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Extensively drug-resistant tuberculosis in Myanmar: burden and mutations causing second-line drug resistance.
Ei, P W; Aung, W W; Nyunt, W W; Swe, T L; Htwe, M M; Win, S M; Aung, S T; Chang, C L; Lee, H-Y; Lee, J S.
  • Ei PW; Advanced Molecular Research Centre, Department of Medical Research, Yangon, Myanmar, Department of Biomedical Laboratory Science, Collage of Health Sciences, Yonsei University, Wonju, Republic of Korea.
  • Aung WW; Advanced Molecular Research Centre, Department of Medical Research, Yangon, Myanmar.
  • Nyunt WW; National Tuberculosis Programme, Department of Public Health, Naypyidaw, Myanmar.
  • Swe TL; National Tuberculosis Programme, Department of Public Health, Naypyidaw, Myanmar.
  • Htwe MM; Advanced Molecular Research Centre, Department of Medical Research, Yangon, Myanmar.
  • Win SM; Advanced Molecular Research Centre, Department of Medical Research, Yangon, Myanmar.
  • Aung ST; National Tuberculosis Programme, Department of Public Health, Naypyidaw, Myanmar.
  • Chang CL; Pusan National University Yangsan Hospital, Yangsan.
  • Lee HY; Department of Biomedical Laboratory Science, Collage of Health Sciences, Yonsei University, Wonju, Republic of Korea.
  • Lee JS; International Tuberculosis Research Center, Changwon, Republic of Korea.
Int J Tuberc Lung Dis ; 22(1): 47-53, 2018 01 01.
Article en En | MEDLINE | ID: mdl-29297425
SETTING: Two tuberculosis (TB) reference laboratories in Myanmar. OBJECTIVES: To determine the proportion of extensively drug-resistant TB (XDR-TB) cases among multidrug-resistant TB (MDR-TB) cases and the mutations that cause resistance to second-line drugs in Myanmar. DESIGN: This was a cross-sectional, retrospective study. Multidrug-resistant Mycobacterium tuberculosis isolates were collected during 2015-2016. Phenotypic drug susceptibility testing (DST) was performed and drug-resistant mutations identified by sequencing. Genotypes were determined to explain relationships between drug resistance patterns and genotypes. RESULTS: Of 89 MDR-TB isolates, 12 were XDR-TB and 24 were pre-XDR-TB, with 21 resistant to fluoroquinolones (FQs) and 3 to second-line injectable agents (SLIDs). High rates of cross-resistance among second-line drugs were observed. Correlations between phenotypic and molecular DST against FQs and SLIDs were 91% in both cases. The most frequent mutation in FQ-resistant isolates was D94G (8/21) in gyrA and A1401G (11/15) in rrs in those resistant to SLIDs. The dominant genotype was the Beijing type (76/89). CONCLUSION: There were high proportions of XDR-TB and pre-XDR-TB among MDR-TB cases; cross-resistance among second-line drugs was high, with various types of genetic mutations. These data suggest that resistance to second-line anti-tuberculosis drugs should be monitored intensively, and molecular DST should be employed.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Tuberculosis Resistente a Múltiples Medicamentos / Tuberculosis Extensivamente Resistente a Drogas / Mycobacterium tuberculosis / Antituberculosos Tipo de estudio: Observational_studies / Prevalence_studies / Risk_factors_studies Límite: Humans País como asunto: Asia Idioma: En Año: 2018 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Tuberculosis Resistente a Múltiples Medicamentos / Tuberculosis Extensivamente Resistente a Drogas / Mycobacterium tuberculosis / Antituberculosos Tipo de estudio: Observational_studies / Prevalence_studies / Risk_factors_studies Límite: Humans País como asunto: Asia Idioma: En Año: 2018 Tipo del documento: Article