii DEDICATORIA …para Federíco, Anaclara y Valeria viii AGRADECIMIENTOS - A Pablo Zunino y Karina Antúnez, gracias por compartir el conocimiento conmigo, abrirme las puertas del IIBCE para poder llevar a cabo este trabajando y por la paciencia y el apoyo en todo momento. - A Daniel Carnevia por el apoyo contínuo y la colaboración brindada en cada uno de mis emprendimientos. - A todo el personal docente y no docente del Instituto de Investigaciones Pesqueras de la Facultad de Veterinaria por tantos años de apoyo y colaboración. - A Belén Branchiccela y todo el personal del Departamento de Microbiología del IIBCE por el apoyo y la colaboración en todas las tareas llevadas a cabo allí. - A Rodrigo Puentes, Uruguaysito Benavides y todo el personal del Área Inmunología de la Facultad de Veterinaria por la colaboración con las taréas de biología molecular llevadas a cabo. -
Isolation, Identification and Phylogenetic Analysis of a Pathogen of Haliotis Diversicolor Supertexta (L.) with Mass Mortalities
Isolation, identification and phylogenetic analysis of a pathogen of Haliotis diversicolor supertexta (L.) with mass mortalities Item Type article Authors Zhou, Jing; Cai, Junpeng Download date 29/09/2021 14:57:43 Link to Item http://hdl.handle.net/1834/37408 Iranian Journal of fisheries Sciences 12(4)843-854 2013 Isolation, identification and phylogenetic analysis of a pathogen of Haliotis diversicolor supertexta (L.) with mass mortalities Zhou Jing*1and Cai Junpeng 2 Received: February2013 Accepted: Abstract This study was conducted to determine a disease outbreak in 14 day old post-larvae of abalone ( Haliotis diversicolor supertexta ) which caused mass mortality in July 2010 in Shanwei, China. Twenty-nine bacterial strains were isolated from a sample pool of 10 diseased post-larval abalones on 2216E marine agar plates during a natural outbreak of the disease. Among them, a dominant isolate (referred to as strain 21) was found to be highly 4 virulent to post-larvae in experimental challenge tests, with an LD 50 value of 1.0 ×10 colony forming units (CFU) mL -1 on day 3. API 20NE kits and 16S rDNA sequence analysis, identified strain 21 as Oceanomonas doudoroffii. It was susceptible to 10 and Downloaded from jifro.ir at 16:31 +0330 on Saturday February 17th 2018 moderately susceptible to 1 of the 16 antibiotics examined when antibiotic sensitivities of the bacterium were assayed. Results of this study implicated Oceanomonas doudoroffii strain 21 as a cause of mortalities in post-larval abalone from Shanwei, China. Keywords : Haliotis -
A Report of 37 Unrecorded Anaerobic Bacterial Species Isolated from the Geum River in South Korea
Journal of Species Research 9(2):105-116, 2020 A report of 37 unrecorded anaerobic bacterial species isolated from the Geum River in South Korea Changsu Lee, Joon Yong Kim, Yeon Bee Kim, Juseok Kim, Seung Woo Ahn, Hye Seon Song and Seong Woon Roh* Microbiology and Functionality Research Group, World Institute of Kimchi, Gwangju 61755, Republic of Korea *Correspondent: [email protected] A total of 37 anaerobic bacteria strains within the classes Alphaproteobacteria, Betaproteobacteria, Gammaproteobacteria, Bacteroidia, Flavobacteriia, Bacilli, Clostridia, and Fusobacteriia were isolated from freshwater and sediment of the Geum River in Korea. The unreported species were related with Rhizobium and Oleomonas of the class Alphaproteobacteria; Acidovorax, Pseudogulbenkiania, and Aromatoleum of the class Betaproteobacteria; Tolumonas, Aeromonas, Cronobacter, Lonsdalea, and Phytobacter of the class Gammaproteobacteria; Bacteroides, Dysgonomonas, Macellibacteroides, and Parabacteroides of the class Bacteroidia; Flavobacterium of the class Flavobacteriia; Bacillus and Paenibacillus of the class Bacilli; Clostridium, Clostridioides, Paraclostridium, Romboutsia, Sporacetigenium, and Terrisporobacter of the class Clostridia; and Cetobacterium and Ilyobacter of the class Fusobacteriia. A total of 37 strains, with >98.7% 16S rRNA gene sequence similarity with validly published bacterial species, but not reported in Korea, were determined to be unrecorded anaerobic bacterial species in Korea. Keywords: 16S rRNA, anaerobic bacteria, bacterial diversity, taxonomy, unrecorded species Ⓒ 2020 National Institute of Biological Resources DOI:10.12651/JSR.2020.9.2.105 INTRODUCTION lated culture in Korea. In the present study, we attempted to isolate anaerobic Since the Nagoya Protocol and the Convention on Bi- microorganisms from freshwater and sediment in the ological Diversity, securing and managing of biological Geum River of Korea. -
