Rapid antigen tests for dengue virus serotypes and Zika virus in patient serum.
Irene BoschHelena de PuigMegan HileyMarc Carré-CampsFederico Perdomo-CelisCarlos F NarváezDoris M SalgadoDewahar SenthoorMadeline O'GradyElizabeth PhillipsAnn F DurbinDiana FandosHikaru MiyazakiChun-Wan YenRosa Margarita GelvezRajas V WarkeLucas S RibeiroMauro Martins TexeiraRoque Pacheco de AlmeidaJosé Esteban Muñoz-MedinaJuan E LudertMauricio L NogueiraTatiana E ColomboAna C B TerzianPatrícia Torres BozzaAndrea S CalheirosYasmine R VieiraGiselle Barbosa-LimaAlexandre VizzoniJosé Cerbino-NetoFernando A BozzaThiago M L SouzaMonique Ramos de Oliveira TrugilhoAna M B de FilippisPatricia C de SequeiraErnesto Torres de Azevedo MarquesTereza MagalhaesFrancisco J DiazBerta N RestrepoKaterine MarínSalim Mattar VelillaDaniel OlsonEdwin J AsturiasMark LuceraMohit SinglaGuruprasad R MedigeshiNorma de BoschJustina TamJose Gómez-MárquezCharles ClavetLuis VillarKimberly Hamad-SchifferliLee GehrkePublished in: Science translational medicine (2018)
The recent Zika virus (ZIKV) outbreak demonstrates that cost-effective clinical diagnostics are urgently needed to detect and distinguish viral infections to improve patient care. Unlike dengue virus (DENV), ZIKV infections during pregnancy correlate with severe birth defects, including microcephaly and neurological disorders. Because ZIKV and DENV are related flaviviruses, their homologous proteins and nucleic acids can cause cross-reactions and false-positive results in molecular, antigenic, and serologic diagnostics. We report the characterization of monoclonal antibody pairs that have been translated into rapid immunochromatography tests to specifically detect the viral nonstructural 1 (NS1) protein antigen and distinguish the four DENV serotypes (DENV1-4) and ZIKV without cross-reaction. To complement visual test analysis and remove user subjectivity in reading test results, we used image processing and data analysis for data capture and test result quantification. Using a 30-μl serum sample, the sensitivity and specificity values of the DENV1-4 tests and the pan-DENV test, which detects all four dengue serotypes, ranged from 0.76 to 1.00. Sensitivity/specificity for the ZIKV rapid test was 0.81/0.86, respectively, using a 150-μl serum input. Serum ZIKV NS1 protein concentrations were about 10-fold lower than corresponding DENV NS1 concentrations in infected patients; moreover, ZIKV NS1 protein was not detected in polymerase chain reaction-positive patient urine samples. Our rapid immunochromatography approach and reagents have immediate application in differential clinical diagnosis of acute ZIKV and DENV cases, and the platform can be applied toward developing rapid antigen diagnostics for emerging viruses.
Keyphrases
- dengue virus
- zika virus
- aedes aegypti
- data analysis
- loop mediated isothermal amplification
- monoclonal antibody
- sars cov
- case report
- amino acid
- deep learning
- pregnant women
- autism spectrum disorder
- big data
- electronic health record
- coronavirus disease
- acute respiratory distress syndrome
- working memory
- extracorporeal membrane oxygenation
- gestational age
- single cell
- quantum dots