Abstract
We assayed Zika virus–infected mosquitoes stored at room temperature for ≤30 days for live virus by using plaque assay and virus RNA by using real-time reverse transcription PCR. Viable virus was detected in samples stored ≤10 days, and virus RNA was detected in samples held for 30 days.
Cite
CITATION STYLE
APA
Burkhalter, K. L., & Savage, H. M. (2017). Detection of zika virus in desiccated mosquitoes by real-time reverse transcription PCR and plaque assay. Emerging Infectious Diseases, 23(4), 680–681. https://doi.org/10.3201/eid2304.161772
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