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      Bradyrhizobium septentrionale sp. nov. (sv. septentrionale) and Bradyrhizobium quebecense sp. nov. (sv. septentrionale) associated with legumes native to Canada possess rearranged symbiosis genes and numerous insertion sequences

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          Abstract

          Six bacterial strains isolated from root nodules of soybean plants that had been inoculated with root-zone soil of legumes native to Canada were previously characterized and 1) placed in two novel lineages within the genus Bradyrhizobium and 2) assigned to symbiovar septentrionale. Here we verified the taxonomic status of these strains using genomic and phenotypic analyses. Phylogenetic analyses of five protein encoding partial gene sequences as well as 52 full length ribosome protein subunit gene sequences confirmed placement of the novel strains in two highly supported lineages distinct from named Bradyrhizobium species. The highest average nucleotide identity values of strains representing these two lineages relative to type strains of closest relatives were 90.7 and 92.3% which is well below the threshold value for bacterial species circumscription. The genomes of representative strains 1S1 T, 162S2 and 66S1MB T have sizes of 10598256, 10733150 and 9032145 bp with DNA G+C contents of 63.5, 63.4 and 63.8 mol%, respectively. These strains possess between one and three plasmids based on copy number of plasmid replication and segregation ( repABC) genes. Novel strains also possess numerous insertion sequences, and, relative to reference strain Bradyrhizobium diazoefficiens USDA110 T, exhibit inversion and fragmentation of nodulation ( nod) and nitrogen-fixation ( nif) gene clusters. Phylogenetic analyses of nodC and nifH gene sequences confirmed placement of novel strains in a distinct lineage corresponding to symbiovar septentrionale. Data for morphological, physiological and symbiotic characteristics complement the sequence-based results. The data presented here support the description of two new species for which the names Bradyrhizobium septentrionale sp. nov. (sv. septentrionale) and Bradyrhizobium quebecense sp. nov. (sv. septentrionale) are proposed, with 1S1 T (=LMG 29930 T=HAMBI 3676 T) and 66S1MB T (=LMG 31547 T=HAMBI 3720 T) as type strains, respectively.

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          New algorithms and methods to estimate maximum-likelihood phylogenies: assessing the performance of PhyML 3.0.

          PhyML is a phylogeny software based on the maximum-likelihood principle. Early PhyML versions used a fast algorithm performing nearest neighbor interchanges to improve a reasonable starting tree topology. Since the original publication (Guindon S., Gascuel O. 2003. A simple, fast and accurate algorithm to estimate large phylogenies by maximum likelihood. Syst. Biol. 52:696-704), PhyML has been widely used (>2500 citations in ISI Web of Science) because of its simplicity and a fair compromise between accuracy and speed. In the meantime, research around PhyML has continued, and this article describes the new algorithms and methods implemented in the program. First, we introduce a new algorithm to search the tree space with user-defined intensity using subtree pruning and regrafting topological moves. The parsimony criterion is used here to filter out the least promising topology modifications with respect to the likelihood function. The analysis of a large collection of real nucleotide and amino acid data sets of various sizes demonstrates the good performance of this method. Second, we describe a new test to assess the support of the data for internal branches of a phylogeny. This approach extends the recently proposed approximate likelihood-ratio test and relies on a nonparametric, Shimodaira-Hasegawa-like procedure. A detailed analysis of real alignments sheds light on the links between this new approach and the more classical nonparametric bootstrap method. Overall, our tests show that the last version (3.0) of PhyML is fast, accurate, stable, and ready to use. A Web server and binary files are available from http://www.atgc-montpellier.fr/phyml/.
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            ISfinder: the reference centre for bacterial insertion sequences

            ISfinder () is a dedicated database for bacterial insertion sequences (ISs). It has superseded the Stanford reference center. One of its functions is to assign IS names and to provide a focal point for a coherent nomenclature. It is also the repository for ISs. Each new IS is indexed together with information such as its DNA sequence and open reading frames or potential coding sequences, the sequence of the ends of the element and target sites, its origin and distribution together with a bibliography where available. Another objective is to continuously monitor ISs to provide updated comprehensive groupings or families and to provide some insight into their phylogenies. The site also contains extensive background information on ISs and transposons in general. Online tools are gradually being added. At present an online Blast facility against the entire bank is available. But additional features will include alignment capability, PsiBLAST and HMM profiles. ISfinder also includes a section on bacterial genomes and is involved in annotating the IS content of these genomes. Finally, this database is currently recommended by several microbiology journals for registration of new IS elements before their publication.
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              Shifting the genomic gold standard for the prokaryotic species definition.

