Repurposing Ionophores as novel antimicrobial agents for the treatment of bovine mastitis caused by Gram-positive pathogens.
Elizabeth E HickeyHui San WongManouchehr KhazandiAbiodun D OgunniyiKiro R PetrovskiSanjay GargStephen W PageRyan O'HandleyDarren J TrottPublished in: Journal of veterinary pharmacology and therapeutics (2018)
Increasing reports of multidrug-resistant bacterial infections in animals has created a need for novel antimicrobial agents that do not promote cross-resistance to critically important antimicrobial classes used in human medicine. In response to the recent emergence of antimicrobial resistance in several bovine mastitis pathogens, in vitro antimicrobial susceptibility was determined for four polyether ionophores (lasalocid, monensin, narasin and salinomycin) against Staphylococcus spp. and Streptococcus spp. isolated from clinical cases. In addition, erythrocyte haemolysis and WST-1 cell proliferation assays were used to assess in vitro mammalian cell cytotoxicity and biofilm susceptibility testing was performed using the minimum biofilm eradication concentration (MBEC™) biofilm assay. Lasalocid, monensin, narasin and salinomycin exhibited bacteriostatic antimicrobial activity against all pathogens tested, including methicillin-resistant staphylococci, with MIC90 values <16 μg/ml. Narasin and monensin displayed the least toxicity against mammalian cell lines and all compounds significantly reduced viable cell numbers in a Staphylococcus aureus biofilm. Based on in vitro characterization, all four ionophores offer potentially novel treatments against bovine mastitis but in vivo studies will be essential to determine whether acceptable safety and efficacy is present following intramammary administration.
Keyphrases
- staphylococcus aureus
- antimicrobial resistance
- biofilm formation
- gram negative
- multidrug resistant
- methicillin resistant staphylococcus aureus
- cell proliferation
- single cell
- cell therapy
- high throughput
- candida albicans
- endothelial cells
- drug resistant
- stem cells
- induced pluripotent stem cells
- escherichia coli
- mesenchymal stem cells
- emergency department
- pluripotent stem cells
- oxide nanoparticles