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Updated: Aug 14, 2026

DNA Fingerprinting of Mycobacterium leprae Strains Using Variable Number Tandem Repeat (VNTR) - Fragment Length Analysis (FLA)
Published on: July 15, 2011
Dihydropteroate synthase mutations in the folP1 gene predict dapsone resistance in relapsed cases of leprosy
Emmanuelle Cambau1, Laetitia Carthagena, Aurélie Chauffour
1Laboratoire de Bacteriologie-Hygiene, Centre National de Reference pour la Resistance des Mycobacteries aux Antituberculeux, Faculte de Medecine Pitie-Salpetriere, Universite Paris, Paris, France.
Abstract:
Molecular detection was compared with the mouse footpad inoculation test for detection of dapsone resistance in 38 strains of Mycobacterium leprae. Mutations of the folP1 gene (at codons 53 or 55) were found in 6 of 6 strains with high-level resistance, in 3 of 4 strains with intermediate-level resistance, and in 1 of 6 strains with low-level resistance, but not in 22 dapsone-susceptible strains. In cases of infection with strains of M. leprae carrying the folP1 mutation, therapy with dapsone may be replaced by therapy with a fluoroquinolone.
Insights
Molecular detection identified mutations in the folP1 gene linked to dapsone resistance in Mycobacterium leprae. This finding suggests fluoroquinolones as an alternative treatment for dapsone-resistant leprosy.
Area of Science:
- Microbiology
- Genetics
- Pharmacology
Background:
- Dapsone is a primary treatment for leprosy.
- Emerging dapsone resistance in Mycobacterium leprae poses a treatment challenge.
- Accurate detection of resistance is crucial for effective therapy.
Purpose of the Study:
- To compare molecular detection with the mouse footpad test for identifying dapsone resistance in Mycobacterium leprae.
- To investigate the association between folP1 gene mutations and dapsone resistance levels.
Main Methods:
- Tested 38 Mycobacterium leprae strains using both molecular detection and mouse footpad inoculation.
- Analyzed mutations in the folP1 gene at codons 53 and 55.
Main Results:
- folP1 gene mutations were detected in strains with high, intermediate, and low-level dapsone resistance.
- No folP1 mutations were found in dapsone-susceptible strains.
- Molecular detection correlated with resistance levels.
Conclusions:
- Molecular detection of folP1 mutations is a reliable method for identifying dapsone resistance in Mycobacterium leprae.
- The presence of folP1 mutations indicates potential treatment failure with dapsone.
- Fluoroquinolones may be a suitable alternative therapy for infections with dapsone-resistant Mycobacterium leprae strains carrying folP1 mutations.
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