# The Probiotic Effects of Lactobacillus intestinalis Y10 Isolated From Feces of Wild Brown Rat (Rattus norvegicus)

**Authors:** Sijia Yu, Peihang Hong, Chao-Min Wang, Shyun Chou, Cheng-Hung Lai

PMC · DOI: 10.1155/ijm/6537388 · International Journal of Microbiology · 2026-03-08

## TL;DR

This study identifies a probiotic strain from wild rat feces that survives harsh conditions and inhibits harmful bacteria, showing potential for rodent-specific probiotic use.

## Contribution

The study characterizes Lactobacillus intestinalis Y10 as a novel probiotic candidate with strong survival and antimicrobial properties from wild rat feces.

## Key findings

- L. intestinalis Y10 showed 72.4% viability after 2 hours in acidic conditions (pH 2.5).
- The strain exhibited high hydrophobicity (93.80%) and auto-aggregation (81.68%), indicating strong mucosal adhesion.
- It demonstrated concentration-dependent antimicrobial activity against E. coli, P. aeruginosa, and S. aureus.

## Abstract

The gut microbiota of wild mice exhibits a significant correlation with their environmental adaptability, particularly highlighted by the dominance of Lactobacillus spp. This study evaluated the probiotic traits of Lactobacillus intestinalis Y10, a fecal isolate from Rattus norvegicus, through in vitro assays. The strain demonstrated two‐hour survival in acidic conditions (pH 2.5; 72.4% viability) and maintained viability under 0.3% bile salts for 24 h. It also showed high hydrophobicity index (93.80%) and auto‐aggregation percentage (81.68%), indicative of superior mucosal adhesion potential. Organic acid–mediated antimicrobial and antibiofilm activity of strain Y10 against Escherichia coli, Pseudomonas aeruginosa, and Staphylococcus aureus subsp. aureus exhibited concentration dependence. Antibiotic susceptibility profiling identified sensitivity to cell wall–targeting agents (penicillin and cephalosporin) but resistant to antibiotics that inhibit nucleic acid synthesis and cytoplasmic membrane function, suggesting the possibility of clinical compatibility with fluoroquinolones or diaminopyrimidines for treatment of specific infections to minimize gut microbiota disruption. These findings position L. intestinalis Y10 as a promising candidate for rodent‐specific probiotic applications, combining environmental resilience with pathogen exclusion capabilities. Further in vivo validation and mechanistic studies are required to translate these traits into therapeutic interventions for gastrointestinal dysbiosis.

## Linked entities

- **Chemicals:** penicillin (PubChem CID 2349), cephalosporin (PubChem CID 25058126)
- **Species:** Rattus norvegicus (taxon 10116), Escherichia coli (taxon 562), Pseudomonas aeruginosa (taxon 287)

## Full-text entities

- **Genes:** malate dehydrogenase [NCBI Gene 3252907]
- **Diseases:** dysbiosis (MESH:D064806), mercury (MESH:D020262), inflammation (MESH:D007249), AAD (MESH:D004761), diarrhea (MESH:D003967), gastrointestinal disorders (MESH:D005767), colitis (MESH:D003092), infection (MESH:D007239), toxicity (MESH:D064420), atherosclerotic (MESH:D050197)
- **Chemicals:** amoxicillin-clavulanic acid (MESH:D019980), lactic acid (MESH:D019344), norfloxacin (MESH:D009643), ceftiofur (MESH:C053503), cholic acid (MESH:D019826), streptomycin (MESH:D013307), ciprofloxacin (MESH:D002939), agar (MESH:D000362), methanol (MESH:D000432), deoxycholic acid sodium salt (MESH:D003840), saline (MESH:D012965), enrofloxacin (MESH:D000077422), doxycycline (MESH:D004318), Acid (MESH:D000143), aminoglycoside (MESH:D000617), acetic acid (MESH:D019342), gentamicin (MESH:D005839), hydrogen chloride (MESH:D006851), inulin (MESH:D007444), sodium hydroxide (MESH:D012972), amoxicillin (MESH:D000658), kanamycin (MESH:D007612), tylosin (MESH:D015645), clindamycin (MESH:D002981), phenol (MESH:D019800), vitamin A (MESH:D014801), penicillin G (MESH:D010400), macrolide (MESH:D018942), amino acids (MESH:D000596), toluene (MESH:D014050), trimethoprim (MESH:D014295), cephalosporin (MESH:D002511), cephalothin (MESH:D002512), fluoroquinolones (MESH:D024841), amikacin (MESH:D000583), crystal violet (MESH:D005840), bile salt (MESH:D001647), ATCC 25923 (-), glycerol (MESH:D005990), penicillin (MESH:D010406), retinoic acid (MESH:D014212), mercury (MESH:D008628), lincomycin (MESH:D008034), beta-lactams (MESH:D047090), PBS (MESH:D007854), neomycin (MESH:D009355), florfenicol (MESH:C035534), chloramphenicol (MESH:D002701), trehalose (MESH:D014199), bacitracin (MESH:D001414), ofloxacin (MESH:D015242), trimethoprim-sulfamethoxazole (MESH:D015662), chloroform (MESH:D002725), minocycline (MESH:D008911), lipid (MESH:D008055)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Pseudomonas aeruginosa (species) [taxon 287], Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932], Escherichia coli (E. coli, species) [taxon 562], aureus [taxon 46170], Pediococcus damnosus (species) [taxon 51663], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Lactobacillales (order) [taxon 186826], Lactobacillus johnsonii (species) [taxon 33959], Rattus norvegicus (brown rat, species) [taxon 10116], Staphylococcus aureus (species) [taxon 1280], Lactobacillus intestinalis (species) [taxon 151781], Bifidobacterium (genus) [taxon 1678], Homo sapiens (human, species) [taxon 9606], Bacillus (genus) [taxon 55087], Lactobacillus crispatus (species) [taxon 47770], Escherichia coli ATCC 25922 (strain) [taxon 1322345]
- **Cell lines:** ATCC 25923 — Homo sapiens (Human), Lung adenocarcinoma, Cancer cell line (CVCL_0023)

## Full text

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## Figures

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## References

70 references — full list in the complete paper: https://tomesphere.com/paper/PMC12968329/full.md

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Source: https://tomesphere.com/paper/PMC12968329