Construction and characterization of a full-length infectious clone (pMEV) of mink enteritis virus are described. Feline kidney cells (F81) were transfected with pMEV containing an engineered BamHI site that served as a genetic marker. The rescued virus was indistinguishable from its parental virus. The availability of a MEV infectious clone will facilitate studies of viral replication and pathogenicity and will permit the elucidation of determinants of the host range of the parvovirus.
Keywords: Biological properties; Genetic marker; Infectious clone; Mink enteritis virus; Rescue virus; Reverse genetics.
Copyright © 2014 Elsevier B.V. All rights reserved.