6533b852fe1ef96bd12aa507

RESEARCH PRODUCT

Shifts in diversity and microscale distribution of the adapted bacterial phenotypes due to Hg(II) spiking in soil.

Sylvie NazaretLionel RanjardElisabeth Brothier

subject

DNA BacterialRibosomal Intergenic Spacer analysisMolecular Sequence DataAdaptation BiologicalSoil ScienceStreptomycesPolymerase Chain Reaction03 medical and health sciencesXanthomonasPseudomonasRNA Ribosomal 16SGenotypeEcology Evolution Behavior and SystematicsComputingMilieux_MISCELLANEOUSEcosystemSoil Microbiology2. Zero hungerGenetics[SDV.EE]Life Sciences [q-bio]/Ecology environment0303 health sciencesEcologyPhylogenetic treebiologyBase Sequence030306 microbiology04 agricultural and veterinary sciencesMercuryBIOLOGIE MOLECULAIREbiology.organism_classification16S ribosomal RNAAmplified Ribosomal DNA Restriction AnalysisSpatial heterogeneity[SDV.EE] Life Sciences [q-bio]/Ecology environment040103 agronomy & agriculture0401 agriculture forestry and fisheriesDNA Intergenic

description

In a previous experiment [Ranjard et al. (2000) FEMS Microbiol Ecol 31:107–115], the spatial heterogeneity of a mercury impact on soil bacterial community was revealed by an increase of mercury-resistant (HgR) bacterial numbers in the outer fraction and the sand fractions when compared to those in the silt fractions. The objectives of the present study were (i) to investigate whether mercury exposure affects the diversity and the distribution within the various fractions of the HgR populations and (ii) to evaluate the contribution of the HgR populations to the overall community adaptation. A total of 236 strains isolated before (104 isolates) and 30 days (132 isolates) after spiking were characterized by an amplified ribosomal DNA restriction analysis (ARDRA) and grouped into 30 different genotypes. Whereas almost the same numbers of different genotypes were observed at both sampling times when considering all microenvironments, important changes in their evenness were observed. At the microscale level, we also noticed a heterogeneous distribution of the genotypes. Partial 16S rDNA sequences of each genotype were determined to permit phylogenetic affiliation. Whereas Pseudomonas-like species were dominant in all microenvironments at T = 0, genotypes not detected before spiking such as genotypes closely related to Xanthomonas, Pseudoaminobacter, and Sphingomonas-like species became dominant at T = 30. Similarly, several genotypes close to Bacillus, Streptomyces, and Rhodococcus species were only detected in the sand fractions at T = 0 and could not be detected in these fractions at T = 30. Probes defined within the intergenic spacer between the rrs and rrl genes were designed for the dominant genotypes and were hybridized toward the RISA (Ribosomal Intergenic Spacer Analysis) profiles derived from the T = 0 and T = 30 bacterial communities associated to the unfractionated soil. Results showed that the culturable dominant HgR genotypes partially contributed to the adaptation of the whole bacterial community.

10.1007/s00248-002-2035-7https://pubmed.ncbi.nlm.nih.gov/12658524