- Turkish Journal of Veterinary and Animal Sciences
- Volume:42 Issue:3
- Evaluation of real-time PCR, MAT, and recombinant LipL32-based ELISA for the diagnosis of canine lep...
Evaluation of real-time PCR, MAT, and recombinant LipL32-based ELISA for the diagnosis of canine leptospirosis in a disease-endemic South Indian state, Kerala
Authors : Siju JOSEPH, Mangattumuruppel MINI, Vamshi Krishna SRIRAM, Ramachandran AMBILY, Thazathuveettil ARAVINDAKSHAN, Sreedharannair Ajith KUMAR
Pages : 191-197
View : 8 | Download : 6
Publication Date : 0000-00-00
Article Type : Research Paper
Abstract :Canine samples insert ignore into journalissuearticles values(n = 425); collected from cases of suspected leptospirosis over a period of 6 years were tested using the microscopic agglutination test insert ignore into journalissuearticles values(MAT);, recombinant LipL32-based IgM and IgG ELISA, and real-time PCR insert ignore into journalissuearticles values(RT PCR);. A prevalence of 69.41% was recorded by MAT. Among the different tests, IgG ELISA was observed to have maximum agreement with that of MAT insert ignore into journalissuearticles values(k-0.810);, followed by IgM ELISA insert ignore into journalissuearticles values(k-0.762.);. RT PCR had only slight agreement with MAT insert ignore into journalissuearticles values(k-0.156);. However, the percentage positivity of RT PCR with samples with MAT titers of 1:100 and 1:200 were 76.47% and 85.96%, respectively, indicating the reliability of RT PCR in the early phase of the disease. The values for the samples at higher MAT titers of 1:400 and 1:800 were 10.58% and 1.2%, respectively, clearly indicating the unreliability of the test for samples having high antibody titers. It was concluded that IgG ELISA could be used as the routine test for the diagnosis of canine leptospirosis in this disease-endemic region. Samples with negative results that have high symptomatic correlation with leptospirosis may be tested by PCR/RT PCR for the detection of the pathogen well ahead of antibody generation.Keywords : Microscopic agglutination test, ELISA, real time PCR, leptospirosis, disease endemic region