Abstract

Cache Valley virus (CVV) is a mosquito-borne virus in the genus Orthobunyavirus, family Peribunyaviridae. It was first isolated from a Culiseta inorata mosquito in Cache Valley, Utah in 1956 and is known to circulate widely in the Americas. While only a handful of human cases have been reported since its discovery, it is the causative agent of fetal death and severe malformations in livestock. CVV has recently emerged as a potential viral pathogen causing severe disease in humans. Currently, the only serological assay available for diagnostic testing is plaque reduction neutralization test which takes several days to perform and requires biocontainment. To expand diagnostic capacity to detect CVV infections by immunoassays, 12 hybridoma clones secreting anti-CVV murine monoclonal antibodies (MAbs) were developed. All MAbs developed were found to be non-neutralizing and specific to the nucleoprotein of CVV. Cross-reactivity experiments with related orthobunyaviruses revealed several of the MAbs reacted with Tensaw, Fort Sherman, Tlacotalpan, Maguari, Playas, and Potosi viruses. Our data shows that MAbs CVV14, CVV15, CVV17, and CVV18 have high specific reactivity as a detector in an IgM antibody capture test with human sera.

Highlights

  • Cache Valley virus (CVV) is a member of the Bunyamwera serogroup in the genus Orthobunyavirus, family Peribunyaviridae

  • Cache Valley virus is a mosquito-borne virus found throughout the Americas

  • The only serological diagnostic assay available to detect recent viral infection is plaque reduction neutralization test which requires the use of live virus in biocontainment

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Summary

Introduction

Cache Valley virus (CVV) is a member of the Bunyamwera serogroup in the genus Orthobunyavirus, family Peribunyaviridae. CVV was first isolated from a Culiseta inorata mosquito in Cache Valley, Utah in 1956 [4] Since it has been isolated from several mosquito species and mammals throughout the Americas and is considered the most widely distributed member of the Bunyamwera serogroup [1,2,5]. The nucleocapsid core is surrounded by a lipid bilayer with viral glycoproteins, Gc (108–125 kDa) and Gn (29–41 kDa), displayed on the surface of the virion. These glycoproteins are involved in receptor-mediated endocytosis and viral-cell membrane fusion [6]

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