Abstract

The Evaluation of the Speed-Oligo® Mycobacteria Assay for Identification of Mycobacterium spp. from Smear Positive and Negative Sputum Samples

Highlights

  • Tuberculosis (TB) is a chronic infectious disease that is common all over the World [1]

  • Nontuberculous mycobacteria (NTM) infections are getting increase depend on a immunosuppression, AIDS, malignancy, drug abuse, bad living conditions or medical intervention

  • The aim of this study was to evaluate Speed-oligo® Direct Mycobacterium tuberculosis (SO-DMT) by using 25 type reference strains of mycobacteria (18 non-tuberculosis mycobacteria, M. tuberculosis H37Rv and M. tuberculosis H37Ra), 60 sputum samples (40 smear positive, 20 smear negative) collected from patient with suspected TB

Read more

Summary

Introduction

Tuberculosis (TB) is a chronic infectious disease that is common all over the World [1]. Speed-oligo® Direct Mycobacterium tuberculosis (SO-DMT) is an oligochromatographic test (Vircell SL, Santa Fe, Granada, Spain) for the specific identification of M. tuberculosis complex (MTC) from Mycobacterium genus in respiratory specimens. It is based on polymerase chain reaction targeting 16S rRNA and 16S-23S rRNA regions and double-reverse hybridization on a dipstick using probes bound to colloidal gold and to the membrane. It may represent a fast and easy alternative for differentiating between MTBC and NTM in direct samples at laboratories with standard laboratory equipment (thermocycler and thermoblock) [5,6,7,8]. The aim of this study was to evaluate SO-DMT by using 25 type reference strains of mycobacteria (18 non-tuberculosis mycobacteria, M. tuberculosis H37Rv and M. tuberculosis H37Ra), 60 sputum samples (40 smear positive, 20 smear negative) collected from patient with suspected TB

Objectives
Methods
Findings
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.