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Substances released from probiotic L actobacillus rhamnosus GR ‐1 potentiate NF ‐κB activity in E scherichia coli ‐stimulated urinary bladder cells
Author(s) -
Karlsson Mattias,
Scherbak Nikolai,
Khalaf Hazem,
Olsson PerErik,
Jass Jana
Publication year - 2012
Publication title -
fems immunology & medical microbiology
Language(s) - English
Resource type - Journals
eISSN - 1574-695X
pISSN - 0928-8244
DOI - 10.1111/j.1574-695x.2012.00994.x
Subject(s) - lactobacillus rhamnosus , microbiology and biotechnology , escherichia coli , probiotic , biology , immune system , immunogenicity , lactobacillus , bacteria , immunology , biochemistry , genetics , gene
L actobacillus rhamnosus GR ‐1 is a probiotic bacterium used to maintain urogenital health. The putative mechanism for its probiotic effect is by modulating the host immunity. Urinary tract infections ( UTI ) are often caused by uropathogenic E scherichia coli that frequently evade or suppress immune responses in the bladder and can target pathways, including nuclear factor‐kappaB ( NF ‐κ B ). We evaluated the role of L . rhamnosus GR ‐1 on NF ‐κ B activation in E . coli ‐stimulated bladder cells. Viable L . rhamnosus GR ‐1 was found to potentiate NF ‐κ B activity in E . coli ‐stimulated T 24 bladder cells, whereas heat‐killed lactobacilli demonstrated a marginal increase in NF ‐κ B activity. Surface components released by trypsin‐ or LiCl treatment, or the resultant heat‐killed shaved lactobacilli, had no effect on NF ‐κ B activity. Isolation of released products from L . rhamnosus GR ‐1 demonstrated that the induction of NF ‐κ B activity was owing to released product(s) with a relatively large native size. Several putative immunomodulatory proteins were identified, namely G ro EL , elongation factor T u and NLP / P 60. G ro EL and elongation factor T u have previously been shown to elicit immune responses from human cells. Isolating and using immune‐augmenting substances produced by lactobacilli is a novel strategy for the prevention or treatment of UTI caused by immune‐evading E . coli .