High diversity NVP-AUY922 price of PFGE genomotypes The genomic DNA of 56 O. anthropi strains (32 human and 24 environmental) were analysed by PFGE. At a 100% similarity level, PFGE discriminated all the strains except LR1 and LR2, which came from the same environmental sample. The pulsotypes were highly diverse even among strains belonging to the same clonal complex and/or sharing the same ST. The clinical strains originating from a same French hospital were epidemiologically unrelated by PFGE analysis (Fig. 5).
PFGE Selleck Napabucasin clusters appeared only below a 60% similarity level (Tables 1 and 2), suggesting that PFGE was unable to structure the population studied. Members of the different clonal complexes appeared intermingled among the PFGE clusters (Tables 1 and 2). The PFGE clusters defined at 60% similarity level could not be related to any characteristic of the strains such as isolation niche, geography, lifestyle, date of isolation, or antibiotype. Figure 5 Representative PFGE profiles obtained for French clinical strains isolated in the same hospital and belonging to the major clonal complex MSCC4/eBCC4. PFGE clusters at a 60% buy I-BET-762 similarity level are indicated at the bottom of the gel. (*) ADN of the strain
ADV77 was deposited twice on the gel to check reproducibility and to help profiles comparison. Antibiotypes of O. anthropi clinical and environmental strains Both clinical and environmental strains appeared highly resistant to all β-lactams, but imipenem. We observed a general susceptibility to aminoglycosides, fluoroquinolones, tetracycline, trimethoprim-sulfamethoxazole and an overall resistance to chloramphenicol and fosfomycin. The strains isolated from hospitalized patients did not show particular resistance characteristics when compared to environmental strains. This suggested that the high level of
resistance observed in O. anthropi is a natural trait of the species mostly unrelated to the medical use of antibiotics. Discussion We proposed here the first application of MLST to O. anthropi. Our MLST scheme contains 6 housekeeping and 1 outer-membrane Methocarbamol protein (omp25) genes, scattered on the large chromosome of strain ATCC 49188T. The sequences of bipartite genomes in alphaproteobacteria suggested the plasmidic origin of the smaller chromosome [40]. In this MLST scheme, no loci were chosen on the small chromosome to avoid bias due to the potential difference in the evolution history of the two chromosomes. The construction of another complete MLST scheme based on genes carried by this second chromosome would be of great interest to assess the emergence and the evolution of the complex genome in O. anthropi. At each locus examined by MLST, even at omp25, genetic variation appears to be mostly neutral. The 7 loci had mol%G+C contents similar to that of the rest of the genome. This suggests that these genes were not recently acquired through horizontal gene transfer. ST diversity in O.