Abstract

SummaryBackgroundCertain Clostridium difficile ribotypes have been associated with complex disease phenotypes including recurrence and increased severity, especially the well-described hypervirulent RT027. This study aimed to determine the pattern of ribotypes causing infection and the association, if any, with severity.MethodsAll faecal samples submitted to a large diagnostic laboratory for C. difficile testing between 2011 and 2013 were subject to routine testing and culture. All C. difficile isolates were ribotyped, and associated clinical and demographic patient data were retrieved and linked to ribotyping data.ResultsIn total, 86 distinct ribotypes were identified from 705 isolates of C. difficile. RT002 and RT015 were the most prevalent (22.5%, N=159). Only five isolates (0.7%) were hypervirulent RT027. Ninety of 450 (20%) patients with clinical information available died within 30 days of C. difficile isolation. RT220, one of the 10 most common ribotypes, was associated with elevated median C-reactive protein and significantly increased 30-day all-cause mortality compared with RT002 and RT015, and with all other ribotypes found in the study.ConclusionsA wide range of C. difficile ribotypes were responsible for C. difficile infection presentations. Although C. difficile-associated mortality has reduced in recent years, expansion of lineages associated with increased severity could herald increases in future mortality. Enhanced surveillance for emerging lineages such as RT220 that are associated with more severe disease is required, with genomic approaches to dissect pathogenicity.

Highlights

  • Clostridium difficile infections (CDI) remain a significant cause of mortality and morbidity [1]

  • 758 glutamate dehydrogenase (GDH) and polymerase chain reaction (PCR) toxin-B-positive C. difficile episodes were identified in the study period, from which 705 C. difficile isolates were ribotyped (Figure S1, see online supplementary material)

  • RT027 was isolated in only five patients (0.7%)

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Summary

Introduction

Clostridium difficile infections (CDI) remain a significant cause of mortality and morbidity [1]. CDI rates in the UK have decreased since 2007, likely due to a number of infection control and antibiotic stewardship interventions, and in part, to a decline in the epidemic ribotype RT027, which had been associated with poor clinical outcomes [1e4]. Ribotypes such as RT018, RT027, RT056, RT078, RT176 and RT244 have all been reported to be associated with complicated disease outcomes, recurrences and increased severity [4e11]. It is not yet known whether ribotype can predict the severity of infection per se [12,13]

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