Loop-Mediated Isothermal Amplification for Direct Detection of Mycobacterium tuberculosis Complex, M. avium , and M. intracellulare in Sputum Samples
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Open Access
- 1 June 2003
- journal article
- research article
- Published by American Society for Microbiology in Journal of Clinical Microbiology
- Vol. 41 (6) , 2616-2622
- https://doi.org/10.1128/jcm.41.6.2616-2622.2003
Abstract
Loop-mediated isothermal amplification (LAMP) is a novel nucleic acid amplification method in which reagents react under isothermal conditions with high specificity, efficiency, and rapidity. We used LAMP for detection of Mycobacterium tuberculosis complex, Mycobacterium avium , and Mycobacterium intracellulare directly from sputum specimens as well as for detection of culture isolates grown in a liquid medium (MGIT; Nippon Becton Dickinson Co., Ltd., Tokyo, Japan) or on a solid medium (Ogawa's medium). Species-specific primers were designed by targeting the gyrB gene, and their specificities were validated on 24 mycobacterial species and 7 nonmycobacterial species. The whole procedure is quite simple, starting with the mixing of all reagents in a single tube, followed by an isothermal reaction during which the reaction mixture is held at 63°C. The resulting amplicons are visualized by adding SYBR Green I to the reaction tube. The only equipment needed for the amplification reaction is a regular laboratory water bath or heat block that furnishes a constant temperature of 63°C. The assay had a detection limit of 5 to 50 copies of purified DNA with a 60-min incubation time. The reaction time could be shortened to 35 min for the species identification of M. tuberculosis complex, M. avium , and M. intracellulare from a solid-medium culture. Residual DNA lysates prepared for the Amplicor assay (Roche Diagnostics GmbH) from 66 sputum specimens were tested in the LAMP assay. Although the sample size used for the latter assay was small, 2.75 μl of the DNA lysates, it showed a performance comparable with that of the Amplicor assay, which required 50 μl of the lysates. This LAMP-based assay is simple, rapid, and sensitive; a result is available in 35 min for a solid-medium culture and in 60 min for a liquid-medium culture or for a sputum specimen that contains a corresponding amount of DNA available for testing.Keywords
This publication has 38 references indexed in Scilit:
- Rapid-Cycle PCR and Fluorimetry for Detection of MycobacteriaJournal of Clinical Microbiology, 2002
- Accelerated reaction by loop-mediated isothermal amplification using loop primersMolecular and Cellular Probes, 2002
- Isolation of Single-Stranded DNA from Loop-Mediated Isothermal Amplification ProductsBiochemical and Biophysical Research Communications, 2002
- RIDOM: Ribosomal Differentiation of Medical Micro-organisms DatabaseNucleic Acids Research, 2002
- Detection of Loop-Mediated Isothermal Amplification Reaction by Turbidity Derived from Magnesium Pyrophosphate FormationBiochemical and Biophysical Research Communications, 2001
- Application of a Simple Multiplex PCR To Aid in Routine Work of the Mycobacterium Reference LaboratoryJournal of Clinical Microbiology, 2001
- Loop-mediated isothermal amplification of DNANucleic Acids Research, 2000
- Intuitive hypertext-based molecular identification of micro-organismsThe Lancet, 1999
- Nucleic acid sequence-based amplification (NASBA) for the identification of mycobacteriaJournal of General Microbiology, 1993
- Evaluation of Gen-Probe DNA hybridization systems for the identification of mycobacterium tuberculosis and mycobacterium avium-intracellulareDiagnostic Microbiology and Infectious Disease, 1987