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2394. Different Clostridioides difficile Ribotypes Among Patients With Colonization, Initial Clinical Disease, and Recurrent Clinical Disease
BACKGROUND: C. difficile is the most common cause of hospital infections with a spectrum of presentation from asymptomatic carriage to severe recurrent diarrhea. Certain C. difficile ribotypes are associated with severe disease, but there are little data on ribotypes in asymptomatic carriers or seve...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254634/ http://dx.doi.org/10.1093/ofid/ofy210.2047 |
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author | Khoury, Kevin Yen, Eugene Grant, Jennifer Park, Se Hyuk Thaparee, Talent Schora, Donna Smith, Becky Singh, Kamaljit Das, Sanchita |
author_facet | Khoury, Kevin Yen, Eugene Grant, Jennifer Park, Se Hyuk Thaparee, Talent Schora, Donna Smith, Becky Singh, Kamaljit Das, Sanchita |
author_sort | Khoury, Kevin |
collection | PubMed |
description | BACKGROUND: C. difficile is the most common cause of hospital infections with a spectrum of presentation from asymptomatic carriage to severe recurrent diarrhea. Certain C. difficile ribotypes are associated with severe disease, but there are little data on ribotypes in asymptomatic carriers or severe recurrent disease. The aim of this study was to compare virulence potential of C.diff ribotypes with clinical disease severity. METHODS: This retrospective study included patients aged ≥18 years at NorthShore University HealthSystem (NUHS) from February 1, 2015 to May 30, 2017. Three groups of patients with positive PCR test for C. diff toxin gene were selected: (1) Asymptomatic patients positive for rectal carriage; (2) symptomatic outpatients with a single positive test (CDI); and (3) patients with recurrent CDI who underwent FMT. Clinical data were extracted from the Enterprise Database Warehouse. Isolates underwent fluorescent PCR ribotyping and were assigned to clades. Ribotypes with “high” (e.g., 027 and 078) and “low” (e.g., 106) virulence potential were defined as such. Virulence potential of cryptic ribotypes were considered “unknown.” We used Χ(2) and independent samples median tests to compare categorical and continuous variables, respectively. RESULTS: 129 C. diff isolates (asymptomatic, N = 66; CDI, N = 33; FMT, N = 30) were ribotyped with 60 types identified. Median age was higher in asymptomatic patients [80.5 (IQR 70.8–90) years] compared with both CDI and FMT [69 (58–81) and 69 (51–83.5) years, respectively, P = 0.004] Low virulence ribotypes were identified more frequently in asymptomatic carriers than those with CDI or FMT (22/66 vs. 8/33 vs. 1/30, respectively, P = 0.006). High virulence ribotypes were found in all groups, with highest frequency in the FMT group (23/30) vs. asymptomatic (25/67) or CDI (13/33), P = 0.001). CONCLUSION: Patients with severe or recurrent CDI had ribotypes associated with high virulence potential. In addition, asymptomatic carriers were more likely to have ribotypes of C.diff historically associated with a low virulence potential. Molecular C.diff typing may have a role in evaluating asymptomatic C.diff colonization vs. clinical disease. DISCLOSURES: All authors: No reported disclosures. |
format | Online Article Text |
id | pubmed-6254634 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-62546342018-11-28 2394. Different Clostridioides difficile Ribotypes Among Patients With Colonization, Initial Clinical Disease, and Recurrent Clinical Disease Khoury, Kevin Yen, Eugene Grant, Jennifer Park, Se Hyuk Thaparee, Talent Schora, Donna Smith, Becky Singh, Kamaljit Das, Sanchita Open Forum Infect Dis Abstracts BACKGROUND: C. difficile is the most common cause of hospital infections with a spectrum of presentation from asymptomatic carriage to severe recurrent diarrhea. Certain C. difficile ribotypes are associated with severe disease, but there are little data on ribotypes in asymptomatic carriers or severe recurrent disease. The aim of this study was to compare virulence potential of C.diff ribotypes with clinical disease severity. METHODS: This retrospective study included patients aged ≥18 years at NorthShore University HealthSystem (NUHS) from February 1, 2015 to May 30, 2017. Three groups of patients with positive PCR test for C. diff toxin gene were selected: (1) Asymptomatic patients positive for rectal carriage; (2) symptomatic outpatients with a single positive test (CDI); and (3) patients with recurrent CDI who underwent FMT. Clinical data were extracted from the Enterprise Database Warehouse. Isolates underwent fluorescent PCR ribotyping and were assigned to clades. Ribotypes with “high” (e.g., 027 and 078) and “low” (e.g., 106) virulence potential were defined as such. Virulence potential of cryptic ribotypes were considered “unknown.” We used Χ(2) and independent samples median tests to compare categorical and continuous variables, respectively. RESULTS: 129 C. diff isolates (asymptomatic, N = 66; CDI, N = 33; FMT, N = 30) were ribotyped with 60 types identified. Median age was higher in asymptomatic patients [80.5 (IQR 70.8–90) years] compared with both CDI and FMT [69 (58–81) and 69 (51–83.5) years, respectively, P = 0.004] Low virulence ribotypes were identified more frequently in asymptomatic carriers than those with CDI or FMT (22/66 vs. 8/33 vs. 1/30, respectively, P = 0.006). High virulence ribotypes were found in all groups, with highest frequency in the FMT group (23/30) vs. asymptomatic (25/67) or CDI (13/33), P = 0.001). CONCLUSION: Patients with severe or recurrent CDI had ribotypes associated with high virulence potential. In addition, asymptomatic carriers were more likely to have ribotypes of C.diff historically associated with a low virulence potential. Molecular C.diff typing may have a role in evaluating asymptomatic C.diff colonization vs. clinical disease. DISCLOSURES: All authors: No reported disclosures. Oxford University Press 2018-11-26 /pmc/articles/PMC6254634/ http://dx.doi.org/10.1093/ofid/ofy210.2047 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Abstracts Khoury, Kevin Yen, Eugene Grant, Jennifer Park, Se Hyuk Thaparee, Talent Schora, Donna Smith, Becky Singh, Kamaljit Das, Sanchita 2394. Different Clostridioides difficile Ribotypes Among Patients With Colonization, Initial Clinical Disease, and Recurrent Clinical Disease |
title | 2394. Different Clostridioides difficile Ribotypes Among Patients With Colonization, Initial Clinical Disease, and Recurrent Clinical Disease |
title_full | 2394. Different Clostridioides difficile Ribotypes Among Patients With Colonization, Initial Clinical Disease, and Recurrent Clinical Disease |
title_fullStr | 2394. Different Clostridioides difficile Ribotypes Among Patients With Colonization, Initial Clinical Disease, and Recurrent Clinical Disease |
title_full_unstemmed | 2394. Different Clostridioides difficile Ribotypes Among Patients With Colonization, Initial Clinical Disease, and Recurrent Clinical Disease |
title_short | 2394. Different Clostridioides difficile Ribotypes Among Patients With Colonization, Initial Clinical Disease, and Recurrent Clinical Disease |
title_sort | 2394. different clostridioides difficile ribotypes among patients with colonization, initial clinical disease, and recurrent clinical disease |
topic | Abstracts |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254634/ http://dx.doi.org/10.1093/ofid/ofy210.2047 |
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