Establishing a novel realtime RT-PCR to detect Zika and Chikungunya viruses
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Abstract
Objective: To establish of a real-time RT-PCR method for the detection of Zika and Chikungunia viruses. Subject and method: This real-time RT-PCR-based method is for the amplification of target genes, using relevant negative, ZIKV and CHIKV controls that were provided by NIHE and WHO, respectively. Detection limits and sensitivity were determined by a range of spiking assays from 105÷100 copies/µl. Result: Our data demonstrated that the LOD of our newly developed method for detecting Zika virus and Chikungunia virus were 5 and 3 RNA copies/µl that are equal to 500 and 300 copies/ml. Specificity and sensitivity were 100 - 95%, respectively. Conclusion: A real-time RT-PCR assay for the detection of Zika virus and Chikungunia virus was succesfully established.
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References
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