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1.
Syst Appl Microbiol ; 41(4): 333-339, 2018 Jul.
Article in English | MEDLINE | ID: mdl-29656850

ABSTRACT

We have characterized genetic, phenotypic and symbiotic properties of bacterial strains previously isolated from nitrogen-fixing nodules of Retama sphaerocarpa from Northern Algeria. Phylogenetic analyses of 16S rRNA genes and three concatenated housekeeping genes, recA, atpD and glnII, placed them in a new divergent group that is proposed to form a new Bradyrhizobium species, Bradyrhizobium algeriense sp. nov. (type strain RST89T, LMG 27618 and CECT 8363). Based on these phylogenetic markers and on genomic identity data derived from draft genomic sequences, Bradyrhizobium valentinum LmjM3T, Bradyrhizobium lablabi CCBAU 23086T, Bradyrhizobium retamae Ro19T, and Bradyrhizobium jicamae PAC68T are the closest relatives of B. algeriense RST89T, with sequence identities of 92-94% and Average Nucleotide Identities (ANIm) under 90%, well below the 95-96% species circumscription threshold. Likewise, a comparison of whole-cell proteomic patterns, estimated by Matrix-Assisted Laser Desorption/Ionization-Time-of-Flight (MALDI-TOF) mass spectrometric analysis, yielded almost identical spectra between B. algeriense strains but significant differences with B. valentinum, Bradyrhizobium paxllaeri, Bradyrhizobium icense, B. lablabi, B. jicamae and B. retamae. A phylogenetic tree based on symbiotic gene nodC revealed that the B. algeriense sequences cluster with sequences from the Bradyrhizobium symbiovar retamae, previously defined with B. retamae strains isolated from Retama monosperma. B. algeriense strains were able to establish effective symbioses with Retama raetam, Lupinus micranthus, Lupinus albus and Genista numidica, but not with Lupinus angustifolius or Glycine max.


Subject(s)
Bradyrhizobium , Fabaceae/microbiology , Root Nodules, Plant/microbiology , Algeria , Bradyrhizobium/classification , Bradyrhizobium/genetics , Bradyrhizobium/isolation & purification , DNA, Bacterial/genetics , Fatty Acids/analysis , Genes, Bacterial/genetics , Genes, Essential/genetics , Multilocus Sequence Typing , Phylogeny , RNA, Ribosomal, 16S/genetics , Sequence Analysis, DNA , Symbiosis
2.
Syst Appl Microbiol ; 39(4): 266-274, 2016 Jun.
Article in English | MEDLINE | ID: mdl-27236566

ABSTRACT

Lupinus micranthus is a lupine distributed in the Mediterranean basin whose nitrogen fixing symbiosis has not been described in detail. In this study, 101 slow-growing nodule isolates were obtained from L. micranthus thriving in soils on both sides of the Western Mediterranean. The diversity of the isolates, 60 from Algeria and 41 from Spain, was addressed by multilocus sequence analysis of housekeeping genes (16S rRNA, atpD, glnII and recA) and one symbiotic gene (nodC). Using genomic fingerprints from BOX elements, 37 different profiles were obtained (22 from Algeria and 15 from Spain). Phylogenetic analysis based on 16S rRNA and concatenated atpD, glnII and recA sequences of a representative isolate of each BOX profile displayed a homogeneous distribution of profiles in six different phylogenetic clusters. All isolates were taxonomically ascribed to the genus Bradyrhizobium. Three clusters comprising 24, 6, and 4 isolates, respectively, accounted for most of the profiles. The largest cluster was close to the Bradyrhizobium canariense lineage, while the other two were related to B. cytisi/B. rifense. The three remaining clusters included only one isolate each, and were close to B. canariense, B. japonicum and B. elkanii species, respectively. In contrast, phylogenetic clustering of BOX profiles based on nodC sequences yielded only two phylogenetic groups. One of them included all the profiles except one, and belonged to symbiovar genistearum. The remaining profile, constituted by a strain related to B. elkanii, was not related to any well-defined symbiotic lineage, and may constitute both a new symbiovar and a new genospecies.


Subject(s)
Bradyrhizobium/classification , Bradyrhizobium/genetics , Lupinus/microbiology , Multilocus Sequence Typing , Root Nodules, Plant/microbiology , Soil Microbiology , Algeria , Bradyrhizobium/isolation & purification , N-Acetylglucosaminyltransferases/genetics , Nitrogen Fixation/physiology , Phylogeny , Plant Root Nodulation , RNA, Ribosomal, 16S/genetics , Rec A Recombinases/genetics , Spain , Symbiosis , Transcription Factors/genetics
3.
Antonie Van Leeuwenhoek ; 105(6): 1121-9, 2014 Jun.
Article in English | MEDLINE | ID: mdl-24756908

ABSTRACT

Fifty-one rhizobial strains isolated from root nodules of Cytisus villosus growing in Northeastern Algeria were characterized by genomic and phenotypic analyses. Isolates were grouped into sixteen different patterns by PCR-RAPD. The phylogenetic status of one representative isolate from each pattern was examined by multilocus sequence analyses of four housekeeping genes (16S rRNA, glnII, recA, and atpD) and one symbiotic gene (nodC). Analysis of 16S rRNA gene sequences showed that all the isolates belonged to the genus Bradyrhizobium. Phylogenetic analyses based on individual or concatenated genes glnII, recA, and atpD indicated that strains cluster in three distinct groups. Ten out of the sixteen strains grouped together with Bradyrhizobium japonicum, while a second group of four clustered with Bradyrhizobium canariense. The third group, represented by isolates CTS8 and CTS57, differed significantly from all other bradyrhizobia known to nodulate members of the Genisteae tribe. In contrast with core genes, sequences of the nodC symbiotic gene from all the examined strains form a homogeneous group within the genistearum symbiovar of Bradyrhizobium. All strains tested nodulated Lupinus angustifolius, Lupinus luteus, and Spartium junceum but not Glycine max. From these results, it is concluded that C. villosus CTS8 and CTS57 strains represent a new lineage within the Bradyrhizobium genus.


Subject(s)
Bradyrhizobium/classification , Bradyrhizobium/isolation & purification , Cytisus/microbiology , Cytisus/physiology , Plant Root Nodulation , Algeria , Bacterial Proteins/genetics , Bradyrhizobium/genetics , Cluster Analysis , DNA, Bacterial/chemistry , DNA, Bacterial/genetics , DNA, Ribosomal/chemistry , DNA, Ribosomal/genetics , Genes, Bacterial , Lupinus/microbiology , Lupinus/physiology , Molecular Sequence Data , Multilocus Sequence Typing , Phylogeny , Polymerase Chain Reaction , RNA, Ribosomal, 16S/genetics , Random Amplified Polymorphic DNA Technique , Spartium/microbiology , Spartium/physiology
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