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Involvement of lipoprotein PpiA of Streptococcus gordonii in evasion of phagocytosis by macrophages.

Authors
  • Cho, K
  • Arimoto, T
  • Igarashi, T
  • Yamamoto, M
Type
Published Article
Journal
Molecular oral microbiology
Publication Date
Oct 01, 2013
Volume
28
Issue
5
Pages
379–391
Identifiers
DOI: 10.1111/omi.12031
PMID: 23734737
Source
Medline
Keywords
License
Unknown

Abstract

Streptococcus gordonii is a commensal gram-positive bacterium that resides in the human oral cavity, and is one of the most common causes of infective endocarditis (IE). Bacterial surface molecules play an important role in establishing IE, and several S. gordonii proteins have been implicated in binding to host cells during the establishment of IE. In this study, we identified a putative lipoprotein, peptidyl-prolyl cis/trans isomerase (PpiA), and clarified its role in evasion of phagocytosis by macrophages. Attenuation of the gene encoding prolipoprotein diacylglyceryl transferase (Lgt) altered the localization of PpiA from the cell surface to the culture supernatant, indicating that PpiA is lipid-anchored in the cell membrane by Lgt. Both human and murine macrophages showed higher phagocytic activity towards ppiA and lgt mutants than the wild-type, indicating that the presence of PpiA suppresses phagocytosis of S. gordonii. Human macrophages treated with dextran sulfate had significantly impaired phagocytosis of S. gordonii, suggesting that class A scavenger receptors in human macrophages are involved in the phagocytosis of S. gordonii. These results provide evidence that S. gordonii lipoprotein PpiA plays an important role in inhibiting phagocytic engulfment and in evasion of the host immune response.

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