              DNA-DNA hybridization (DDH) has been used for nearly 50 years as the gold standard for prokaryotic species circumscriptions at the genomic level. It has been the only taxonomic method that offered a numerical and relatively stable species boundary, and its use has had a paramount influence on how the current classification has been constructed. However, now, in the era of genomics, DDH appears to be an outdated method for classification that needs to be substituted. The average nucleotide identity (ANI) between two genomes seems the most promising method since it mirrors DDH closely. Here we examine the work package JSpecies as a user-friendly, biologist-oriented interface to calculate ANI and the correlation of the tetranucleotide signatures between pairwise genomic comparisons. The results agreed with the use of ANI to substitute DDH, with a narrowed boundary that could be set at approximately 95-96%. In addition, the JSpecies package implemented the tetranucleotide signature correlation index, an alignment-free parameter that generally correlates with ANI and that can be of help in deciding when a given pair of organisms should be classified in the same species. Moreover, for taxonomic purposes, the analyses can be produced by simply randomly sequencing at least 20% of the genome of the query strains rather than obtaining their full sequence.
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                Author and article information

                Journal
                Int J Syst Evol Microbiol
                Int J Syst Evol Microbiol
                ijsem
                ijsem
                International Journal of Systematic and Evolutionary Microbiology
                Microbiology Society
                1466-5026
                1466-5034
                2021
                9 June 2021
                9 June 2021
                : 71
                : 6
                : 004831
                Affiliations
                [ 1]departmentOttawa Research and Development Centre , Agriculture and Agri-Food Canada , 960 Carling Avenue, Ottawa, Ontario K1A OC6, Canada
                Author notes

                The GenBank/EMBL/DDBJ accession numbers for gene sequences of strains Bradyrhizobium quebecense 66S1MB T and 12S5, Bradyrhizobium septentrionale 1S1 T, 162S2, 75S4 and 28S5 respectively, are: KP768782, KP768768, KP768787, KP768799, KP768813, and KP768772 (16S rRNA); KP768550, KP768536, KP768555, KP768567, KP768581 and KP768540 ( atpD); KP768608, KP768652, KP768613, KP768625, KP768639 and KP768656 ( glnII); KF615025, KF615584, KF615049, KF615372, KF615511 and KF615598 ( recA); KP768724, KP768710, KP768729, KP768741, KP768755 and KP768714 ( gyrB); KP768666, KP768652, KP768671, KP768683, KP768697 and KP768656 ( rpoB); KF615618, KF615654, KF615620, KF615633, KF615645 and KF615658 ( nodC) and, KF615665, KF615701, KF615667, KF615680, KF615692 and KF615705 ( nifH). The whole genome shotgun projects for strains 66S1MB T, 1S1 T and 162S2 were deposited at DDBJ/ENA/GenBank under the accession numbers JABWSX000000000, JAAOLE000000000 and JABXFA000000000, respectively. Raw PacBio data for strain 66S1MB T, 1S1 T and 162S2 were deposited in the NCBI Sequence Read Archive under the BioProject accession numbers PRJNA640100, PRJNA612041 and PRJNA640156, respectively. Strains 66S1MB T, 1S1 T and 162S2 were deposited in the BCCM/LMG Bacteria Collection, Belgium as LMG 31547 T, LMG 29930 T and LMG 31550 and in the HAMBI Microbial Culture Collection, Finland as HAMBI 3720 T, HAMBI 3676 T and HAMBI 3724, respectively.

                *Correspondence: Eden S. P. Bromfield, eden.bromfield@ 123456canada.ca
                Author information
                https://orcid.org/0000-0001-5385-7815
                Article
                004831
                10.1099/ijsem.0.004831
                8374602
                34106824
                9b56a121-230a-4bcb-8f60-00f2b6870949
                © 2021 Her Majesty the Queen in right of Canada by the Minister of Agriculture and Agri-Food

                This is an open-access article distributed under the terms of the Creative Commons Attribution License.

                History
                : 08 February 2021
                : 26 April 2021
                Funding
                Funded by: Agriculture and Agri-Food Canada
                Award ID: J-002272
                Award Recipient : ApplicableNot
                Categories
                New Taxa
                Proteobacteria
                Custom metadata
                0

                Microbiology & Virology
                bradyrhizobium septentrionale (sv. septentrionale),bradyrhizobium quebecense (sv. septentrionale),insertion sequences,symbiosis genes,genetic rearrangements,canada

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