INVESTIGADORES
CASTILLO Daniela Susana
congresos y reuniones científicas
Título:
Development of a highly sensitive NS1 capture Enzyme-linked Immunosorbent Assay for the detection of acute Zika Virus infection
Autor/es:
ROLDÁN JS; CASSOLA A; CASTILLO DS
Reunión:
Congreso; LXVI Reunión anual de la Sociedad Argentina de Investigación Clínica; 2021
Resumen:
Zika virus (ZIKV) is a flavivirus that is primarily transmitted from bites of infected Aedes aegypti or Aedes albopictus mosquitoes. There are currently no vaccines to prevent ZIKV infection nor commercially available clinical diagnostic tests demonstrated to identify ZIKV without cross-reactive interference of other related flaviviruses. In this context, the development of sensitive and accurate diagnostic methods is urgently needed for the early detection of ZIKV. Nonstructural protein 1 (NS1) is a highly conserved glycoprotein that is secreted as a hexamer and circulates at high levels in the bloodstream of acute patients. These properties turn ZIKV NS1 (ZNS1) into a good diagnostic marker, allowing early detection and diagnosis of ZIKV infection. In order to develop a highly specific and sensitive capture ELISA, we aimed at obtaining monoclonal antibodies (mAbs) against hexameric ZNS1 protein. We selected 6F6 specific hybridoma clone, which binds to a ZNS1 linear epitope. Cross-reaction studies through Western blotting, indirect ELISA and immunofluoresence staining indicated that 6F6 specifically recognizes ZNS1, and does not cross-react with the NS1 protein from other related flaviviruses. The 6F6 mAb enabled the development of a sensitive, reliable and reproducible capture ELISA with a limit of detection (LOD) of 10.8 ng/ml and a limit of quantification (LOQ) of 29.4 ng/ml. The accuracy of the 6F6 sandwich ELISA was assessed by spike-and-recovery tests, obtaining average recoveries between the ideal range from 80 to 120%. In conclusion, we established a valid capture ELISA that allows the detection and quantification of small amounts of ZNS1 in human sera, and constitutes a promising bioanalytical method for control strategies and the prevention of ZIKV propagation.