Intestinal Dysbiosis in Carriers of Carbapenem-Resistant <italic toggle="yes">Enterobacteriaceae</italic>

ABSTRACT Infection with carbapenem-resistant Enterobacteriaceae (CRE) has become an important challenge in health care settings and a growing concern worldwide. Since infection is preceded by colonization, an understanding of the latter may reduce CRE infections. We aimed to characterize the gut mic...

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Autores principales: Hila Korach-Rechtman, Maysaa Hreish, Carmit Fried, Shiran Gerassy-Vainberg, Zaher S. Azzam, Yechezkel Kashi, Gidon Berger
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Publicado: American Society for Microbiology 2020
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spelling oai:doaj.org-article:c98c43228e514623946fa8371fc3a7ec2021-11-15T15:29:16ZIntestinal Dysbiosis in Carriers of Carbapenem-Resistant <italic toggle="yes">Enterobacteriaceae</italic>10.1128/mSphere.00173-202379-5042https://doaj.org/article/c98c43228e514623946fa8371fc3a7ec2020-04-01T00:00:00Zhttps://journals.asm.org/doi/10.1128/mSphere.00173-20https://doaj.org/toc/2379-5042ABSTRACT Infection with carbapenem-resistant Enterobacteriaceae (CRE) has become an important challenge in health care settings and a growing concern worldwide. Since infection is preceded by colonization, an understanding of the latter may reduce CRE infections. We aimed to characterize the gut microbiota in CRE carriers, assuming that microbiota alterations precede CRE colonization. We evaluated the gut microbiota using 16S rRNA gene sequencing extracted of fecal samples collected from hospitalized CRE carriers and two control groups, hospitalized noncarriers and healthy adults. The microbiota diversity and composition in CRE-colonized patients differed from those of the control group participants. These CRE carriers displayed lower phylogenetic diversity and dysbiotic microbiota, enriched with members of the family Enterobacteriaceae. Concurrent with the enrichment in Enterobacteriaceae, a depletion of anaerobic commensals was observed. Additionally, changes in several predicted metabolic pathways were observed for the CRE carriers. Concomitantly, we found higher prevalence of bacteremia in the CRE carriers. Several clinical factors that might induce changes in the microbiota were examined and found to be insignificant between the groups. The compositional and functional changes in the microbiota of CRE-colonized patients are associated with increased risk for systemic infection. Our study results provide justification for attempts to restore the dysbiotic microbiota with probiotics or fecal transplantation. IMPORTANCE The gut microbiota plays important roles in the host’s normal function and health, including protection against colonization by pathogenic bacteria. Alterations in the gut microbial profile can potentially serve as an early diagnostic tool, as well as a therapeutic strategy against colonization by and carriage of harmful bacteria, including antibiotic-resistant pathogens. Here, we show that the microbiota of hospitalized patients demonstrated specific taxa which differed between carriers of carbapenem-resistant Enterobacteriaceae (CRE) and noncarriers. The difference in the microbiota also dictates alterations in microbiome-specific metabolic capabilities, in association with increased prevalence of systemic infection. Reintroducing specific strains and/or correction of dysbiosis with probiotics or fecal transplantation may potentially lead to colonization by bacterial taxa responsible for protection against or depletion of antibiotic-resistant pathogens.Hila Korach-RechtmanMaysaa HreishCarmit FriedShiran Gerassy-VainbergZaher S. AzzamYechezkel KashiGidon BergerAmerican Society for Microbiologyarticlecarbapenem-resistant EnterobacteriaceaeCREmicrobiomeintestinal dysbiosisantibiotic resistanceMicrobiologyQR1-502ENmSphere, Vol 5, Iss 2 (2020)
institution DOAJ
collection DOAJ
language EN
topic carbapenem-resistant Enterobacteriaceae
CRE
microbiome
intestinal dysbiosis
antibiotic resistance
