The lack of a suitable animal model of Aeromonas-associated diarrhoea has h
ampered investigations into Aeromonas pathogenic mechanisms. Hence, a publi
shed report that clindamycin-pretreated rats developed signs and symptoms o
f enteritis following intragastric inoculation of an Aeromonas strain requi
red further investigation. Although we could demonstrate long-term colonisa
tion (>12 days) and histological damage in this animal model with Pseudomon
as aeruginosa isolated from patients with chronic diarrhoea, this was not s
een with Aeromonas spp. Six Aeromonas strains, selected for their potential
virulence and colonising abilities and including the strain from the origi
nal report, were either not recovered from stools or were recovered for no
longer than 2 days post inoculation. Intestinal histology remained normal.
Destruction of bacteria in vivo appeared to be due to immune mechanisms as
inoculum strains were not 'suicidal' or unduly sensitive to low pH or clind
amycin. This study was, therefore, unable to validate the clindamycin-treat
ed rat model as a useful one for investigating the enteropathogenicity of A
eromonas species. Possible reasons for the discrepancy between our study an
d the original report are discussed. (C) 2000 Federation of European Microb
iological Societies. Published by Elsevier Science B.V. All rights reserved
.