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19 Cards in this Set

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Staphylococcus aureus: Microbiology
Gram-positive cocci, arranged in grape-like clusters
From Greek staphyle – bunch of grapes
Initially white colonies turn buff-golden (aureus)
Most colonies β-hemolytic, facultative
Ability to grow in 7.5% NaCl, mannitol salt agar (selective/indicator medium)
Staphylococcus aureus: Identification and subtyping
Coagulase distinguishes S. aureus from other staphylococci
Most strains produce clumping factor
-“bound coagulase”
-Binds fibrinogen
Staphylococcus aureus: Epidemiology
Any age
Risk factors: open wound
Outbreaks: Hospital/healthcare associated - primarily MRSA, nasal carriers (30% of population). Community - MSSA (wrestlers), MRSA (drug addicts, children)
New evidence indicates increase in CA-MRSA from 14% to 35% of cases
CA-MRSA infections, general
1st or 2nd cause of soft tissue infections
2nd or 3rd cause of pneumonia
1st cause of osteomyelitis
1st cause of infectious arthritis (excluding STDs)
CA-MRSA Skin Infections
Mimic Spider Bites
Fagan SP, Spider bites presenting with MRSA soft tissue infection require early aggressive treatment.

Houston, TX ; 3/00 - 11/01

38 patients presented with infected “spider bites”

87% grew MRSA
CA-MRSA: differentiating from HA-MRSA, virulence factor
Panton-Valentine leukocidin (PVL, pore forming cytotoxin)
-targets leukocytes
HA - MRSA infections, general
1st cause of surgical site infections
2nd cause of pneumonia
2nd cause of bloodstream infections
10th cause of urinary tract infections
HA - MRSA: Pathogenesis
Colonization mediated by number of surface proteins which bind host elements/foreign bodies
Trauma/foreign matter lower infectious dose
Resistance to phagocytosis permits accumulation of toxins
Resolution depends on ability to isolate the infection
Granulation and fibrosis of boil
In organs other than skin, spread and destruction prominent
S. aureus toxin mediated disease
Food Poisoning:
Preformed enterotoxin resistant to boiling, action within hours of ingestion
Exfoliative toxin:
causes blisters when localized to site of infection, scalded skin syndrome when absorbed
Staphylococcal toxic shock syndrome:
Toxin(s) absorbed and circulated
Not limited to TSST-1
S. aureus clinical manifestations
Furuncle and Carbuncle:
-Superficial infection of follicle
-Infection resolves upon spontaneous drainage
-Multiple boils yield a carbuncle
Bullous impetigo:
-Often secondary invader of GAS pustular impetigo
-Exfoliative toxin strains
Wide variety of deep tissue infections:
-osteomyelitis (90% of acute cases in children)
-pneumonia and deep tissue lesions highly destructive
Scalded skin syndrome
-exfoliative toxin
Toxic shock syndrome
TSST-1 and Toxic Shock
S. aureus
Superantigen:
-non specific binding of TCR and MHC class II
-hyperactivation of immune response, cytokine storm
S. aureus immunity
Immunity poorly understood
Role of cellular and humoral components unclear
Relapsing infections can occur over many years
-Chronic furunculosis
Current efforts directed at multicomponent vaccine
-Fibronectin-binding protein, collagen-binding protein, fibrinogen-binding protein, capsular polysaccharide, alpha toxin mutant
S. aureus nasal carriage
Nasal carriage of CA-MRSA is on the rise
-From 2001 – 2004, rates climbed from 0.8% to 9% for MRSA
-36% carriage of MSSA
-Similar studies showing increased carriage of PVL strains as well
S. aureus treatment
80-90% of strains penicillin resistant
Penicillin sensitive – penicillin
Pen resistant/Ox sensitive – oxacillin, nafcillin or cefazolin
Methicillin resistant (MRSA) – vancomycin, synercid, linezolid, daptomycin
Vancomycin resistant (VRSA) - synercid, linezolid, daptomycin
Total resistance to antibiotics seems likely
CA-MRSA treatment
10d - 3 weeks of clindamycin, minocycline; occasionally vancomycin or newer parenteral agents
Topical skin antiseptics
Povidone iodine (10%)
Chlorhexidine (4%)
Phisohex soap
Topical nasal agents
Mupirocin, Bacitracin
House cleaning
Decolonize family members
New Approaches to Preventing S. aureus Infection: Vaccination
Vaccination
polysaccharide-based vaccine known as StaphVAX
Ineffective in a confirmatory phase 3 trial – halted
human IgG preparation known as INH-A21 (Veronate)
Ineffective at phase 3
An effective vaccine will have to be multicomponent, incorporating several surface proteins, toxoids, and surface polysaccharides
New Approaches to Preventing S. aureus Infection: Nasal decolonization
Topical decolonization with mupirocin reduced the overall Staphylococcus aureus infection rate after surgery in Staphylococcus aureus nasal carriers
Topical decolonization with chlorhexidine gluconate resulted in a reduced overall nosocomial infection rate, but no effect was found on the Staphylococcus aureus infection rate
New Approaches to Preventing S. aureus Infection: anti-infective vascular catheters
Minocycline/rifampin coated catheters significantly reduce adherence (P = 0.001)
M/R catheters significantly longer antimicrobial durability (28 days, P = 0.01)
Downside: possible resistance to coating
Anti-infective catheter flush solutions
Minocycline/EDTA used as a flush solution in hemodialysis patients reduces the risk of CRB by up to 10-fold
Coagulase-negative Staphylococci
S. epidermidis and other lesser recognized species
Commensals of skin, anterior nares, ear canals
Commonly colonize implanted medical devices
Viscous extracellular polysaccharide provides mechanical barrier to host defenses/antimicrobial agents – biofilm
Most common skin contaminant in cultures