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Long-term administration of oral macrolides for acne treatment increases macrolide-resistant Propionibacterium acnes
Keisuke Nakase1, Yuhei Okamoto1, Sae Aoki1
1Department of Microbiology, School of Pharmacy, Tokyo University of Pharmacy and Life Sciences, Tokyo, Japan.
Abstract:
Macrolide-resistant Propionibacterium acnes are frequently isolated from patients with acne vulgaris, and the most resistant isolates (>90% resistance) have the 23S rRNA mutation. An increase in resistant P. acnes with this mutation is thought to be caused by the inappropriate use of antimicrobials. Therefore, we studied the mutation frequency of macrolide resistance in P. acnes in vitro. When P. acnes mutants were exposed to clarithromycin after being incubated in broth without antimicrobials, resistant mutants with the 23S rRNA mutation were not isolated. However, the mutants were obtained at the frequency of 10-6 after being pre-incubated with 0.03 μg/mL of antimicrobials. This is the estimated epidermal concentration of clarithromycin after p.o. administration. The resistant mutants had the 23S rRNA mutations A2058G, A2059G and C2611G. When pre-incubated with clarithromycin, C2611G mutants which showed resistance to clarithromycin were obtained 32.1% more often than pre-incubated with clindamycin (P < 0.01). By contrast, when pre-incubated with clindamycin, A2058G mutants, which show high-level resistance to both clarithromycin and clindamycin, were more frequently obtained than pre-incubated with clarithromycin (87.5%, P < 0.01). No difference in the isolation rate of A2059G mutants, which show high-level resistance to macrolides but low-level resistance to clindamycin, was found with either treatment. These results indicate the possibility that long-term use of oral macrolides for acne treatment facilitate the increase of macrolide-resistant P. acnes.
Insights
Macrolide resistance in acne-causing bacteria (Propionibacterium acnes) with specific 23S rRNA mutations increases with antimicrobial exposure. Long-term oral macrolide use may drive this rise in resistant P. acnes.
Area of Science:
- Microbiology
- Dermatology
- Molecular Biology
Background:
- Macrolide-resistant Propionibacterium acnes (P. acnes) are common in acne vulgaris.
- The 23S rRNA mutation is prevalent in highly resistant P. acnes isolates.
- Antimicrobial misuse is suspected to increase resistant P. acnes strains.
Purpose of the Study:
- To investigate the in vitro mutation frequency of macrolide resistance in P. acnes.
- To determine the impact of sub-inhibitory antimicrobial concentrations on resistance development.
Main Methods:
- P. acnes mutants were exposed to clarithromycin after incubation with or without antimicrobials.
- Resistant mutants were selected and their 23S rRNA mutations (A2058G, A2059G, C2611G) analyzed.
- Mutation frequencies were compared following pre-incubation with clarithromycin or clindamycin.
Main Results:
- Resistant P. acnes with 23S rRNA mutations were not isolated without antimicrobial pre-incubation.
- Mutants emerged at a frequency of 10^-6 after pre-incubation with 0.03 μg/mL clarithromycin.
- Pre-incubation with clarithromycin favored C2611G mutants, while clindamycin favored A2058G mutants.
Conclusions:
- Sub-inhibitory concentrations of antimicrobials can select for specific macrolide resistance mutations in P. acnes.
- Long-term oral macrolide therapy for acne may contribute to the increasing prevalence of resistant P. acnes.
- Understanding resistance mechanisms is crucial for effective acne treatment strategies.
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