Emergence and Transmission of Drug-/Multidrug-resistant Mycobacterium leprae in a Former Leprosy Colony in the Brazilian Amazon

Author:

Rosa Patrícia S1,D’Espindula Helena R S2,Melo Ana C L3,Fontes Amanda N B4,Finardi Amanda J1,Belone Andréa F F1,Sartori Beatriz G C1,Pires Carla A A5,Soares Cleverson T1,Marques Flávio B1,Branco Francisco J D3,Baptista Ida M F D1,Trino Lázara M1,Fachin Luciana R V1,Xavier Marília B56,Floriano Marcos C7,Ura Somei1,Diório Suzana M1,Delanina Wladimir F B1,Moraes Milton O4,Virmond Marcos C L1,Suffys Philip N4,Mira Marcelo T2

Affiliation:

1. Division of Research and Education, Instituto Lauro de Souza Lima, Bauru, São Paulo, Brazil

2. Graduate Program in Health Sciences, School of Medicine, Pontifícia Universidade Católica do Paraná, Curitiba, Brazil

3. Centro de Referência Nacional em Dermatologia Sanitária Dona Libânia, Fortaleza, Ceará, Brazil

4. Laboratory of Molecular Biology Applied in Mycobacteria, Fundação Oswaldo Cruz, Rio de Janeiro, Brazil

5. Core of Tropical Diseases, Universidade Federal do Pará, Belém, Brazil

6. Center for Biological and Health Sciences, Universidade do Estado do Pará, Belém, Brazil

7. Department of Dermatology, Universidade Federal de São Paulo, Brazil

Abstract

AbstractBackgroundLeprosy has been treated with multidrug therapy, which has been distributed for free across the globe and regarded as highly efficient. However, the impossibility of growing Mycobacterium leprae in axenic media has historically impaired assessments of M. leprae resistance, a parameter only recently detectable through molecular methods.MethodsA systematic, population-based search for M. leprae resistance in suspected leprosy relapse cases and contacts was performed in Prata Village, an isolated, hyperendemic, former leprosy colony located in the Brazilian Amazon. Results led to an extended active search involving the entire Prata population. Confirmed leprosy cases were investigated for bacterial resistance using a combination of in vivo testing and direct sequencing of resistance genes folP1, rpoB, and gyrA. A molecular epidemiology analysis was performed using data from 17 variable number tandem repeats (VNTR).ResultsMycobacterium leprae was obtained from biopsies of 37 leprosy cases (18 relapses and 19 new cases): 16 (43.24%) displayed drug-resistance variants. Multidrug resistance to rifampicin and dapsone was observed in 8 relapses and 4 new cases. Single resistance to rifampicin was detected in 1 new case. Resistance to dapsone was present in 2 relapses and 1 new case. Combined molecular resistance and VNTR data revealed evidence of intra-familial primary transmission of resistant M. leprae.ConclusionsA comprehensive, population-based systematic approach to investigate M. leprae resistance in a unique population revealed an alarming scenario of the emergence and transmission of resistant strains. These findings may be used for the development of new strategies for surveillance of drug resistance in other populations.

Funder

Conselho Nacional de Desenvolvimento Científico e Tecnológico

Fundação Araucária

Damien Foundation

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

Reference27 articles.

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3. Primary dapsone-resistant leprosy;Pearson;Lepr Rev,1977

4. Rifampin-resistant leprosy;Jacobson;Lancet,1976

5. Chemotherapy of leprosy for control programmes;World Health Organization;World Health Organ Tech Rep Ser,1982

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