Abstract

The determination of antibiotic potency against bacterial strains by assessment of their minimum inhibitory concentration normally uses a standardized broth microdilution assay procedure developed more than 50 years ago. However, certain antibiotics require modified assay conditions in order to observe optimal activity. For example, daptomycin requires medium supplemented with Ca2+, and the lipoglycopeptides dalbavancin and oritavancin require Tween 80 to be added to the growth medium to prevent the depletion of free drug via adsorption to the plastic microplate. In this report, we examine systematically the effects of several different plate types on microdilution broth MIC values for a set of antibiotics against Gram-positive and Gram-negative bacteria, both in medium alone and in medium supplemented with the commonly used additives Tween 80, lysed horse blood, and 50% human serum. We observed very significant differences in measured MICs (up to 100-fold) for some lipophilic antibiotics, such as the Gram-positive lipoglycopeptide dalbavancin and the Gram-negative lipopeptide polymyxins, and found that nonspecific binding plates can replace the need for surfactant additives. Microtiter plate types and any additives should be specified when reporting broth dilution MIC values, as results can vary dramatically for some classes of antibiotics.

Highlights

  • The determination of antibiotic potency against bacterial strains by assessment of their minimum inhibitory concentration normally uses a standardized broth microdilution assay procedure developed more than 50 years ago

  • Our studies were designed to examine the effects of different plate types on broth microdilution MIC determinations

  • One Gram-positive organism was tested against seven antibiotics and one Gram-negative organism against seven antibiotics

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Summary

Introduction

The determination of antibiotic potency against bacterial strains by assessment of their minimum inhibitory concentration normally uses a standardized broth microdilution assay procedure developed more than 50 years ago. The adherence of cationic AMPs to PS ( tissue-culture treated PS) is mentioned in a note in a 2007 Methods in Molecular Biology chapter, which recommended the use of PP plates [9] Some antibiotics, such as the lipoglycopeptides teicoplanin (compound 1), telavancin (compound 2), dalbavancin (compound 3), oritavancin (compound 4), and ramoplanin (compound 6) (Fig. 1), must be solubilized in dimethyl sulfoxide (DMSO) or 0.002% polysorbate 80 (Tween 80) in water to prevent adherence to plastic surfaces, including assay plates [10,11,12,13,14], with other additives, such as 2% lysed horse blood (LHB) [10] or 0.02% bovine serum albumin (BSA) [15, 16] found to have a similar blocking effect as surfactant. Other binding surfaces include a high binding surface to bind biomolecules that possess ionic groups and/or hydrophobic regions, and surfaces coated with poly-D-lysine, sulfhydryl, carbohydrate, amine, or photoreactive groups that can be used to covalently immobilize biomolecules

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