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      Whole Genome Analyses Suggests that Burkholderia sensu lato Contains Two Additional Novel Genera ( Mycetohabitans gen. nov., and Trinickia gen. nov.): Implications for the Evolution of Diazotrophy and Nodulation in the Burkholderiaceae

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          Abstract

          Burkholderia sensu lato is a large and complex group, containing pathogenic, phytopathogenic, symbiotic and non-symbiotic strains from a very wide range of environmental (soil, water, plants, fungi) and clinical (animal, human) habitats. Its taxonomy has been evaluated several times through the analysis of 16S rRNA sequences, concantenated 4–7 housekeeping gene sequences, and lately by genome sequences. Currently, the division of this group into Burkholderia, Caballeronia, Paraburkholderia, and Robbsia is strongly supported by genome analysis. These new genera broadly correspond to the various habitats/lifestyles of Burkholderia s.l., e.g., all the plant beneficial and environmental (PBE) strains are included in Paraburkholderia (which also includes all the N 2-fixing legume symbionts) and Caballeronia, while most of the human and animal pathogens are retained in Burkholderia sensu stricto. However, none of these genera can accommodate two important groups of species. One of these includes the closely related Paraburkholderia rhizoxinica and Paraburkholderia endofungorum, which are both symbionts of the fungal phytopathogen Rhizopus microsporus. The second group comprises the Mimosa-nodulating bacterium Paraburkholderia symbiotica, the phytopathogen Paraburkholderia caryophylli, and the soil bacteria Burkholderia dabaoshanensis and Paraburkholderia soli. In order to clarify their positions within Burkholderia sensu lato, a phylogenomic approach based on a maximum likelihood analysis of conserved genes from more than 100 Burkholderia sensu lato species was carried out. Additionally, the average nucleotide identity (ANI) and amino acid identity (AAI) were calculated. The data strongly supported the existence of two distinct and unique clades, which in fact sustain the description of two novel genera Mycetohabitans gen. nov. and Trinickia gen. nov. The newly proposed combinations are Mycetohabitans endofungorum comb. nov., Mycetohabitans rhizoxinica comb. nov., Trinickia caryophylli comb. nov., Trinickia dabaoshanensis comb. nov., Trinickia soli comb. nov., and Trinickia symbiotica comb. nov. Given that the division between the genera that comprise Burkholderia s.l. in terms of their lifestyles is often complex, differential characteristics of the genomes of these new combinations were investigated. In addition, two important lifestyle-determining traits—diazotrophy and/or symbiotic nodulation, and pathogenesis—were analyzed in depth i.e., the phylogenetic positions of nitrogen fixation and nodulation genes in Trinickia via-à-vis other Burkholderiaceae were determined, and the possibility of pathogenesis in Mycetohabitans and Trinickia was tested by performing infection experiments on plants and the nematode Caenorhabditis elegans. It is concluded that (1) T. symbiotica nif and nod genes fit within the wider Mimosa-nodulating Burkholderiaceae but appear in separate clades and that T. caryophylli nif genes are basal to the free-living Burkholderia s.l. strains, while with regard to pathogenesis (2) none of the Mycetohabitans and Trinickia strains tested are likely to be pathogenic, except for the known phytopathogen T. caryophylli.

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            Since 2006, numerous cases of bacterial symbionts with extraordinarily small genomes have been reported. These organisms represent independent lineages from diverse bacterial groups. They have diminutive gene sets that rival some mitochondria and chloroplasts in terms of gene numbers and lack genes that are considered to be essential in other bacteria. These symbionts have numerous features in common, such as extraordinarily fast protein evolution and a high abundance of chaperones. Together, these features point to highly degenerate genomes that retain only the most essential functions, often including a considerable fraction of genes that serve the hosts. These discoveries have implications for the concept of minimal genomes, the origins of cellular organelles, and studies of symbiosis and host-associated microbiota.
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              The KEGG databases at GenomeNet.

