
AbstractAlthough many lactic acid bacteria (LAB) influence the consumer’s immune status it is not completely understood how this is established. Bacteria-host interactions between bacterial cell-wall components and toll-like receptors (TLRs) have been suggested to play an essential role. Here we investigated the interaction between LABs with reported health effects and TLRs. By using cell-lines expressing single or combination of TLRs, we show that LABs can signal via TLR-dependent and independent pathways. The strains only stimulated and did not inhibit TLRs. We found that several strains such as L. plantarum CCFM634, L. plantarum CCFM734, L. fermentum CCFM381, L. acidophilus CCFM137 and S. thermophilus CCFM218 stimulated TLR2/TLR6. TLR2/TLR6 is essential in immune regulatory processes and of interest for prevention of diseases. Specificity of the TLR2/TLR6 stimulation was confirmed with blocking antibodies. Immunomodulatory properties of LABs were also studied by assessing IL-10 and IL-6 secretion patterns in bacteria-stimulated THP1-derived macrophages, which confirmed species and strain specific effects of the LABs. With this study we provide novel insight in LAB specific host-microbe interactions. Our data demonstrates that interactions between pattern recognition receptors such as TLRs is species and strain specific and underpins the importance of selecting specific strains for promoting specific health effects.
TOLL-LIKE RECEPTORS, Interleukin-6, THP-1 Cells, Macrophages, NF-KAPPA-B, BARRIER, Article, Toll-Like Receptor 2, Interleukin-10, Lactobacillus, Toll-Like Receptor 6, LACTOBACILLUS-RHAMNOSUS GG, INFLAMMATION, HUMAN DENDRITIC CELLS, T-CELLS, Humans, INTESTINAL EPITHELIAL-CELLS, COLITIS, RESPONSES, Signal Transduction
TOLL-LIKE RECEPTORS, Interleukin-6, THP-1 Cells, Macrophages, NF-KAPPA-B, BARRIER, Article, Toll-Like Receptor 2, Interleukin-10, Lactobacillus, Toll-Like Receptor 6, LACTOBACILLUS-RHAMNOSUS GG, INFLAMMATION, HUMAN DENDRITIC CELLS, T-CELLS, Humans, INTESTINAL EPITHELIAL-CELLS, COLITIS, RESPONSES, Signal Transduction
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