Probiotic Bacillus spp. enhance TLR3-mediated TNF signalling in macrophages

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Probiotics have been reported to have immunomodulatory properties in the context of infectious disease and inflammation, although the underlying mechanisms are not fully understood. Here, we aimed to determine how different probiotic bacterial strains modulated macrophage function during TLR3 stimulation mimicking viral infection. We screened 14 different strains for their ability to modulate TNF-α, IL-6 IL-10, IFN-α, IFN-β and IFN-γ secretion in RAW 264.7 macrophages with or without poly(I:C) stimulation. Seven strains were selected for further analysis using primary porcine alveolar macrophages. In-depth transcriptomic analysis on alveolar macrophages was conducted for two strains. Most strains induced a synergistic effect when co-incubated with poly(I:C) resulting in increased levels of IL-6 and TNF-α secretion from RAW 264.7 cells. This synergistic effect was found to be TLR2 independent. Only strains of Bacillus spp. could induce this effect in alveolar macrophages. Transcriptomic analysis indicated that the increased TNF-α secretion in alveolar macrophages after co-incubation with poly(I:C) correlated with significant upregulation of TNF and IL23A-related pathways. Collectively, our data show that probiotic bacteria possess strain-dependent immunomodulatory properties that may be harnessed to enhance innate immune responses to pathogens.
OriginalsprogEngelsk
TidsskriftImmunology
Vol/bind171
Udgave nummer3
Sider (fra-til)402-412
Antal sider11
ISSN0019-2805
DOI
StatusUdgivet - 2024

Bibliografisk note

Funding Information:
The authors thank Audrey Inge Schytz Andersen-Civil for help with cell line studies and ELISA. This work was financially supported by Chr. Hansen A/S (Denmark) and Innovation Foundation Denmark via a PhD grant (grant number: 0153-00153A) for the first author.

Funding Information:
The authors thank Audrey Inge Schytz Andersen‐Civil for help with cell line studies and ELISA. This work was financially supported by Chr. Hansen A/S (Denmark) and Innovation Foundation Denmark via a PhD grant (grant number: 0153‐00153A) for the first author.

Publisher Copyright:
© 2023 John Wiley & Sons Ltd.

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