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      Characterization and complete genome analysis of the surfactin-producing, plant-protecting bacterium Bacillus velezensis 9D-6

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          Abstract

          Background

          Bacillus velezensis is an endospore-forming, free-living soil bacterium with potential as a biopesticide against a broad spectrum of microbial pathogens of plants. Its potential for commercial development is enhanced by rapid replication and resistance to adverse environmental conditions, typical of Bacillus species. However, the use of beneficial microbes against phytopathogens has not gained dominance due to limitations that may be overcome with new biopesticidal strains and/or new biological knowledge.

          Results

          Here, we isolated B. velezensis strain 9D-6 and showed that it inhibits the in vitro growth of prokaryotic and eukaryotic pathogens, including the bacteria Bacillus cereus , Clavibacter michiganensis, Pantoea agglomerans, Ralstonia solanacearum, Xanthomonas campestris, and Xanthomonas euvesicatoria; and the fungi Alternaria solani, Cochliobolus carbonum, Fusarium oxysporum, Fusarium solani, Gibberella pulicaris, Gibberella zeae, Monilinia fructicola, Pyrenochaeta terrestris and Rhizoctonia solani. Antimicrobial compounds with activity against Clavibacter michiganensis were isolated from B. velezensis 9D-6 and characterized by high resolution LC-MS/MS, yielding formulae of C 52H 91N 7O 13 and C 53H 93N 7O 13, which correspond to [Leu 7] surfactins C 14 and C 15 (also called surfactin B and surfactin C), respectively. We further sequenced the B. velezensis 9D-6 genome which consists of a single circular chromosome and revealed 13 gene clusters expected to participate in antimicrobial metabolite production, including surfactin and two metabolites that have not typically been found in this species - ladderane and lantipeptide. Despite being unable to inhibit the growth of Pseudomonas syringae DC3000 in an in vitro plate assay, B. velezensis 9D-6 significantly reduced root colonization by DC3000, suggesting that 9D-6 uses methods other than antimicrobials to control phytopathogens in the environment. Finally, using in silico DNA-DNA hybridization ( isDDH), we confirm previous findings that many strains currently classified as B. amyloliquefaciens are actually B. velezensis.

          Conclusions

          The data presented here suggest B. velezensis 9D-6 as a candidate plant growth promoting bacterium (PGPB) and biopesticide, which uses a unique complement of antimicrobials, as well as other mechanisms, to protect plants against phytopathogens. Our results may contribute to future utilization of this strain, and will contribute to a knowledge base that will help to advance the field of microbial biocontrol.

          Electronic supplementary material

          The online version of this article (10.1186/s12866-018-1380-8) contains supplementary material, which is available to authorized users.

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          Most cited references41

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          Probiotic bacteria as biological control agents in aquaculture.

          There is an urgent need in aquaculture to develop microbial control strategies, since disease outbreaks are recognized as important constraints to aquaculture production and trade and since the development of antibiotic resistance has become a matter of growing concern. One of the alternatives to antimicrobials in disease control could be the use of probiotic bacteria as microbial control agents. This review describes the state of the art of probiotic research in the culture of fish, crustaceans, mollusks, and live food, with an evaluation of the results obtained so far. A new definition of probiotics, also applicable to aquatic environments, is proposed, and a detailed description is given of their possible modes of action, i.e., production of compounds that are inhibitory toward pathogens, competition with harmful microorganisms for nutrients and energy, competition with deleterious species for adhesion sites, enhancement of the immune response of the animal, improvement of water quality, and interaction with phytoplankton. A rationale is proposed for the multistep and multidisciplinary process required for the development of effective and safe probiotics for commercial application in aquaculture. Finally, directions for further research are discussed.
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            Insights into secondary metabolism from a global analysis of prokaryotic biosynthetic gene clusters.

            Although biosynthetic gene clusters (BGCs) have been discovered for hundreds of bacterial metabolites, our knowledge of their diversity remains limited. Here, we used a novel algorithm to systematically identify BGCs in the extensive extant microbial sequencing data. Network analysis of the predicted BGCs revealed large gene cluster families, the vast majority uncharacterized. We experimentally characterized the most prominent family, consisting of two subfamilies of hundreds of BGCs distributed throughout the Proteobacteria; their products are aryl polyenes, lipids with an aryl head group conjugated to a polyene tail. We identified a distant relationship to a third subfamily of aryl polyene BGCs, and together the three subfamilies represent the largest known family of biosynthetic gene clusters, with more than 1,000 members. Although these clusters are widely divergent in sequence, their small molecule products are remarkably conserved, indicating for the first time the important roles these compounds play in Gram-negative cell biology. Copyright © 2014 Elsevier Inc. All rights reserved.
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              DNASTAR's Lasergene sequence analysis software.

              Lasergene's eight modules provide tools that enable users to accomplish each step of sequence analysis, from trimming and assembly of sequence data, to gene discovery, annotation, gene product analysis, sequence similarity searches, sequence alignment, phylogenetic analysis, oligonucleotide primer design, cloning strategies, and publication of the results. The Lasergene software suite provides the functions and customization tools needed so that users can perform analyses the software writers never imagined.
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                Author and article information

                Contributors
                egrady@uwo.ca
                jmacdon2@uwo.ca
                mho246@uwo.ca
                brian.weselowski@agr.gc.ca
                tim.mcdowell@agr.gc.ca
                osolomon@uwo.ca
                justin.renaud@agr.gc.ca
                001-519-953-6641 , zyuan27@uwo.ca , yuanz@agr.gc.ca
                Journal
                BMC Microbiol
                BMC Microbiol
                BMC Microbiology
                BioMed Central (London )
                1471-2180
                8 January 2019
                8 January 2019
                2019
                : 19
                : 5
                Affiliations
                [1 ]ISNI 0000 0004 1936 8884, GRID grid.39381.30, Department of Microbiology & Immunology, Schulich School of Medicine & Dentistry, , Dental Science Building Rm. 3014, University of Western Ontario, ; London, ON N6A 5C1 Canada
                [2 ]ISNI 0000 0001 1302 4958, GRID grid.55614.33, London Research and Development Centre, , Agriculture & Agri-Food Canada, ; 1391 Sandford Street, London, ON N5V 4T3 Canada
                Author information
                http://orcid.org/0000-0002-2685-1669
                Article
                1380
                10.1186/s12866-018-1380-8
                6325804
                30621587
                b1109b17-85c6-483f-9035-7c7f29094119
                © The Author(s). 2019

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 21 August 2018
                : 25 December 2018
                Funding
                Funded by: Agriculture & Agri-Food Canada
                Award ID: Growing Forward-II [project J‐001332 and project J‐001589]
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100000038, Natural Sciences and Engineering Research Council of Canada;
                Award ID: Discovery grant RGPIN‐2015‐06052
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100004489, Mitacs;
                Award ID: Mitacs-Accelerate [Fund IT07941-Yuan_OGVG]
                Award Recipient :
                Categories
                Research Article
                Custom metadata
                © The Author(s) 2019

                Microbiology & Virology
                antibacterial,antifungal,genome sequencing,induced systemic resistance (isr),plant-microbe interactions,secondary metabolites

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