Intranasal administration of Lactobacillus rhamnosus GG protects mice from H1N1 influenza virus infection by regulating respiratory immune responses

Lett Appl Microbiol. 2010 Jun 1;50(6):597-602. doi: 10.1111/j.1472-765X.2010.02844.x. Epub 2010 Mar 29.

Abstract

Aims: To investigate whether intranasal Lactobacillus administration protects host animals from influenza virus (IFV) infection by enhancing respiratory immune responses in a mouse model.

Methods and results: After 3 days of intranasal exposure to Lactobacillus rhamnosus GG (LGG), BALB/c mice were infected with IFV A/PR/8/34 (H1N1). Mice treated with LGG showed a lower frequency of accumulated symptoms and a higher survival rate than control mice (P < 0.05). The YAC-1 cell-killing activity of lung cells isolated from mice treated with LGG was significantly greater than those isolated from control mice (P < 0.01). Intranasal administration of LGG significantly increased mRNA expression of interleukin (IL)-1 beta, tumour necrosis factor (TNF) and monocyte chemotactic protein (MCP)-1 (P < 0.01).

Conclusions: These results suggest that intranasal administration of LGG protects the host animal from IFV infection by enhancing respiratory cell-mediated immune responses following up-regulation of lung natural killer (NK) cell activation.

Significance and impact of study: We have demonstrated that probiotics might protect host animals from viral infection by stimulating immune responses in the respiratory tract.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Intranasal
  • Animals
  • Disease Models, Animal
  • Female
  • Humans
  • Influenza A Virus, H1N1 Subtype / immunology
  • Influenza A Virus, H1N1 Subtype / physiology*
  • Influenza, Human / genetics
  • Influenza, Human / immunology*
  • Influenza, Human / prevention & control*
  • Influenza, Human / virology
  • Interleukin-1beta / genetics
  • Interleukin-1beta / immunology
  • Killer Cells, Natural / immunology
  • Lacticaseibacillus rhamnosus / immunology*
  • Lung / immunology
  • Lung / virology
  • Mice
  • Mice, Inbred BALB C
  • Respiratory System / immunology*
  • Respiratory System / virology

Substances

  • Interleukin-1beta