Publication | Closed Access
Real‐time PCR with internal amplification control for detecting tuberculosis: method design and validation
15
Citations
9
References
2009
Year
Internal Amplification ControlTuberculosis PreventionDiagnosisNucleic Acid Amplification TestDiagnosticsMedical MicrobiologyReal-time PcrBioanalysisReal-time Pcr TestDiagnostic TestTuberculosis DiagnosticsAntimicrobial ResistanceRadiologyHealth SciencesPulmonary TuberculosisMethod DesignTuberculosisClinical MicrobiologyReal‐time PcrInnovative DiagnosticsMicrobiologyMedicineDiagnostic Microbiology
Real-time PCR has been a major development in the diagnosis of tuberculosis. However, most tests do not include an internal amplification control (IAC), which therefore limits it clinical application. In this study a new, easy to perform real-time PCR test with IAC was designed and validated in clinical samples. The primers amplified a 163-bp fragment of IS6110 of Mycobacterium tuberculosis and the IAC was designed with a fragment of a different microorganism (Chlamydia trachomatis). The interassay and intraassay variation of this test were very low (0.45-1.65% and 0.18-1.80%, respectively). The detection accuracy was validated in 50 samples (25 urine, 25 sputum) with different concentrations of M. tuberculosis, 18 clinical isolates of non-tuberculous mycobacteria and 148 samples with clinical suspicion of pulmonary tuberculosis. The specificity was 100%. The detection limit of this PCR test without IAC was approximately 15 bacteria and with IAC approximately 32 bacteria. This real-time PCR with IAC assay can improve the detection of M. tuberculosis and contribute to standardization of this diagnostic technique.
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