# Shengjiang Xiexin decoction combined with vancomycin for Clostridioides difficile infection: impact of vancomycin dose-reduction strategy on gut microbiota homeostasis and recurrence risk

**Authors:** Lin Zhu, Li-sheng Chen, Fu-zhi Ma, Jin-e Peng, Yu-bu Wang, Yu-qing Ma, Yue Xu, Yi Wang, Ayiman Yeerjiang, Cong-en Zhang, Zhi-jie Ma

PMC · DOI: 10.3389/fcimb.2025.1740179 · Frontiers in Cellular and Infection Microbiology · 2026-02-11

## TL;DR

This study shows that combining a Chinese herbal formula with vancomycin for treating Clostridioides difficile infection requires standard antibiotic dosing to prevent relapse and restore gut health.

## Contribution

The study reveals that reducing vancomycin dosage in combination therapy with Shengjiang Xiexin decoction compromises therapeutic synergy and increases recurrence risk.

## Key findings

- Dose deescalation strategies led to worse relapse rates and sustained gut dysbiosis in a murine model.
- Only standard vancomycin dosing with Shengjiang Xiexin decoction restored gut microbiota diversity and stability.
- Reduced vancomycin doses blunted the synergistic effect and increased inflammation.

## Abstract

Even though relapse rates for Clostridioides difficile infection (CDI) are high, vancomycin—a medication that targets C. difficile and works well during acute episodes—has gut microbiota-disrupting effects. The Chinese herbal formula Shengjiang Xiexin decoction (SXD) is helpful for microbial reversion, justifying the use of combination therapy. One often invoked tactic in such bundles of care is to minimize patients’ antibiotic exposure. In this work, we challenged this paradigm in a murine CDI model. Divergently with regard to the dose deescalation (low-dose vs. short-course), we found that it significantly undermined the synergy between the drugs. Despite the resolution of acute symptoms by all combination regimens containing SXD, deescalation strategies (CDR2 and CDR3) resulted in significantly worse relapse, enhanced inflammation and sustained gut dysbiosis. Conversely, only the CDR1 regimen with SXD co-treatment resulted in a full recovery of gut microbiota alpha-diversity and long-term ecological stability, associated with a better shift of metabolic pathways. Accordingly, our key finding is that standard vancomycin dosing is necessary for this therapeutic synergy to be realized and that dose deescalation blunts it and raises the risk of relapse. Such evidence invites a more sophisticated antibiotic stewardship approach with concomitant treatments, favoring preservation of synergistic effect over simplistic dose reduction.

## Linked entities

- **Chemicals:** vancomycin (PubChem CID 14969)

## Full-text entities

- **Genes:** Gapdh (glyceraldehyde-3-phosphate dehydrogenase) [NCBI Gene 14433] {aka Gapd}
- **Diseases:** PMC (MESH:D004761), inflammation (MESH:D007249), mucosal disruption (MESH:D019958), gut dysbiosis (MESH:D064806), neurotoxicity (MESH:D020258), mucosal irritation (MESH:D001523), diarrhea (MESH:D003967), vomiting (MESH:D014839), malnutrition (MESH:D044342), dysentery (MESH:D004403), C. difficile Infection (MESH:D003015), cytotoxic (MESH:D064420), gastrointestinal ailments (MESH:D005767), infection (MESH:D007239), mucosal damage (MESH:D052016), bacterial (MESH:D001424), infectious diarrhea (MESH:D003141), intestinal diseases (MESH:D007410), mucosal destruction (MESH:D008105)
- **Chemicals:** paraffin (MESH:D010232), Pentobarbital sodium (MESH:D010424), Metronidazole (MESH:D008795), nitrogen (MESH:D009584), Van (MESH:D014640), Clindamycin (MESH:D002981), water (MESH:D014867), Gentamicin (MESH:D005839), Hematoxylin (MESH:D006416), bile acid (MESH:D001647), H&amp;E (MESH:D006371), DCA (-), lipid (MESH:D008055), paraformaldehyde (MESH:C003043), SYBR Green (MESH:C098022), berberine (MESH:D001599), CA (MESH:D002118), baicalin (MESH:C038044), short-chain fatty acids (MESH:D005232), Eosin (MESH:D004801)
- **Species:** Petrachloros mirabilis (species) [taxon 2918835], Ligilactobacillus murinus (species) [taxon 1622], Escherichia coli (E. coli, species) [taxon 562], Coptis chinensis (species) [taxon 261450], Scutellaria baicalensis (Baikal skullcap, species) [taxon 65409], Helicobacter (genus) [taxon 209], Mus musculus (house mouse, species) [taxon 10090], Pinellia ternata (species) [taxon 199225], Bacteroides stercorirosoris (species) [taxon 871324], Bacteroides thetaiotaomicron (species) [taxon 818], Panax ginseng (Asiatic ginseng, species) [taxon 4054], Parabacteroides goldsteinii (species) [taxon 328812], Akkermansia muciniphila (species) [taxon 239935], Ziziphus jujuba (Chinese jujube, species) [taxon 326968], Homo sapiens (human, species) [taxon 9606], Clostridioides difficile (species) [taxon 1496], Lactobacillus johnsonii (species) [taxon 33959], Lactobacillales (order) [taxon 186826], Bacillota (clostridial firmicutes, phylum) [taxon 1239], Blautia (genus) [taxon 572511], Limosilactobacillus reuteri (species) [taxon 1598], gut metagenome (species) [taxon 749906]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12932506/full.md

## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12932506/full.md

## References

52 references — full list in the complete paper: https://tomesphere.com/paper/PMC12932506/full.md

---
Source: https://tomesphere.com/paper/PMC12932506