[HTML][HTML] Contribution of human thrombospondin-1 to the pathogenesis of gram-positive bacteria

U Binsker, TP Kohler, S Hammerschmidt - Journal of Innate Immunity, 2019 - karger.com
U Binsker, TP Kohler, S Hammerschmidt
Journal of Innate Immunity, 2019karger.com
A successful colonization of different compartments of the human host requires multifactorial
contacts between bacterial surface proteins and host factors. Extracellular matrix proteins
and matricellular proteins such as thrombospondin-1 play a pivotal role as adhesive
substrates to ensure a strong interaction with pathobionts like the Gram-positive
Streptococcus pneumoniae and Staphylococcus aureus. The human glycoprotein
thrombospondin-1 is a component of the extracellular matrix and is highly abundant in the …
Abstract
A successful colonization of different compartments of the human host requires multifactorial contacts between bacterial surface proteins and host factors. Extracellular matrix proteins and matricellular proteins such as thrombospondin-1 play a pivotal role as adhesive substrates to ensure a strong interaction with pathobionts like the Gram-positive Streptococcus pneumoniae and Staphylococcus aureus. The human glycoprotein thrombospondin-1 is a component of the extracellular matrix and is highly abundant in the bloodstream during bacteremia. Human platelets secrete thrombospondin-1, which is then acquired by invading pathogens to facilitate colonization and immune evasion. Gram-positive bacteria express a broad spectrum of surface-exposed proteins, some of which also recognize thrombospondin-1. This review highlights the importance of thrombospondin-1 as an adhesion substrate to facilitate colonization, and we summarize the variety of thrombospondin-1-binding proteins of S. pneumoniae and S. aureus.
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