Publication | Open Access
Diminished virulence of a sar-/agr- mutant of Staphylococcus aureus in the rabbit model of endocarditis.
327
Citations
36
References
1994
Year
Microbial PathogensBacteriologyImmunologyPathologyStaphylococcus AureusSar-/agr- MutantRabbit ModelBacterial PathogensVirulence GenesBacterial PathogenesisMedical MicrobiologyMicrobial PathogenicityInfection ControlAntimicrobial ResistanceHost-pathogen InteractionsVirulence FactorInfective EndocarditisPathogen CharacterizationMolecular MicrobiologyClinical MicrobiologyPathogenesisMicrobiologyMedicine
Staphylococcus aureus pathogenicity is governed by multiple virulence genes regulated by global systems such as sar and agr. The study aimed to assess how sar and agr loci influence virulence by creating sar-/agr- mutants of strains RN6390 and RN450 and comparing their phenotypes to single mutants and wild-type parents. The authors generated sar-/agr- mutants of RN6390 and RN450 and compared their phenotypes to single sar- and agr- mutants and parental strains. The sar-/agr- double mutants lacked hemolysin secretion, showed markedly reduced fibronectin binding, and in rabbit endocarditis exhibited lower infectivity, bacterial densities, and valvular adhesion compared to the parent, indicating sar and agr are critical for adherence, persistence, and multiplication in endocarditis.
Microbial pathogenicity in Staphylococcus aureus is a complex process involving a number of virulence genes that are regulated by global regulatory systems including sar and agr. To evaluate the roles of these two loci in virulence, we constructed sar-/agr- mutants of strains RN6390 and RN450 and compared their phenotypic profiles to the corresponding single sar- and agr- mutants and parents. The secretion of all hemolysins was absent in the sar-/agr- mutants while residual beta-hemolysin activity remained in single agr- mutants. The fibronectin binding capacity was significantly diminished in both single sar- mutants and double mutants when compared with parents while the reduction in fibrinogen binding capacity in the double mutants was modest. In the rabbit endocarditis model, there was a significant decrease in both infectivity rates and intravegetation bacterial densities with the double mutant as compared to the parent (RN6390) at 10(3)-10(6) CFU inocula despite comparable levels of early bacteremia among various challenge groups. Notably, fewer bacteria in the double mutant group adhered to valvular vegetations at 30 min after challenge (10(6) CFU) than the parent group. These studies suggest that both the sar and agr loci are involved in initial valvular adherence, intravegetation persistence and multiplication of S. aureus in endocarditis.
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