Gut resistome plasticity in pediatric patients undergoing hematopoietic stem cell transplantation

Federica D'Amico1, Matteo Soverini1, Daniele Zama2

  • 1Unit of Microbial Ecology of Health, Department of Pharmacy and Biotechnology, University of Bologna, Via Belmeloro 6, Bologna, 40126, Italy.

Scientific Reports
|April 6, 2019
PubMed

Insights

Pediatric patients undergoing stem cell transplants with Graft-versus-Host Disease show increased gut antibiotic resistance genes. This highlights the need to monitor the gut resistome for better infection treatment post-transplant.

Area of Science:

  • Microbiology
  • Immunology
  • Hematology

Background:

  • The gut microbiome is a reservoir for antimicrobial resistance (AMR).
  • AMR in pediatric patients undergoing allogeneic hematopoietic stem cell transplantation (HSCT) impacts mortality.
  • Understanding gut resistome dynamics post-HSCT is crucial.

Purpose of the Study:

  • To explore the gut resistome dynamics in pediatric HSCT patients.
  • To investigate the association between acute Graft-versus-Host Disease (aGvHD) and gut resistome expansion.
  • To identify specific antibiotic resistance patterns in aGvHD patients.

Main Methods:

  • Shotgun metagenomics was employed to analyze the gut microbiome.
  • Eight pediatric HSCT patients were studied, with half developing aGvHD.
  • Resistome patterns were analyzed before and after HSCT.

Main Results:

  • Patients with aGvHD exhibited significant post-HSCT expansion of their gut resistome.
  • New antibiotic resistance genes were acquired, and pre-existing ones were consolidated in aGvHD patients.
  • The aGvHD-associated resistome bloom included multidrug resistance and resistance to macrolides, aminoglycosides, tetracyclines, and beta-lactams.

Conclusions:

  • Acute Graft-versus-Host Disease is linked to an expanded gut resistome in pediatric HSCT patients.
  • The observed resistance patterns extend beyond administered antibiotics, indicating broader AMR implications.
  • Mapping the gut resistome is essential for optimizing anti-infective strategies in HSCT recipients.

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