Microevolution and origins of Bradyrhizobium populations associated with soybeans at two field sites (A and B, 280 km apart in Canada) with contrasting histories of inoculation was investigated using probabilistic analyses of six core (housekeeping) gene sequences. These analyses supported division of 220 isolates in five lineages corresponding either to B. japonicum groups 1 and 1a or to one of three novel lineages within the genus Bradyrhizobium. None of the isolates from site A and about 20% from site B (the only site with a recent inoculation history) were attributed to inoculation sources. The data suggest that most isolates were of indigenous origin based on sequence analysis of 148 isolates of soybean-nodulating bacteria from native legumes (Amphicarpaea bracteata and Desmodium canadense). Isolates from D. canadense clustered with B. japonicum group 1, whereas those from A. bracteata were placed in two novel lineages encountered at soybean field sites. One of these novel lineages predominated at soybean sites and exhibited a significant clonal expansion likely reflecting selection by the plant host. Homologous recombination events detected in the 35 sequence types from soybean sites had an effect on genetic diversification that was approximately equal to mutation. Interlineage transfer of core genes was infrequent and mostly attributable to gyrB that had a history of frequent recombination. Symbiotic gene sequences (nodC and nifH) of isolates from soybean sites and native legumes clustered in two lineages corresponding to B. japonicum and B. elkani with the inheritance of these genes appearing predominantly by vertical transmission. The data suggest that soybean-nodulating bacteria associated with native legumes represent a novel source of ecologically adapted bacteria for soybean inoculation.

Phage-resistant and -susceptible bacteria from nodules of alfalfa and sweet clover, grown at a site without a known history of cultivation, were identified as diverse genotypes of Ensifer, Rhizobium and Phyllobacterium species based on sequence analysis of ribosomal (16S and 23S rRNA) and protein-encoding (atpD and recA) genes, Southern hybridization/RFLP and a range of phenotypic characteristics. Among phage-resistant bacteria, one genotype of Rhizobium sp. predominated on alfalfa (frequency~68 %) but was recovered infrequently (~1 %) from sweet clover. A second genotype was isolated infrequently only from alfalfa. These genotypes fixed nitrogen poorly in association with sweet clover and Phaseolus vulgaris, but were moderately effective with alfalfa. They produced a near-neutral reaction on mineral salts agar containing mannitol, which is atypical of the genus Rhizobium. A single isolate of Ensifer sp. and two of Phyllobacterium sp. were recovered only from sweet clover. All were highly resistant to multiple antibiotics. Phylogenetic analysis indicated that Ensifer sp. strain T173 is closely related to, but separate from, the non-symbiotic species 'Sinorhizobium morelense'. Strain T173 is unique in that it possesses a 175 kb symbiotic plasmid and elicits ineffective nodules on alfalfa, sweet clover, Medicago lupulina and Macroptilium atropurpureum. The two Phyllobacterium spp. were non-symbiotic and probably represent bacterial opportunists. Three genotypes of E. meliloti that were symbiotically effective with alfalfa and sweet clover were encountered infrequently. Among phage-susceptible isolates, two genotypes of E. medicae were encountered infrequently and were highly effective with alfalfa, sweet clover and Medicago polymorpha. The ecological and practical implications of the findings are discussed.

