Fungal chitin-binding glycoprotein induces Dectin-2-mediated allergic airway inflammation synergistically with chitin

PLoS Pathog. 2024 Jan 3;20(1):e1011878. doi: 10.1371/journal.ppat.1011878. eCollection 2024 Jan.

Abstract

Although chitin in fungal cell walls is associated with allergic airway inflammation, the precise mechanism underlying this association has yet to be elucidated. Here, we investigated the involvement of fungal chitin-binding protein and chitin in allergic airway inflammation. Recombinant Aspergillus fumigatus LdpA (rLdpA) expressed in Pichia pastoris was shown to be an O-linked glycoprotein containing terminal α-mannose residues recognized by the host C-type lectin receptor, Dectin-2. Chitin particles were shown to induce acute neutrophilic airway inflammation mediated release of interleukin-1α (IL-1α) associated with cell death. Furthermore, rLdpA-Dectin-2 interaction was shown to promote phagocytosis of rLdpA-chitin complex and activation of mouse bone marrow-derived dendritic cells (BMDCs). Moreover, we showed that rLdpA potently induced T helper 2 (Th2)-driven allergic airway inflammation synergistically with chitin, and Dectin-2 deficiency attenuated the rLdpA-chitin complex-induced immune response in vivo. In addition, we showed that serum LdpA-specific immunoglobulin levels were elevated in patients with pulmonary aspergillosis.

MeSH terms

  • Animals
  • Aspergillus fumigatus
  • Chitin* / metabolism
  • Glycoproteins / metabolism
  • Humans
  • Inflammation
  • Lectins, C-Type* / genetics
  • Lectins, C-Type* / metabolism
  • Mice
  • Phagocytosis

Substances

  • dectin-2, mouse
  • Chitin
  • Lectins, C-Type
  • Glycoproteins

Grants and funding

This work was supported by JSPS KAKENHI (Grant Number 20K07476 and 23K06535 to YM). This work was also partially supported by the Japan Agency for Medical Research and Development (AMED) (Grant Number JP18ek0410026 to KK). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.