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Updated: Nov 8, 2025

Cefoperazone-treated Mouse Model of Clinically-relevant Clostridium difficile Strain R20291
Published on: December 10, 2016
Complete genome sequence of the Clostridium difficile LCL126
Jianfeng Wang1,2, Chu Yang2, Chao Zhang2
1School of Life Sciences, Lanzhou University, Lanzhou, Gansu Province, China.
This study sequenced the Clostridium difficile LCL126 genome, identifying key genes related to virulence and metabolic processes. Findings reveal potential toxicological factors, aiding in understanding C. difficile pathogenesis.
Area of Science:
- Genomics
- Microbiology
- Molecular Biology
Background:
- Clostridium difficile (C. difficile) is an anaerobic, gram-positive bacillus linked to intestinal diseases and antibiotic use.
- Understanding the C. difficile genome is crucial for developing targeted treatments.
Purpose of the Study:
- To perform whole-genome sequencing and functional analysis of the C. difficile LCL126 strain.
- To identify genes associated with virulence, pathogenicity, and metabolic functions.
Main Methods:
- Metagenomic technology and genome sequencing were employed.
- Bioinformatic analyses included gene prediction, functional annotation, and pathogenicity assessment.
- Methylation expression patterns were visualized.
Main Results:
- The C. difficile LCL126 genome is 4,301,949 bp with 27.97% GC content, containing 4119 coding genes.
- Analysis revealed 127 carbohydrate-active enzyme genes, 133 reduced and 22 increased virulence genes.
- Dominant methylation types (m4C, m5C, m6C) were identified, with m5C being the most abundant.
Conclusions:
- Whole genome sequencing of C. difficile LCL126 provides comprehensive genetic information.
- Functional predictions highlight the presence of genes with potential toxicological significance.
- This data can inform strategies for combating C. difficile infections.
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