# Combination of bacteriophage–probiotics alleviates intestinal barrier dysfunction by regulating gut microbiome in a chick model of multidrug-resistant Salmonella infection

**Authors:** Youbin Choi, Anna Kang, Eunsol Seo, Daniel Junpyo Lee, Junha Park, Yeonsoo Kim, Keesun Yu, Cheol‑Heui Yun, Ki Beom Jang, Woo Kyun Kim, Kwanseob Shim, Darae Kang, Younghoon Kim

PMC · DOI: 10.1186/s40104-025-01324-4 · 2026-01-23

## TL;DR

A combination of bacteriophages and a probiotic improved gut health and reduced Salmonella infection in chicks, offering a potential alternative to antibiotics.

## Contribution

The study introduces a novel phage–probiotic combination therapy that enhances Salmonella clearance and intestinal health in poultry.

## Key findings

- Co-administration of phages and probiotics reduced Salmonella colonization and improved body-weight gain in infected chicks.
- The treatment improved intestinal barrier function by increasing tight-junction gene expression and reducing inflammation.
- The gut microbiota showed a more balanced composition with increased beneficial bacteria like Lactobacillus and Blautia.

## Abstract

The rapid emergence of multidrug-resistant Salmonella in poultry demands alternative control strategies beyond conventional antibiotics. In this study, we evaluated a combination of lytic Salmonella-infecting bacteriophages (SLAM_phiST45 and SLAM_phiST56) and a probiotic bacterium Limosilactobacillus reuteri (SLAM_LAR11) in a chick model challenged with Salmonella enterica serovar Typhimurium infection.

Co-administration with two-phage cocktail and a probiotic showed markedly reduced Salmonella colonization in the gut and systemic organs of chicks, comparable to the effect of phage-only treatment. In contrast with phage-only treatment, the combined therapy significantly improved the rate of body-weight change from the day of infection to necropsy (P < 0.0001) and alleviated infection-associated splenomegaly (P = 0.028) and hepatomegaly (P = 0.011). In the ileum, the villus height-to-crypt depth ratio (VH/CD) increased significantly (P = 0.044). In the colon, expression of tight-junction genes OCLN (P = 0.014), TJP1 (P < 0.0001), and MUC2 (P = 0.011) was elevated, whereas the pro-inflammatory cytokine IL6 was reduced (P = 0.018). These improvements were accompanied, in the cecum, by trends toward decreases in Escherichia–Shigella (P = 0.09) and Clostridium (P = 0.16) and a trend toward an increase in Blautia (P = 0.11); additionally, in the ileum, Lactobacillus (P = 0.037) and Blautia (P = 0.016) increased significantly, yielding a more balanced microbiota than with phage-only treatment. Consistently, levels of functional metabolites, including acetic acid (LDA = 3.32) and lactic acid (LDA = 5.29), were increased.

Taken together, these findings demonstrate that phage–probiotic co-administration not only enhances the clearance of multidrug-resistant Salmonella more effectively than phage treatment alone but also promotes intestinal health, highlighting its potential as an antibiotic-alternatives strategy to improve intestinal health and ensure food safety in poultry production systems.

The online version contains supplementary material available at 10.1186/s40104-025-01324-4.

## Linked entities

- **Genes:** OCLN (occludin) [NCBI Gene 100506658], TJP1 (tight junction protein 1) [NCBI Gene 7082], MUC2 (mucin 2, oligomeric mucus/gel-forming) [NCBI Gene 4583], IL6 (interleukin 6) [NCBI Gene 3569]
- **Chemicals:** acetic acid (PubChem CID 176), lactic acid (PubChem CID 612)
- **Diseases:** Salmonella infection (MONDO:0000827)
- **Species:** Limosilactobacillus reuteri (taxon 1598), Clostridium (taxon 1485), Blautia (taxon 572511), Lactobacillus (taxon 1578)

