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Journal of Clinical Microbiology, May 1997, 1131-1137, Vol 35, No. 5
J Van Ostaaijen, J Frey, S Rosendal and JI MacInnes
Actinobacillus suis isolates recovered from both healthy and diseased pigs
were characterized by biochemical testing, serotyping, restriction
endonuclease fingerprinting, and apx toxin gene typing. The clinical
isolates analyzed were collected over a 10-year period from approximately
40 different locations in southwestern Ontario, Canada. Little variation in
the biochemical profiles of these isolates was seen, and all isolates
reacted strongly with rabbit antisera prepared against one of the strains.
Similarly, by using BamHI and BglII for restriction endonuclease
fingerprinting (REF) analysis, all isolates were found to belong to a
single REF group. Minor variations could be detected, especially in the
BglII fingerprints, but overall the patterns were remarkably similar.
Sequences that could be amplified by PCR with primers to the apxICA and
apxIICA genes of Actinobacillus pleuropneumoniae were detected in all
strains. Although no amplification was obtained with primers to the A.
pleuropneumoniae apxIBD genes, sequences with homology to apxIBD were
detected by hybridization. There was no evidence of apxIII homologs. Taken
together, these data suggest that A. suis isolates are genotypically and
phenotypically very similar, regardless of their source, and that they
contain genes similar to, but not identical to, the apxICABD and apxIICA
genes of A. pleuropneumoniae.
Copyright © 1997 by the American Society for Microbiology. All rights reserved.
Actinobacillus suis strains isolated from healthy and diseased swine are clonal and carry apxICABDvar. suis and apxIICAvar. suis toxin genes
Department of Pathobiology, University of Guelph, Ontario, Canada.
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