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1.
Environ Microbiol ; 19(9): 3423-3438, 2017 09.
Article in English | MEDLINE | ID: mdl-28618121

ABSTRACT

Rhizobia are α- and ß-proteobacteria that associate with legumes in symbiosis to fix atmospheric nitrogen. The chemical communication between roots and rhizobia begins in the rhizosphere. Using signature-tagged-Tn5 mutagenesis (STM) we performed a genome-wide screening for Ensifer meliloti genes that participate in colonizing the rhizospheres of alfalfa and other legumes. The analysis of ca. 6,000 mutants indicated that genes relevant for rhizosphere colonization account for nearly 2% of the rhizobial genome and that most (ca. 80%) are chromosomally located, pointing to the relevance and ancestral origin of the bacterial ability to colonize plant roots. The identified genes were related to metabolic functions, transcription, signal transduction, and motility/chemotaxis among other categories; with several ORFs of yet-unknown function. Most remarkably, we identified a subset of genes that impacted more severely the colonization of the roots of alfalfa than of pea. Further analyses using other plant species revealed that such early differential phenotype could be extended to other members of the Trifoliae tribe (Trigonella, Trifolium), but not the Fabeae and Phaseoleae tribes. The results suggest that consolidation of E. meliloti into its current symbiotic state should have occurred in a rhizobacterium that had already been adapted to rhizospheres of the Trifoliae tribe.


Subject(s)
Medicago sativa/microbiology , Pisum sativum/microbiology , Plant Roots/microbiology , Rhizosphere , Sinorhizobium meliloti/growth & development , Symbiosis/genetics , Genome-Wide Association Study , Phenotype , Plant Root Nodulation/genetics , Root Nodules, Plant/microbiology , Sinorhizobium meliloti/genetics
2.
Int J Syst Evol Microbiol ; 66(11): 4451-4457, 2016 Nov.
Article in English | MEDLINE | ID: mdl-27499008

ABSTRACT

Strains LPU83T and Or191 of the genus Rhizobium were isolated from the root nodules of alfalfa, grown in acid soils from Argentina and the USA. These two strains, which shared the same plasmid pattern, lipopolysaccharide profile, insertion-sequence fingerprint, 16S rRNA gene sequence and PCR-fingerprinting pattern, were different from reference strains representing species of the genus Rhizobium with validly published names. On the basis of previously reported data and from new DNA-DNA hybridization results, phenotypic characterization and phylogenetic analyses, strains LPU83T and Or191 can be considered to be representatives of a novel species of the genus Rhizobium, for which the name Rhizobium favelukesii sp. nov. is proposed. The type strain of this species is LPU83T (=CECT 9014T=LMG 29160T), for which an improved draft-genome sequence is available.


Subject(s)
Medicago sativa/microbiology , Phylogeny , Rhizobium/classification , Root Nodules, Plant/microbiology , Argentina , Bacterial Typing Techniques , Base Composition , DNA, Bacterial/genetics , Nucleic Acid Hybridization , RNA, Ribosomal, 16S/genetics , Rhizobium/genetics , Rhizobium/isolation & purification , Sequence Analysis, DNA , United States
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