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Origin and transmission of carbapenemase-producing Enterobacterales and vancomycin-resistant enterococci in hospitalized patients: a genomic and epidemiological analysis

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dc.contributor.authorKim, J. H.-
dc.contributor.authorSeong, J. E.-
dc.contributor.authorLee, Y. S.-
dc.contributor.authorLee, J. A.-
dc.contributor.authorAhn, J. Y.-
dc.contributor.authorJeong, S. J.-
dc.contributor.authorKu, N. S.-
dc.contributor.authorYeom, J. -S.-
dc.contributor.authorYong, D.-
dc.contributor.authorChoi, J. Y.-
dc.date.accessioned2025-12-02T06:29:53Z-
dc.date.available2025-12-02T06:29:53Z-
dc.date.created2026-01-02-
dc.date.issued2025-11-
dc.identifier.issn0195-6701-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/209233-
dc.description.abstractBackground: Antimicrobial resistance is an emerging threat, with carbapenemaseproducing Enterobacterales (CPE) and vancomycin-resistant enterococci (VRE) posing substantial challenges. This study investigated CPE/VRE acquisition and spread in hospitalized patients by analysing resistance genes and microbiomes using whole-genome sequencing (WGS), and exploring epidemiological and clinical risk factors. Methods: This retrospective study included patients from the infectious disease department of a tertiary hospital. Stool samples were collected weekly, together with clinical and epidemiological information. Those in which CPE/VRE were isolated underwent WGS to evaluate the presence of resistance genes. Microbiome analysis was performed at admission and discharge. WGS was also performed for all positive samples collected within the hospital during the study period. Results: Of the 102 participants, 16 (15.7%) had CPE/VRE at admission. Key risk factors for harbouring CPE/VRE at admission included recent hospitalization, surgery and antibiotic use. The first week of hospitalization was critical for acquiring CPE/VRE, with dementia, central or urinary catheters, and carbapenem use being significant risk factors. CPE/VRE acquired post-admission shared resistance genes with circulating hospital strains, whereas those present at admission featured novel genes such as blaOXY-4-1 and optrA. Microbiome analysis revealed significant differences in species abundance and reduced diversity at discharge. Conclusions: The probability of having CPE/VRE at admission to the infectious disease department was high. Stringent infection control measures are essential for preventing the spread of CPE/VRE and the introduction of novel resistance genes. (c) 2025 The Healthcare Infection Society. Published by Elsevier Ltd. All rights are reserved, including those for text and data mining, AI training, and similar technologies.-
dc.description.statementOfResponsibilityrestriction-
dc.languageEnglish-
dc.publisherW.B. Saunders For The Hospital Infection Society-
dc.relation.isPartOfJOURNAL OF HOSPITAL INFECTION-
dc.relation.isPartOfJOURNAL OF HOSPITAL INFECTION-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.subject.MESHAdult-
dc.subject.MESHAged-
dc.subject.MESHAged, 80 and over-
dc.subject.MESHBacterial Proteins* / genetics-
dc.subject.MESHBacterial Proteins* / metabolism-
dc.subject.MESHCarbapenem-Resistant Enterobacteriaceae* / genetics-
dc.subject.MESHCarbapenem-Resistant Enterobacteriaceae* / isolation & purification-
dc.subject.MESHCross Infection* / epidemiology-
dc.subject.MESHCross Infection* / microbiology-
dc.subject.MESHCross Infection* / transmission-
dc.subject.MESHEnterobacteriaceae Infections* / epidemiology-
dc.subject.MESHEnterobacteriaceae Infections* / microbiology-
dc.subject.MESHEnterobacteriaceae Infections* / transmission-
