Amoxicillin/clavulanate in combination with rifampicin/clarithromycin is bactericidal against Mycobacterium ulcerans

PLoS Negl Trop Dis. 2024 Apr 4;18(4):e0011867. doi: 10.1371/journal.pntd.0011867. eCollection 2024 Apr.

Abstract

Background: Buruli ulcer (BU) is a skin neglected tropical disease (NTD) caused by Mycobacterium ulcerans. WHO-recommended treatment requires 8-weeks of daily rifampicin (RIF) and clarithromycin (CLA) with wound care. Treatment compliance may be challenging due to socioeconomic determinants. Previous minimum Inhibitory Concentration and checkerboard assays showed that amoxicillin/clavulanate (AMX/CLV) combined with RIF+CLA were synergistic against M. ulcerans. However, in vitro time kill assays (TKA) are a better approach to understand the antimicrobial activity of a drug over time. Colony forming units (CFU) enumeration is the in vitro reference method to measure bacterial load, although this is a time-consuming method due to the slow growth of M. ulcerans. The aim of this study was to assess the in vitro activity of RIF, CLA and AMX/CLV combinations against M. ulcerans clinical isolates by TKA, while comparing four methodologies: CFU enumeration, luminescence by relative light unit (RLU) and optical density (at 600 nm) measurements, and 16S rRNA/IS2404 genes quantification.

Methodology/principal findings: TKA of RIF, CLA and AMX/CLV alone and in combination were performed against different M. ulcerans clinical isolates. Bacterial loads were quantified with different methodologies after 1, 3, 7, 10, 14, 21 and 28 days of treatment. RIF+AMX/CLV and the triple RIF+CLA+AMX/CLV combinations were bactericidal and more effective in vitro than the currently used RIF+CLA combination to treat BU. All methodologies except IS2404 quantitative PCR provided similar results with a good correlation with CFU enumeration. Measuring luminescence (RLU) was the most cost-effective methodology to quantify M. ulcerans bacterial loads in in vitro TKA.

Conclusions/significance: Our study suggests that alternative and faster TKA methodologies can be used in BU research instead of the cumbersome CFU quantification method. These results provide an in vitro microbiological support to of the BLMs4BU clinical trial (NCT05169554, PACTR202209521256638) to shorten BU treatment.

MeSH terms

  • Amoxicillin-Potassium Clavulanate Combination / pharmacology
  • Amoxicillin-Potassium Clavulanate Combination / therapeutic use
  • Anti-Bacterial Agents / pharmacology
  • Anti-Bacterial Agents / therapeutic use
  • Buruli Ulcer* / drug therapy
  • Buruli Ulcer* / microbiology
  • Clarithromycin / pharmacology
  • Clarithromycin / therapeutic use
  • Humans
  • Mycobacterium ulcerans* / genetics
  • RNA, Ribosomal, 16S
  • Rifampin / pharmacology
  • Rifampin / therapeutic use

Substances

  • Clarithromycin
  • Rifampin
  • RNA, Ribosomal, 16S
  • Anti-Bacterial Agents
  • Amoxicillin-Potassium Clavulanate Combination

Associated data

  • ClinicalTrials.gov/NCT05169554

Grants and funding

This work was partially supported by grants from the Tres Cantos Open Lab Foundation (Grant No. TC281) and from Anesvad Foundation, both to SRG. ACMP was recipient of a fellowship from the Spanish Government (Programa de Formación de Profesorado Universitario) Ref. FPU 17/01812. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.