Targeting E. coli invasion of the blood-brain barrier for investigating the pathogenesis and therapeutic development of E. coli meningitis

Cell Microbiol. 2020 Oct;22(10):e13231. doi: 10.1111/cmi.13231. Epub 2020 Jul 12.

Abstract

Escherichia coli is the most common Gram-negative bacillary organism causing neonatal meningitis. Escherichia coli meningitis remains an important cause of mortality and morbidity, but the pathogenesis of E. coli penetration of the blood-brain barrier remains incompletely understood. Escherichia coli entry into the brain occurs in the meningeal and cortex capillaries, not in the choroid plexus, and exploits epidermal growth factor receptor (EGFR) and cysteinyl leukotrienes (CysLTs) for invasion of the blood-brain barrier. The present study examined whether EGFR and CysLTs are inter-related in their contribution to E. coli invasion of the blood-brain barrier and whether counteracting EGFR and CysLTs is a beneficial adjunct to antibiotic therapy of E. coli meningitis. We showed that (a) meningitis isolates of E. coli exploit EGFR and CysLTs for invasion of the blood-brain barrier, (b) the contribution of EGFR is upstream of that of CysLTs, and (c) counteracting EGFR and CysLTs as an adjunctive therapy improved the outcome (survival, neuronal injury and memory impairment) of animals with E. coli meningitis. These findings suggest that investigation of host factors contributing to E. coli invasion of the blood-brain barrier will help in enhancing the pathogenesis and development of new therapeutic targets for E. coli meningitis in the era of increasing resistance to conventional antibiotics.

Keywords: CysLTs; E. coli meningitis; EGFR; blood-brain barrier; therapy.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Acetates / therapeutic use*
  • Animals
  • Anti-Bacterial Agents / therapeutic use
  • Blood-Brain Barrier / microbiology*
  • Blood-Brain Barrier / physiopathology
  • Brain / blood supply
  • Ceftriaxone / therapeutic use
  • Cells, Cultured
  • Cyclopropanes / therapeutic use*
  • Cysteine / metabolism*
  • Drug Therapy, Combination
  • Endothelial Cells
  • ErbB Receptors / antagonists & inhibitors
  • ErbB Receptors / metabolism*
  • Escherichia coli / pathogenicity*
  • Female
  • Gefitinib / therapeutic use*
  • Humans
  • Infant, Newborn
  • Leukotriene Antagonists / therapeutic use
  • Leukotrienes / metabolism*
  • Male
  • Meningitis, Escherichia coli / drug therapy
  • Meningitis, Escherichia coli / microbiology*
  • Mice
  • Permeability
  • Phospholipases A2, Cytosolic / metabolism
  • Quinolines / therapeutic use*
  • Sphingosine-1-Phosphate Receptors / metabolism
  • Sulfides / therapeutic use*

Substances

  • Acetates
  • Anti-Bacterial Agents
  • Cyclopropanes
  • Leukotriene Antagonists
  • Leukotrienes
  • Quinolines
  • Sphingosine-1-Phosphate Receptors
  • Sulfides
  • cysteinyl-leukotriene
  • sphingosine-1-phosphate receptor-2, mouse
  • Ceftriaxone
  • ErbB Receptors
  • Phospholipases A2, Cytosolic
  • Cysteine
  • montelukast
  • Gefitinib