Evaluation of multiplex PCR assay for detection of Babesia spp, Ehrlichia canis and Trypanosoma evansi in dogs

• Published in: Acta tropica 2018-12, Vol.188, p.58-67
• Main Authors: Azhahianambi, Palavesam, G, Jyothimol, GR, Baranidharan, M, Aravind, R, Ram Narendran, Latha, Bhaskaran Ravi, M, Raman
• Format: Article
• Language: English
• Subjects: Babesia spp; Diagnostic sensitivity and specificity; Ehrlichia canis; Haemoparasite; Multiplex PCR; Singular PCR; Trypanosoma evansi
• ISSN: 0001-706X; 1873-6254
• DOI: 10.1016/j.actatropica.2018.08.028

[Display omitted] •A multiplex PCR to detect the DNA of two intracellular blood parasites (Babesia spp and Ehrlichia canis) and an extracellular blood parasite (Trypanosoma evansi) of dog was evaluated using field samples with high level of diagnostic specificity (97.5, E = 0.025–100%, E = 0.008).•The diagnostic sensitivity of multiplex PCR was low (40.45%, E = 0.1) to moderate (66.7%, E = 0.11) in detection of Babesia spp and E. canis, respectively when compared with singular PCR. However, the diagnostic sensitivity of multiplex PCR in the detection of T. evansi (95%, E = 0.065) is comparable with singular PCR.•The strength of agreement between singular PCR and multiplex PCR in detection of Babesia spp (Kappa value = 0.445 ± 0.057) and E. canis (Kappa value = 0.708 ± 0.052) was designated as ‘moderate’ and ‘good’, respectively. Whereas, the strength of agreement was ‘very good’ between the two tests in detection of T. evansi (Kappa value = 0.968 ± 0.018).•The multiplex PCR amplicon size is negatively correlated with sensitivity (R= -0.99) and specificity (R= −0.83).The GC content of forward and reverse primers is positively correlated (R = 0.62, R = 0.78) with specificity.•The multiplex PCR was found to be 10 fold less sensitive when compared to the singular PCR counterpart. A multiplex PCR test was evaluated to detect the DNA of three important dog haemoparasites by comparing with singular PCR counterpart on clinical blood samples of dogs in and around Chennai, Tamil Nadu, India. Initial screening of samples was done by microscopic examination of peripheral blood smear and singular PCR and those found exclusively positive for Babesia spp, Ehrlichia canis and Trypanosoma evansi and concurrent infections were used to standardize multiplex PCR. Amplicons of 619 bp, 377 bp and 227 bp corresponding to Babesia spp (18S rRNA gene), E. canis (VirB9 gene), and T.evansi (VSG gene) respectively were amplified, without any non-specific amplification. The laboratory sensitivity (91.7% to 100%) and specificity (100%) of the multiplex PCR were calculated using ‘true positive’ and ‘true negative’ dog blood samples obtained in the initial screening process. Clinical blood samples from 287 dogs were screened using singular PCR and multiplex PCR tests for the presence of genome of Babesia spp, E. canis and T. evansi. The multiplex PCR was found to have high level of diagnostic specificity (97.5%–100%) in the detection of all three dog blood parasites and high level of diag