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Infection and Immunity, April 1999, p. 1962-1966, Vol. 67, No. 4
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
0019-9567/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Vaccination and Protection of Pigs against Pleuropneumonia with a
Vaccine Strain of Actinobacillus pleuropneumoniae
Produced by Site-Specific Mutagenesis of the ApxII Operon
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.
*
Corresponding author. CSIRO, Division of Animal Health,
Animal Health Laboratory, Private Bag No. 24, Geelong, Victoria
3120, Australia. Phone: 61-3-5227 5000. Fax: 61-3-5227 5531. E-mail: Christopher.Prideaux{at}dah.csiro.au.
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