Effects of Pseudomonas aeruginosa mannose-sensitive hemagglutinin (PA-MSHA) pretreatment on septic rats

Int Immunopharmacol. 2013 Nov;17(3):836-42. doi: 10.1016/j.intimp.2013.09.006. Epub 2013 Sep 18.

Abstract

To evaluate the effects of Pseudomonas aeruginosa mannose-sensitive hemagglutinin (PA-MSHA) injection on the survival rate of rats post cecal ligation and puncture (CLP), Sprague-Dawley (SD) rats were subcutaneously injected with 0.125 ml, 0.25 ml or 0.5 ml PA-MSHA for 8 days or 16 days before CLP. The survival rate and physiological appearance of rats in each group were monitored daily post CLP. The expression of Toll-like receptor 4 (TLR4) and cytokines related to inflammation was evaluated. We found that the 0.5 ml-8d (0.5 ml PA-MSHA injected for 8 days) group had the highest 7-day survival rate (91.7%), which was significantly improved compared with the CLP-only group (33.3%). Furthermore, our results showed that PA-MSHA effectively increased serum pro-inflammatory mediators (TNF-α, IL-1β and IL-6) at the early stage (8 days) but increased anti-inflammatory mediators (IL-4 and IL-10) at the late stage (16 days). PA-MSHA significantly up-regulated the mRNA expression of TLR4 at 8 and 16 days. After PA-MSHA pretreatment, CLP had no marked effect on the levels of most inflammatory factors. To explore potential protective mechanisms of PA-MSHA against CLP, we examined the effect of PA-MSHA on murine macrophage-like RAW264.7 cells and found that PA-MSHA induced endotoxin tolerance. In conclusion, this study suggested that precisely controlling the dosage and time of PA-MSHA administration can effectively increase the rat survival rate post CLP, which may be mediated through regulating inflammatory mediators and inducing endotoxin tolerance.

Keywords: Cecal ligation and puncture (CLP); Cytokines; Endotoxin tolerance; Pseudomonas aeruginosa mannose-sensitive hemagglutinin (PA-MSHA); Sepsis; Toll-like receptor 4.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adjuvants, Immunologic / pharmacology*
  • Animals
  • Cell Line
  • Cytokines / blood
  • Hemagglutinins / pharmacology*
  • Immune Tolerance
  • Lipopolysaccharides
  • Lung / drug effects
  • Lung / immunology
  • Male
  • Mannose / pharmacology*
  • Mice
  • Pseudomonas aeruginosa*
  • Rats
  • Rats, Sprague-Dawley
  • Sepsis / drug therapy*
  • Sepsis / immunology
  • Toll-Like Receptor 4 / immunology

Substances

  • Adjuvants, Immunologic
  • Cytokines
  • Hemagglutinins
  • Lipopolysaccharides
  • Tlr4 protein, rat
  • Toll-Like Receptor 4
  • Mannose