Transduction as a Potential Dissemination Mechanism of a Clonal -Carrying Plasmid Isolated From of Multiple Serotypes and Isolation Sources.

Antimicrobial resistance is an increasing problem worldwide, and spp. resistance to quinolone was classified by WHO in the high priority list. Recent studies in Europe and in the US reported the presence of small plasmids carrying quinolone resistance in isolated from poultry and poultry products. The aims of this study were to identify and characterize plasmid-mediated quinolone resistance in spp. and to investigate transduction as a possible mechanism associated to its dissemination. First, we assessed resistance to nalidixic acid and/or ciprofloxacin in 64 spp. and detected resistance in eight of them. Genomic analyses determined that six isolates of different serotypes and sources carried an identical 2.7-kb plasmid containing the gene which confers quinolone resistance. The plasmid detected also has high identity with plasmids reported in the US, Europe, and South America. The presence of similar plasmids was later surveyed by PCR in a local collection ( = 113) obtained from diverse sources: food (eggs), wild and domestic animals (pigs, horse, chicken), and human clinical cases. -carrying plasmids were found in 8/113 tested strains. A bioinformatics analysis including Chilean and previously described plasmids revealed over 95.0% of nucleotide identity among all the sequences obtained in this study. Furthermore, we found that a -carrying plasmid can be transferred between of different serotypes through a P22-mediated transduction. Altogether our results demonstrate that plasmid-mediated quinolone resistance (PMQR) is widespread in of different serotypes isolated from human clinical samples, wild and domestic animals, and food in Chile and suggest that transduction could be a plausible mechanism for its dissemination. The occurrence of these antimicrobial resistance elements in in a widespread area is of public health and food safety concern, and it indicates the need for increased surveillance for the presence of these plasmids in strains and to assess their actual impact in the rise and spread of quinolone resistance.