Streptococcus pyogenes: Difference between revisions

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Streptococcus pyogenes
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== Microbiology ==
 
== Microbiology ==
   
* [[Has Gram stain::Gram-positive]] coccus, typically in pairs or short chains
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* [[Has Gram stain::Gram-positive]] coccus, typically in short chains
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* Non-motile, non–spore forming, catalase-negative, and facultatively anaerobic
  +
* [[Has hemolysis pattern::β hemolytic]] on blood agar (complete hemolysis)
  +
  +
== Pathophysiology ==
  +
  +
=== Virulence factors ===
  +
  +
* Capsular hyaluronic acid is similar to human
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* M protein is the main factor imparting virulence
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** M protein differences given ''S. pyogenes'' its serotypes
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** Confers resistance to phagocytosis by modulating host immune response
   
 
== Clinical Presentation ==
 
== Clinical Presentation ==
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== Prognosis ==
 
== Prognosis ==
   
* Highest risk of streptococcal toxic shock syndrome (TSS) or death
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* Highest risk of streptococcal [[toxic shock syndrome]] (TSS) or death
** Necrotizing fasciitis (50% and 50%)
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** [[Necrotizing fasciitis]] (50% and 50%)
 
** Pneumonia (30% and 30%)
 
** Pneumonia (30% and 30%)
 
** Bacteremia (15% and 25%)
 
** Bacteremia (15% and 25%)

Revision as of 21:13, 11 September 2019

  • Also commonly referred to as Group A Streptococcus

Microbiology

  • Gram-positive coccus, typically in short chains
  • Non-motile, non–spore forming, catalase-negative, and facultatively anaerobic
  • β hemolytic on blood agar (complete hemolysis)

Pathophysiology

Virulence factors

  • Capsular hyaluronic acid is similar to human
  • M protein is the main factor imparting virulence
    • M protein differences given S. pyogenes its serotypes
    • Confers resistance to phagocytosis by modulating host immune response

Clinical Presentation

  • Skin and soft tissue infections, including necrotizing fasciitis
  • Upper and lower respiratory tract infections
  • Bacteremia without a focus
  • Septic arthritis and osteomyelitis
  • Pelvic infections, including postpartum endometritis
  • Many other foci

Prognosis

References

  1. ^  Athanasios G. Michos, Chrysanthi G. Bakoula, Maria Braoudaki, Foteini I. Koutouzi, Eleftheria S. Roma, Anastasia Pangalis, Georgia Nikolopoulou, Elena Kirikou, Vassiliki P. Syriopoulou. Macrolide resistance in Streptococcus pyogenes: prevalence, resistance determinants, and emm types. Diagnostic Microbiology and Infectious Disease. 2009;64(3):295-299. doi:10.1016/j.diagmicrobio.2009.03.004.
  2. ^  Walter H. Traub, Birgit Leonhard. Comparative Susceptibility of Clinical Group A, B, C, F, and G β-Hemolytic Streptococcal Isolates to 24 Antimicrobial Drugs. Chemotherapy. 1997;43(1):10-20. doi:10.1159/000239529.
  3. a b  Matthias Imöhl, Mark van der Linden. Jose Melo-Cristino. Antimicrobial Susceptibility of Invasive Streptococcus pyogenes Isolates in Germany during 2003-2013. PLOS ONE. 2015;10(9):e0137313. doi:10.1371/journal.pone.0137313.
  4. ^  A. C. Bowen, R. A. Lilliebridge, S. Y. C. Tong, R. W. Baird, P. Ward, M. I. McDonald, B. J. Currie, J. R. Carapetis. Is Streptococcus pyogenes Resistant or Susceptible to Trimethoprim-Sulfamethoxazole?. Journal of Clinical Microbiology. 2012;50(12):4067-4072. doi:10.1128/jcm.02195-12.