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      Genome analysis of two novel Pseudomonas strains exhibiting differential hypersensitivity reactions on tobacco seedlings reveals differences in nonflagellar T3SS organization and predicted effector proteins

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          Abstract

          Multilocus sequence analysis ( MLSA) of two new biological control strains (S1E40 and S3E12) of Pseudomonas was performed to assess their taxonomic position relative to close lineages, and comparative genomics employed to investigate whether these strains differ in key genetic features involved in hypersensitivity responses ( HRs). Strain S3E12, at high concentration, incites HRs on tobacco and corn plantlets while S1E40 does not. Phylogenies based on individual genes and 16S rRNAgyrB‐ rpoB‐ rpoD concatenated sequence data show strains S1E40 and S3E12 clustering in distinct groups. Strain S3E12 consistently clustered with Pseudomonas marginalis, a bacterium causing soft rots on plant tissues. MLSA data suggest that strains S1E40 and S3E12 are novel genotypes. This is consistent with the data of genome‐based DNADNA homology values that are below the proposed cutoff species boundary. Comparative genomics analysis of the two strains revealed major differences in the type III secretion systems (T3 SS) as well as the predicted T3 SS secreted effector proteins (T3Es). One nonflagellar ( NF‐T3 SS) and two flagellar T3 SSs (F‐T3 SS) clusters were identified in both strains. While F‐T3 SS clusters in both strains were relatively conserved, the NF‐T3 SS clusters differed in the number of core components present. The predicted T3Es also differed in the type and number of CDSs with both strains having unique predicted protease‐related effectors. In addition, the T1 SS organization of the S3E12 genome has protein‐coding sequences ( CDSs) encoding for key factors such as T1 SS secreted agglutinin repeats‐toxins (a group of cytolysins and cytotoxins), a membrane fusion protein (LapC), a T1 SS ATPase of LssB family (LapB), and T1 SS‐associated transglutaminase‐like cysteine proteinase (LapP). In contrast, strain S1E40 has all CDSs for the seven‐gene operon ( pelA‐ pelG) required for Pel biosynthesis but not S3E12, suggesting that biofilm formation in these strains is modulated differently. The data presented here provide an insight of the genome organization of these two phytobacterial strains.

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          Major facilitator superfamily.

          The major facilitator superfamily (MFS) is one of the two largest families of membrane transporters found on Earth. It is present ubiquitously in bacteria, archaea, and eukarya and includes members that can function by solute uniport, solute/cation symport, solute/cation antiport and/or solute/solute antiport with inwardly and/or outwardly directed polarity. All homologous MFS protein sequences in the public databases as of January 1997 were identified on the basis of sequence similarity and shown to be homologous. Phylogenetic analyses revealed the occurrence of 17 distinct families within the MFS, each of which generally transports a single class of compounds. Compounds transported by MFS permeases include simple sugars, oligosaccharides, inositols, drugs, amino acids, nucleosides, organophosphate esters, Krebs cycle metabolites, and a large variety of organic and inorganic anions and cations. Protein members of some MFS families are found exclusively in bacteria or in eukaryotes, but others are found in bacteria, archaea, and eukaryotes. All permeases of the MFS possess either 12 or 14 putative or established transmembrane alpha-helical spanners, and evidence is presented substantiating the proposal that an internal tandem gene duplication event gave rise to a primordial MFS protein prior to divergence of the family members. All 17 families are shown to exhibit the common feature of a well-conserved motif present between transmembrane spanners 2 and 3. The analyses reported serve to characterize one of the largest and most diverse families of transport proteins found in living organisms.
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            genoPlotR: comparative gene and genome visualization in R

            Summary: The amount of gene and genome data obtained by next-generation sequencing technologies generates a need for comparative visualization tools. Complementing existing software for comparison and exploration of genomics data, genoPlotR automatically creates publication-grade linear maps of gene and genomes, in a highly automatic, flexible and reproducible way. Availability: genoPlotR is a platform-independent R package, available with full source code under a GPL2 license at R-Forge: http://genoplotr.r-forge.r-project.org/ Contact: lionel.guy@ebc.uu.se
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              GenBank

              GenBank® is a comprehensive database that contains publicly available nucleotide sequences for more than 380 000 organisms named at the genus level or lower, obtained primarily through submissions from individual laboratories and batch submissions from large-scale sequencing projects, including whole genome shotgun (WGS) and environmental sampling projects. Most submissions are made using the web-based BankIt or standalone Sequin programs, and accession numbers are assigned by GenBank staff upon receipt. Daily data exchange with the European Nucleotide Archive (ENA) and the DNA Data Bank of Japan (DDBJ) ensures worldwide coverage. GenBank is accessible through the NCBI Entrez retrieval system that integrates data from the major DNA and protein sequence databases along with taxonomy, genome, mapping, protein structure and domain information, and the biomedical journal literature via PubMed. BLAST provides sequence similarity searches of GenBank and other sequence databases. Complete bimonthly releases and daily updates of the GenBank database are available by FTP. To access GenBank and its related retrieval and analysis services, begin at the NCBI Homepage: www.ncbi.nlm.nih.gov.
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                Author and article information

                Contributors
                james.tambong@agr.gc.ca
                Journal
                Microbiologyopen
                Microbiologyopen
                10.1002/(ISSN)2045-8827
                MBO3
                MicrobiologyOpen
                John Wiley and Sons Inc. (Hoboken )
                2045-8827
                21 February 2018
                April 2018
                : 7
                : 2 ( doiID: 10.1002/mbo3.2018.7.issue-2 )
                : e00553
                Affiliations
                [ 1 ] Ottawa Research and Development Centre Ottawa ON Canada
                [ 2 ] Institut des sciences de santé et de la vie Collège La Cité Ottawa ON Canada
                Author notes
                [*] [* ] Correspondence

                James T. Tambong,

                Ottawa Research and Development Centre, Ottawa, ON, Canada.

                Email: james.tambong@ 123456agr.gc.ca

                Author information
                http://orcid.org/0000-0001-5325-8038
                Article
                MBO3553
                10.1002/mbo3.553
                5911992
                29464939
                329939ad-fa0a-4120-9db0-7b7b9b5b9a0f
                © 2017 The Authors. MicrobiologyOpen published by John Wiley & Sons Ltd.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 17 February 2017
                : 17 July 2017
                : 18 July 2017
                Page count
                Figures: 6, Tables: 2, Pages: 13, Words: 10092
                Funding
                Funded by: Agriculture and Agri‐Food Canada
                Funded by: Manitoba Corn Growers Association
                Categories
                Original Research
                Original Research
                Custom metadata
                2.0
                mbo3553
                April 2018
                Converter:WILEY_ML3GV2_TO_NLMPMC version:version=5.3.4 mode:remove_FC converted:23.04.2018

                Microbiology & Virology
                digital dna‐dna hybridization,genome sequencing,mummer average nucleotide identity,pseudomonas,t1ss,t3ss

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