The SAG-2 modified live rabies vaccine was tested for innocuity when a
dministered by the oral route in several potential wild non-target bai
t-consuming species, as follows: ten chacma baboons (Papio ursinus), s
ix African civets (Civettictis civetta), six slender mongooses (Galere
lla sanguinea), six honey badgers (Mellivora capensis), six large-spot
ted genets (Genetta tigrina), 39 multi-mammate mice (Mastomys natalens
is), 26 bushveld gerbils (Tatera leucogaster) and six pied crows (Corv
us albus). At least 9.0 log(10) median tissue culture infectious doses
(TCID50), given in a volume of I mi was administered orally to each o
f the animals, except the rodents which received 8.0 log(10) TCID50, g
iven in 0.1 ml. All the animals were observed for not <90 days for sig
ns of vaccine-induced rabies. Most of the species were also tested for
vaccine virus replication in the oral cavity and persistent virus inf
ection in the brain, salivary gland and tonsil. None of the animals di
ed of rabies and no persistent infection was found Rabies virus which
was pathologically and serotypically, indistinguishable from the vacci
nal strain was isolated from the saliva of one genet 1 day after vacci
ne administration From this study it was concluded that SAG-2 rabies v
accine would be safe for use in most situations where oral vaccination
campaigns for jackals are required in Zimbabwe. (C) 1997 Elsevier Sci
ence Ltd.