Digital Repository

Application of a Real Time Polymerase Chain Reaction (PCR) for Detection of Pathogenic Leptospira in Clinical Samples

Show simple item record

dc.contributor.author Denipitiya, D.T.H. en_US
dc.contributor.author Jiffrey, A.M. en_US
dc.contributor.author Abeyewickreme, W. en_US
dc.contributor.author Wellawaththge, C. en_US
dc.contributor.author Hapugoda, M.D. en_US
dc.date.accessioned 2015-06-11T04:39:09Z en_US
dc.date.available 2015-06-11T04:39:09Z en_US
dc.date.issued 2012 en_US
dc.identifier.citation Proceedings of the Annual Research Symposium, Faculty of Graduate Studies, University of Kelaniya. 2012; 13: 38. en_US
dc.identifier.uri en_US
dc.identifier.uri http://repository.kln.ac.lk/handle/123456789/8170 en_US
dc.description.abstract Leptospirosis, is a zoonotic disease with worldwide distribution, caused by pathogenic species of the genus Leptospira. It has the greatest impact on health in developing countries where it is often grossly under-recognized. Clinical features are similar to a range of other infectious diseases that occur in the same environmental and climatologic conditions. Therefore, laboratory confirmation is essential for proper management of leptospirosis patients. Molecular assays offer definitive laboratory confirmation of leptospirosis at the early phase of infection (1-5 days of fever) within a few hours. The objective of this study was to establish and evaluate potential use of a real time- PCR assay for early, definitive laboratory confirmation of leptospirosis patients. A SYBR green-based real time PCR assay targeting a 203 bp fragment on the secY gene which is conserved among pathogenic serovars of Leptospira was established using a reference DNA sample (Leptospira interrogans strain RGA). Analytical specificity of the assay was tested with the DNA from pathogenic and non-pathogenic Leptospira spp. and five other micro organisms. Analytical sensitivity of the assay was tested using serial dilutions of the reference sample. A panel of acute blood samples (n=150) collected during early phase of infection (1-5 days of fever) from leptospirosis suspected patients was used for evaluation of real time PCR vs qualitative PCR. The results show, real time PCR assay with high analytical specificity (100%) was established and the assay shows 100 times higher sensitivity over qualitative PCR assay (1.3 pg/ml). Real time PCR and qualitative PCR could diagnose current leptospirosis infection in 37.3% (56/150) and 19.3% (29/150) suspected patients respectively. These results indicate high sensitivity of real time PCR over qualitative PCR for diagnosis of leptospirosis patients. In conclusion, this study shows that real time PCR has the potential to facilitate rapid and sensitive diagnosis of acute leptospirosis during early phase of infection. en_US
dc.language.iso en en_US
dc.publisher University of Kelaniya en_US
dc.subject.mesh Leptospirosis en
dc.subject.mesh Leptospirosis-diagnosis en
dc.subject.mesh Real-Time Polymerase Chain Reaction en
dc.subject.mesh Real-Time Polymerase Chain Reaction-methods en
dc.title Application of a Real Time Polymerase Chain Reaction (PCR) for Detection of Pathogenic Leptospira in Clinical Samples en_US
dc.type Conference Abstract en_US
dcterms.description Annual Research Symposium Abstracts, FGS, University of Kelaniya, November, 2012, Kelaniya en
dc.identifier.department Parasitology en
dc.identifier.department Molecular Medicine Unit en


Files in this item

This item appears in the following Collection(s)

Show simple item record

Search Digital Repository


Browse

My Account