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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Format: | Article |
Language: | English |
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Cambridge University Press
2022-07-01
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Series: | Antimicrobial Stewardship & Healthcare Epidemiology |
Online Access: | https://www.cambridge.org/core/product/identifier/S2732494X22001103/type/journal_article |
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author | Brenda Tesini Samantha Taffner Trupti Hatwar Steven Gill Ghinwa Dumyati Nicole Pecora |
author_facet | Brenda Tesini Samantha Taffner Trupti Hatwar Steven Gill Ghinwa Dumyati Nicole Pecora |
author_sort | Brenda Tesini |
collection | DOAJ |
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. |
first_indexed | 2024-04-10T05:03:53Z |
format | Article |
id | doaj.art-9573f1f42f8d4bceb84f607c775c4881 |
institution | Directory Open Access Journal |
issn | 2732-494X |
language | English |
last_indexed | 2024-04-10T05:03:53Z |
publishDate | 2022-07-01 |
publisher | Cambridge University Press |
record_format | Article |
series | Antimicrobial Stewardship & Healthcare Epidemiology |
spelling | doaj.art-9573f1f42f8d4bceb84f607c775c48812023-03-09T12:28:10ZengCambridge University PressAntimicrobial Stewardship & Healthcare Epidemiology2732-494X2022-07-012s29s3010.1017/ash.2022.110Evaluation of the genomic epidemiology and transmission of Clostridioides difficile infection across a communityBrenda TesiniSamantha TaffnerTrupti HatwarSteven GillGhinwa DumyatiNicole PecoraBackground: 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.https://www.cambridge.org/core/product/identifier/S2732494X22001103/type/journal_article |
spellingShingle | Brenda Tesini Samantha Taffner Trupti Hatwar Steven Gill Ghinwa Dumyati Nicole Pecora Evaluation of the genomic epidemiology and transmission of Clostridioides difficile infection across a community Antimicrobial Stewardship & Healthcare Epidemiology |
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 |
url | https://www.cambridge.org/core/product/identifier/S2732494X22001103/type/journal_article |
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