Comparison of Bacterial Diversity from Solar Salterns and a Simulated Laboratory Study
Ann Microbiol (2015) 65:995–1005 DOI 10.1007/s13213-014-0944-6 ORIGINAL ARTICLE Comparison of bacterial diversity from solar salterns and a simulated laboratory study Kabilan Mani & Sivaraman Chandrasekaran & Bhakti B. Salgaonkar & Srikanth Mutnuri & Judith M. Bragança Received: 8 January 2014 /Accepted: 14 July 2014 /Published online: 2 August 2014 # Springer-Verlag Berlin Heidelberg and the University of Milan 2014 Abstract Bacterial diversity in solar salterns and a simulated Introduction solar saltern under laboratory conditions was studied. The two systems were compared at the pre-salt harvesting phase and Hypersaline environments like salt lakes and solar salterns are salt harvesting phase using Denaturing Gradient Gel Electro- extreme ecosystems in which the change in salinity is the phoresis (DGGE). Bacterial composition was dominated by dictating factor which determines microbial diversity at any Gammaproteobacteria and more specifically with members of given point of time (Rodríguez-Valera et al. 1985). Prokary- Alteromonas, Vibrio, Pseudomonas, Tolumonas, otic diversity in any ecosystem is an important factor to be Marinobacter, Pseudoalteromonas and novel uncultured bac- considered because of its role in nutrient turnover, element teria. The Shannon–Weaver index (H), Simpson diversity recycling and as a potential hub for recovery of microorgan- index (D) and Equitability index (E) values showed that isms for industrially important metabolic products (Garcia- salterns can support a wide range of microbes during the Martinez et al. 1999; Lorenz and Eck 2005). Solar salterns pre-salt harvesting phase (3–4 % salinity) when compared to serve as a good model for studying the changes in biodiversity the salt harvesting phase (21–29 % salinity). -
Identification of the Potential Role of the Rumen Microbiome in Milk
animals Article Identification of the Potential Role of the Rumen Microbiome in Milk Protein and Fat Synthesis in Dairy Cows Using Metagenomic Sequencing Xin Wu 1, Shuai Huang 2, Jinfeng Huang 1, Peng Peng 1, Yanan Liu 1, Bo Han 1 and Dongxiao Sun 1,* 1 National Engineering Laboratory for Animal Breeding, Key Laboratory of Animal Genetics, Breeding and Reproduction of Ministry of Agriculture and Rural Affairs, Department of Animal Genetics, Breeding and Reproduction, College of Animal Science and Technology, China Agricultural University, Beijing 100193, China; [email protected] (X.W.); [email protected] (J.H.); [email protected] (P.P.); [email protected] (Y.L.); [email protected] (B.H.) 2 State Key Laboratory of Animal Nutrition, Beijing Engineering Technology Research Center of Raw Milk Quality and Safety Control, College of Animal Science and Technology, China Agricultural University, Beijing 100193, China; [email protected] * Correspondence: [email protected] Simple Summary: The rumen is the main digestive and absorption organ of dairy cows. It contains abundant microorganisms and can effectively use human-indigestible plant mass. Therefore, we used metagenomics to explore the role of rumen microbes in the regulation of milk protein and fat in dairy cows. This study showed that Prevotella species and Neocallimastix californiae in the rumen of cows are related to the synthesis of milk components due to their important functions in carbohydrate, amino acid, pyruvate, insulin, and lipid metabolism and transportation metabolic pathways. Citation: Wu, X.; Huang, S.; Huang, Abstract: The rumen contains abundant microorganisms that aid in the digestion of lignocellulosic J.; Peng, P.; Liu, Y.; Han, B.; Sun, D.