Homologues of the plasmid replicator gene repC were detected and chara
cterized in a sample of Rhizobium leguminosarum strains. Conserved PCR
primers were designed from published sequences of repC; they amplifie
d a fragment of about 750 bp from 39 out of 41 strains tested, and als
o from several Sinorhizobium strains, including S. meliloti. Restricti
on endonuclease digestion showed that the PCR product from individual
strains, though uniform in size, was often heterogeneous in sequence,
PCR products from 24 field isolates of R. leguminosarum from Prance, G
ermany and the Uh were cloned and partially sequenced from both ends.
Phylogenies constructed from the 5' and 3' ends (200 bp each) were lar
gely congruent and demonstrated four clearly defined groups plus sever
al unique strains. Published Agrobacterium repC sequences fall within
the phylogeny of R. leguminosarum sequences, though not within any of
the four groups. Specific pairs of PCR primers were designed for each
of the four groups; 29 out of 41 R. leguminosarum strains gave a PCR p
roduct of the expected size with more than one group-specific primer p
air, We hypothesize that the sequence groups correspond to incompatibi
lity groups of Rhizobium plasmids.