Nod2 is required for the early innate immune clearance of Acinetobacter baumannii from the lungs

Sci Rep. 2017 Dec 12;7(1):17429. doi: 10.1038/s41598-017-17653-y.

Abstract

Acinetobacter baumannii (A. baumannii) is a significant cause of severe nosocomial pneumonia in immunocompromised individuals world-wide. With limited treatment options available, a better understanding of host immnity to A. baumannii infection is critical to devise alternative control strategies. Our previous study has identified that intracellular Nod1/Nod2 signaling pathway is required for the immune control of A. baumannii in airway epithelial cells in vitro. In the current study, using Nod2-/- mice and an in vivo sublethal model of pulmonary infection, we show that Nod2 contributes to the early lung defense against A. baumannii infection through reactive oxygen species (ROS)/reactive nitrogen species (RNS) production as Nod2-/- mice showed significantly reduced production of ROS/RNS in the lungs following A. baumannii infection. Consistent with the higher bacterial load, A. baumannii-induced neutrophil recruitment, cytokine/chemokine response and lung pathology was also exacerbated in Nod2-/- mice at early time points post-infection. Finally, we show that administration of Nod2 ligand muramyl dipeptide (MDP) prior to infection protected the wild- type mice from A. baumannii pulmonary challenge. Collectively, Nod2 is an important player in the early lung immunity against A. baumannii and modulating Nod2 pathway could be considered as a viable therapeutic strategy to control A. baumannii pulmonary infection.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylmuramyl-Alanyl-Isoglutamine / pharmacology
  • Acinetobacter Infections / drug therapy
  • Acinetobacter Infections / immunology*
  • Acinetobacter Infections / pathology
  • Acinetobacter baumannii / immunology*
  • Animals
  • Anti-Infective Agents / pharmacology
  • Female
  • Immunity, Innate / physiology*
  • Lung / drug effects
  • Lung / immunology*
  • Lung / pathology
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Nod2 Signaling Adaptor Protein / genetics
  • Nod2 Signaling Adaptor Protein / metabolism*
  • Reactive Nitrogen Species / metabolism
  • Reactive Oxygen Species / metabolism

Substances

  • Anti-Infective Agents
  • Nod2 Signaling Adaptor Protein
  • Nod2 protein, mouse
  • Reactive Nitrogen Species
  • Reactive Oxygen Species
  • Acetylmuramyl-Alanyl-Isoglutamine