Molecular Events Underlying Group B Streptococcal Bloodstream Infection: The Role of the Platelet and Endothelium

Autor: Emagha, Unwana
Rok vydání: 2022
Předmět:
Epidemiology not elsewhere classified
Cell Physiology
Receptors and Membrane Biology
Medical bacteriology
Molecular Targets
blood platelets
Other health sciences not elsewhere classified
Diseases
FOS: Basic medicine
Medical Microbiology not elsewhere classified
Pathogenesis
Signal transduction
Cell Development
Proliferation and Death

FOS: Health sciences
Microbiology
Host-Parasite Interactions
sepsis
Streptococcal Infections
Cellular interactions (incl. adhesion
matrix
cell wall)

111601 Cell Physiology
Microbiology not elsewhere classified
60103 Cell Development
Proliferation and Death

110899 Medical Microbiology not elsewhere classified
111403 Paediatrics
Clinical microbiology
Pathology (excl. oral pathology)
FOS: Clinical medicine
60110 Receptors and Membrane Biology
Streptococcus
Bacteriology
Paediatrics
110303 Clinical Microbiology
60111 Signal Transduction
Paediatrics not elsewhere classified
119999 Medical and Health Sciences not elsewhere classified
111207 Molecular Targets
Infectious Diseases
FOS: Other medical sciences
FOS: Biological sciences
60106 Cellular Interactions (incl. Adhesion
Matrix
Cell Wall)

60307 Host-Parasite Interactions
110309 Infectious Diseases
Endothelium
Vascular

Medical and Health Sciences not elsewhere classified
60501 Bacteriology
110801 Medical Bacteriology
DOI: 10.25419/rcsi.20513229.v1
Popis: Bloodstream infections carry a high economic and health burdenand can develop into invasive life-threatening conditions such as sepsis, meningitis and infective endocarditis, characterised byaberrant thrombus formation and endothelial dysregulation. The intestinal and vaginal microflora, Streptococcus agalactiae, commonly known as Group B Streptococcus (GBS), is the mostcommonneonatalinvasive bloodstream infection pathogenin the western world. The aim of this thesis was to investigate the molecularinteractions between GBS,platelets and endothelial cells and the potential value of these interactions inGBS bloodstream infectionmanagement.Here, we demonstrate a GBS strain dependent platelet and endothelialcell interaction. GBS signal driven platelet aggregation was dependent on the bacterial strain, trypsin sensitive bacterial surface proteins and immunoglobulin G.We have delineated the functional role of the platelet receptor FcγRIIain GBS driven thrombus formation using a microfluidic physiological shear flow system coupled with real time microscopy, revealingits non-involvement in the initial platelet rolling and adhesion interaction with GBSeven as GBS was shown to interact withplatelets optimally only at low shear rate (≤ 200 s-1). GBS strain dependent endothelial cell invasion was accompanied by endothelial cell damage and necrosis as seen in our flow cytometric analysis and electron micrograph of GBS infected endothelial cells. These endothelial abnormalities coincided with an increase in endothelial permeability as seenin our FITC-dextran monolayer flux analysis.While epidemiological studies suggest an association between GBS serotype and clonal complex groups with GBS pathogenicity,our observation of GBS strain dependent platelet and endothelial dysregulation reveals that predicting disease outcome, particularly thrombotic and endothelial dysfunction, based on serotype or clonal complex group could be misleading.Our studyhas revealedthe usefulness of the flow system in studying GBS platelet-bacterial interactions andadds to theevidence of FcγRIIaas a potential target in bacterial induced thrombosis.
Databáze: OpenAIRE