Mouse adenovirus type 1 infection of adipose tissue

Virus Res. 2018 Jan 15:244:90-98. doi: 10.1016/j.virusres.2017.11.014. Epub 2017 Nov 12.

Abstract

Human adenovirus (HAdV) type 36 seropositivity has been linked to obesity in humans. That link is supported by a small number of studies using HAdV-36 infection of animals that are not natural hosts for HAdVs. In this study, we infected mice with mouse adenovirus type 1 (MAV-1), a mouse pathogen, to determine whether MAV-1 infected adipose tissue and was associated with adipose tissue inflammation and obesity. We detected MAV-1 in adipose tissue during acute MAV-1 infection, but we did not detect virus-induced increases in adipose tissue cytokine expression or histological evidence of adipose tissue inflammation during acute infection. MAV-1 did not persist in adipose tissue at later times, and we did not detect long-term adipose inflammation, increased adipose tissue mass, or body weight in infected mice. Our data indicate that MAV-1 is not associated with obesity in infected mice.

Keywords: Adenovirus; Adipose tissue; Inflammation; Mouse model; Obesity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenoviridae Infections / genetics
  • Adenoviridae Infections / immunology
  • Adenoviridae Infections / virology*
  • Adipose Tissue / immunology
  • Adipose Tissue / virology*
  • Animals
  • Body Weight
  • CCAAT-Enhancer-Binding Protein-beta / genetics
  • CCAAT-Enhancer-Binding Protein-beta / immunology
  • Cell Line
  • Chemokine CCL2 / genetics
  • Chemokine CCL2 / immunology
  • DNA, Viral / genetics*
  • DNA, Viral / immunology
  • Female
  • Fibroblasts / virology
  • Gene Expression Regulation / immunology*
  • Host-Pathogen Interactions*
  • Interferon-gamma / genetics
  • Interferon-gamma / immunology
  • Interleukin-17 / genetics
  • Interleukin-17 / immunology
  • Male
  • Mastadenovirus / genetics*
  • Mastadenovirus / growth & development
  • Mastadenovirus / metabolism
  • Mice
  • Mice, Inbred C57BL
  • PPAR gamma / genetics
  • PPAR gamma / immunology
  • Tumor Necrosis Factor-alpha / genetics
  • Tumor Necrosis Factor-alpha / immunology
  • Virus Replication

Substances

  • CCAAT-Enhancer-Binding Protein-beta
  • Ccl2 protein, mouse
  • Cebpb protein, mouse
  • Chemokine CCL2
  • DNA, Viral
  • Interleukin-17
  • PPAR gamma
  • Tumor Necrosis Factor-alpha
  • Interferon-gamma