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Updated: Jun 21, 2026

Cefoperazone-treated Mouse Model of Clinically-relevant Clostridium difficile Strain R20291
Published on: December 10, 2016
Simulating interventions to prevent gastro-intestinal transmission of Clostridioides difficile and
Alessandro Gerada1, Yinzheng Zhong2, Charlotte Brookefield1
1Antimicrobial Pharmacodynamics and Therapeutics, Department of Pharmacology and Therapeutics, Institute of Systems, Molecular & Integrative Biology, University of Liverpool, Liverpool, United Kingdom; Department of Infection and Immunity, Liverpool Clinical Laboratories, Clinical Support Services Building (CSSB), Liverpool University Hospitals NHS Foundation Trust, Liverpool, United Kingdom.
Background:
Hospital-acquired infections caused by pathogens such as Clostridioides difficile and antimicrobial-resistant bacteria are a major burden to healthcare systems. Infection prevention and control (IPC) measures are used to limit transmission, but quantifying the impact of individual interventions remains challenging.
Methods:
Here, we describe an agent-based model (ABM) that simulates faecal-oral transmission of pathogens under antimicrobial selection pressure in hospital settings. The model was calibrated to a C. difficile outbreak using approximate Bayesian computation.
Findings:
The calibrated model reproduced the observed outbreak dynamics with rates of nosocomial infection that were similar to those of the true outbreak. In simulated scenarios, the pre-outbreak baseline rate was a median of 1.22 cases per 1000 patient-days (interquartile range [IQR] range: 1.02-1.44), compared with the real rate of 1.25 cases per 1000 (IQR: 0.94-1.56). During the outbreak period, simulations had a median rate of 2.42 (IQR: 1.51-3.92) cases, compared with the real median rate of 3.74 (IQR: 3.32-4.41). Sensitivity analyses revealed that toilet cleaning frequency had the greatest impact on reducing nosocomial infections; antimicrobial stewardship and patient cohorting into single-occupancy rooms also reduced cases.
Conclusion:
This ABM provides a flexible framework for evaluating IPC interventions and supporting outbreak preparedness. The approach is readily adaptable to other faecal-orally transmitted pathogens, including vancomycin-resistant Enterococcus and carbapenemase-producing Enterobacterales.
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