Staphylococcus aureus is a commensal bacterium and pathogen. Identifying biomarkers for the transition from colonization to disease caused by this organism would be useful. Several S. aureus small RNAs (sRNAs) regulate virulence. We investigated presence and expression of 8 sRNAs in 83 S. aureus strains from 42 patients with sepsis or septic shock and 41 asymptomatic colonized carriers. Small pathogenicity island sRNAs sprB and sprC were clade specific. Six sRNAs had variable expression not correlated with clinical status. Expression of RNAIII was lower in strains from septic shock patients than in strains from colonized patients. When RNAIII was associated with expression of sprD, colonizing strains could be discriminated from strains in patients with bloodstream infections, including patients with sepsis and septic shock. Isolates associated with colonization might have sRNAs with target expression different from those of disease isolates. Monitoring expression of RNAIII and sprD could help determine severity of bloodstream infections.
Keywords: RNAIII; S. aureus protein A typing; Staphylococcus aureus; bacteria; biomarkers; bloodstream infections; immune evasion protein; multilocus sequence typing; nasal carrier; nasal colonization; second immunoglobulin-binding protein; sepsis; septic shock; small RNAs; small pathogenicity island RNAs; spa typing; spr RNAs; staphylococci; transfer–messenger RNA.