TABLE 2.
Summary of key epidemiologic and virulence factors for ocular strains of P. aeruginosa, S. aureus, and S pneumoniae.
Pathogen | P. aeruginosa | S. aureus | S. pneumoniae |
---|---|---|---|
Key epidemiologic features |
|
|
|
Minimum infectious dose in cornea (CFUs) | ~50 | ~100 | Unknown |
Cell surface features | Lipopolysaccharide (LPS) Pili (fimbriae) Flagella Alginate Glycocalyx (biofilm)-forming peptides Type III secretion systems |
Lipoprotein Lipoteichoic acid (LTA) MSCRAMMs including collagen, elastin, fibronectin, fibrinogen, and laminin-binding proteins, as well as clumping factor Peptidoglycans Protein A |
Lipoteichoic acid (LTA) Peptidoglycans Polysaccharide capsule Pneumococcal adherence and virulence factors A and B (PavA and PavB) Pneumococcal choline-binding protein Pneumococcal surface antigen A (PsaA) Pneumococcal surface protein A (PspA) Pneumococcal surface protein C (PspC) Protein A |
Secreted virulence factors | Exotoxin A Hemolysins Large exoprotease Leucocidin Metalloproteinases (Las A protease, Las B protease, alkaline protease, modified protease) Phospholipases Protease IV P. aeruginosa small protease (PASP) |
α-toxin Catalase Coagulase DNAse Hemolysins (α-, β-, δ-, and γ- toxins) Hyaluronidase Leucocidin Staphylokinase Superantigens (enterotoxins A – D) |
Autolysin Pneumolysin Reactive oxygen species (e.g., hydrogen peroxide) Secretory IgA protease |
Antimicrobial resistance in ocular strains (in the US) | Low; <10% of ocular isolates resistant to fluoroquinolones and aminoglycosides (tobramycin). However, multi-drug resistant strains requiring last-line carbapenems and colistin are becoming of increasing concern. | High and rapidly accumulating:
|
Low; <10% of ocular isolates resistant to fluoroquinolones. |