We adapted a rat model of gastrointestinal candidiasis for studies of
in vivo gastric colonization with Candida albicans. Whereas normal rat
s cleared a single intragastric inoculum of 5 X 10(6) C. albicans from
the stomach within 4 hours, rats pretreated with chloramphenicol and
gentamicin achieved stable gastric colonization for at least 5 days af
ter administration of this inoculum. We next used this model to study
host modifications hypothesized to alter gastric colonization. A first
group received dilute HCl 4 hr before yeast inoculation, to induce ac
ute superficial gastric erosions; another group was treated with gluco
corticosteroid beginning 12 days before yeast inoculation; and another
group received famotidine therapy beginning 3 days before yeast inocu
lation, to neutralize gastric acidity. Recovery of yeasts from stomach
s was significantly different from the control group only in rats trea
ted with steroids; greater colonization was found in the rats so treat
ed. In a final group of experiments, we attempted to inhibit in vivo g
astric colonization with yeasts by preincubation of yeasts in vitro wi
th a polyclonal antiserum raised in rabbits against heat-killed C. alb
icans. We were not able to demonstrate inhibition of gastric colonizat
ion by preincubation with this antiserum in this model system.