Laboratory Evaluation of the Rapid Analyte Measurement Platform Assay to Detect Dengue Virus in Mosquito Pools

• Published in: Journal of the American Mosquito Control Association Vol. 37; no. 3; pp. 152 - 156
• Main Authors: Burkhalter, Kristen L., Savage, Harry M.
• Format: Journal Article
• Language: English
• Published: Mount Laurel American Mosquito Control Association 01.09.2021
• Subjects: Antigens; Aquatic insects; Assaying; Biosafety; Buffers; Deactivation; Dengue fever; Detergents; Human diseases; Inactivation; Microbiological strains; Mosquitoes; Sensitivity analysis; Serotypes; Specificity; Vector-borne diseases; Viruses
• ISSN: 8756-971X; 1943-6270; 1943-6270
• DOI: 10.2987/21-7013.1

We report the results of a laboratory sensitivity and specificity evaluation of the Rapid Analyte Measurement Platform (RAMP®) Dengue Virus (DENV) antigen detection assay, which is designed to detect all serotypes of DENV in mosquito pools. The RAMP DENV assay was able to detect geographically distinct strains of all 4 DENV serotypes in virus-spiked mosquito pools that contained at least 4.3 log 10 plaque forming units/ml, although discrete sensitivity limits varied slightly for each serotype. The RAMP DENV assay also detected DENV 1–4 in mosquito pools containing a single infected mosquito and 24 laboratory-reared uninfected mosquitoes. No false positives were detected in negative control mosquito pools or in samples containing high titers of nontarget arboviruses. We found that while the kit-supplied RAMP buffer reduced the infectious titer of DENV, it did not completely inactivate all serotypes. We recommend adding a detergent, Triton X-100, to the buffer to ensure complete inactivation of DENV if the assay is to be conducted at a lower biosafety level than required for DENV handling.