Infection and Immunity, April 1999, p. 1962-1966, Vol. 67, No. 4
0019-9567/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Animal Health Laboratory, CSIRO Division of Animal Health, Geelong, Victoria 3120, Australia
Received 16 April 1998/Returned for modification 6 July 1998/Accepted 26 January 1999
The production of toxin (Apx)-neutralizing antibodies during
infection plays a major role in the induction of protective immunity to
Actinobacillus pleuropneumoniae reinfection. In the present study, the gene encoding the ApxII-activating protein,
apxIIC, was insertionally inactivated on the chromosome of
a serovar 7 strain, HS93. Expression of the structural toxin, ApxIIA,
and of the two genes required for its secretion, apxIB and
apxID, still occurs in this strain. The resulting mutant
strain, HS93C
Ampr, was found to secrete the
unactivated toxin. Pigs vaccinated with live HS93C
Ampr via the intranasal route were protected against a
cross-serovar challenge with a virulent serovar 1 strain of
A. pleuropneumoniae. This is the first reported
vaccine strain of A. pleuropneumoniae which can be
delivered live to pigs and offers cross-serovar protection against
porcine pleuropneumonia.
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