Two-year analysis of Clostridium difficile ribotypes associated with increased severity
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Published version
Author(s)
Type
Journal Article
Abstract
Background
Certain Clostridium difficile ribotypes have been associated with complex disease phenotypes including recurrence and increased severity, especially the well-described hypervirulent ribotype RT027. In this study we set out to determine the pattern of ribotypes causing infection and association if any with severity.
Methods
All faecal samples submitted to a large diagnostic laboratory for C. difficile testing between 2011 and 2013 were subject to routine testing and cultured. All C. difficile isolates were ribotyped and associated clinical and demographic patient data were retrieved then linked to ribotyping data.
Results
A total of 86 distinct ribotypes were identified from 705 isolates of C. difficile. Ribotypes RT002 and RT015 were the most prevalent (22.5%, n=159). Only five isolates (0.7%) were the hypervirulent RT027. Ninety of 450 (20%) patients with clinical information available died within 30-days of C. difficile isolation. Ribotype RT220, one of the ten commonest ribotypes, was associated with elevated median C-reactive protein and significantly increased 30-day all-cause mortality when compared with ribotypes RT002 and RT015, and with all other ribotypes found in the study.
Conclusions
A 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.
Certain Clostridium difficile ribotypes have been associated with complex disease phenotypes including recurrence and increased severity, especially the well-described hypervirulent ribotype RT027. In this study we set out to determine the pattern of ribotypes causing infection and association if any with severity.
Methods
All faecal samples submitted to a large diagnostic laboratory for C. difficile testing between 2011 and 2013 were subject to routine testing and cultured. All C. difficile isolates were ribotyped and associated clinical and demographic patient data were retrieved then linked to ribotyping data.
Results
A total of 86 distinct ribotypes were identified from 705 isolates of C. difficile. Ribotypes RT002 and RT015 were the most prevalent (22.5%, n=159). Only five isolates (0.7%) were the hypervirulent RT027. Ninety of 450 (20%) patients with clinical information available died within 30-days of C. difficile isolation. Ribotype RT220, one of the ten commonest ribotypes, was associated with elevated median C-reactive protein and significantly increased 30-day all-cause mortality when compared with ribotypes RT002 and RT015, and with all other ribotypes found in the study.
Conclusions
A 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.
Date Issued
2019-12
Date Acceptance
2019-06-10
Citation
Journal of Hospital Infection, 2019, 103 (4), pp.388-394
ISSN
0195-6701
Publisher
Elsevier
Start Page
388
End Page
394
Journal / Book Title
Journal of Hospital Infection
Volume
103
Issue
4
Copyright Statement
© 2019 The Authors. Published by Elsevier Ltd on behalf of The Healthcare Infection Society. This is an open access articleunder the CC BY license (http://creativecommons.org/licenses/by/4.0/
Sponsor
Medical Research Council (MRC)
Medical Research Council (MRC)
National Institute for Health Research
National Institute for Health Research
Wellcome Trust
Imperial College Healthcare NHS Trust- BRC Funding
Imperial College Healthcare NHS Trust- BRC Funding
Imperial College Healthcare NHS Trust- BRC Funding
Medical Research Council (MRC)
Grant Number
G0800777
G0800777
HPRU-2012-10047
HPRU-2012-10047
087732/Z/08/Z
RDA02 79560
RDA02
RDF04
MR/R015600/1
Subjects
Science & Technology
Life Sciences & Biomedicine
Public, Environmental & Occupational Health
Infectious Diseases
Clostridium difficile
Ribotype
Severe infection
C-reactive protein
tcdA
tcdB
RISK-FACTORS
INFECTION
STRAIN
EMERGENCE
MORTALITY
EPIDEMIOLOGY
SURVEILLANCE
PREDICTORS
C-reactive protein
Clostridium difficile
Ribotype
Severe infection
tcdA
tcdB
1103 Clinical Sciences
1117 Public Health and Health Services
Epidemiology
Publication Status
Published
Date Publish Online
2019-06-18