In order to develop a model of Mycobacterium bovis infection with pathogene
tical relevance, a modified version of the Henderson apparatus was used to
deliver infectious aerosols directly to the snouts of guinea pigs. Aerosols
generated from 10(6), 10(7), 10(8) CFU/ml M. bovis suspensions established
disease in every animal, with estimated retained doses of 10, 100, 1000 CF
U, respectively. For comparison, other guinea pigs were inoculated with 100
CFU M. bovis intramuscularly (i.m.). Pathology and bacterial colonisation
of lungs and spleen varied according to the dose and route of inoculation.
Animals inoculated i.m. gave a significant cutaneous tuberculin hypersensit
ivity reaction earlier after testing than those infected aerogenically. A s
erological response to M. bovis antigens was detected in all infected anima
ls. Intensity of antigen recognition was dose-dependent and although the ra
nge of antigens recognised varied between animals, a 25 kDa antigen present
in the cell fraction was serodominant. Thus, a reproducible guinea pig mod
el has been defined that may be suitable for virulence, vaccination, and im
munological studies. Crown Copyright (C) 2001 Published by Elsevier Science
B.V. All rights reserved.