A single feeding of milk containing 2 x 10(7) TCID50 of infectious cap
rine arthritis-encephalitis virus (CAEV) infected 50% of newborn kids.
Lesser amounts were not infectious when given as a single ingestion,
indicating that 2 x 10(7) TCID50 was near the minimal infective oral d
ose. Seroconversion following intravenous innoculation of infectious C
AEV was observed to occur more rapidly (4 weeks post-innoculation), at
a lower level of exposure (2 x 10(6) TCID50), and more efficiently (1
00%) when compared to other routes of exposure. The occurrence of mate
rnal-fetal transmission was supported by experiments in which kids wer
e removed from their mothers immediately at birth and reared in isolat
ion on virus-free milk or milk replacers. Five percent of a group of 4
0 kids born to naturally CAEV-infected does and handled in this manner
seroconverted within 8 weeks. This indicated that at least two kids i
n the group were infected prior to birth or during the birth process.
When seronegative kids were housed in intimate contact with CAEV-infec
ted animals, an additional 10% became seropositive within 20 weeks, su
ggesting that contact transmission of CAEV also occurs later in life b
etween infected and susceptible goats. Intramammary infusion of 2 x 10
(7) TCID50 infectious CAEV resulted in seroconversion in three of thre
e lactating seronegative does within 4-8 weeks post-infusion. Thus, go
ats may be infected by a single oral exposure to infectious CAEV, by c
ontact with infected individuals as occurs in normal husbandry practic
es, by intramammary route as might occur during routine machine milkin
g of lactating does, and from doe to fetus either prior to or during t
he birth process. Control of CAEV on commercial goat dairies will be e
nhanced by incorporation of the findings of these studies in a prevent
ive program.