              The Kyoto Encyclopedia of Genes and Genomes (KEGG) is the primary database resource of the Japanese GenomeNet service (http://www.genome.ad.jp/) for understanding higher order functional meanings and utilities of the cell or the organism from its genome information. KEGG consists of the PATHWAY database for the computerized knowledge on molecular interaction networks such as pathways and complexes, the GENES database for the information about genes and proteins generated by genome sequencing projects, and the LIGAND database for the information about chemical compounds and chemical reactions that are relevant to cellular processes. In addition to these three main databases, limited amounts of experimental data for microarray gene expression profiles and yeast two-hybrid systems are stored in the EXPRESSION and BRITE databases, respectively. Furthermore, a new database, named SSDB, is available for exploring the universe of all protein coding genes in the complete genomes and for identifying functional links and ortholog groups. The data objects in the KEGG databases are all represented as graphs and various computational methods are developed to detect graph features that can be related to biological functions. For example, the correlated clusters are graph similarities which can be used to predict a set of genes coding for a pathway or a complex, as summarized in the ortholog group tables, and the cliques in the SSDB graph are used to annotate genes. The KEGG databases are updated daily and made freely available (http://www.genome.ad.jp/kegg/).
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                Author and article information

                Journal
                Genes (Basel)
                Genes (Basel)
                genes
                Genes
                MDPI
                2073-4425
                01 August 2018
                August 2018
                : 9
                : 8
                : 389
                Affiliations
                [1 ]Instituto Politécnico Nacional, Escuela Nacional de Ciencias Biológicas, 11340 Cd. de Mexico, Mexico; belcha06@ 123456yahoo.com.mx
                [2 ]Department of Microbiology and Plant Pathology, Forestry and Agricultural Biotechnology Institute, University of Pretoria, Pretoria 0083, South Africa; marike.duplessis@ 123456fabi.up.ac.za (M.P.); chrizelle.beukes@ 123456fabi.up.ac.za (C.B.); emma.steenkamp@ 123456up.ac.za (E.T.S.)
                [3 ]Department of Molecular, Cell, and Developmental Biology and Molecular Biology Institute, University of California, Los Angeles, CA 90095, USA; lbriscoep81@ 123456ucla.edu (L.B.); noor.612@ 123456gmail.com (N.K.); ehumm@ 123456ucla.edu (E.H.); mnarrabit@ 123456ucla.edu (M.A.)
                [4 ]The James Hutton Institute, Dundee DD2 5DA, UK; Marta.Maluk@ 123456hutton.ac.uk (M.M.); marcel.lafos@ 123456hutton.ac.uk (M.L.)
                [5 ]450G Tracy Hall Science Building, Weber State University, Ogden, 84403 UT, USA; matthewcrook@ 123456weber.edu
                [6 ]Center for Electron Microscopy, Department of Agricultural and Environmental Sciences, Santa Cruz State University, 45662-900 Ilheus, BA, Brazil; egross@ 123456uesc.br
                [7 ]Embrapa CENARGEN, 70770-917 Brasilia, Distrito Federal, Brazil; marcelo.simon@ 123456embrapa.br
                [8 ]Embrapa Cerrados, 73310-970 Planaltina, Distrito Federal, Brazil; fabio.reis@ 123456embrapa.br
                [9 ]Department of Microbiology, University of Georgia, Athens, GA 30602, USA; whitman@ 123456uga.edu
                [10 ]DOE Joint Genome Institute, Walnut Creek, CA 94598, USA; nrshapiro@ 123456lbl.gov
                [11 ]Department of Plant Sciences, University of Oxford, South Parks Road, Oxford OX1 3RB, UK; philip.poole@ 123456plants.ox.ac.uk
                Author notes
                [* ]Correspondence: pestradadelossantos@ 123456gmail.com (P.E.-d.l.S.); ahirsch@ 123456ucla.edu (A.M.H.); fanus.venter@ 123456fabi.up.ac.za (S.N.V.); euan.james@ 123456hutton.ac.uk (E.K.J.); Tel.: +44-1382-568873 (E.K.J.)
                [†]

                These authors made an equal contribution.

                Author information
                https://orcid.org/0000-0003-2407-0284
                https://orcid.org/0000-0001-7975-2907
                https://orcid.org/0000-0002-1057-0432
                https://orcid.org/0000-0002-9633-1538
                https://orcid.org/0000-0002-5726-4918
                https://orcid.org/0000-0001-7969-6570
                Article
                genes-09-00389
                10.3390/genes9080389
                6116057
                30071618
                017d08af-2e9e-4529-b2fa-37e47414cc46
                © 2018 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 24 May 2018
                : 24 July 2018
                Categories
                Article

                burkholderia,paraburkholderia,caballeronia,robbsia,mimosa,rhizopus,symbionts,diazotrophy,root nodulation

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