Insertion sequence (IS) hybridization was used to define the structure of a population of Rhirobium meliloti isolated directly from soil and from nodules of Medicago sativn (alfalfa) and Melilotus alba (sweet clover) grown under controlled conditions and inoculated with a suspension of the same soil. The detection of R. meliloti isolated from soil on agar plates was facilitated by use of a highly species specific DNA probe derived from ISRm5. All R. meliloti o'btained directly from soil proved to be symbiotic (i.e. noddated and fixed nitrogen with alfalfa). Analysis of 293 R. meliloti isolates revealed a total of 17 distinct I S genotypes of which 9,9 and 15 were from soil, M. alba and M. satina, respectively; 8 genotypes were common to soil and both plant species. The frequency of R. meliloti genotypes from soil differed markedly from that sampled from nodules of both legume species: 5 genotypes represented about 90% of the isolates from soil whereas a single genotype predominated among isolates from nodules accounting for more than 55% of the total. The distribution of genotypes differed between M. satiaa and M. alba indicating species variation in nodulation preferences for indigenous R. meliloti. The data are discussed in the context of competition for nodalation of the host plant and the selection of Rhizobium strains for use in legume inoculants. This study has ecological implications and suggests that the composition of R meliloti populations sampled by the traditionally used host legume may not be representative of that actually present in soil. Segovia L, Pincro D, Palaaos R, Marthez-Romem E (1991) Genetic structure of a soil population of nonsymbiotic Rhbbium legumintmrum. Applied and Environmental Microbiology, 57, 426-433. Smith GE, Summers MD (1980) The bidirectional transfer of DNA and RNA to nitroceIlulose or diazobenzyloxymethyl paper. Analyticnl Biochemistry, 109,123-129. Snedecor CW, Cochran WG (1980) Statistical Methods, Iowa State University Press. SoberonChdvez G, Ndkra R, Olivera H, Segovia L (1986) Genetic rearrangements of a Rhizobium phnsmli symbiotic plasmid. Journal of Bacteriology, 167,487-491. SoberonChdvez G, Ndjera R (1989) Isolation from Soil of Rhiwbium leguminosnrum lacking symbiotic information. Canadian Journal of Microbiology, 35,464-468. Thurman NP, Bromfield ESP (1988) Effect of variation within and between Medicago and Melilotus species on the composition and dynamics of indigenous populations of Rhizqbium meliloti.Soil Biology and Biochemistry, 20,31-38. Vincent J M (1970) A Manual for the Practical Study of Root-nodule Bacteria I.B.P. Blackwell Scientific Publications, Oxford. Wheatcroft R, Watson RJ (1988) Distribution of insertion sequence ISRml in Rhizobium meliloti and other Gram-negative bacteria. Journal of Gcneml Microbiology, 134,113-121. Wheatcroft R, Bromfield ESP, Laberge S, Barran LR (1993) Species specific DNA probe and colony hybridization of Rhizobium rneliloti. In: New Horizons in Nitrogen Fixation (eds Palacios R, Mora J, Newton WE) p. 661. Kluwer, Bosto...

Sixteen strains of symbiotic bacteria from root nodules of Glycine max grown in Ottawa, Canada, were previously characterized and placed in a novel group within the genus Bradyrhizobium. To verify their taxonomic status, these strains were further characterized using a polyphasic approach. All strains possessed identical 16S rRNA gene sequences that were 99.79 % similar to the closest relative, Bradyrhizobium liaoningense LMG 18230T. Phylogenetic analysis of concatenated atpD, glnII, recA, gyrB, rpoB and dnaK genes divided the 16 strains into three multilocus sequence types that were placed in a highly supported lineage distinct from named species of the genus Bradyrhizobium consistent with results of DNA–DNA hybridization. Based on analysis of symbiosis gene sequences (nodC and nifH), all novel strains were placed in a phylogenetic group with five species of the genus Bradyrhizobium that nodulate soybeans. The combination of phenotypic characteristics from several tests including carbon and nitrogen source utilization and antibiotic resistance could be used to differentiate representative strains from recognized species of the genus Bradyrhizobium. Novel strain OO99T elicits effective nodules on Glycine max, Glycine soja and Macroptilium atropurpureum, partially effective nodules on Desmodium canadense and Vigna unguiculata, and ineffective nodules on Amphicarpaea bracteata and Phaseolus vulgaris. Based on the data presented, we conclude that our strains represent a novel species for which the name Bradyrhizobium ottawaense sp. nov. is proposed, with OO99T ( = LMG 26739T = HAMBI 3284T) as the type strain. The DNA G+C content is 62.6 mol%.

An assessment was made of the evolutionary relationships of soybean nodulating bacteria associated with legumes native to eastern Canada to identify potential new sources of soybean inoculant strains. Short season soybeans were used to selectively trap bacteria from root zone soils of four native legume species. Screening of more than 800 bacterial isolates from soybean root nodules by analysis of recA gene sequences followed by analyses of selected genotypes using six core and two symbiosis (nodC and nifH) gene sequences permitted identification of diverse taxa that included eight novel and four named Bradyrhizobium species as well as lineages attributed to the genera Afipia and Tardiphaga. Plant tests showed that symbionts related to four named species as well as a novel Bradyrhizobium lineage were highly efficient with regard to nitrogen fixation on soybeans relative to an inoculant strain. A new symbiovar (sv. septentrionalis) is proposed based on a group of four novel Bradyrhizobium spp. that possess distinctive nodC and nifH gene sequences and symbiotic characteristics. Evidence is provided for horizontal transfer of sv. septentrionalis symbiosis genes between novel Bradyrhizobium spp., a process that rendered recipient bacteria ineffective on soybeans. Diverse lineages of non-symbiotic and symbiotic Bradyrhizobium spp. co-occured within monophyletic clusters in a phylogenetic tree of concatenated core genes, suggesting that loss and/or gain of symbiosis genes has occurred in the evolutionary history of the bacterial genus. Our data suggest that symbiont populations associated with legumes native to eastern Canada harbour elite strains of Bradyrhizobium for soybean inoculation.

