West Nile virus was recovered from the brain of a red-tailed hawk that died
in Westchester County, N.Y., in February 2000, Multiple foci of glial cell
s, lymphocytes, and a few pyknotic nuclei were observed in the brain. Three
to 4 days after inoculation of Vero cells with brain homogenates, cytopath
ic changes were detected. The presence of West Nile virus antigen in fixed
cells or cell lysates was revealed by fluorescent antibody testing or enzym
e-linked immunosorbent assay, respectively. Furthermore, Reverse transcript
ase-PCR with primers specific for the NS3 gene of West Nile virus resulted
in an amplicon of the expected size (470 bp), Electron microscopy of thin s
ections of infected Vero cells revealed the presence of viral particles app
roximately 40 nm in diameter, within cytoplasmic vesicles. The demonstratio
n of infection with the West Nile virus in the dead of the winter, long aft
er mosquitoes ceased to be active, is significant in that it testifies to t
he survival of the virus in the region beyond mosquito season and suggests
another route of transmission: in this case, prey to predator.