Rabies virus variants obtained by recombinant DNA techniques enabled us to
use the high neurotropism of rabies virus to express foreign genes (e.g: Ch
loramphenicol Acetyl Transferase gene) in neuronal cell cultures as well as
in rodent brain. The foreign gene was inserted in the viral pseudogene reg
ion; this insertion did not affect the neurotropism of rabies virus, as sho
wn by infection of neuronal cell cultures without any major cytopathic effe
cts for several days. Stereotaxic inoculation of these rabies virus variant
s into rat striatum indicated that insertion of the foreign gene did not al
ter the viral axonal transport and the subsequent widespread brain infectio
n. These data allow to consider rabies virus as a vector for the selective
expression of foreign genes in neurons.