# Gut-Centric Multi-System Regulation by Bacillus subtilis and Bacillus natto: A Review of Their Probiotic Functions in Nutrition, Immunity, and Metabolism

**Authors:** Mei Hua, Jing Wang, Yueqiao Li, Yuguang He, Zhengyang Luo, Da Li, Mubai Sun, Xinyu Miao, Honghong Niu, Tong Pan, Jinghui Wang, Chengshan Wan

PMC · DOI: 10.3390/nu18050802 · Nutrients · 2026-02-28

## TL;DR

This review explores how Bacillus subtilis and Bacillus natto improve gut health, immunity, and metabolism through multiple mechanisms.

## Contribution

The paper introduces a novel 'triple mechanism' framework for BS and BN's probiotic effects on nutrition, immunity, and metabolism.

## Key findings

- BS and BN enhance digestion and absorption in the small intestine and promote animal growth.
- They improve immune defenses by regulating mucins, tight junctions, and inflammatory factors.
- BS and BN reshape gut microbiota and metabolic pathways to reduce insulin resistance and liver injury.

## Abstract

Background: Compared with lactic acid-producing probiotics, spore-producing probiotics such as Bacillus subtilis (BS) and Bacillus natto (BN) exhibited superior metabolic capacity and stress resistance and are more suitable for industrial applications. However, limited understanding of their nutritional and intestinal health mechanisms has constrained their food potential. Objectives: This review systematically expounded on the ‘triple mechanism’ of BS and BN and their effects on intestinal nutrition, immunity and metabolism benefit for the first time. Methods: We searched PubMed, Scopus, Web of Science, and Google Scholar for studies on livestock, model organisms, and human research from 2000 to 2025. After evaluating relevance and eligibility, 115 articles were included. Results: Firstly, by secreting various digestive enzymes, BS and BN directly enhanced the small intestine digestive and absorptive efficiency and promoted animal growth. In particular, BN significantly increases calcium absorption in postmenopausal women. Secondly, as the antigen carrier that induced intestinal mucosal immunity, BS and BN enhanced the host’s defense ability by strengthening the expression of tight junction proteins, mucins, and inflammatory factors and bidirectionally regulated constipation and acute diarrhea in the human body. Thirdly, they reshaped the structure of the intestinal microbiota and their metabolic profile in the form of the gut–liver/gut–adipose axis, including enriching beneficial bacteria, activating lipid metabolism pathways such as PI3K/AKT and AMPK/SREBP, and regulating liver targets such as PPAR and CD36, thereby reducing insulin resistance and liver injury and maintaining overall metabolic homeostasis. Conclusions: Bacillus subtilis and Bacillus natto mediated their probiotic benefits through a gut-centric, multi-system regulatory strategy, involving nutrient utilization, immune homeostasis, and microbial–host metabolic interactions. This integrated mechanism provided a robust foundation for their targeted application in functional formulations and fermented food science.

## Linked entities

- **Genes:** PIK3CA (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha) [NCBI Gene 5290], AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207], PRKAA1 (protein kinase AMP-activated catalytic subunit alpha 1) [NCBI Gene 5562], SREBP (Sterol regulatory element binding protein) [NCBI Gene 40155], PPARA (peroxisome proliferator activated receptor alpha) [NCBI Gene 5465], CD36 (CD36 molecule (CD36 blood group)) [NCBI Gene 948]
- **Species:** Bacillus subtilis (taxon 1423)

## Full-text entities

- **Diseases:** liver injury (MESH:D017093), inflammatory (MESH:D007249), acute diarrhea (MESH:D000208), insulin resistance (MESH:D007333), constipation (MESH:D003248)
- **Chemicals:** lipid (MESH:D008055), calcium (MESH:D002118), lactic acid (MESH:D019344)
- **Species:** Bacillus subtilis (species) [taxon 1423], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12987042/full.md

## References

117 references — full list in the complete paper: https://tomesphere.com/paper/PMC12987042/full.md

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Source: https://tomesphere.com/paper/PMC12987042