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- Ringdahl, Ulrika, et al.
(författare)
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A role for the fibrinogen-binding regions of streptococcal M proteins in phagocytosis resistance
- 2000
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Ingår i: Molecular Microbiology. - : Wiley. - 1365-2958 .- 0950-382X. ; 37:6, s. 1318-1326
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Tidskriftsartikel (refereegranskat)abstract
- All virulent group A streptococcal isolates bind fibrinogen, a property that is closely linked to expression of type-specific antiphagocytic surface molecules designated M proteins. Here we show that although the M proteins from two different strains, M1 and M5, both bind fibrinogen with high affinity, they interact with different regions in the ligand. Moreover, mapping experiments demonstrated that the fibrinogen-binding regions in the M1 and M5 proteins are quite dissimilar at the amino acid sequence level and that they bind to different regions in the plasma protein. In spite of these differences, the fibrinogen-binding regions of M1 and M5 could both be shown to contribute to streptococcal survival in human blood, providing evidence for the distinct function of a plasma protein interaction in bacterial pathogenesis.
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- Weineisen, Maria, et al.
(författare)
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Streptococcal M5 protein prevents neutrophil phagocytosis by interfering with CD11b/CD18 receptor-mediated association and signaling.
- 2004
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Ingår i: J Immunol. - 0022-1767. ; 172:6, s. 3798-3807
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Tidskriftsartikel (refereegranskat)abstract
- Group A streptococci (GAS) are common human pathogens that express major surface-associated virulence factors designated M proteins. In this study, we explored directly the cellular mechanisms behind their supposed ability to prevent phagocytosis. Isolated human neutrophils killed an M-negative GAS mutant (DeltaM5), but not the wild-type parent strain (M5). After 3 h, 3-4 times as many DeltaM5 as M5 bacteria were associated with the neutrophils, and more DeltaM5 than M5 bacteria were ingested. However, there was no statistically significant difference between DeltaM5 and M5 bacteria in regard to the percentage of the neutrophil-associated bacteria that were ingested, indicating that M5 protein prevents an adhesion receptor-dependent association with neutrophils and not the phagocytic machinery per se. Different Abs against CD11b/CD18 (CR3) blocked adhesion and killing of DeltaM5 bacteria, whereas the blocking of two other complement receptors, CD11c/CD18 (CR4) and CD35 (CR1), did not. The CD11b/CD18-mediated killing of DeltaM5 bacteria resulted in protein tyrosine phosphorylations and Cdc42 activation. Furthermore, inhibition of CD11b/CD18 receptor engagement or tyrosine kinase activity blocked the DeltaM5-induced activation of Cdc42 as well as the killing of these bacteria. We conclude that M5 protein interferes with the CD11b/CD18-dependent association between GAS and neutrophils, and thereby blocks subsequent ingestion of the bacteria.
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- Weineisen, Maria
(författare)
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Interactions between Streptococcus pyogenes and the Human Immune System
- 2006
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Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
- Streptococcus pyogenes is a common human pathogen causing mild infections such as tonsillitis and pharyngitis, but is also the cause of life-threatening conditions. To be able to infect the human host, S. pyogenes express different virulence factors. The surface-expressed M protein is a major virulence factor of S. pyogenes, mediating resistance to killing by human neutrophils. Results presented in this thesis show that in the presence of plasma from non-immune individuals, S. pyogenes avoids killing by human neutrophils by M protein-mediated inhibition of adhesion to the neutrophils. By comparing a wild type strain and a strain deficient in M protein-expression, the interactions between S. pyogenes and human neutrophils were studied. The interactions between S. pyogenes and human neutrophils in the presence of non-immune plasma are mediated mainly by complement components deposited on the bacterial surface and CD11b/CD18 expressed on the neutrophil surface. This interaction leads to the effective ingestion and killing of the bacteria. The activation of CD11b/CD18 leads to the activation of tyrosine kinases and the subsequent activation of the small Rho GTPase Cdc42. In blood from immune humans, S. pyogenes are opsonized and killed. In this thesis, we show that killing is mediated by Abs directed against the N-terminal part of the M protein and that these Abs activate the complement system. In the presence of serum from immune individuals, the killing of S. pyogenes is mediated through activation of the complement system by M protein-specific Abs and activation of CD11b/CD18 and Cdc42 and subsequently phagocytosis. Almost all strains of S. pyogenes bind fibrinogen (Fg) and the Fg-binding is associated with members of the M protein family. We mapped the binding of Fg to the B repeats of the M1 and M5 proteins and demonstrated that the Fg-binding is important for these bacteria to resist killing when incubated in human blood. The conditions under which the interactions between S. pyogenes and human neutrophils were investigated in the studies described above resemble the situation in bacteremia (a low multiplicity of infection, MOI, i.e. bacteria: neutrophil ratio). However, at the initial stages of infection, occurring at skin or mucosal surfaces, the bacteria to neutrophil ratio is much higher. Using two different model systems to study the interactions of S. pyogenes and phagocytes at a higher MOI, we found that this interaction is mediated by fibronectin deposited at the bacterial surface and the integrins ?5?1 and ?v?3 expressed on the phagocytes.
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