Staphylococcus aureus infection pathophysiology: Difference between revisions

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# Imbalance in ion homeostasis occur as a result of the pore formation (efflux of potassium cations and ATP or influx of calcium ions). This eventually result in cell death. Alpha-toxin targets a variety of cell types including epithelial and endothelial cells, platelets and blood cells.
# Imbalance in ion homeostasis occur as a result of the pore formation (efflux of potassium cations and ATP or influx of calcium ions). This eventually result in cell death. Alpha-toxin targets a variety of cell types including epithelial and endothelial cells, platelets and blood cells.
# Alpha-hemolysin activates alpha-hemolysin receptor (a disintegrin and metalloprotease 10), contributing to proteolysis of E-cadherin. This results in the disruption of the adherens junction in the epithelial layer. Remodeling of the epithelial layer occurs and pathogen dissemination ensues.
# Alpha-hemolysin activates alpha-hemolysin receptor (a disintegrin and metalloprotease 10), contributing to proteolysis of E-cadherin. This results in the disruption of the adherens junction in the epithelial layer. Remodeling of the epithelial layer occurs and pathogen dissemination ensues.
# Proteolysis of the extracellular domain of vascular endothelial cadherin contribute to the breach of blood vessel endothelium integrity
# Proteolysis of the extracellular domain of vascular endothelial cadherin can also occur, contributing to the breach of blood vessel endothelium integrity.
# Alpha-toxin has been shown to promote strong host inflammatory responses which has been linked to increased morbidity and mortality.
# Alpha-toxin has been shown to promote strong host inflammatory responses which has been linked to increased morbidity and mortality.
# Alpha-toxin can activate intracellular host sensor molecules such as nucleotide-binding domain leucine-rich repeat containing (NLR) family (NLRC2 and NLRP3).
# Alpha-toxin can activate intracellular host sensor molecules such as nucleotide-binding domain leucine-rich repeat containing (NLR) family (NLRC2 and NLRP3).
Line 27: Line 27:
# Sizes of abscesses have been shown to significantly reduce following functional inactivation of the gene encoding alpha-hemolysin.
# Sizes of abscesses have been shown to significantly reduce following functional inactivation of the gene encoding alpha-hemolysin.
* '''Bicomponent leukocidins'''
* '''Bicomponent leukocidins'''
# These include Panton-Valentine leukocidin, γ-hemolysins,  
# These include Panton-Valentine leukocidin (LukF-PV and LukS-PV), γ-hemolysins (HlgAB and HlgCB), LukED, and LukAB.     
# Similar to the alpha-toxin, this is also a Staphylococcus aureus pore-forming toxin.
# Similar to the alpha-toxin, leukocidins are also Staphylococcus aureus pore-forming toxins.
# More than one leukocidin is often encoded by a S. aureus strain, and different leukocidins can target the same cell types and receptors.
# Leukocidins have been associated with staphylococcal skin and soft tissue infections, bacteremia, severe pneumonia.


==References==
==References==

Latest revision as of 19:39, 16 May 2017

Staphylococcus aureus infection Main page

Overview

Classification

Pathophysiology

Causes

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief: Fatimo Biobaku M.B.B.S [2]

Overview

Staphylococcus aureus is a recognized cause of a wide variety of human infections with approximately half of the world's population colonized with this highly virulent bacteria.[1][2] Different strains of S. aureus bacteria have been identified, the attribute of a particular strain (toxins and extracellular factors, invasive properties such as adherence, biofilm formation, and resistance to phagocytosis), and the host immune defense mechanisms, largely determine the pathogenesis of the infection.[1][3]

Pathophysiology

Staphylococcus aureus is a highly virulent bacteria that has been recognized as a cause of a wide variety of diseases in humans. Approximately 60% of humans are colonized with Staphylococcus aureus (the nasal membranes and skin are the common habitat).[1][2] Several strains of Staphylococcus aureus bacteria exist. The characteristic attribute of a particular strain such as toxins and extracellular factors, invasive properties (such as adherence, biofilm formation, and resistance to phagocytosis), as well as the immune defense mechanisms of the host, majorly determine the pathogenesis of Staphylococcus aureus infection.[1][3] Staphylococcus aureus causes several infections ranging from mild infections to invasive diseases that are life threatening. Infections caused by Staphylococcus aureus include skin and soft tissue infections, osteomyelitis, food poisoning, pneumonia, infective endocarditis and sepsis. Some of the virulence factors that have been recognized in the pathogenesis of Staphylococcus aureus infections include:[4][5][2][3][6][7]

