Your browser doesn't support javascript.
loading
Detection of multidrug-resistant Mycobacterium tuberculosis strains isolated in Brazil using a multimarker genetic assay for katG and rpoB genes
Café Oliveira, Luita Nice; Muniz-Sobrinho, Jairo da Silva; Viana-Magno, Luiz Alexandre; Oliveira Melo, Sônia Cristina; Macho, Antonio; Rios-Santos, Fabrício.
  • Café Oliveira, Luita Nice; Universidade Estadual de Santa Cruz (UESC). Laboratório de Farmacogenômica e Epidemiologia Molecular (LAFEM). Ilhéus. BR
  • Muniz-Sobrinho, Jairo da Silva; Universidade Estadual de Santa Cruz (UESC). Laboratório de Farmacogenômica e Epidemiologia Molecular (LAFEM). Ilhéus. BR
  • Viana-Magno, Luiz Alexandre; Universidade Estadual de Santa Cruz (UESC). Laboratório de Farmacogenômica e Epidemiologia Molecular (LAFEM). Ilhéus. BR
  • Oliveira Melo, Sônia Cristina; Universidade Estadual de Santa Cruz (UESC). Laboratório de Farmacogenômica e Epidemiologia Molecular (LAFEM). Ilhéus. BR
  • Macho, Antonio; Universidade Estadual de Santa Cruz (UESC). Laboratório de Farmacogenômica e Epidemiologia Molecular (LAFEM). Ilhéus. BR
  • Rios-Santos, Fabrício; Universidade Estadual de Santa Cruz (UESC). Laboratório de Farmacogenômica e Epidemiologia Molecular (LAFEM). Ilhéus. BR
Braz. j. infect. dis ; 20(2): 166-172, Mar.-Apr. 2016. tab, graf
Article in English | LILACS | ID: lil-780813
ABSTRACT
Abstract Multidrug-resistant tuberculosis (MDRTB) is a serious world health problem that limits public actions to control tuberculosis, because the most used anti-tuberculosis first-line drugs fail to stop mycobacterium spread. Consequently, a quick detection through molecular diagnosis is essential to reduce morbidity and medical costs. Despite the availability of several molecular-based commercial-kits to diagnose multidrug-resistant tuberculosis, their diagnostic value might diverge worldwide since Mycobacterium tuberculosis genetic variability differs according to geographic location. Here, we studied the predictive value of four common mycobacterial mutations in strains isolated from endemic areas of Brazil. Mutations were found at the frequency of 41.9% for katG, 25.6% for inhA, and 69.8% for rpoB genes in multidrug-resistant strains. Multimarker analysis revealed that combination of only two mutations (“katG/S315T + rpoB/S531L”) was a better surrogate of multidrug-resistant tuberculosis than single-marker analysis (86% sensitivity vs. 62.8%). Prediction of multidrug-resistant tuberculosis was not improved by adding a third or fourth mutation in the model. Therefore, rather than using diagnostic kits detecting several mutations, we propose a simple dual-marker panel to detect multidrug-resistant tuberculosis, with 86% sensitivity and 100% specificity. In conclusion, this approach (previous genetic study + analysis of only prevalent markers) would considerably decrease the processing costs while retaining diagnostic accuracy.
Subject(s)


Full text: Available Index: LILACS (Americas) Main subject: Bacterial Proteins / DNA-Directed RNA Polymerases / Catalase / Drug Resistance, Multiple, Bacterial / Isoniazid / Antitubercular Agents Type of study: Diagnostic study / Prognostic study Limits: Humans Country/Region as subject: South America / Brazil Language: English Journal: Braz. j. infect. dis Journal subject: Communicable Diseases Year: 2016 Type: Article Affiliation country: Brazil Institution/Affiliation country: Universidade Estadual de Santa Cruz (UESC)/BR

Similar

MEDLINE

...
LILACS

LIS


Full text: Available Index: LILACS (Americas) Main subject: Bacterial Proteins / DNA-Directed RNA Polymerases / Catalase / Drug Resistance, Multiple, Bacterial / Isoniazid / Antitubercular Agents Type of study: Diagnostic study / Prognostic study Limits: Humans Country/Region as subject: South America / Brazil Language: English Journal: Braz. j. infect. dis Journal subject: Communicable Diseases Year: 2016 Type: Article Affiliation country: Brazil Institution/Affiliation country: Universidade Estadual de Santa Cruz (UESC)/BR