Contribution of Human Thrombospondin-1 to the Pathogenesis of Gram-Positive Bacteria

J Innate Immun. 2019;11(4):303-315. doi: 10.1159/000496033. Epub 2019 Feb 27.

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.

Keywords: Colonization; Dissemination; Human thrombospondin-1; Staphylococcus aureus; Streptococcus pneumoniae.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Bacterial Adhesion
  • Bacterial Proteins / metabolism*
  • Blood Platelets / physiology*
  • Gram-Positive Bacteria / physiology*
  • Gram-Positive Bacterial Infections / immunology*
  • Humans
  • Immune Evasion
  • Immunity, Innate
  • Protein Binding
  • Thrombospondin 1 / metabolism*

Substances

  • Bacterial Proteins
  • Thrombospondin 1
  • thrombospondin-1, human