Staphylococci
Gram positive cocci that:
- Typically occur in bunches
- Culture well on enriched media
e.g. Blood. - All produce catalase
Key distinguishing feature from Streptococci. - Grouped by their ability to produce coagulase
Enzyme which cleaves fibrinogen and leads to clot production. This clot also covers the bacteria in a film of clot, which protects them from immune detection and subsequent phagocytosis.- Coagulase positive
Confined to S. Aureus. - Coagulase negative
All the rest.
- Coagulase positive
Staphylococcus Aureus
Common skin commensal that:
- Causes illness by local infection and toxin production
- Generally requires host compromise to cause infection:
- Skin breaks
- Foreign body
- Immunosuppression
- May lead to infection in:
- B
- HAP
Classically necrotising.
- HAP
- C
- Infective endocarditis
May be associated with local abscesses if related to injection. - Invasive vascular devices
- CLABSI
- Pacemaker
- Infective endocarditis
- D
- Osteomyelitis
- Discitis
- Epidural abscess
- E
- Skin
- Soft tissue infections
- Joint prostheses
- B
Staphylococcal toxic shock is a complication of S. Aureus colonisation, and is covered under Toxic Shock Syndrome.
Methicillin-Resistant Staphylococcus Aureus
MRSA is a common mutation of S. Aureus that:
- Alters the Penicillin Binding Protein
- Significantly ↓ affinity of β-lactams for the cell wall so they become non-responsive
- Require treatment with a much more limited arsenal of antimicrobials
Coagulase Negative Staphylococcus
Coagulase-negative Staphylococcus:
- Include several strains, the most common which are:
- S. Epidermidis
IE, line infections. - S. Saprophyticus
UTIs. - S. lugdunensis
IE. - S. haemolyticus
IE. - S. schleiferi
IE. - S. warneri
- S. hominis
- S. capitis
- S. Epidermidis
- Usually exist as skin and nares commensals
Common cause of false-positive blood cultures. True infection can be distinguished on:- Clinical suspicion
- Number of positive cultures
- Differential time to positivity
Time between the bottle from an infected line (classically a CVC) flagging positive, and a peripheral culture taken at the same time; if the CVC culture becomes positive earlier it is more likely to be the source. - Positive in aerobic and anaerobic bottles
85% of “true” infections, compared to ~35% of potentially contaminated specimens. - Culture positive in <16 hours
- Cause infections in:
- Areas obscured from the immune system:
- Septic arthritis
- Endocarditis
- Invasive devices
- Lines
- Pacemakers
- Prosthetics
- Valves
- Joints
- VP shunts
- Immunocompromised host
- Disrupted integumentary barriers
- Burns
- Areas obscured from the immune system:
- Are generally multiresistant, and sensitive to glycopeptides and linezolid
Investigations
Bedside:
- TTE
For vegetations. Does not exclude IE, but can rule-in. - TOE
Should be performed if TTE is negative.
Management
Specific therapy:
- Pharmacological
- MSSA
- β-lactams
- Flucloxacillin
- Cefazolin
- Clindamycin
- Moxifloxacin
- Vancomycin
Failure rates ~4× that of β-lactams.
- β-lactams
- MRSA
- Glycopeptides
- Vancomycin
- Teicoplanin
- Linezolid 600mg IV Q12H
No dose adjustments required for renal or hepatic impairment. - 5th generation cephalosporins:
- Ceftaroline 600mg IV Q8H
- Ceftobiprole 500mg Q8H
- Daptomycin
- Rifampicin/fusidic acid
- Trimethoprim/sulfamethoxazole
- Glycopeptides
- Coagulase-negative
- Vancomycin as empiric therapy
- Flucloxacillin/Cephalosporin
May be appropriate de-escalation once sensitivity testing completed.
- MSSA
- Procedural
- Source Control
Desensitisation for β-lactam allergic patients is preferable - these are by far and away the best agents.
Prognosis
Mortality varies on site of origin, but can reach 50% with:
- Lung
- CLABSI
- Infective endocarditis
References
- Harvey RA, Cornelissen CN, Fisher BD. Lippincott Illustrated Reviews: Microbiology (Lippincott Illustrated Reviews Series). 3rd Ed. LWW.