The live modified rabies virus vaccine strain SAG-2 was selected from
SADBerne in a two step process employing anti-rabies glycoprotein mono
clonal antibodies. The first two nucleotides coding for the amino acid
in position 333 of the rabies glycoprotein are mutated. Arginine at p
osition 333, which is associated with rabies pathogenicity, was substi
tuted first by lysine and then by glutamic acid. The two nucleotide di
fferences at position 333 in SAG-2 to any of six possible arginine tri
plets translated into excellent genetic stability and apathogenicity f
or adult mice, foxes, cats and dogs. The vaccination of foxes and dogs
by the oral route provided protection against a lethal challenge with
rabies virus.