ArticleAntibiotics (Basel, Switzerland)2025
Agar-Dilution Is Comparable to Broth Dilution for MIC Determination in
Article in Antibiotics (Basel, Switzerland), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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Who cites it
3 citing papers in PubMed.
- Design, synthesis, and antibacterial efficacy of new methylene disalicylic acid/1,3,4-oxadiazole hybrids as dual inhibitors of DNA gyrase and topoisomerase IV.Molecular diversity · 2026Article
- Electroporation of pLI50 harboring qacA or qacB increases chlorhexidine minimal inhibitory concentrations in transformed Staphylococcus aureus strain RN4220.Scientific reports · 2026Article
- In-vitro and in-silico antibacterial and antibiofilm activities of an aromatic heterocyclic metabolite from a novel halo-thermophilic Streptomyces sp. strain CBN-1 against bacteria causing nosocomial infections.Molecular biology reports · 2025Article
Corrections and comments
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Authors and funding
8 authors.
Funding
Abstract
background
objectiveTo demonstrate that agar-dilution AST provides equivalent results to broth dilution methods, with superior capacity for high-throughput screening.
methodsAgar-dilution and microdilution AST methods were compared using a panel of 24 characterised susceptible and resistant GBS strains for benzylpenicillin, chloramphenicol, clindamycin, erythromycin, gentamicin, levofloxacin, tetracycline, and vancomycin. Minimum inhibitory concentration (MIC) agreements were evaluated, and resistance profile correlations were assessed using Cohen's kappa values.
resultsAgar-dilution demonstrated >90% agreement with BMD MIC for most antimicrobials, except vancomycin (87.5%), erythromycin (83.33%), and tetracycline (52.78%). Cohen's kappa values indicated strong agreement (0.88-1.00) for resistance determination. Agar-dilution avoided "trailing growth" issues associated with BMD and facilitated easier detection of non-GBS contaminants.
conclusionsAgar-dilution is a valid method for high-throughput AMR surveillance of retrospective cohorts (96 isolates per plate) and is critical for identifying emerging GBS resistance trends and informing therapeutic guidelines. However, due to the large number of plates required per antimicrobial, it is impractical for routine clinical diagnostics.
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