Abstract
Enterococcus faecalisblood isolates were probed for the serine protease activator of cytolysin (cylA) and aggregation substance (asa1), traits that generally reside on pheromone-responsive plasmids, to determine how commonly these genotypes were associated with disease. In dot blot assays, no significant difference was found in the frequency ofasa1for blood isolates [55 of 103 (54%)] and isolates recovered from stool [9 of 14 (60%);P> 0.1, χ2test]. In contrast,cylAoccurred more frequently among bacteremia isolates [34 of 68 (50%)] than endocarditis [4 of 35 (11%)] or stool isolates (0 of 14;P< 0.001; χ2test). However, when the clonality of isolates was accounted for, the frequency ofasa1andcylAamong unrelated strains was not significantly different among the three sets of strains (P> 0.2, χ2test). The lack of enrichment forasa1orcylAamong clonally unrelatedE. faecalisbloodstream isolates fails to support a role for plasmid-encoded aggregation substance or cytolysin in the transition from bacteremia to endocarditis. Clonally related, cytolytic strains, however, demonstrated an increased propensity to cause bloodstream infection.
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