Cargando…
Fecal Transplant in Children With Clostridioides difficile Gives Sustained Reduction in Antimicrobial Resistance and Potential Pathogen Burden
BACKGROUND: Fecal microbiota transplantation (FMT) treats Clostridioides difficile infection (CDI). Little is known regarding the changes in antimicrobial resistance (AMR) genes and potential pathogen burden that occur in pediatric recipients of FMT. The aim of this study was to investigate changes...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6790402/ https://www.ncbi.nlm.nih.gov/pubmed/31660343 http://dx.doi.org/10.1093/ofid/ofz379 |
_version_ | 1783458789450579968 |
---|---|
author | Hourigan, Suchitra K Ahn, Michelle Gibson, Keylie M Pérez-Losada, Marcos Felix, Grace Weidner, Melissa Leibowitz, Ian Niederhuber, John E Sears, Cynthia L Crandall, Keith A Oliva-Hemker, Maria |
author_facet | Hourigan, Suchitra K Ahn, Michelle Gibson, Keylie M Pérez-Losada, Marcos Felix, Grace Weidner, Melissa Leibowitz, Ian Niederhuber, John E Sears, Cynthia L Crandall, Keith A Oliva-Hemker, Maria |
author_sort | Hourigan, Suchitra K |
collection | PubMed |
description | BACKGROUND: Fecal microbiota transplantation (FMT) treats Clostridioides difficile infection (CDI). Little is known regarding the changes in antimicrobial resistance (AMR) genes and potential pathogen burden that occur in pediatric recipients of FMT. The aim of this study was to investigate changes in AMR genes, potential pathogens, species, and functional pathways with FMT in children. METHODS: Nine children with recurrent CDI underwent FMT. Stool was collected from donor and recipient pre-FMT and longitudinally post-FMT for up to 24 weeks. Shotgun metagenomic sequencing was performed. Reads were analyzed using PathoScope 2.0. RESULTS: All children had resolution of CDI. AMR genes decreased post-FMT (P < .001), with a sustained decrease in multidrug resistance genes (P < .001). Tetracycline resistance genes increased post-FMT (P < .001). Very low levels of potential pathogens were identified in donors and recipients, with an overall decrease post-FMT (P < .001). Prevotella sp. 109 expanded in all recipients post-FMT, and no recipients had any clinical infection. Alpha diversity was lower in recipients vs donors pre-FMT (P < .001), with an increase post-FMT (P ≤ .002) that was sustained. Beta diversity differed significantly in pre- vs post-FMT recipient samples (P < .001). Bacterial species Faecalibacterium prausnitzii and Bacteroides ovatus showed higher abundance in donors than recipients (P = .008 and P = .040, respectively), with expansion post-FMT. Biosynthetic pathways predominated in the donor and increased in the recipient post-FMT. CONCLUSIONS: FMT for CDI in children decreases AMR genes and potential pathogens and changes microbiota composition and function. However, acquisition of certain AMR genes post-FMT combined with low levels of potential pathogens found in donors suggests that further study is warranted regarding screening donors using metagenomics sequencing before FMT. |
format | Online Article Text |
id | pubmed-6790402 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-67904022019-10-21 Fecal Transplant in Children With Clostridioides difficile Gives Sustained Reduction in Antimicrobial Resistance and Potential Pathogen Burden Hourigan, Suchitra K Ahn, Michelle Gibson, Keylie M Pérez-Losada, Marcos Felix, Grace Weidner, Melissa Leibowitz, Ian Niederhuber, John E Sears, Cynthia L Crandall, Keith A Oliva-Hemker, Maria Open Forum Infect Dis Major Article BACKGROUND: Fecal microbiota transplantation (FMT) treats Clostridioides difficile infection (CDI). Little is known regarding the changes in antimicrobial resistance (AMR) genes and potential pathogen burden that occur in pediatric recipients of FMT. The aim of this study was to investigate changes in AMR genes, potential pathogens, species, and functional pathways with FMT in children. METHODS: Nine children with recurrent CDI underwent FMT. Stool was collected from donor and recipient pre-FMT and longitudinally post-FMT for up to 24 weeks. Shotgun metagenomic sequencing was performed. Reads were analyzed using PathoScope 2.0. RESULTS: All children had resolution of CDI. AMR genes decreased post-FMT (P < .001), with a sustained decrease in multidrug resistance genes (P < .001). Tetracycline resistance