Thirty-three isolates of indigenous Rhizobium meliloti, either possessing cryptic plasmids that hybridize to probes for symbiotic genes or lacking a 1500-kb megaplasmid band in Eckhardt gels, were tested for infectivity on 10 legume species grown under axenic conditions. A previous study had shown that all but two isolates were symbiotically effective with Medicago sativa. All indigenous isolates and two reference strains of R. meliloti induced nodules which were symbiotically ineffective on Trigonella foenum-graecum (100% plants nodulated) and Phaseolus vulgaris (40 to 100% plants nodulated). Eighteen indigenous isolates of R. meliloti elicited ineffective nodules on Macroptilium atropurpureum (2 to 25% plants nodulated) and Leucaena leucocephala (11 to 75% plants nodulated). The identity of single colony nodule isolates from each R. meliloti inoculant and host combination was verified by phage typing and analysis of plasmid profiles; tests with subsamples of these isolates showed that all were capable of nodulating M. sativa. There was no apparent relationship between the host range of indigenous R. meliloti and either the presence of cryptic plasmids that hybridize to probes for symbiotic genes or the absence of a megaplasmid band in Eckhardt gels. The data suggest that nodulation promiscuity may be a relatively common characteristic of R. meliloti. Key words: host range, Rhizobium meliloti, Leucaena, Macroptilium, Phaseolus.

An assessment was made of the impact of temporal separation on the composition of a population of Sinorhizobium meliloti associated with Medicago sativa (alfalfa) and Melilotus alba (sweet clover) grown at a single site that had no known history of alfalfa cultivation. Root nodules were sampled on six occasions over two seasons, and a total of 1620 isolates of S. meliloti were characterized on the basis of phage sensitivity using 16 typing phages. Plant infection tests indicated that symbiotic S. meliloti were deficient in the soil at the time of planting and that these bacteria were present at low density during the first season (<10(2)/g of soil); in the second season numbers increased markedly to about 10(5)/g of soil. Overall, 37 and 51 phage types, respectively, were encountered among the nodule isolates from M. sativa and M. alba. The data indicate significant temporal shifts in the frequency and diversity of types associated with the two legume species. Apparent temporal variation with respect to the frequency of types appeared largely unpredictable and was not attributable to any one sampling time. The results indicate an apparent reduction in phenotypic diversity over the course of the experiment. Differential host plant selection of specific types with respect to nodule occupancy was indicated by significant interactions between legume species and either the frequency or diversity of phage types. Isolates from M. sativa that were resistant to lysis by all typing phages (type 14) were unusual in that they were predominant on this host at all sampling times (between 53% and 82% nodule occupancy) and were relatively homogeneous on the basis of DNA hybridization with 98% of the isolates analysed sharing the same nod EFG hybridization profile. In contrast, those isolates from M. alba comprising type 14 were encountered at low total frequency (2%) and were genetically heterogeneous on the basis of Southern hybridization. The implications of the observed temporal and host plant variation for ecological studies are discussed.

Phage types representative of the population of indigenous Rhizobium mezilotiat each of two sites were evaluated for plasmid content by agarose gel electrophoresis and for symbiotic effectiveness with Medicago sativa cv. Saranac. Relative to four strains used commercially, 55 and 65 phage types representing these populations showed a high average level of symbiotic effectiveness; only a single type from one site was relatively ineffective in symbiosis. On the basis of plasmid number and molecular mass, 160 isolates comprising 45 and 48 types from both sites were placed in 22 different groups with 17 and 13 groups from the respective sites. The number of plasmids varied between one and five per isolate with molecular masses ranging from 5 MDa to considerably greater than 267 MDa. Only five isolates lacked a plasmid with mobility in agarose gels corresponding to that of a reference megaplasmid but instead showed a band of lesser mobility and therefore greater molecular mass. Phage types, which were divided into plasmid groups solely on the basis of differences between isolates from each site, may reflect adaptation of R. meIiIoti to their respective sites. Differences between isolates within certain phage types due to the presence or absence of a single plasmid May have resulted from genetic interchange between indigenous R. meliloti. There was no significant correlation between plasmid number or mass and symbiotic effectiveness or phage sensitivity of the phage types from either site.