Abstract

Tuberculosis (TB) remains as a major public health issue in developing countries. Accurate detection is essential for the proper management of patients with active disease. Here, we present a simple DNAzol-LAMP (loop-mediated isothermal amplification) procedure for the detection of Mycobacterium tuberculosis in sputum specimens. Twenty smear-positive sputum samples were analyzed as follows: (i) Genetic material was extracted by a standard DNAzol protocol, and (ii) mycobacterial DNA was detected by a typical TB-specific loop-mediated isothermal amplification method. Results and diagnostic test performance attests to the suitability of the proposed procedure.

Highlights

  • Tuberculosis (TB) continues among the major threats to public health

  • The study was conducted in accordance with the Declaration of Helsinki, and the protocol was approved by the Ethics Committee of the General Hospital of Tijuana (Project identification code 10/05/2016)

  • AAnmalpyslisficoaf tAiomnplpifirocadtuiocntsPwroedruectsseparated by agarose gel electrophoresis, stained with ethidium bromide, visualized under UV light, and documented using a Bio‐Rad GelDoc EZ System

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Summary

Introduction

Tuberculosis (TB) continues among the major threats to public health. In 2015, the WHO estimated 10.4 million new cases [2], suggesting that both late detection and misdiagnosis sustain the disease prevalence [3]. Smear microscopy, and bacterial culture, are the foremost means for the detection of Mycobacterium tuberculosis, the leading causative agent of TB in humans [4]. But has low sensitivity, while bacterial culture (the gold standard) is sensitive, but it takes up to six weeks to provide a reliable result. Despite their intrinsic disadvantages, to date, these methods are applied for routine mycobacteriology [5,6]

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