Ribotype variability of Clostridioides difficile strains in patients with hospital-acquired C. difficile infections, community-acquired C. difficile infections, and colonization with toxigenic and non-toxigenic strains of C. difficile

被引:7
作者
Kim, Bongyoung [1 ]
Seo, Mi-Ran [1 ]
Kim, Jieun [1 ]
Pai, Hyunjoo [1 ]
机构
[1] Hanyang Univ, Coll Med, Dept Internal Med, 222 Wangsimni Ro, Seoul 04763, South Korea
基金
新加坡国家研究基金会;
关键词
Clostridioides difficile; Colonization; Infection; Ribotype; CLINICAL-PRACTICE GUIDELINES; HEALTH-CARE EPIDEMIOLOGY; DISEASES SOCIETY; ADULTS; SURVEILLANCE; UPDATE;
D O I
10.1016/j.anaerobe.2019.102086
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
There have been few available data that presented a direct comparison between polymerase chain reaction ribotype (RT) distribution of Clostridioides difficile strains from C. difficile infection (CDI) and colonization. To understand the epidemiology of CDI in a hospital setting, we compared RTs of C. difficile strains from hospital-acquired CDI (HA-CDI) and toxigenic colonization and from community-acquired CDI (CA-CDI) and non-toxigenic colonization using the stool samples submitted for C. difficile cultures at an institution during 2009, 2012, and 2014. Overall, 721 C. difficile strains were identified from 607 patients. Among them, 450 (62.4%) were HA-CDI, 20 (2.8%) were CA-CDI, 126 (17.5%) were toxigenic colonization, and 125 (17.3%) were non-toxigenic colonization. RT018, RT017, RT002, RT015, and RT001 isolates were the most prevalent RTs in HA-CDI, and they comprised 74.9% of the total HA-CDI isolates but accounted for 60.4% of isolates from toxigenic colonization. In total, 32 strain compromising 18 RTs from HA-CDI (7.1%) were not seen among the toxigenic colonization group, and 3 RTs with 5 strains from toxigenic colonization were not seen among the HA-CDI group. The distribution of RTs was the most diverse in CA-CDI and the least diverse in HA-CDI. Although 5 RT strains, which were prevalent in HA-CDI, comprised 40% of CA-CDI, 5 isolates (25%) revealed unknown RTs, which were uncommon in HA-CDI or toxigenic colonization. In 12 patients with both episodes of CDI and toxigenic colonization, 8 had 2 isolates with different RTs and 4 had isolates with identical RTs. In conclusion, although RT017 and RT018 were the most common in HA-CDI and toxigenic colonization, C. difficile strains from toxigenic colonization were more diverse than those from HA-CDI. (C) 2019 Elsevier Ltd. All rights reserved.
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页数:6
相关论文
共 21 条
[1]  
Barbut F, 2000, J CLIN MICROBIOL, V38, P2386
[2]   Development of a new PCR-ribotyping method for Clostridium difficile based on ribosomal RNA gene sequencing [J].
Bidet, P ;
Barbut, F ;
Lalande, V ;
Burghoffer, B ;
Petit, JC .
FEMS MICROBIOLOGY LETTERS, 1999, 175 (02) :261-266
[3]   ACQUISITION OF CLOSTRIDIUM-DIFFICILE BY HOSPITALIZED-PATIENTS - EVIDENCE FOR COLONIZED NEW ADMISSIONS AS A SOURCE OF INFECTION [J].
CLABOTS, CR ;
JOHNSON, S ;
OLSON, MM ;
PETERSON, LR ;
GERDING, DN .
JOURNAL OF INFECTIOUS DISEASES, 1992, 166 (03) :561-567
[4]   Clinical Practice Guidelines for Clostridium difficile Infection in Adults: 2010 Update by the Society for Healthcare Epidemiology of America (SHEA) and the Infectious Diseases Society of America (IDSA) [J].
Cohen, Stuart H. ;
Gerding, Dale N. ;
Johnson, Stuart ;
Kelly, Ciaran P. ;
Loo, Vivian G. ;
McDonald, L. Clifford ;
Pepin, Jacques ;
Wilcox, Mark H. .
INFECTION CONTROL AND HOSPITAL EPIDEMIOLOGY, 2010, 31 (05) :431-455
[5]   Understanding Clostridium difficile Colonization [J].
Crobach, Monique J. T. ;
Vernon, Jonathan J. ;
Loo, Vivian G. ;
Kong, Ling Yuan ;
Pechine, Severine ;
Wilcox, Mark H. ;
Kuijper, Ed J. .
CLINICAL MICROBIOLOGY REVIEWS, 2018, 31 (02)
[6]   Use of Multilocus Variable Number of Tandem Repeats Analysis Genotyping to Determine the Role of Asymptomatic Carriers in Clostridium difficile Transmission [J].
Curry, Scott R. ;
Muto, Carlene A. ;
Schlackman, Jessica L. ;
Pasculle, A. William ;
Shutt, Kathleen A. ;
Marsh, Jane W. ;
Harrison, Lee H. .
CLINICAL INFECTIOUS DISEASES, 2013, 57 (08) :1094-1102
[7]   Diverse Sources of C. difficile Infection Identified on Whole-Genome Sequencing [J].
Eyre, David W. ;
Cule, Madeleine L. ;
Wilson, Daniel J. ;
Griffiths, David ;
Vaughan, Alison ;
O'Connor, Lily ;
Ip, Camilla L. C. ;
Golubchik, Tanya ;
Batty, Elizabeth M. ;
Finney, John M. ;
Wyllie, David H. ;
Didelot, Xavier ;
Piazza, Paolo ;
Bowden, Rory ;
Dingle, Kate E. ;
Harding, Rosalind M. ;
Crook, Derrick W. ;
Wilcox, Mark H. ;
Peto, Tim E. A. ;
Walker, A. Sarah .
NEW ENGLAND JOURNAL OF MEDICINE, 2013, 369 (13) :1195-1205
[8]   The Changing Epidemiology of Clostridium difficile Infections [J].
Freeman, J. ;
Bauer, M. P. ;
Baines, S. D. ;
Corver, J. ;
Fawley, W. N. ;
Goorhuis, B. ;
Kuijper, E. J. ;
Wilcox, M. H. .
CLINICAL MICROBIOLOGY REVIEWS, 2010, 23 (03) :529-+
[9]   Health Care-Associated Clostridium difficile Infection in Adults Admitted to Acute Care Hospitals in Canada: A Canadian Nosocomial Infection Surveillance Program Study [J].
Gravel, Denise ;
Miller, Mark ;
Simor, Andrew ;
Taylor, Geoffrey ;
Gardam, Michael ;
McGeer, Allison ;
Hutchinson, James ;
Moore, Dorothy ;
Kelly, Sharon ;
Boyd, David ;
Mulvey, Michael .
CLINICAL INFECTIOUS DISEASES, 2009, 48 (05) :568-576
[10]   The host immune response to Clostridium difficile [J].
Kelly, Ciaran P. ;
Kyne, Lorraine .
JOURNAL OF MEDICAL MICROBIOLOGY, 2011, 60 (08) :1070-1079