# Clostridioides difficile infection cases and the causative strains in a large Chinese tertiary hospital in 2023–2024

**Authors:** Xin Lu, Yiqi Liang, Yu Feng, Tingting Wang, Zhiyong Zong, Xiaohui Wang

PMC · DOI: 10.3389/fmicb.2026.1749145 · Frontiers in Microbiology · 2026-02-11

## TL;DR

This study examines Clostridioides difficile infections in a Chinese hospital, identifying prevalent strains and resistance patterns post-pandemic.

## Contribution

The study reports the emergence of ST81 as a dominant fluoroquinolone-resistant strain in Southwest China.

## Key findings

- ST3 remains the most prevalent clone, while ST81 has become the second-most prevalent with high fluoroquinolone resistance.
- Moxifloxacin resistance in isolates is primarily due to mutations in gyrA and gyrB genes.
- The cfr(B) resistance gene was first detected in a ST54 isolate in China.

## Abstract

Clostridioides difficile is a global urgent-threat pathogen, with prevalence and clinical impact varying over time and across regions. This study aims to elucidate the landscape of C. difficile infection (CDI) and its causative strains in Southwest China after the COVID-19 pandemic.

This retrospective study enrolled CDI patients hospitalized between June 2023 and May 2024 at a large tertiary hospital in Southwest China, who were diagnosed via glutamate dehydrogenase (GDH) combined with toxin A/B testing. Toxigenic isolates from positive stool samples were submitted for antimicrobial susceptibility testing and whole-genome sequencing (WGS). Multilocus sequence typing (ST), identification of resistance determinants, and core-genome SNP (cgSNP) analysis were integrated with clinical data.

One hundred fifty-seven CDI patients were identified among 2,917 suspected patients with diarrhea. 67.5% of patients were male, 51.0% were ≥65 years, 20.4% had severe CDI, and two patients were fulminant. All 109 isolates remained susceptible to vancomycin and fidaxomicin. The moxifloxacin resistance rate reached as high as 56.0%, primarily driven by gyrA Thr82Ile and gyrB Asp426Val/Ser366Ala mutations. ST3 (23.9%) remains the most prevalent clone. ST81 (18.3%), all resistant to moxifloxacin and 20% resistant to metronidazole, has replaced ST37 (7.3%) as the second-most prevalent clone. ST5 (4.6%) was the main prevalent clone producing the binary toxin, and no ST1/RT027 was identified. The cfr(B) resistance gene was first detected in a ST54 isolate from China. CgSNP analysis identified 4 genetically highly related ST3 clone groups (≤2 SNPs within 124 days).

In the post-pandemic era, the clinical burden of CDI in Southwest China cannot be overlooked. ST81 with high-level fluoroquinolone resistance has increased significantly and deserves more attention. Integration of data on clinical cases and their pathogenic strains through sustained clinical case monitoring, genomic surveillance of isolates, and antimicrobial resistance (AMR) pattern surveys provides early warning for future clonal dissemination and supports clinical management and public health decisions.

## Linked entities

- **Genes:** GYRA (DNA GYRASE A) [NCBI Gene 820238], gyrB (DNA gyrase subunit B) [NCBI Gene 857440]
- **Chemicals:** vancomycin (PubChem CID 14969), fidaxomicin (PubChem CID 10034073), moxifloxacin (PubChem CID 152946), metronidazole (PubChem CID 4173)
- **Diseases:** diarrhea (MONDO:0001673)
- **Species:** Clostridioides difficile (taxon 1496)

## Full-text entities

- **Genes:** GyrB [NCBI Gene 4915789], GyrA [NCBI Gene 4915790], GLUD1 (glutamate dehydrogenase 1) [NCBI Gene 2746] {aka GDH, GDH1, GLUD, hGDH1}, ST11 (suppression of tumorigenicity 11 (pancreas)) [NCBI Gene 8466] {aka PETS1}, CADM1 (cell adhesion molecule 1) [NCBI Gene 23705] {aka BL2, IGSF4, IGSF4A, NECL2, Necl-2, RA175}, TcdB [NCBI Gene 4914074]
- **Diseases:** Infectious Diseases (MESH:D003141), hematological malignancies (MESH:D019337), hypotension (MESH:D007022), diarrhea (MESH:D003967), ileus (MESH:D045823), toxicity (MESH:D064420), fulminant (MESH:D017114), diabetes (MESH:D003920), COVID (MESH:D000086382), AMR (MESH:D060467), tumors (MESH:D009369), megacolon (MESH:D008531), infected (MESH:D007239), shock (MESH:D012769), C. difficile (MESH:D003015)
- **Chemicals:** creatinine (MESH:D003404), chloramphenicol (MESH:D002701), moxifloxacin (MESH:D000077266), beta-lactam (MESH:D047090), levofloxacin (MESH:D064704), tetracyclines (MESH:D013754), vancomycin (MESH:D014640), carbapenems (MESH:D015780), D-cycloserine (MESH:D003523), Lincosamides (MESH:D055231), linezolid (MESH:D000069349), metronidazole (MESH:D008795), fluoroquinolone (MESH:D024841), agar (MESH:D000362), pleuromutilins (MESH:C004262), ciprofloxacin (MESH:D002939), macrolides (MESH:D018942), fidaxomicin (MESH:D000077732), trimethoprim (MESH:D014295), Tetracycline (MESH:D013752), Streptogramins (MESH:D025361), Phosphomycin (MESH:D005578), streptogramin A (MESH:D025364), Aminoglycoside (MESH:D000617), Oxazolidinones (MESH:D023303), Macrolide-lincosamide-streptogramin B (-), cefoxitin (MESH:D002440)
- **Species:** Streptomyces sp. t54 (species) [taxon 1828162], Ovis aries (domestic sheep, species) [taxon 9940], Clostridioides difficile (species) [taxon 1496], Homo sapiens (human, species) [taxon 9606], Bacteroides fragilis (species) [taxon 817], Clostridioides difficile 630 (strain) [taxon 272563]
- **Mutations:** Asp426Val, Ser366Ala, Ser366Ala, Asp426Val, Thr82Ile, Thr82Ile
- **Cell lines:** ST37 — Homo sapiens (Human), Lung non-small cell carcinoma, Cancer cell line (CVCL_7025)

## Full text

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## Figures

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## References

51 references — full list in the complete paper: https://tomesphere.com/paper/PMC12932564/full.md

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Source: https://tomesphere.com/paper/PMC12932564