Exopolysaccharides from Lactobacillus kiferi as adjuvant enhanced the immuno-protective against Staphylococcus aureus infection

Int J Biol Macromol. 2020 Oct 15:161:10-23. doi: 10.1016/j.ijbiomac.2020.06.005. Epub 2020 Jun 5.

Abstract

Exopolysaccharides from lactic acid bacteria (LAB) have gained more attention due to their health benefits. Most research on LAB EPS focuses on antitumor and antioxidant activities. To our knowledge, the immunoadjuvant activity of LAB EPS has not been thoroughly studied. In this study, the EPS produced by Lactobacillus kiferi WXD029 were purified by ethanol precipitation and column chromatography fractionation. The molecular weight of the EPS was 3.423 × 105 Da and was mainly composed of Glu, GlcN, and GalN in a molar ratio of 3.1:1:1. In vitro, EPS could significantly enhance the proliferation and phagocytic activity as well as induce the production of NO, TNF-α, IL-1β, and IL-6 in RAW264.7 cells. In vivo, the EPS adjuvant could increase the titers of S.aureus antigen-specific antibodies and markedly enhanced T cell proliferation. Notably, EPS adjuvant also induced a strong potential Th1, Th2 and Th17-cell mixture responses. Furthermore, immunization with S.aureus antigen plus EPS adjuvant induced a protective effect when compared with S.aureus antigen alone in murine bacteremia, pneumonia and mastitis model. Collectively, these results suggest that EPS derived from probiotic Lactobacillus kiferi strain is promising as an efficient adjuvant candidate for the prevention of S. aureus infections.

Keywords: Adjuvant; Exopolysaccharides; Staphylococcus aureus.

MeSH terms

  • Adjuvants, Immunologic / chemistry*
  • Animals
  • Cytokines / metabolism
  • Disease Models, Animal
  • Female
  • Immunologic Factors / chemistry*
  • Immunologic Factors / pharmacology*
  • Inflammation Mediators / metabolism
  • Lactobacillus / chemistry*
  • Mice
  • Molecular Weight
  • Polysaccharides, Bacterial / chemistry*
  • Polysaccharides, Bacterial / pharmacology*
  • RAW 264.7 Cells
  • Spectrum Analysis
  • Staphylococcal Infections / drug therapy
  • Staphylococcal Infections / immunology
  • Staphylococcal Infections / microbiology
  • Staphylococcus aureus / drug effects*
  • Staphylococcus aureus / immunology
  • T-Lymphocytes / drug effects
  • T-Lymphocytes / immunology
  • T-Lymphocytes / metabolism

Substances

  • Adjuvants, Immunologic
  • Cytokines
  • Immunologic Factors
  • Inflammation Mediators
  • Polysaccharides, Bacterial