Glycolytic Metabolism Is Critical for the Innate Antibacterial Defense in Acute Streptococcus pneumoniae Otitis Media

Front Immunol. 2021 Apr 19:12:624775. doi: 10.3389/fimmu.2021.624775. eCollection 2021.

Abstract

Objective: Streptococcus pneumoniae (S.pn) is a common respiratory pathogen and a frequent cause of acute otitis media (AOM) in children. However, little is known about the immunometabolism during AOM. This study was to assess the presence of glucose metabolic reprogramming during AOM and its underlying mechanism affecting inflammatory response and middle ear injury.

Methods: The levels of glycolytic metabolism were evaluated by measuring the expression of glycolysis-related genes and the production of metabolites. HE stain, immunofluorescence, immunohistochemistry, enzyme-linked immunosorbent assay (ELISA) and Western blot were performed to measure the effect of glucose metabolic reprogramming on inflammatory response, pneumococcal clearance, hypoxia-inducible factor 1 alpha (HIF-1α) expression and cytokine secretion during AOM, respectively.

Results: The analysis of microarray revealed an increase of the expression of glycolysis-related genes during S.pn-induced AOM, which was verified by real-time PCR. Increased glycolysis promoted the production of IL-1β and TNF-α and facilitated the clearance of S.pn by enhancing phagocytosis and killing capability of neutrophils, but also aggravated the middle ear injury. Furthermore, these pathogenic effects could be reversed after glycolytic inhibitor 2DG treatment. Additionally, HIF-1α was observed to involve in glycolytic metabolism during AOM.

Conclusion: S.pn infection induced increased glycolysis conversion during AOM, which promoted inflammatory responses and bacterial clearance, but also aggravated tissue damage.

Keywords: glycolysis; hypoxia inducible factor-1α; innate immunity; neutrophils; otitis media.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Disease Models, Animal
  • Ear, Middle / immunology
  • Ear, Middle / metabolism*
  • Ear, Middle / microbiology
  • Ear, Middle / pathology
  • Gene Expression Regulation, Enzymologic
  • Glycolysis*
  • Host-Pathogen Interactions
  • Hypoxia-Inducible Factor 1, alpha Subunit / genetics
  • Hypoxia-Inducible Factor 1, alpha Subunit / metabolism
  • Inflammation Mediators / metabolism
  • Interleukin-1beta / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Neutrophils / immunology
  • Neutrophils / metabolism
  • Neutrophils / microbiology
  • Otitis Media / immunology
  • Otitis Media / metabolism*
  • Otitis Media / microbiology
  • Otitis Media / pathology
  • Phagocytosis
  • Pneumococcal Infections / immunology
  • Pneumococcal Infections / metabolism*
  • Pneumococcal Infections / microbiology
  • Pneumococcal Infections / pathology
  • Streptococcus pneumoniae / immunology
  • Streptococcus pneumoniae / pathogenicity*
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Hif1a protein, mouse
  • Hypoxia-Inducible Factor 1, alpha Subunit
  • IL1B protein, mouse
  • Inflammation Mediators
  • Interleukin-1beta
  • Tnf protein, mouse
  • Tumor Necrosis Factor-alpha