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. 2013 Nov 12;8(11):e78445.
doi: 10.1371/journal.pone.0078445. eCollection 2013.

Asymptomatic Clostridium difficile colonisation and onward transmission

Affiliations

Asymptomatic Clostridium difficile colonisation and onward transmission

David W Eyre et al. PLoS One. .

Abstract

Introduction: Combined genotyping/whole genome sequencing and epidemiological data suggest that in endemic settings only a minority of Clostridium difficile infection, CDI, is acquired from other cases. Asymptomatic patients are a potential source for many unexplained cases.

Methods: We prospectively screened a cohort of medical inpatients in a UK teaching hospital for asymptomatic C. difficile carriage using stool culture. Electronic and questionnaire data were used to determine risk factors for asymptomatic carriage by logistic regression. Carriage isolates were compared with all hospital/community CDI cases from the same geographic region, from 12 months before the study to 3 months after, using whole genome sequencing and hospital admission data, assessing particularly for evidence of onward transmission from asymptomatic cases.

Results: Of 227 participants recruited, 132 provided ≥1 stool samples for testing. 18 participants were culture-positive for C. difficile, 14/132(11%) on their first sample. Independent risk factors for asymptomatic carriage were patient reported loose/frequent stool (but not meeting CDI criteria of ≥3 unformed stools in 24 hours), previous overnight hospital stay within 6 months, and steroid/immunosuppressant medication in the last 6 months (all p≤0.02). Surprisingly antibiotic exposure in the last 6 months was independently associated with decreased risk of carriage (p = 0.005). The same risk factors were identified excluding participants reporting frequent/loose stool. 13/18(72%) asymptomatically colonised patients carried toxigenic strains from common disease-causing lineages found in cases. Several plausible transmission events to asymptomatic carriers were identified, but in this relatively small study no clear evidence of onward transmission from an asymptomatic case was seen.

Conclusions: Transmission events from any one asymptomatic carrier are likely to be relatively rare, but as asymptomatic carriage is common, it may still be an important source of CDI, which could be quantified in larger studies. Risk factors established for asymptomatic carriage may help identify patients for inclusion in such studies.

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Conflict of interest statement

Competing Interests: The authors have read the journal’s policy and have the following conflicts: The institution of DWC and TEAP received per-case funding from Optimer Pharmaceuticals to support fidaxomicin trial patient expenses. DWC and TEAP also received honoraria from Optimer Pharmaceuticals for participation in additional meetings related to investigative planning for fidaxomicin. No other author has a conflict of interest. This does not alter the authors’ adherence to all the PLOS ONE policies on sharing data and materials.

Figures

Figure 1
Figure 1. Asymptomatic study participants and samples.
Figure 2
Figure 2. Temporal pattern of samples in participants with ≥1 positive sample.
Asymptomatic positive and negative relate to samples obtained during the carriage study. Matching of study participants with the hospital admission and microbiology data allowed 4 participants with a subsequent symptomatic CDI positive samples to be identified, denoted symptomatic positive. 118 participants had consistently negative samples and are not plotted.
Figure 3
Figure 3. Epidemiological relationships between 4 asymptomatic study participants and genetically related cases.
Study participants are shown in blue, with the exception of participant 3, shown in red in the first panel. Symptomatic cases are shown as different colours, and are distinct across different panels. Positive asymptomatic samples from study participants are shown as filled circles. Positive symptomatic samples are shown as crosses. EIA-negative culture-positive samples are shown as diamonds. Ward stays are shown as horizontal lines with capped ends. Wards sharing the same specialty and hospital share the same initial letter; adjacent wards forming a single unit have the same letter and number and are followed by a lower case letter.

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