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Molecular epidemiology of community‐ and hospital‐associated Clostridioides difficile infections in Jönköping, Sweden, October 2017 – March 2018

Clostridioides difficile infections (CDIs) in Sweden are mostly hospital‐associated (HA) with limited knowledge regarding community‐associated (CA) infections. Here, we investigated the molecular epidemiology of clinical isolates of CA‐CDI and HA‐CDI in a Swedish county. Data and isolates (n = 156)...

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Autores principales: Enkirch, Theresa, Mernelius, Sara, Magnusson, Cecilia, Kühlmann‐Berenzon, Sharon, Bengnér, Malin, Åkerlund, Thomas, Rizzardi, Kristina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9826108/
https://www.ncbi.nlm.nih.gov/pubmed/35980252
http://dx.doi.org/10.1111/apm.13270
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author Enkirch, Theresa
Mernelius, Sara
Magnusson, Cecilia
Kühlmann‐Berenzon, Sharon
Bengnér, Malin
Åkerlund, Thomas
Rizzardi, Kristina
author_facet Enkirch, Theresa
Mernelius, Sara
Magnusson, Cecilia
Kühlmann‐Berenzon, Sharon
Bengnér, Malin
Åkerlund, Thomas
Rizzardi, Kristina
author_sort Enkirch, Theresa
collection PubMed
description Clostridioides difficile infections (CDIs) in Sweden are mostly hospital‐associated (HA) with limited knowledge regarding community‐associated (CA) infections. Here, we investigated the molecular epidemiology of clinical isolates of CA‐CDI and HA‐CDI in a Swedish county. Data and isolates (n = 156) of CDI patients (n = 122) from Jönköping county, October 2017–March 2018, were collected and classified as CA (without previous hospital care or onset ≤2 days after admission or >12 weeks after discharge from hospital) or HA (onset >3 days after hospital admission or within 4 weeks after discharge). Molecular characterization of isolates included PCR ribotyping (n = 156 isolates) and whole genome sequencing with single nucleotide polymorphisms (SNP) analysis (n = 53 isolates). We classified 47 patients (39%) as CA‐CDI and 75 (61%) as HA‐CDI. Between CA‐CDI and HA‐CDI patients, we observed no statistically significant differences regarding gender, age, 30‐day mortality or recurrence. Ribotype 005 (RR 3.1; 95% CI: 1.79–5.24) and 020 (RR 2.5; 95% CI: 1.31–4.63) were significantly associated with CA‐CDI. SNP analysis identified seven clusters (0–2 SNP difference) involving 17/53 isolates of both CA‐CDI and HA‐CDI. Molecular epidemiology differed between CA‐CDI and HA‐CDI and WGS analysis suggests transmission of CDI within and between hospitals and communities.
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spelling pubmed-98261082023-01-09 Molecular epidemiology of community‐ and hospital‐associated Clostridioides difficile infections in Jönköping, Sweden, October 2017 – March 2018 Enkirch, Theresa Mernelius, Sara Magnusson, Cecilia Kühlmann‐Berenzon, Sharon Bengnér, Malin Åkerlund, Thomas Rizzardi, Kristina APMIS Original Articles Clostridioides difficile infections (CDIs) in Sweden are mostly hospital‐associated (HA) with limited knowledge regarding community‐associated (CA) infections. Here, we investigated the molecular epidemiology of clinical isolates of CA‐CDI and HA‐CDI in a Swedish county. Data and isolates (n = 156) of CDI patients (n = 122) from Jönköping county, October 2017–March 2018, were collected and classified as CA (without previous hospital care or onset ≤2 days after admission or >12 weeks after discharge from hospital) or HA (onset >3 days after hospital admission or within 4 weeks after discharge). Molecular characterization of isolates included PCR ribotyping (n = 156 isolates) and whole genome sequencing with single nucleotide polymorphisms (SNP) analysis (n = 53 isolates). We classified 47 patients (39%) as CA‐CDI and 75 (61%) as HA‐CDI. Between CA‐CDI and HA‐CDI patients, we observed no statistically significant differences regarding gender, age, 30‐day mortality or recurrence. Ribotype 005 (RR 3.1; 95% CI: 1.79–5.24) and 020 (RR 2.5; 95% CI: 1.31–4.63) were significantly associated with CA‐CDI. SNP analysis identified seven clusters (0–2 SNP difference) involving 17/53 isolates of both CA‐CDI and HA‐CDI. Molecular epidemiology differed between CA‐CDI and HA‐CDI and WGS analysis suggests transmission of CDI within and between hospitals and communities. John Wiley and Sons Inc. 2022-09-06 2022-11 /pmc/articles/PMC9826108/ /pubmed/35980252 http://dx.doi.org/10.1111/apm.13270 Text en © 2022 The Authors. APMIS published by John Wiley & Sons Ltd on behalf of Scandinavian Societies for Pathology, Medical Microbiology and Immunology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Enkirch, Theresa
Mernelius, Sara
Magnusson, Cecilia
Kühlmann‐Berenzon, Sharon
Bengnér, Malin
Åkerlund, Thomas
Rizzardi, Kristina
Molecular epidemiology of community‐ and hospital‐associated Clostridioides difficile infections in Jönköping, Sweden, October 2017 – March 2018
title Molecular epidemiology of community‐ and hospital‐associated Clostridioides difficile infections in Jönköping, Sweden, October 2017 – March 2018
title_full Molecular epidemiology of community‐ and hospital‐associated Clostridioides difficile infections in Jönköping, Sweden, October 2017 – March 2018
title_fullStr Molecular epidemiology of community‐ and hospital‐associated Clostridioides difficile infections in Jönköping, Sweden, October 2017 – March 2018
title_full_unstemmed Molecular epidemiology of community‐ and hospital‐associated Clostridioides difficile infections in Jönköping, Sweden, October 2017 – March 2018
title_short Molecular epidemiology of community‐ and hospital‐associated Clostridioides difficile infections in Jönköping, Sweden, October 2017 – March 2018
title_sort molecular epidemiology of community‐ and hospital‐associated clostridioides difficile infections in jönköping, sweden, october 2017 – march 2018
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9826108/
https://www.ncbi.nlm.nih.gov/pubmed/35980252
http://dx.doi.org/10.1111/apm.13270
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