## Full-text entities

- **Genes:** IL10 (interleukin 10) [NCBI Gene 428264] {aka IL-10, interleukin-10}, IL6 (interleukin 6) [NCBI Gene 395337] {aka CHIL-6, IL-6, interleukin-6}, INFG (interferon gamma) [NCBI Gene 396054] {aka IFNG}, IL8L2 (interleukin 8 like 2) [NCBI Gene 396495] {aka CEF4, CXCL8, CXCLi2, EMF-1, EMF1, IL8}, IL1B (interleukin 1, beta) [NCBI Gene 395196] {aka IL-1BETA, IL1beta}
- **Diseases:** PR (MESH:D054331), cytotoxic (MESH:D064420), SA (MESH:D012480), stunted (MESH:D006130), colitis (MESH:D003092), mucosal damage (MESH:D052016), gut injury (MESH:C536735), crypt hyperplasia (MESH:D006965), bacterial (MESH:D001424), splenomegaly (MESH:D013163), hepatosplenomegaly (MESH:C535727), Infection (MESH:D007239), weight gain (MESH:D015430), colonic inflammation (MESH:D007249), foodborne illness (MESH:D005517), hypertrophy (MESH:D006984), enteric infections (MESH:D004751), dysbiosis (MESH:D064806), hepatomegaly (MESH:D006529)
- **Chemicals:** zinc (MESH:D015032), tetracyclines (MESH:D013754), phosphorus (MESH:D010758), IAA (MESH:C030737), bacitracin (MESH:D001414), vancomycin (MESH:D014640), pyridine (MESH:C023666), SCFA (MESH:D005232), lactate (MESH:D019344), fosfomycin (MESH:D005578), MgSO4 (MESH:D008278), indole (MESH:C030374), aminoglycosides (MESH:D000617), 4,4-dimethyl-thiazolidine (-), methionine (MESH:D008715), macrolides (MESH:D018942), amino acid (MESH:D000596), 1,3-propanediol (MESH:C041787), propionate (MESH:D011422), propionic acid (MESH:C029658), p-cresol (MESH:C032538), methanol (MESH:D000432), tryptophan (MESH:D014364), beta-lactams (MESH:D047090), choline chloride (MESH:D002794), formalin (MESH:D005557), calcium (MESH:D002118), TRIzol (MESH:C411644), limestone (MESH:D002119), lipid (MESH:D008055), butyrate (MESH:D002087), glycopeptide (MESH:D006020), N,O-bis(trimethylsilyl)trifluoroacetamide (MESH:C103255), NaCl (MESH:D012965), LPS (MESH:D008070), water (MESH:D014867), polysaccharides (MESH:D011134), dicalcium phosphate (MESH:C494366), L-alanine (MESH:D000409), bile acid (MESH:D001647), hematoxylin (MESH:D006416), Phenol (MESH:D019800), cholesterol (MESH:D002784), paraffin (MESH:D010232), H&amp;E (MESH:D006371), tyrosine (MESH:D014443), Acetic acid (MESH:D019342), copper (MESH:D003300), cystine (MESH:D003553), DL-methionine (MESH:D064697), eosin (MESH:D004801), L-threonine (MESH:D013912), glycerol (MESH:D005990), methoxyamine hydrochloride (MESH:C005214), Acetate (MESH:D000085)
- **Species:** Faecalibacterium (genus) [taxon 216851], Eisenbergiella (genus) [taxon 1432051], Gallus gallus (bantam, species) [taxon 9031], Blautia (genus) [taxon 572511], Limosilactobacillus reuteri (species) [taxon 1598], Salmonella (genus) [taxon 590], Butyricicoccus (genus) [taxon 580596], Bifidobacterium (genus) [taxon 1678], Clostridium butyricum (species) [taxon 1492], gut metagenome (species) [taxon 749906], Lactobacillus (genus) [taxon 1578], Clostridium perfringens (species) [taxon 1502], Bacteroides (genus) [taxon 816], Ruminococcus (genus) [taxon 1263], Homo sapiens (human, species) [taxon 9606], Bacteriophage sp. (species) [taxon 38018], Clostridium (genus) [taxon 1485], Mus musculus (house mouse, species) [taxon 10090], Salmonella enterica subsp. enterica serovar Typhimurium (no rank) [taxon 90371], Enterococcus (genus) [taxon 1350], Escherichia coli (E. coli, species) [taxon 562]

## Figures

10 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12829087/full.md

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Source: https://tomesphere.com/paper/PMC12829087