genes increased post-FMT (P < .001). Very low levels of potential pathogens were identified in donors and recipients, with an overall decrease post-FMT (P < .001). Prevotella sp. 109 expanded in all recipients post-FMT, and no recipients had any clinical infection. Alpha diversity was lower in recipients vs donors pre-FMT (P < .001), with an increase post-FMT (P ≤ .002) that was sustained. Beta diversity differed significantly in pre- vs post-FMT recipient samples (P < .001). Bacterial species Faecalibacterium prausnitzii and Bacteroides ovatus showed higher abundance in donors than recipients (P = .008 and P = .040, respectively), with expansion post-FMT. Biosynthetic pathways predominated in the donor and increased in the recipient post-FMT. CONCLUSIONS: FMT for CDI in children decreases AMR genes and potential pathogens and changes microbiota composition and function. However, acquisition of certain AMR genes post-FMT combined with low levels of potential pathogens found in donors suggests that further study is warranted regarding screening donors using metagenomics sequencing before FMT. Oxford University Press 2019-08-26 /pmc/articles/PMC6790402/ /pubmed/31660343 http://dx.doi.org/10.1093/ofid/ofz379 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Major Article Hourigan, Suchitra K Ahn, Michelle Gibson, Keylie M Pérez-Losada, Marcos Felix, Grace Weidner, Melissa Leibowitz, Ian Niederhuber, John E Sears, Cynthia L Crandall, Keith A Oliva-Hemker, Maria Fecal Transplant in Children With Clostridioides difficile Gives Sustained Reduction in Antimicrobial Resistance and Potential Pathogen Burden |
title | Fecal Transplant in Children With Clostridioides difficile Gives Sustained Reduction in Antimicrobial Resistance and Potential Pathogen Burden |
title_full | Fecal Transplant in Children With Clostridioides difficile Gives Sustained Reduction in Antimicrobial Resistance and Potential Pathogen Burden |
title_fullStr | Fecal Transplant in Children With Clostridioides difficile Gives Sustained Reduction in Antimicrobial Resistance and Potential Pathogen Burden |
title_full_unstemmed | Fecal Transplant in Children With Clostridioides difficile Gives Sustained Reduction in Antimicrobial Resistance and Potential Pathogen Burden |
title_short | Fecal Transplant in Children With Clostridioides difficile Gives Sustained Reduction in Antimicrobial Resistance and Potential Pathogen Burden |
title_sort | fecal transplant in children with clostridioides difficile gives sustained reduction in antimicrobial resistance and potential pathogen burden |
topic | Major Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6790402/ https://www.ncbi.nlm.nih.gov/pubmed/31660343 http://dx.doi.org/10.1093/ofid/ofz379 |
work_keys_str_mv | AT hourigansuchitrak fecaltransplantinchildrenwithclostridioidesdifficilegivessustainedreductioninantimicrobialresistanceandpotentialpathogenburden AT ahnmichelle fecaltransplantinchildrenwithclostridioidesdifficilegivessustainedreductioninantimicrobialresistanceandpotentialpathogenburden AT gibsonkeyliem fecaltransplantinchildrenwithclostridioidesdifficilegivessustainedreductioninantimicrobialresistanceandpotentialpathogenburden AT perezlosadamarcos fecaltransplantinchildrenwithclostridioidesdifficilegivessustainedreductioninantimicrobialresistanceandpotentialpathogenburden AT felixgrace fecaltransplantinchildrenwithclostridioidesdifficilegivessustainedreductioninantimicrobialresistanceandpotentialpathogenburden AT weidnermelissa fecaltransplantinchildrenwithclostridioidesdifficilegivessustainedreductioninantimicrobialresistanceandpotentialpathogenburden AT leibowitzian fecaltransplantinchildrenwithclostridioidesdifficilegivessustainedreductioninantimicrobialresistanceandpotentialpathogenburden AT niederhuberjohne fecaltransplantinchildrenwithclostridioidesdifficilegivessustainedreductioninantimicrobialresistanceandpotentialpathogenburden AT searscynthial fecaltransplantinchildrenwithclostridioidesdifficilegivessustainedreductioninantimicrobialresistanceandpotentialpathogenburden AT crandallkeitha fecaltransplantinchildrenwithclostridioidesdifficilegivessustainedreductioninantimicrobialresistanceandpotentialpathogenburden AT olivahemkermaria fecaltransplantinchildrenwithclostridioidesdifficilegivessustainedreductioninantimicrobialresistanceandpotentialpathogenburden |