Abstract:
Rabies is a highly fatal viral disease transmitted through the saliva of infected animals, especially dogs and cats. In the Philippines, rabies is a serious public health problem, causing 200 to 500 deaths annually. This study was designed to develop a Reverse Transcription - Polymerase Chain Reaction (RT-PCR) protocol for the detection of rabies virus from human saliva. Specifically, this study aimed to optimize RT-PCR conditions such as primer pair combination and annealing temperature; validate the optimized protocol using human saliva samples; and determine the limit of detection. SuperScript ® III Reverse Transcriptase Platinum® Taq DNA polymerase was used for the RT-PCR run and QIAGEN RNeasy extraction kit was used for the extraction of RNA from human saliva samples. Results showed that the RT-PCR protocol developed was useful for the diagnosis of rabies virus using human saliva. The best primer pair combination is the forward primer JW 12(C) (ATGTAACACCCCTACAATG); and reverse primer JW6(DPL) (CAATTCGCACACATTTTGTG). The optimum annealing temperature for this primer pair combination is 60°C. The protocol developed is useful for a template concentration of 58 pg/mL.
