Lactiplantibacillus plantarum Postbiotics Suppress Salmonella Infection via Modulating Bacterial Pathogenicity, Autophagy and Inflammasome in Mice.
Aixin HuWenxia HuangXin ShuShiyue MaCaimei YangRuiqiang ZhangXiao XiaoYanping WuPublished in: Animals : an open access journal from MDPI (2023)
Our study aimed to explore the effects of postbiotics on protecting against Salmonella infection in mice and clarify the underlying mechanisms. Eighty 5-week-old C57BL/6 mice were gavaged daily with Lactiplantibacillus plantarum (LP)-derived postbiotics (heat-killed bacteria, LPB inactive ; culture supernatant, LPC) or the active bacteria (LPB active ), and gavaged with Salmonella enterica Typhimurium (ST). The Turbidimetry test and agar diffusion assay indicated that LPC directly inhibited Salmonella growth. Real-time PCR and biofilm inhibition assay showed that LPC had a strong ability in suppressing Salmonella pathogenicity by reducing virulence genes ( SopE , SopB , InvA , InvF , SipB , HilA , SipA and SopD 2), pili genes ( FilF , SefA , LpfA , FimF ), flagellum genes ( FlhD , FliC , FliD ) and biofilm formation. LP postbiotics were more effective than LP on attenuating ST-induced intestinal damage in mice, as indicated by increasing villus/crypt ratio and increasing the expression levels of tight junction proteins (Occludin and Claudin-1). Elisa assay showed that LP postbiotics significantly reduced ST-induced inflammation by regulating the levels of inflammatory cytokines (the increased IL-4 and IL-10 and the decreased TNF-α) in serum and ileum ( p < 0.05). Furthermore, LP postbiotics inhibited the activation of NOD-like receptor thermal protein domain-associated protein 3 (NLRP3) inflammasome by decreasing the protein expression of NLRP3 and Caspase-1, and the gene expression of Caspase - 1 , IL-1β and IL - 18 . Meanwhile, both LPC and LPB observably activated autophagy under ST infection, as indicated by the up-regulated expression of LC3 and Beclin1 and the downregulated p62 level ( p < 0.05). Finally, we found that LP postbiotics could trigger an AMP-activated protein kinase (AMPK) signaling pathway to induce autophagy. In summary, Lactiplantibacillus plantarum -derived postbiotics alleviated Salmonella infection via modulating bacterial pathogenicity, autophagy and NLRP3 inflammasome in mice. Our results confirmed the effectiveness of postbiotics agents in the control of Salmonella infection.
Keyphrases
- biofilm formation
- escherichia coli
- signaling pathway
- nlrp inflammasome
- cell death
- listeria monocytogenes
- pseudomonas aeruginosa
- oxidative stress
- staphylococcus aureus
- high fat diet induced
- gene expression
- induced apoptosis
- protein kinase
- candida albicans
- endoplasmic reticulum stress
- high throughput
- poor prognosis
- genome wide
- pi k akt
- rheumatoid arthritis
- systematic review
- high glucose
- epithelial mesenchymal transition
- binding protein
- dna methylation
- mass spectrometry
- wild type
- real time pcr
- small molecule
- cystic fibrosis
- skeletal muscle
- cell proliferation
- heat stress
- protein protein
- endothelial cells
- adipose tissue
- stress induced
- innate immune