dc.subject.MESHEnterobacteriaceae* / enzymology-
dc.subject.MESHEnterobacteriaceae* / genetics-
dc.subject.MESHEnterobacteriaceae* / isolation & purification-
dc.subject.MESHFeces / microbiology-
dc.subject.MESHFemale-
dc.subject.MESHGram-Positive Bacterial Infections* / epidemiology-
dc.subject.MESHGram-Positive Bacterial Infections* / microbiology-
dc.subject.MESHGram-Positive Bacterial Infections* / transmission-
dc.subject.MESHHospitalization-
dc.subject.MESHHumans-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHMolecular Epidemiology-
dc.subject.MESHRetrospective Studies-
dc.subject.MESHRisk Factors-
dc.subject.MESHTertiary Care Centers-
dc.subject.MESHVancomycin-Resistant Enterococci* / genetics-
dc.subject.MESHVancomycin-Resistant Enterococci* / isolation & purification-
dc.subject.MESHWhole Genome Sequencing-
dc.subject.MESHbeta-Lactamases* / genetics-
dc.subject.MESHbeta-Lactamases* / metabolism-
dc.titleOrigin and transmission of carbapenemase-producing Enterobacterales and vancomycin-resistant enterococci in hospitalized patients: a genomic and epidemiological analysis-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.googleauthorKim, J. H.-
dc.contributor.googleauthorSeong, J. E.-
dc.contributor.googleauthorLee, Y. S.-
dc.contributor.googleauthorLee, J. A.-
dc.contributor.googleauthorAhn, J. Y.-
dc.contributor.googleauthorJeong, S. J.-
dc.contributor.googleauthorKu, N. S.-
dc.contributor.googleauthorYeom, J. -S.-
dc.contributor.googleauthorYong, D.-
dc.contributor.googleauthorChoi, J. Y.-
dc.identifier.doi10.1016/j.jhin.2025.07.017-
dc.relation.journalcodeJ01445-
dc.identifier.eissn1532-2939-
dc.identifier.pmid40803378-
dc.identifier.urlhttps://www.sciencedirect.com/science/article/pii/S0195670125002336-
dc.subject.keywordAntimicrobial resistance-
dc.subject.keywordCarbapenemase-producing-
dc.subject.keywordEnterobacterales-
dc.subject.keywordVancomycin-resistant-
dc.subject.keywordenterococci-
dc.subject.keywordWhole-genome sequencing-
dc.subject.keywordRisk factors-
dc.contributor.alternativeNameKu, Nam Su-
dc.contributor.affiliatedAuthorKim, J. H.-
dc.contributor.affiliatedAuthorSeong, J. E.-
dc.contributor.affiliatedAuthorLee, Y. S.-
dc.contributor.affiliatedAuthorLee, J. A.-
dc.contributor.affiliatedAuthorAhn, J. Y.-
dc.contributor.affiliatedAuthorJeong, S. J.-
dc.contributor.affiliatedAuthorKu, N. S.-
dc.contributor.affiliatedAuthorYeom, J. -S.-
dc.contributor.affiliatedAuthorYong, D.-
dc.contributor.affiliatedAuthorChoi, J. Y.-
dc.identifier.scopusid2-s2.0-105017437073-
dc.identifier.wosid001589354600004-
dc.citation.volume165-
dc.citation.startPage100-
dc.citation.endPage108-
dc.identifier.bibliographicCitationJOURNAL OF HOSPITAL INFECTION, Vol.165 : 100-108, 2025-11-
dc.identifier.rimsid90652-
dc.type.rimsART-
dc.description.journalClass1-
dc.description.journalClass1-
dc.subject.keywordAuthorAntimicrobial resistance-
dc.subject.keywordAuthorCarbapenemase-producing-
dc.subject.keywordAuthorEnterobacterales-
dc.subject.keywordAuthorVancomycin-resistant-
dc.subject.keywordAuthorenterococci-
dc.subject.keywordAuthorWhole-genome sequencing-
dc.subject.keywordAuthorRisk factors-
dc.subject.keywordPlusSTOOL MINI KIT-
dc.subject.keywordPlusCLINICAL MICROBIOLOGY-
dc.subject.keywordPlusBACTERIAL-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalWebOfScienceCategoryPublic, Environmental & Occupational Health-
dc.relation.journalWebOfScienceCategoryInfectious Diseases-
dc.relation.journalResearchAreaPublic, Environmental & Occupational Health-
dc.relation.journalResearchAreaInfectious Diseases-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Laboratory Medicine (진단검사의학교실) > 1. Journal Papers

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