Skip to main navigation Skip to search Skip to main content

High glucose levels increase influenzaassociated damage to the pulmonary epithelial-endothelial barrier

  • Katina D. Hulme
  • , Limin Yan
  • , Rebecca J. Marshall
  • , Conor J. Bloxham
  • , Kyle R. Upton
  • , Sumaira Z. Hasnain
  • , Helle Bielefeldt-Ohmann
  • , Zhixuan Loh
  • , Katharina Ronacher
  • , Keng Yih Chew
  • , Linda A. Gallo
  • , Kirsty R. Short*
  • *Corresponding author for this work
  • University of Queensland

Research output: Contribution to journalArticleAcademicpeer-review

17 Downloads (Pure)

Abstract

Diabetes mellitus is a known susceptibility factor for severe influenza virus infections. However, the mechanisms that underlie this susceptibility remain incompletely understood. Here, the effects of high glucose levels on influenza severity were investigated using an in vitro model of the pulmonary epithelial-endothelial barrier as well as an in vivo murine model of type II diabetes. In vitro we show that high glucose conditions prior to IAV infection increased virus-induced barrier damage. This was associated with an increased pro-inflammatory response in endothelial cells and the subsequent damage of the epithelial junctional complex. These results were subsequently validated in vivo. This study provides the first evidence that hyperglycaemia may increase influenza severity by damaging the pulmonary epithelial-endothelial barrier and increasing pulmonary oedema. These data suggest that maintaining long-term glucose control in individuals with diabetes is paramount in reducing the morbidity and mortality associated with influenza virus infections.

Original languageEnglish
Article numbere56907
Pages (from-to)1-20
Number of pages20
JournaleLife
Volume9
DOIs
Publication statusPublished - Jul 2020

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Fingerprint

Dive into the research topics of 'High glucose levels increase influenzaassociated damage to the pulmonary epithelial-endothelial barrier'. Together they form a unique fingerprint.

Cite this