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<jats:title>ABSTRACT</jats:title> <jats:p>Most cases of severe <jats:italic>Staphylococcus aureus</jats:italic> disease cannot be explained by the action of a single virulence determinant, and it is likely that a number of factors act in combination during the infective process. This study examined the relationship between disease in humans and a large number of putative virulence determinants, both individually and in combination. <jats:italic>S. aureus</jats:italic> isolates (<jats:italic>n</jats:italic> = 334) from healthy blood donors and from patients with invasive disease were compared for variation in the presence of 33 putative virulence determinants. After adjusting for the effect of clonality, seven determinants (<jats:italic>fnbA</jats:italic>, <jats:italic>cna</jats:italic>, <jats:italic>sdrE</jats:italic>, <jats:italic>sej</jats:italic>, <jats:italic>eta</jats:italic>, <jats:italic>hlg</jats:italic>, and <jats:italic>ica</jats:italic>) were significantly more common in invasive isolates. All seven factors contributed independently to virulence. No single factor predominated as the major predictor of virulence, their effects appearing to be cumulative. No combinations of the seven genes were either more or less likely to cause disease than others with the same number of virulence-associated genes. There was evidence of considerable horizontal transfer of genes on a background of clonality. Our findings also suggested that allelic variants of a polymorphic locus can make different contributions to the disease process, further study of which is likely to expand our understanding of staphylococcal disease pathogenesis.</jats:p>

Original publication

DOI

10.1128/iai.70.9.4987-4996.2002

Type

Journal article

Journal

Infection and Immunity

Publisher

American Society for Microbiology

Publication Date

09/2002

Volume

70

Pages

4987 - 4996