Affiliation:
1. National Laboratory for Enteric Pathogens
2. National Laboratory for Bacteriology, National Microbiology Laboratory, Winnipeg, Manitoba, Canada
Abstract
ABSTRACT
A multiplex PCR assay was designed to amplify the
Aeromonas hydrophila
and
A. veronii
bv. sobria hemolysin and aerolysin genes. The assay was evaluated by using 121 clinical isolates and 7 reference strains of
Aeromonas
spp., and these were divided into five genotypes on the basis of the results of the multiplex PCR. The five genotypes were characterized as type 1 for those carrying the
ahh1
gene only (36% of isolates), type 2 for those carrying the
asa1
gene only (8.5% of isolates), type 3 for those carrying both the
ahh1
and the
asa1
genes (4% of isolates), type 4 for those carrying the
ahh1
gene and the A. hydrophila aerA (aerolysin) gene (37.5% of isolates), and type 5 for those in which no hemolysin genes were detected (14% of isolates). The most common single hemolysin gene carried among all the
Aeromonas
isolates examined was
ahh1
, with 99 of 128 (77%) of isolates testing positive for this gene either alone or in combination with other hemolysin genes. Phenotypic expression of toxins was evaluated in a Vero cell culture cytotoxicity assay. These results indicated that there is a statistically significant correlation between the cytotoxin titers and the hemolysin genotype. Isolates belonging to genotype 4 (carrying both the
ahh1
gene and the aerolysin and hemolysin
aerA
genes) expressed higher cytotoxin titers than isolates of the other genotypes (
P
< 0.001). These isolates were more cytotoxic in cell culture and may have greater clinical significance.
Publisher
American Society for Microbiology
Cited by
167 articles.
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