| Literature DB >> 28551732 |
Elaine Martins da Costa1,2, Amanda Azarias Guimarães1, Rayssa Pereira Vicentin1, Paula Rose de Almeida Ribeiro1, Aniele Carolina Ribas Leão3, Eduardo Balsanelli3, Liesbeth Lebbe4, Maarten Aerts4, Anne Willems4, Fatima Maria de Souza Moreira5.
Abstract
Four strains of rhizobia isolated from nodules of Vigna unguiculata (UFLA03-321T, UFLA03-320 and UFLA03-290) and Macroptilium atropurpureum (UFLA04-0212) in Brazilian soils were previously reported as a new group within the genus Bradyrhizobium. To determine their taxonomic position, these strains were characterized in this study using a polyphasic approach. The analysis of the 16S rRNA gene grouped the four strains with Bradyrhizobium pachyrhizi PAC48T. However, the concatenated sequence analysis of the two (recA and glnII) or three (atpD, gyrB and recA) housekeeping genes indicated that these strains represent a novel species of Bradyrhizobium, which is very closely related to B. pachyrhizi PAC48T and B. elkanii USDA 76T. Genomic relatedness analyses between the UFLA03-321T strain and B. elkanii USDA 76T and B. pachyrhizi PAC48T revealed an average nucleotide identity below 96% and values of estimated DNA-DNA hybridization below 70%, confirming that they represent genomically distinct species. Analysis of MALDI-TOF MS (Matrix-assisted laser desorption ionization-time-of-flight mass spectrometry) profiles and phenotypic characteristics also allowed differentiation of the novel species from its two neighboring species. In phylogenetic analysis of nodC and nifH genes, UFLA03-321T exhibited maximum similarity with B. tropiciagri CNPSo 1112T. The data suggest that these four UFLA strains represent a novel species, for which the name Bradyrhizobium brasilense sp. nov. is proposed, with UFLA03-321T (=LMG 29353 =CBAS645) as type strain. G + C content in the DNA of UFLA03-321T is 63.9 mol %.Entities:
Keywords: Bradyrhizobium; Genomics; MALDI-TOF MS; Polyphasic taxonomy; Vigna unguiculata L.
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Year: 2017 PMID: 28551732 DOI: 10.1007/s00203-017-1390-1
Source DB: PubMed Journal: Arch Microbiol ISSN: 0302-8933 Impact factor: 2.552