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Heterogeneous persistence of Mycobacterium leprae in oral and nasal mucosa of multibacillary patients during multidrug therapy.
Neumann, Arthur da Silva; Fontes, Amanda Nogueira Brum; Lopes, Márcia Quinhones Pires; Suffys, Philip Noel; Moraes, Milton Ozório; Lara, Flávio Alves.
  • Neumann ADS; Fundação Oswaldo Cruz-Fiocruz, Instituto Oswaldo Cruz, Laboratório de Microbiologia Celular, Rio de Janeiro, RJ, Brasil.
  • Fontes ANB; Universidade Federal do Rio de Janeiro, Instituto de Ciências Biomédicas, Laboratório de Investigação em Neuroprogramação, Rio de Janeiro, RJ, Brasil.
  • Lopes MQP; Ministério da Saúde, Secretaria de Ciência, Tecnologia e Insumos Estratégicos, Departamento de Ciência e Tecnologia, Brasília, DF, Brasil.
  • Suffys PN; Fundação Oswaldo Cruz-Fiocruz, Laboratório de Biologia Molecular Aplicada à Micobactérias, Rio de Janeiro, RJ, Brasil.
  • Moraes MO; Fundação Oswaldo Cruz-Fiocruz, Laboratório de Biologia Molecular Aplicada à Micobactérias, Rio de Janeiro, RJ, Brasil.
  • Lara FA; Fundação Oswaldo Cruz-Fiocruz, Laboratório de Biologia Molecular Aplicada à Micobactérias, Rio de Janeiro, RJ, Brasil.
Mem Inst Oswaldo Cruz ; 117: e220058, 2022.
Article en En | MEDLINE | ID: mdl-36259791
ABSTRACT

BACKGROUND:

Leprosy is curable by multidrug therapy (MDT) treatment regimen ranging from six to 12 months. The variable levels of tolerance and adherence among patients can, however, result in treatment failure and the emergence of drug-resistant strains.

OBJECTIVES:

Describe the impact of MDT over Mycobacterium leprae viability in patient's oral and nasal mucosa along treatment.

METHODS:

Mycobacterium leprae viability was monitored by quantitative polymerase chain reaction (qPCR) quantification of 16S rRNA in lateral and contralateral scrapings of oral and nasal mucosa of 10 multibacillary patients along the initial five months of treatment.

FINDINGS:

The results demonstrated high heterogenicity of M. leprae viability among patients and between nasal and oral samples. Of six patients who presented good adherence and tolerance to the treatment, only four displayed absence of M. leprae viability in both samples three months after the first MDT dose, while for the other two, the absence of M. leprae viability in the oral and nasal cavities was only detected five months after the first dose. MAIN

CONCLUSIONS:

We concluded that qPCR of 16S rRNA for the determination of M. leprae viability in nasal and oral scraping samples could represent an interesting approach to monitor treatment efficacy.
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