Detection and discrimination of two Brucella species by multiplex real-time PCR and high-resolution melt analysis curve from human blood and comparison of results using RFLP

Objective(s): Rapid and accurate detection of Brucella abortus and Brucella melitensis from clinical samples is so important because antibiotic treatment has major side effects. This study reveals a new method in detection of clinical samples of brucellosis using real-time PCR and high-resolution melt (HRM) curve analysis. Materials and Methods: ۱۶۰ brucellosis suspicious samples with more than ۱/۸۰ serum antibody titers were collected and the results were compared with the RFLP method. In order to amplify the sequences for HRM analysis, vdcc, int-hyp and glk and for RFLP, omp۲a and omp۲b with PstI and Hinf۱ restriction endonuclease were used. At last, the accuracy and specificity of the two methods were compared with each other. Results: Out of these ۱۶۰ samples, multiplex real time PCR showed ۱۰۸ positive samples (۶۷.۵%), including ۵۶% B. melitensis and ۴۴% B. abortus; whereas in PCR-RFLP ۵۲ out of ۱۶۰ samples were positive, where recognition of two species were accordant with HRM analysis, separation was based on the size of the amplified fragment. Using the designed primers and performing the assay, we confirmed this method to be much faster and have lower cost with more than ۹۹% accuracy compared to methods such as RFLP. Conclusion: The present study showed that this technique, which scans gene segments and creates an analysis pattern for detection of clinical samples, is useful and more dominant compared with PCR-RFLP. Thus, this method can be used for brucellosis detection, and clinical and epidemiological research.

Keywords:

Brucella , High-resolution melt - analysis , Multiplex PCR , RFLP