A rapid and quantitative method for the detection of Leptospira species in human leptospirosis

摘要

Prompt laboratory diagnosis of leptospirosis infection facilitates patient management and initiation of therapy. A cost effective real-time PCR assay using SYBR Green I was developed for detection of pathogenic leptospires in serum specimens. Specific PCR products were obtained only with DNA of pathogenic Leptospira genomospecies. LightCycler PCR ability to distinguish between species was possible using melting Curves.. providing an approach for identification with a specific Tm assigned to a single species or set of species. Assay sensitivity was approximately 50 leptospires/ml, corresponding to one to two genome copies in a PCR mixture. Fifty-one patients who had clinical symptoms consistent with leptospirosis were tested both with a previously described rrs amplification and our real-time assay. Our LFBI real-time assay confirmed the diagnosis for 25 patients (49%, 25/51) and revealed an estimated density of 8.0 x 10(1)-3.9 x 10(4) leptospires/ml of blood. The total assay time for 12 clinical samples from sample to data analysis was less than 3 h. These data illustrate the potential of our LFBI real-time assay for the rapid detection of leptospires in serum samples and their subsequent quantification in a single run. (c) 2005 Federation of European Microbiological Societies. Published by Elsevier B.V. All rights reserved.