UNIGE document Scientific Article
previous document  unige:25316  next document
add to browser collection

Robustness of a loop-mediated isothermal amplification reaction for diagnostic applications

Hibbs, Jonathan
Bonetti, Eve-Julie
Boehme, Catharina C
Notomi, Tsugunori
Perkins, Mark D
Published in FEMS Immunology and Medical Microbiology. 2011, vol. 62, no. 1, p. 41-8
Abstract We evaluated the robustness of loop-mediated isothermal amplification (LAMP) of DNA for bacterial diagnostic applications. Salmonella enterica serovar Typhi was used as the target organism and compared with a real-time quantitative PCR (qPCR) for testing assay performance and reproducibly, as well as the impact of pH and temperature stability. This isothermal amplification method appeared to be particularly robust across 2 pH units (7.3-9.3) and temperature values (57-67 °C). The detection limit was comparable to that observed using optimized home-brew qPCR assays. The specificity of the amplification reaction remained high even at temperatures markedly different from the optimal one. Exposing reagents to the ambient temperature during the preparation of the reaction mixture as well as prolonging times for preparing the amplification reaction did not yield false-positive results. LAMP remained sensitive and specific despite the addition of untreated biological fluids such as stool or urine that commonly inhibit PCR amplification. Whereas the detection of microorganisms from whole blood or a blood-culture medium typically requires extensive sample purification and removal of inhibitors, LAMP amplification remained more sensitive than conventional qPCR when omitting such preparatory steps. Our results demonstrate that LAMP is not only easy to use, but is also a very robust, innovative and powerful molecular diagnostic method for both industrialized and developing countries.
Keywords Bacteriological TechniquesBlood/microbiologyDNA Primers/geneticsFeces/microbiologyHumansHydrogen-Ion ConcentrationMolecular Diagnostic TechniquesNucleic Acid Amplification Techniques/methodsPolymerase Chain ReactionSalmonella typhi/classification/genetics/isolation & purificationSensitivity and SpecificityTemperatureTyphoid Fever/diagnosis/microbiology
PMID: 21276085
Full text
Article (Published version) (427 Kb) - document accessible for UNIGE members only Limited access to UNIGE
Research group Analyse génomique et fonctionnelle du staphylocoque doré (604)
(ISO format)
FRANCOIS, Patrice et al. Robustness of a loop-mediated isothermal amplification reaction for diagnostic applications. In: FEMS Immunology and Medical Microbiology, 2011, vol. 62, n° 1, p. 41-8. https://archive-ouverte.unige.ch/unige:25316

215 hits

0 download


Deposited on : 2013-01-10

Export document
Format :
Citation style :