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Evaluation of the genomic epidemiology and transmission of Clostridioides difficile infection across a community

Background: Clostridioides difficile infection (CDI) is a major cause of morbidity and healthcare costs in the United States. The epidemiology of CDI has recently shifted, with healthcare-associated (HCA) CDI trending downward and community-associated (CA)-CDI becoming more prominent. The cause of t...

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Autores principales: Tesini, Brenda, Taffner, Samantha, Hatwar, Trupti, Gill, Steven, Dumyati, Ghinwa, Pecora, Nicole
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9615007/
http://dx.doi.org/10.1017/ash.2022.110
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author Tesini, Brenda
Taffner, Samantha
Hatwar, Trupti
Gill, Steven
Dumyati, Ghinwa
Pecora, Nicole
author_facet Tesini, Brenda
Taffner, Samantha
Hatwar, Trupti
Gill, Steven
Dumyati, Ghinwa
Pecora, Nicole
author_sort Tesini, Brenda
collection PubMed
description Background: Clostridioides difficile infection (CDI) is a major cause of morbidity and healthcare costs in the United States. The epidemiology of CDI has recently shifted, with healthcare-associated (HCA) CDI trending downward and community-associated (CA)-CDI becoming more prominent. The cause of this shift is not well understood but may be related to changing genomic epidemiology. We assessed C. difficile strains across a CDC Emerging Infections Program (EIP) site in Western New York, including strains from both HCA-CDI and CA-CDI cases to characterize predominating strains and putative transmission across epidemiological classifications and between index and recurrent cases. Methods: In total, 535 isolates of C. difficile were collected over a 6-month period in 2018 from the Monroe Country, New York, EIP site and were analyzed using whole-genome sequencing (WGS). Standard epidemiological definitions were used to classify cases as hospital onset (HO-CDI); community associated (CA-CDI); community onset, healthcare associated (CO-HCFA-CDI); or long-term care onset (LTCO-CDI). Recurrent cases were defined as those diagnosed within 8 weeks of an initial positive test. Multilocus sequence types (MLSTs) were assigned according to PUBMLST and single-nucleotide polymorphisms (SNPs) were determined using a modified CFSAN analytical pipeline. Cases resulting from putative transmission were defined as those separated by 0–1 core SNPs. Results: Of 535 isolates, 454 were from index and 81 were from recurrent cases. The index cases were comprised of CA-CDI (47.4%), CO-HCFA-CDI (24%), LTCO-CDI (8.1%), and HO-CDI (19.3%). Cases with recurrent disease mirrored the epidemiological distribution of the larger set. Common MLSTs included ST2 (12.3%), ST8 (10.5%), ST42 (7.9%), ST58 (4.9%), ST43 (4.5%), and ST11 (4.3%). The previously widespread epidemic strain, NAP1/ST1/RT027 accounted for Conclusions: The genomic epidemiology of C. difficile across this large community cohort demonstrated a diverse group of strain types that was similarly distributed across epidemiological classifications and between index and recurrent cases. SNP analysis indicated that direct transmission between cases was uncommon. Funding: None Disclosures: None
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spelling pubmed-96150072022-10-29 Evaluation of the genomic epidemiology and transmission of Clostridioides difficile infection across a community Tesini, Brenda Taffner, Samantha Hatwar, Trupti Gill, Steven Dumyati, Ghinwa Pecora, Nicole Antimicrob Steward Healthc Epidemiol C. difficile Background: Clostridioides difficile infection (CDI) is a major cause of morbidity and healthcare costs in the United States. The epidemiology of CDI has recently shifted, with healthcare-associated (HCA) CDI trending downward and community-associated (CA)-CDI becoming more prominent. The cause of this shift is not well understood but may be related to changing genomic epidemiology. We assessed C. difficile strains across a CDC Emerging Infections Program (EIP) site in Western New York, including strains from both HCA-CDI and CA-CDI cases to characterize predominating strains and putative transmission across epidemiological classifications and between index and recurrent cases. Methods: In total, 535 isolates of C. difficile were collected over a 6-month period in 2018 from the Monroe Country, New York, EIP site and were analyzed using whole-genome sequencing (WGS). Standard epidemiological definitions were used to classify cases as hospital onset (HO-CDI); community associated (CA-CDI); community onset, healthcare associated (CO-HCFA-CDI); or long-term care onset (LTCO-CDI). Recurrent cases were defined as those diagnosed within 8 weeks of an initial positive test. Multilocus sequence types (MLSTs) were assigned according to PUBMLST and single-nucleotide polymorphisms (SNPs) were determined using a modified CFSAN analytical pipeline. Cases resulting from putative transmission were defined as those separated by 0–1 core SNPs. Results: Of 535 isolates, 454 were from index and 81 were from recurrent cases. The index cases were comprised of CA-CDI (47.4%), CO-HCFA-CDI (24%), LTCO-CDI (8.1%), and HO-CDI (19.3%). Cases with recurrent disease mirrored the epidemiological distribution of the larger set. Common MLSTs included ST2 (12.3%), ST8 (10.5%), ST42 (7.9%), ST58 (4.9%), ST43 (4.5%), and ST11 (4.3%). The previously widespread epidemic strain, NAP1/ST1/RT027 accounted for Conclusions: The genomic epidemiology of C. difficile across this large community cohort demonstrated a diverse group of strain types that was similarly distributed across epidemiological classifications and between index and recurrent cases. SNP analysis indicated that direct transmission between cases was uncommon. Funding: None Disclosures: None Cambridge University Press 2022-05-16 /pmc/articles/PMC9615007/ http://dx.doi.org/10.1017/ash.2022.110 Text en © The Society for Healthcare Epidemiology of America 2022 https://creativecommons.org/licenses/by/4.0/This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle C. difficile
Tesini, Brenda
Taffner, Samantha
Hatwar, Trupti
Gill, Steven
Dumyati, Ghinwa
Pecora, Nicole
Evaluation of the genomic epidemiology and transmission of Clostridioides difficile infection across a community
title Evaluation of the genomic epidemiology and transmission of Clostridioides difficile infection across a community
title_full Evaluation of the genomic epidemiology and transmission of Clostridioides difficile infection across a community
title_fullStr Evaluation of the genomic epidemiology and transmission of Clostridioides difficile infection across a community
title_full_unstemmed Evaluation of the genomic epidemiology and transmission of Clostridioides difficile infection across a community
title_short Evaluation of the genomic epidemiology and transmission of Clostridioides difficile infection across a community
title_sort evaluation of the genomic epidemiology and transmission of clostridioides difficile infection across a community
topic C. difficile
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9615007/
http://dx.doi.org/10.1017/ash.2022.110
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