  • Staphylococcal superantigens (SAgs)
  1. These have been strongly implicated in a wide range of illnesses such as toxic shock syndrome and staphylococcal food poisoning.
  2. Several studies also suggest staphylococcal superantigens play a role in diseases such as atopic dermatitis, some forms of psoriasis, Kawasaki disease, and chronic rhinosinusitis.
  3. Staphylococcal superantigens are exotoxins with more than 20 distinct types, and most staphylococcus aureus strains encode many superantigen gene. Staphylococcus superantigens include staphylococcal enterotoxins, staphylococcal enterotoxin-like proteins, and toxic shock syndrome toxin-1.
  4. Staphylococcal enterotoxins cause food poisoning via ingestion of contaminated food. These enterotoxins have a very high stability and they are not easily denatured by heat and low pH (mild cooking or food digestion in the stomach cannot easily eradicate these toxins).
  5. Unlike most conventional peptides that stimulate roughly 1% of naive T-cells, a staphylococcal superantigen can simultaneously activate a large proportion of T lymphocytes (up to 20%).
  6. Staphylococcal superantigens are distinct because of their ability to bypass highly specific antigen-driven interaction between T-cells and antigen presenting cells.
  7. The superantigens can uniquely activate T lymphocytes by directly crosslinking certain TCR Vβ (T cell receptor β-chain variable domain).
  8. Numerous superantigen-activated T cells can then release several proinflammatory cytokines (this can lead to a “cytokine storm” phenomenon in severe cases, as seen in toxic shock syndrome). Superantigens also activate antigen presenting cells and this contributes to cytokine release.
  • Alpha-hemolysin (α-toxin)
  1. This has been implicated in skin and soft tissue infections, and invasive Staphylococcus aureus diseases.
  2. It is a pore-forming cytotoxin, it forms transmembrane pores on the surface of target cells.
  3. Imbalance in ion homeostasis occur as a result of the pore formation (efflux of potassium cations and ATP or influx of calcium ions). This eventually result in cell death. Alpha-toxin targets a variety of cell types including epithelial and endothelial cells, platelets and blood cells.
  4. Alpha-hemolysin activates alpha-hemolysin receptor (a disintegrin and metalloprotease 10), contributing to proteolysis of E-cadherin. This results in the disruption of the adherens junction in the epithelial layer. Remodeling of the epithelial layer occurs and pathogen dissemination ensues.
  5. Proteolysis of the extracellular domain of vascular endothelial cadherin can also occur, contributing to the breach of blood vessel endothelium integrity.
  6. Alpha-toxin has been shown to promote strong host inflammatory responses which has been linked to increased morbidity and mortality.
  7. Alpha-toxin can activate intracellular host sensor molecules such as nucleotide-binding domain leucine-rich repeat containing (NLR) family (NLRC2 and NLRP3).
  8. The activation of the NLRP3 inflammasome by alpha-toxin and costimulation of NLRC2 by alpha-toxin and muramyl dipeptide, trigger the activation of caspase 1. This subsequently result in the activation of proinflammatory cytokine IL-1β which majorly contributes to the influx of polymorphonuclear leukocytes to the site of infection.
  9. Sizes of abscesses have been shown to significantly reduce following functional inactivation of the gene encoding alpha-hemolysin.
  • Bicomponent leukocidins
  1. These include Panton-Valentine leukocidin (LukF-PV and LukS-PV), γ-hemolysins (HlgAB and HlgCB), LukED, and LukAB.
  2. Similar to the alpha-toxin, leukocidins are also Staphylococcus aureus pore-forming toxins.
  3. More than one leukocidin is often encoded by a S. aureus strain, and different leukocidins can target the same cell types and receptors.
  4. Leukocidins have been associated with staphylococcal skin and soft tissue infections, bacteremia, severe pneumonia.

References

  1. 1.0 1.1 1.2 1.3 Chessa D, Ganau G, Mazzarello V (2015). "An overview of Staphylococcus epidermidis and Staphylococcus aureus with a focus on developing countries". J Infect Dev Ctries. 9 (6): 547–50. doi:10.3855/jidc.6923. PMID 26142662.
  2. 2.0 2.1 2.2 Kobayashi SD, Malachowa N, DeLeo FR (2015). "Pathogenesis of Staphylococcus aureus abscesses". Am J Pathol. 185 (6): 1518–27. doi:10.1016/j.ajpath.2014.11.030. PMC 4450319. PMID 25749135.
  3. 3.0 3.1 3.2 Krishna S, Miller LS (2012). "Host-pathogen interactions between the skin and Staphylococcus aureus". Curr Opin Microbiol. 15 (1): 28–35. doi:10.1016/j.mib.2011.11.003. PMC 3265682. PMID 22137885.
  4. Grumann D, Nübel U, Bröker BM (2014). "Staphylococcus aureus toxins--their functions and genetics". Infect Genet Evol. 21: 583–92. doi:10.1016/j.meegid.2013.03.013. PMID 23541411.
  5. Xu SX, McCormick JK (2012). "Staphylococcal superantigens in colonization and disease". Front Cell Infect Microbiol. 2: 52. doi:10.3389/fcimb.2012.00052. PMC 3417409. PMID 22919643.
  6. Berube BJ, Bubeck Wardenburg J (2013). "Staphylococcus aureus α-toxin: nearly a century of intrigue". Toxins (Basel). 5 (6): 1140–66. PMC 3717774. PMID 23888516.
  7. Seilie ES, Bubeck Wardenburg J (2017). "Staphylococcus aureus pore-forming toxins: The interface of pathogen and host complexity". Semin Cell Dev Biol. doi:10.1016/j.semcdb.2017.04.003. PMID 28445785.