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Faecal microbiota transplantation reduces amounts of antibiotic resistance genes in patients with multidrug-resistant organisms

DC Field Value Language
dc.contributor.author고홍-
dc.contributor.author용동은-
dc.contributor.author이상길-
dc.contributor.author정수진-
dc.contributor.author천재희-
dc.contributor.author최준용-
dc.date.accessioned2022-05-09T17:12:20Z-
dc.date.available2022-05-09T17:12:20Z-
dc.date.issued2022-01-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/188437-
dc.description.abstractBackground: Multidrug-resistant organisms (MDROs) such as vancomycin-resistant enterococci (VRE) and carbapenemase-producing Enterobacteriaceae (CPE) are associated with prolonged hospitalisation, increased medical costs, and severe infections. Faecal microbiota transplantation (FMT) has emerged as an important strategy for decolonisation. This study aimed to evaluate the genetic response of MDROs to FMT. Methods: A single-centre prospective study was conducted on patients infected with VRE, CPE, or VRE/CPE who underwent FMT between May 2018 and April 2019. Genetic response was assessed as the change in the expression of the resistance genes VanA, blaKPC, blaNDM, and blaOXA on days 1, 7, 14, and 28 by real-time reverse-transcription polymerase chain reaction. Results: Twenty-nine patients received FMT, of which 26 (59.3%) were infected with VRE, 5 (11.1%) with CPE, and 8 (29.6%) with VRE/CPE. The mean duration of MDRO carriage before FMT was 71 days. Seventeen patients (63.0%) used antibiotics within a week of FMT. In a culture-dependent method, the expression of VanA and overall genes significantly decreased (p = 0.011 and p = 0.003 respectively). In a culture-independent method, VanA, blaNDM, and overall gene expression significantly decreased over time after FMT (p = 0.047, p = 0.048, p = 0.002, respectively). Similar results were confirmed following comparison between each time point in both the culture-dependent and -independent methods. Regression analysis did not reveal important factors underlying the genetic response after FMT. No adverse events were observed. Conclusion: FMT in patients infected with MDROs downregulates the expression of resistance genes, especially VanA, and facilitates MDRO decolonisation.-
dc.description.statementOfResponsibilityopen-
dc.languageEnglish-
dc.publisherBioMed Central-
dc.relation.isPartOfANTIMICROBIAL RESISTANCE AND INFECTION CONTROL-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.subject.MESHAdult-
dc.subject.MESHAged-
dc.subject.MESHBacteria / genetics*-
dc.subject.MESHCarbapenem-Resistant Enterobacteriaceae / genetics-
dc.subject.MESHDrug Resistance, Multiple, Bacterial*-
dc.subject.MESHFecal Microbiota Transplantation / statistics & numerical data*-
dc.subject.MESHFemale-
dc.subject.MESHHumans-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHProspective Studies-
dc.subject.MESHRepublic of Korea-
dc.subject.MESHVancomycin-Resistant Enterococci / genetics-
dc.subject.MESHYoung Adult-
dc.titleFaecal microbiota transplantation reduces amounts of antibiotic resistance genes in patients with multidrug-resistant organisms-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Pediatrics (소아과학교실)-
dc.contributor.googleauthorJongHoon Hyun-
dc.contributor.googleauthorSang Kil Lee-
dc.contributor.googleauthorJae Hee Cheon-
dc.contributor.googleauthorDong Eun Yong-
dc.contributor.googleauthorHong Koh-
dc.contributor.googleauthorYun Koo Kang-
dc.contributor.googleauthorMoo Hyun Kim-
dc.contributor.googleauthorYujin Sohn-
dc.contributor.googleauthorYunsuk Cho-
dc.contributor.googleauthorYae Jee Baek-
dc.contributor.googleauthorJung Ho Kim-
dc.contributor.googleauthorJin Young Ahn-
dc.contributor.googleauthorSu Jin Jeong-
dc.contributor.googleauthorJoon Sup Yeom-
dc.contributor.googleauthorJun Yong Choi-
dc.identifier.doi10.1186/s13756-022-01064-4-
dc.contributor.localIdA00156-
dc.contributor.localIdA02423-
dc.contributor.localIdA02812-
dc.contributor.localIdA03638-
dc.contributor.localIdA04030-
dc.contributor.localIdA04191-
dc.relation.journalcodeJ03559-
dc.identifier.eissn2047-2994-
dc.identifier.pmid35093183-
dc.subject.keywordCarbapenemase-producing Enterobacteriaceae-
dc.subject.keywordFaecal microbiota transplantation-
dc.subject.keywordMicrobiome-
dc.subject.keywordMultidrug-resistant organism-
dc.subject.keywordVancomycin-resistant enterococci-
dc.contributor.alternativeNameKoh, Hong-
dc.contributor.affiliatedAuthor고홍-
dc.contributor.affiliatedAuthor용동은-
dc.contributor.affiliatedAuthor이상길-
dc.contributor.affiliatedAuthor정수진-
dc.contributor.affiliatedAuthor천재희-
dc.contributor.affiliatedAuthor최준용-
dc.citation.volume11-
dc.citation.number1-
dc.citation.startPage20-
dc.identifier.bibliographicCitationANTIMICROBIAL RESISTANCE AND INFECTION CONTROL, Vol.11(1) : 20, 2022-01-
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
1. College of Medicine (의과대학) > Dept. of Pediatrics (소아과학교실) > 1. Journal Papers

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