| Literature DB >> 30814475 |
Ulrike Binsker1,2, Thomas P Kohler1, Sven Hammerschmidt3.
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.Entities:
Keywords: Colonization; Dissemination; Human thrombospondin-1; Staphylococcus aureus; Streptococcus pneumoniae
Mesh:
Substances:
Year: 2019 PMID: 30814475 PMCID: PMC6738282 DOI: 10.1159/000496033
Source DB: PubMed Journal: J Innate Immun ISSN: 1662-811X Impact factor: 7.349