Infant feces-derived Lactobacillus gasseri FWJL-4 mitigates experimental necrotizing enterocolitis via acetate production

Gut Microbes. 2024 Jan-Dec;16(1):2430541. doi: 10.1080/19490976.2024.2430541. Epub 2024 Dec 8.

Abstract

Necrotizing enterocolitis (NEC) is a life-threatening disease in premature infants, characterized by high mortality. Recent studies increasingly highlight the role of gut dysbiosis in NEC pathogenesis. Although probiotics have shown some efficacy in preventing NEC, further research is needed to determine potential strains and approaches. In this study, we demonstrated that the novel probiotic strain Lactobacillus gasseri (L. gasseri) FWJL-4, isolated from the feces of healthy infants, significantly enhanced intestinal barrier function, providing substantial protection against NEC. This protective effect was attributed to elevated intestinal acetate levels. Notably, acetate supplementation alone was sufficient to mitigate NEC, mimicking the protective effects of L. gasseri FWJL-4. Mechanistically, we revealed that L. gasseri FWJL-4 inhibited necroptosis and preserved the number of the goblet cells and enterocytes through the production of the short-chain fatty acid acetate, via activation of the acetate receptors G protein-coupled receptor (GPR) 41 and GPR43. Our findings suggest that L. gasseri FWJL-4 enhances intestinal barrier function to protect against NEC, underscoring the potential of probiotic manipulation as a promising strategy for NEC prevention.

Keywords: Lactobacillus gasseri; Necrotizing enterocolitis; acetate; probiotics.

MeSH terms

  • Acetates* / metabolism
  • Animals
  • Disease Models, Animal
  • Enterocolitis, Necrotizing* / metabolism
  • Enterocolitis, Necrotizing* / microbiology
  • Enterocolitis, Necrotizing* / prevention & control
  • Enterocytes / metabolism
  • Enterocytes / microbiology
  • Feces* / microbiology
  • Female
  • Gastrointestinal Microbiome
  • Goblet Cells / metabolism
  • Humans
  • Infant
  • Infant, Newborn
  • Intestinal Mucosa / metabolism
  • Intestinal Mucosa / microbiology
  • Lactobacillus gasseri* / metabolism
  • Male
  • Mice
  • Necroptosis
  • Probiotics*
  • Receptors, G-Protein-Coupled / metabolism

Substances

  • Acetates
  • Receptors, G-Protein-Coupled
  • Ffar2 protein, mouse

Grants and funding

The study was supported by Collaborative Innovation Center of Food Safety and Quality Control in Jiangsu Province, the National Natural Science Foundation of China [Grant Nos. 82470488, 81901517], the Natural Science Foundation of Jiangsu Province [Grant No. BK20242079], the Fundamental Research Funds for the Central Universities [Grant No: JUSRP202406003], the Postgraduate Research & Practice Innovation Program of Jiangsu Province [Grant No. KYCX23_2574], Top medical expert team of Wuxi Taihu Talent Plan [Grant Nos. DJTD202106, GDTD202105], Medical Key Discipline Program of Wuxi Health Commission [Grant No. ZDXK2021007], Top Talent Support Program for young and middle-aged people of Wuxi Health Committee [Grant No. BJ2023090], Scientific Research Program of Wuxi health Commission [Grant Nos. Z202109, M202208] and Wuxi Science and Technology Development Fund [Grant No. Y20222001], Jiangnan University Wuxi School of Medicine Subject Development Fund [Grant No. YXXK2024092615].