O-glycosylation in cell wall proteins in Scedosporium prolificans is critical for phagocytosis and inflammatory cytokines production by macrophages

PLoS One. 2015 Apr 14;10(4):e0123189. doi: 10.1371/journal.pone.0123189. eCollection 2015.

Abstract

In this study, we analyze the importance of O-linked oligosaccharides present in peptidorhamnomannan (PRM) from the cell wall of the fungus Scedosporium prolificans for recognition and phagocytosis of conidia by macrophages. Adding PRM led to a dose-dependent inhibition of conidia phagocytosis, whereas de-O-glycosylated PRM did not show any effect. PRM induced the release of macrophage-derived antimicrobial compounds. However, O-linked oligosaccharides do not appear to be required for such induction. The effect of PRM on conidia-induced macrophage killing was examined using latex beads coated with PRM or de-O-glycosylated PRM. A decrease in macrophage viability similar to that caused by conidia was detected. However, macrophage killing was unaffected when beads coated with de-O-glycosylated PRM were used, indicating the toxic effect of O-linked oligosaccharides on macrophages. In addition, PRM triggered TNF-α release by macrophages. Chemical removal of O-linked oligosaccharides from PRM abolished cytokine induction, suggesting that the O-linked oligosaccharidic chains are important moieties involved in inflammatory responses through the induction of TNF-α secretion. In summary, we show that O-glycosylation plays a role in the recognition and uptake of S. prolificans by macrophages, killing of macrophages and production of pro- inflammatory cytokines.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cells, Cultured
  • Female
  • Flow Cytometry
  • Glycoproteins / immunology
  • Glycoproteins / metabolism*
  • Glycosylation
  • Interleukin-10 / metabolism
  • Macrophages / cytology
  • Macrophages / immunology
  • Macrophages / metabolism
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Microscopy, Fluorescence
  • Nitric Oxide / metabolism
  • Phagocytosis
  • Rabbits
  • Scedosporium / physiology*
  • Spores, Fungal / physiology
  • Tumor Necrosis Factor-alpha / metabolism*

Substances

  • Glycoproteins
  • Tumor Necrosis Factor-alpha
  • peptido-rhamnomannan
  • Interleukin-10
  • Nitric Oxide

Grants and funding

This work was supported by grants from the Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq), Conselho de Pesquisa da UFRJ, Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES), Fundação de Amparo a Pesquisa do Estado do Rio de Janeiro (FAPERJ) and Programa de Núcleos de Excelência (PRONEX). LCLL and EBB are supported by FAPERJ, CNPq and CAPES. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.