Drug and Multidrug Resistance among Mycobacterium leprae Isolates from Brazilian Relapsed Leprosy Patients

Author:

Rocha Adalgiza da Silva1,Cunha Maria das Graças2,Diniz Lucia Martins3,Salgado Claudio4,Aires Maria Araci P.5,Nery José Augusto6,Gallo Eugênia Novisck6,Miranda Alice6,Magnanini Monica M. F.7,Matsuoka Masanori8,Sarno Euzenir Nunes6,Suffys Philip Noel1,de Oliveira Maria Leide W.7

Affiliation:

1. Laboratory of Molecular Biology Applied to Mycobacteria, Oswaldo Cruz Institute, Fiocruz, Rio de Janeiro, RJ, Brazil

2. Tropical Dermatology Foundation Alfredo da Matta (FUAM), Manaus, Amazonas, Brazil

3. Dermatology Service, Santa Casa de Misericordia (EMESCAM), Vitória, Espirito Santo, Brazil

4. Dermato-Immunology Laboratory Universidade Federal do Pará and Dr. Marcello Candia Reference Unit, Marituba, Pará, Brazil

5. Reference Center in Sanitary Dermatology D. Lebanon (CDERM), Fortaleza, SES, Ceara, Brazil

6. Leprosy Laboratory, Oswaldo Cruz Institute, Fiocruz, Rio de Janeiro, RJ, Brazil

7. Training Center on Dermatology, University Hospital HUCFF and Public Health Institute, Federal University of Rio de Janeiro, Rio de Janeiro, RJ, Brazil

8. Leprosy Research Center, National Institute of Infectious Diseases, Tokyo, Japan

Abstract

ABSTRACT Skin biopsy samples from 145 relapse leprosy cases and from five different regions in Brazil were submitted for sequence analysis of part of the genes associated with Mycobacterium leprae drug resistance. Single nucleotide polymorphisms (SNPs) in these genes were observed in M. leprae from 4 out of 92 cases with positive amplification (4.3%) and included a case with a mutation in rpoB only, another sample with SNPs in both folP1 and rpoB , and two cases showing mutations in folP1 , rpoB , and gyrA , suggesting the existence of multidrug resistance (MDR). The nature of the mutations was as reported in earlier studies, being CCC to CGC in codon 55 in folP (Pro to Arg), while in the case of rpoB , all mutations occurred at codon 531, with two being a transition of TCG to ATG (Ser to Met), one TCG to TTC (Ser to Phe), and one TCG to TTG (Ser to Leu). The two cases with mutations in gyrA changed from GCA to GTA (Ala to Val) in codon 91. The median time from cure to relapse diagnosis was 9.45 years but was significantly shorter in patients with mutations (3.26 years; P = 0.0038). More than 70% of the relapses were multibacillary, including three of the mutation-carrying cases; one MDR relapse patient was paucibacillary.

Publisher

American Society for Microbiology

Subject

Microbiology (medical)

Reference39 articles.

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2. Interaction between DNA Gyrase and Quinolones: Effects of Alanine Mutations at GyrA Subunit Residues Ser 83 and Asp 87

3. Brazilian Ministry of Health (Brasil Ministério da Saúde)/SVS. 2009. Monitoramento das recidivas e da resistência medicamentosa em hanseníase no Brasil nota técnica no. 05/2009PNCH/SVS/MS. Brazilian Ministry of Health Federal District Brazil.

4. Brazilian Ministry of Health (Brasil Ministério da Saúde)/SVS. 2010. Instruções Normativas das ações de controle da hanseníase no SUS. Portaria no. 3.125/SVS-SAS. Brazilian Ministry of Health, Federal District, Brazil.

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