# The Protective Effects and Underlying Mechanisms of Taraxacum kok-saghyz Polysaccharides Against Intestinal Dysbiosis-Induced Mastitis Were Elucidated Using a Murine Model of the “Gut–Mammary” Axis

**Authors:** Yuan Liang, Peng Huang, Jianming Li, Zulikeyan Manafu, Rong Wang, Xia Chen, Xiaohui Zhang, Yan Wu, Xieraili Malajiang, Aikebaier Yiming, Selikbuick Duishan, Adelijiang Wusiman

PMC · DOI: 10.3390/ani16050751 · Animals : an Open Access Journal from MDPI · 2026-02-27

## TL;DR

This study shows that polysaccharides from Taraxacum kok-saghyz leaves can reduce mastitis in mice by improving gut health and reducing inflammation.

## Contribution

The novel finding is that TKP-L polysaccharides can target the gut–mammary axis to treat dysbiosis-induced mastitis.

## Key findings

- TKP-L reduced mammary inflammation and improved barrier integrity in gut and mammary tissues.
- TKP-L inhibited bacterial translocation and restored gut and milk microbiota balance.
- Beneficial bacteria like Limosilactobacillus increased with TKP-L treatment.

## Abstract

Mastitis in dairy cows is a costly inflammatory disease that adversely affects milk production and animal health. Although commonly associated with bacterial infections, emerging evidence indicates that dysbiosis of gut microbiota may contribute to mastitis via the “gut–milk axis,” a pathway through which intestinal disturbances influence the mammary gland. This study investigated whether polysaccharides derived from Taraxacum kok-saghyz leaves (TKP-L), a natural compound, could mitigate mastitis by targeting this gut–mammary connection. Using a murine model, we demonstrated that TKP-L significantly reduced mammary inflammation, enhanced barrier integrity in both intestinal and mammary tissues, and inhibited systemic translocation of pathogenic bacteria. Furthermore, TKP-L restored microbial homeostasis in the gut and milk by promoting beneficial genera such as Limosilactobacillus. These findings suggest that TKP-L represents a safe and environmentally sustainable strategy for preventing and treating mastitis through modulation of gut health, with potential implications for advancing sustainable dairy farming practices.

The gut–mammary axis represents a promising therapeutic target for mastitis. Although plant-derived polysaccharides exhibit immunomodulatory properties, their capacity to modulate this axis—and specifically to ameliorate dysbiosis-induced mastitis—remains unexplored. Here, we investigated the therapeutic potential of Taraxacum kok-saghyz leaf-derived polysaccharides (TKP-L) against mastitis in a murine model of gut dysbiosis, with dysbiosis induced by fecal microbiota transplantation (FMT) from donor cows. Pregnant mice (n = 60) with antibiotic-depleted microbiota received FMT suspensions prepared from the feces of healthy dairy cows or cows with clinical mastitis (based on somatic cell count). Mice were randomly divided into five groups: Control (vehicle), M-FMT (mastitis-cow FMT, disease model), H-FMT (healthy-cow FMT), TKP-L (M-FMT + oral TKP-L, 500 mg/kg/day), and Ciprofloxacin (M-FMT + ciprofloxacin, positive Control). After FMT establishment, TKP-L or ciprofloxacin was administered for 14 days. We assessed histopathology, pro-inflammatory mediators (IL-6, IL-1β, TNF-α, MPO), tight junction proteins (occludin, ZO-1, Claudin-3), and bacterial translocation using GFP-E. coli, and gut/milk microbiota via 16S rRNA sequencing. Compared to the M-FMT group, TKP-L treatment significantly alleviated mammary inflammation and pathology, inhibited pro-inflammatory cytokine expression, and enhanced the expression of tight junction proteins in both intestinal and mammary tissues, correlating with reduced bacterial translocation to the mammary gland. Microbiota analysis showed that TKP-L restored microbial homeostasis in the gut and milk, concurrently increasing the relative abundance of beneficial bacteria such as Limosilactobacillus. TKP-L alleviates gut dysbiosis-induced mastitis in mice by concurrently modulating the gut–mammary axis through microbial remodeling, enhancement of epithelial barriers, and anti-inflammatory actions. These findings highlight TKP-L as a promising gut microbiota-targeting candidate for mastitis intervention.

## Linked entities

- **Proteins:** IL6 (interleukin 6), IL1B (interleukin 1 beta), TNF (tumor necrosis factor), MPO (myeloperoxidase), si:ch73-61d6.3 (uncharacterized si:ch73-61d6.3), TJP1 (tight junction protein 1), CLDN3 (claudin 3)
- **Chemicals:** ciprofloxacin (PubChem CID 2764)
- **Diseases:** mastitis (MONDO:0006849)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** TNF (tumor necrosis factor) [NCBI Gene 280943] {aka TNF-a, TNF-alpha, TNFa}, OCLN (occludin) [NCBI Gene 512405], IL1B (interleukin 1 beta) [NCBI Gene 281251], MPO (myeloperoxidase) [NCBI Gene 511206], LOC517016 (interleukin 6 (interferon, beta 2)) [NCBI Gene 517016] {aka IF1DA6}, CLDN3 (claudin 3) [NCBI Gene 404153], TJP1 (tight junction protein 1) [NCBI Gene 407102] {aka zo1}
- **Diseases:** Mastitis (MESH:D008413), inflammation (MESH:D007249), Intestinal Dysbiosis (MESH:D064806)
- **Chemicals:** Ciprofloxacin (MESH:D002939), TKP-L (-), Polysaccharides (MESH:D011134)
- **Species:** Taraxacum kok-saghyz (species) [taxon 333970], Escherichia coli (E. coli, species) [taxon 562], Mus musculus (house mouse, species) [taxon 10090], Bos taurus (bovine, species) [taxon 9913]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12984485/full.md

## Figures

10 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12984485/full.md

## References

33 references — full list in the complete paper: https://tomesphere.com/paper/PMC12984485/full.md

---
Source: https://tomesphere.com/paper/PMC12984485