Microbiology
QR1-502
spellingShingle carbapenem-resistant Enterobacteriaceae
CRE
microbiome
intestinal dysbiosis
antibiotic resistance
Microbiology
QR1-502
Hila Korach-Rechtman
Maysaa Hreish
Carmit Fried
Shiran Gerassy-Vainberg
Zaher S. Azzam
Yechezkel Kashi
Gidon Berger
Intestinal Dysbiosis in Carriers of Carbapenem-Resistant <italic toggle="yes">Enterobacteriaceae</italic>
description ABSTRACT Infection with carbapenem-resistant Enterobacteriaceae (CRE) has become an important challenge in health care settings and a growing concern worldwide. Since infection is preceded by colonization, an understanding of the latter may reduce CRE infections. We aimed to characterize the gut microbiota in CRE carriers, assuming that microbiota alterations precede CRE colonization. We evaluated the gut microbiota using 16S rRNA gene sequencing extracted of fecal samples collected from hospitalized CRE carriers and two control groups, hospitalized noncarriers and healthy adults. The microbiota diversity and composition in CRE-colonized patients differed from those of the control group participants. These CRE carriers displayed lower phylogenetic diversity and dysbiotic microbiota, enriched with members of the family Enterobacteriaceae. Concurrent with the enrichment in Enterobacteriaceae, a depletion of anaerobic commensals was observed. Additionally, changes in several predicted metabolic pathways were observed for the CRE carriers. Concomitantly, we found higher prevalence of bacteremia in the CRE carriers. Several clinical factors that might induce changes in the microbiota were examined and found to be insignificant between the groups. The compositional and functional changes in the microbiota of CRE-colonized patients are associated with increased risk for systemic infection. Our study results provide justification for attempts to restore the dysbiotic microbiota with probiotics or fecal transplantation. IMPORTANCE The gut microbiota plays important roles in the host’s normal function and health, including protection against colonization by pathogenic bacteria. Alterations in the gut microbial profile can potentially serve as an early diagnostic tool, as well as a therapeutic strategy against colonization by and carriage of harmful bacteria, including antibiotic-resistant pathogens. Here, we show that the microbiota of hospitalized patients demonstrated specific taxa which differed between carriers of carbapenem-resistant Enterobacteriaceae (CRE) and noncarriers. The difference in the microbiota also dictates alterations in microbiome-specific metabolic capabilities, in association with increased prevalence of systemic infection. Reintroducing specific strains and/or correction of dysbiosis with probiotics or fecal transplantation may potentially lead to colonization by bacterial taxa responsible for protection against or depletion of antibiotic-resistant pathogens.
format article
author Hila Korach-Rechtman
Maysaa Hreish
Carmit Fried
Shiran Gerassy-Vainberg
Zaher S. Azzam
Yechezkel Kashi
Gidon Berger
author_facet Hila Korach-Rechtman
Maysaa Hreish
Carmit Fried
Shiran Gerassy-Vainberg
Zaher S. Azzam
Yechezkel Kashi
Gidon Berger
author_sort Hila Korach-Rechtman
title Intestinal Dysbiosis in Carriers of Carbapenem-Resistant <italic toggle="yes">Enterobacteriaceae</italic>
title_short Intestinal Dysbiosis in Carriers of Carbapenem-Resistant <italic toggle="yes">Enterobacteriaceae</italic>
title_full Intestinal Dysbiosis in Carriers of Carbapenem-Resistant <italic toggle="yes">Enterobacteriaceae</italic>
title_fullStr Intestinal Dysbiosis in Carriers of Carbapenem-Resistant <italic toggle="yes">Enterobacteriaceae</italic>
title_full_unstemmed Intestinal Dysbiosis in Carriers of Carbapenem-Resistant <italic toggle="yes">Enterobacteriaceae</italic>
title_sort intestinal dysbiosis in carriers of carbapenem-resistant <italic toggle="yes">enterobacteriaceae</italic>
publisher American Society for Microbiology
publishDate 2020
url https://doaj.org/article/c98c43228e514623946fa8371fc3a7ec
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