Abstract

Epidemiological studies of Staphylococcus aureus have shown a relation between certain clones and the presence of specific virulence genes, but how this translates into virulence-associated functional responses is not fully elucidated. Here we addressed this issue by analyses of community-acquired S. aureus strains characterized with respect to antibiotic resistance, ST types, agr types, and virulence gene profiles. Supernatants containing exotoxins were prepared from overnight bacterial cultures, and tested in proliferation assays using human peripheral blood mononuclear cells (PBMC). The strains displayed stable phenotypic response profiles, defined by either a proliferative or cytotoxic response. Although, virtually all strains elicited superantigen-mediated proliferative responses, the strains with a cytotoxic profile induced proliferation only in cultures with the most diluted supernatants. This indicated that the superantigen-response was masked by a cytotoxic effect which was also confirmed by flow cytometry analysis. The cytotoxic supernatants contained significantly higher levels of α-toxin than did the proliferative supernatants. Addition of α-toxin to supernatants characterized as proliferative switched the response into cytotoxic profiles. In contrast, no effect of Panton Valentine Leukocidin, δ-toxin or phenol soluble modulin α-3 was noted in the proliferative assay. Furthermore, a significant association between agr type and phenotypic profile was found, where agrII and agrIII strains had predominantly a proliferative profile whereas agrI and IV strains had a predominantly cytotoxic profile. The differential response profiles associated with specific S. aureus strains with varying toxin production could possibly have an impact on disease manifestations, and as such may reflect specific pathotypes.

Highlights

  • Staphylococcus aureus (S. aureus) is a significant cause of human infections and an emerging health problem globally due to its increasing resistance to beta-lactams

  • Several of the toxins are encoded by mobile genetic elements resulting in great diversity in toxin gene content among S. aureus strains [12,13] Many of these virulence factors are regulated and controlled by a global regulator system called the accessory gene regulator system encoded by the agr locus [14,15,16,17]

  • A proliferation assay was employed in which peripheral blood mononuclear cells (PBMC) were exposed to bacterial supernatants prepared from CA S. aureus strains

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Summary

Introduction

Staphylococcus aureus (S. aureus) is a significant cause of human infections and an emerging health problem globally due to its increasing resistance to beta-lactams (methicillin-resistant S. aureus, MRSA). Several exotoxins have been implicated in disease pathogenesis, such as superantigens [5,6,7], as well as the cytotoxins Panton Valentine Leukocidin (PVL) [8,9,10], alpha-toxin (a-toxin) [8,10], and phenol soluble modulins (PSMs) [10,11]. Several of the toxins are encoded by mobile genetic elements resulting in great diversity in toxin gene content among S. aureus strains [12,13] Many of these virulence factors are regulated and controlled by a global regulator system called the accessory gene regulator (agr) system encoded by the agr locus [14,15,16,17]. A recent study demonstrated the impact of allelic variation on agr induction dynamics, which translated into significant differences in expression of several virulence factors [19]

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