Tick-Borne Pathogens Screening Using a Multiplex Real-Time Polymerase Chain Reaction-Based Method

Purpose This study aims to develop and evaluate a cost-effective, user-friendly multiplex quantitative real-time polymerase chain reaction (qPCR) method for detecting multiple tick-borne pathogens associated with human and veterinary diseases. Methods In silico PCR was performed to design and evaluate primer sequences reported for amplifying Rickettsia spp ., Borrelia spp. , and Ehrlichia spp. Single and multiplex qPCR assays were then standardized to detect individual pathogens and multiple pathogens in a single reaction. Positive controls were generated to determine the dynamic range of the methods. In the validation phase, a total of 800 samples were screened for the presence of tick-borne pathogens. Results Identification in a single qPCR reaction (multiplex) of Ehrlichia spp . , and Borrelia spp. with a limit of detection of 10 copies and Rickettsia spp . with 100 copies, a PCR efficiency (E) of 90–100% and a coefficient of correlation ( R 2 ) of 0.998–0.996 for all pathogens. Conclusion The ability to detect three significant pathogens (Ehrlichia spp ., Rickettsia spp ., and Borrelia spp .) in a single qPCR reaction offers a significant advantage in the field of molecular diagnostics for tick-borne diseases. This advancement has a profound impact on public health as it facilitates the selection of appropriate treatment protocols, thereby reducing complications associated with disease progression. The streamlined approach provided by this method simplifies the diagnostic process and enables timely intervention, ultimately improving patient outcomes and mitigating the potential risks associated with untreated or misdiagnosed tick-borne infections.