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Streptococci
Classification

b
haemolytic streptococci
Main group of pathogenic streptococci
Group A
Virulence
Relates to surface structures and proteins released from
cells during growth
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Surface structures
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M protein shows cross-reactivity with cardiac
muscle proteins and antibodies to these surface proteins may play a role
in the pathogenesis of rheumatic fever.
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M protein appears to inhibit phagocytosis
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Other surface proteins have the ability to inhibits
activation of complement via the classical pathway
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Extracellular products
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Streptolysin O
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Cardiotoxic effect in animals
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Inhibits chemotaxis, neutrophil mobility and
phagocytosis by macrophages
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Streptokinase
Clinical manifestations
Treatment
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Penicillin
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Erythromycin for
penicillin sensitive patients. However incidence of erythromycin resistance
is increasing and in some areas is as high as 40%
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Addition of aminoglycoside to penicillin has a
synergistic effect
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Penicillin should be combined with clindamycin
in the treatment of life-threatening conditions such as necrotizing
fasciitis and streptococcal toxic shock.
Group C and G
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Not associated with rheumatic fever
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Can cause similar infections to group A strep.
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Occasionally reported as cause of nosocomial and
opportunistic infections including:
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Malignancy, diabetes, cardiovascular disease,
alcoholism are important predisposing factors to invasive infection.
Treatment
Group B
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Colonizes the vagina in many adult women
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Transmission to infant during childbirth occurs in
50-75%. However only a small proportion develop infection.
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In recent years increasingly recognized as a cause of
infection amongst adults
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At risk groups: pregnant women, patients with serious
underlying disease.
Manifestations:
Prognosis
Mortality 30-35%. Worse prognosis in those >60 yrs
Treatment
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Penicillin, ampicillin or cephalosporin
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Resistance
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Duration of therapy relatively arbitrary but most
recommend 10 days for bacteraemia, 2-3 weeks for meningitis and 3-4 weeks
for osteomyelitis or endocarditis
Streptococcus pneumoniae
- Alpha haemolytic
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Virulence associated with the production of an
antiphagocytic capsular polysaccharide. Strains that do not produce this are
non-pathogenic
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Also produce hemolysin (similar to streptolysin O of
group A strep.), hyaluronidase and neuraminadase. However none of these
appear to play a direct role in the disease process.
Risk factors for infection
Clinical manifestations
Treatment
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Penicillin-sensitive strains: penicillin
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Intermediate penicillin resistance (MIC 0.12-1 mcg/ml):
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Highly penicillin resistant (MIC 2 mcg/ml or above):
3rd generation cephalosporin and glycopeptide
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However recent data on penicillin resistant
pneumococcal infections suggest that outcome is no different, almost
regardless of the beta-lactam used
Prevention
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Currently available vaccine is a mixture of 23
pneumococcal capsular polysaccharides
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Does not cover all strains
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Insufficient antibody response seen in asplenic and
elderly patients and in young children (ie the at risk groups).
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Antibody levels subside with time and may not be
detectable after 5 years in older patients. Therefore, patients at high risk
of pneumococcal disease should be vaccinated every 3-5 years
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