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DC Field | Value | Language |
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dc.contributor.author | Uduwawala, H. | |
dc.contributor.author | Manamperi, A. | |
dc.contributor.author | Gunaratna, G.P.S. | |
dc.contributor.author | Karunanayake, L. | |
dc.contributor.author | Ceruti, A. | |
dc.contributor.author | Wahed, A.A.E. | |
dc.contributor.author | Fernando, L. | |
dc.contributor.author | Premaratna, R. | |
dc.contributor.author | Hapugoda, M. | |
dc.date.accessioned | 2024-03-21T04:55:48Z | |
dc.date.available | 2024-03-21T04:55:48Z | |
dc.date.issued | 2024 | |
dc.identifier.citation | PLoS One.2024;19(3):e0295287 | en_US |
dc.identifier.issn | 1932-6203 (Electronic) | |
dc.identifier.uri | http://repository.kln.ac.lk/handle/123456789/27784 | |
dc.description | Indexed in MEDLINE | en_US |
dc.description.abstract | Leptospirosis is the most widespread zoonosis in the world. The disease is more prevalent in tropical regions where the majority of developing countries are located. Leptospirosis is considered a protean manifestation zoonosis with severity of the disease ranging from a mild febrile illness to a severe and life-threatening illness. Clinical symptoms of leptospirosis overlap with other tropical febrile illnesses. Early, rapid, and definitive diagnosis is important for effective patient management. Since Polymerase Chain Reaction (PCR)-based assays are not readily available in most clinical settings, there is a need for an affordable, simple, and rapid diagnostic test. Quantitative PCR (qPCR) and Recombinase Polymerase Amplification (RPA) were implemented at the Faculty of Medicine, University of Kelaniya, and a prospective study to evaluate RPA for diagnosis of acute phase of leptospirosis was conducted. Results indicate that RPA and qPCR were positive in 81% (98/121) of the total positive and acute clinical samples. Of the 81 positive MAT confirmed patients 60 (74%) and 53 (65%) were positive with qPCR and RPA respectively. Retrospective evaluation revealed a high diagnostic accuracy (sensitivity-70% and specificity-87%) of RPA compared to MAT as the reference gold standard. Results further suggest that there is no significant difference between the two assays, qPCR and RPA-SwiftX (P = 0.40). Laboratory procedures for the extraction and detection by qPCR in the laboratory have been optimized to obtain results within 6 hours. However, the RPA-SwiftX method under field conditions took 35 minutes. The RPA-SwiftX method could replace the qPCR which shows similar sensitivity and specificity. Therefore, RPA established under the current study presents a powerful tool for the early and rapid diagnosis of leptospirosis at point-of-care. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Public Library of Science | en_US |
dc.subject | polymerase | en_US |
dc.title | Detection of pathogenic Leptospira with rapid extraction followed by recombinase polymerase amplification (RPA) and quantitative polymerase chain reaction (qPCR) assay-A comprehensive study from Sri Lanka | en_US |
dc.type | Article | en_US |
Appears in Collections: | Journal/Magazine Articles |
Files in This Item:
File | Description | Size | Format | |
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pone.0295287.pdf | 818.48 kB | Adobe PDF | View/Open |
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