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. 2018 Jul 2;67(2):229-234.
doi: 10.1093/cid/ciy060.

Clostridium difficile Whole Genome Sequencing Reveals Limited Transmission Among Symptomatic Children: A Single-Center Analysis

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Clostridium difficile Whole Genome Sequencing Reveals Limited Transmission Among Symptomatic Children: A Single-Center Analysis

Larry K Kociolek et al. Clin Infect Dis. .

Abstract

Background: Although pediatric Clostridium difficile infections (CDIs) are increasing, C. difficile transmission patterns among children are poorly understood.

Methods: We performed whole genome sequencing (WGS) on C. difficile isolates collected from children diagnosed with CDI between December 2012 and December 2013 at a single academic medical center. Genome sequences of isolates from CDIs diagnosed ≥8 weeks after study initiation were compared to all study isolate genome sequences. Among patients with isogenic isolates (≤2-3 core genome single nucleotide variants [SNVs] identified by pairwise SNV analyses), common inpatient and/or outpatient healthcare exposures were investigated.

Results: Among 131 CDIs in 107 children, WGS identified 104 genetically distinct isolates. Of 84 incident CDIs occurring ≥8 weeks after study initiation, only 10 (11.9%) were caused by a strain isogenic to another cohort CDI isolate (putative transmission events). Proportions of each CDI class putatively associated with transmission were hospital-onset healthcare facility-associated (HCFA), 2/16 (12.5%); community-onset HCFA, 1/17 (5.9%); indeterminate, 1/11 (9.1%); community-associated (CA), 5/40 (12.5%); and recurrent, 1/21 (4.8%). Transmission events among CA and HCFA CDIs were similarly infrequent (5/40 [12.5%] vs 3/33 [9.1%]; P = .64). Shared healthcare facility exposures were only identified among 7/10 putative transmission events. Potential community transmission (same postal code) was not identified.

Conclusions: WGS identified a highly diverse group of C. difficile isolates among children with CDI, including those with HCFA CDI. Clostridium difficile transmission among symptomatic children was very uncommon. Among putatively transmitted cases, investigation of shared healthcare exposures often did not identify a potential transmission source.

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Figures

Figure 1.
Figure 1.
Chronology of Clostridium difficile infections and associated healthcare exposures among patients involved in the 7 putative transmission events where an epidemiologic link was identified. Event numbers are referred to in Table 1. Abbreviations: CDI, Clostridium difficile infection; IP, inpatient; OP, outpatient.

References

    1. Magill SS, Edwards JR, Bamberg W, et al. ; Emerging Infections Program Healthcare-Associated Infections and Antimicrobial Use Prevalence Survey Team Multistate point-prevalence survey of health care-associated infections. N Engl J Med 2014; 370:1198–208. - PMC - PubMed
    1. Centers for Disease Control and Prevention. Antibiotic Resistance Threats in the United States, 2013 Available at: http://www.cdc.gov/drugresistance/pdf/ar-threats-2013–508.pdf. Accessed 11 December 2017.
    1. Eyre DW, Cule ML, Wilson DJ, et al. . Diverse sources of C. difficile infection identified on whole-genome sequencing. N Engl J Med 2013; 369:1195–205. - PMC - PubMed
    1. Tamma PD, Sandora TJ. Clostridium difficile infection in children: current state and unanswered questions. J Pediatric Infect Dis Soc 2012; 1:230–43. - PMC - PubMed
    1. Wendt JM, Cohen JA, Mu Y, et al. . Clostridium difficile infection among children across diverse US geographic locations. Pediatrics 2014; 133:651–8. - PMC - PubMed

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