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Antibiotic-Induced Shifts in Fecal Microbiota Density and Composition during Hematopoietic Stem Cell Transplantation

Dramatic microbiota changes and loss of commensal anaerobic bacteria are associated with adverse outcomes in hematopoietic cell transplantation (HCT) recipients. In this study, we demonstrate these dynamic changes at high resolution through daily stool sampling and assess the impact of individual an...

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Autores principales: Morjaria, Sejal, Schluter, Jonas, Taylor, Bradford P., Littmann, Eric R., Carter, Rebecca A., Fontana, Emily, Peled, Jonathan U., van den Brink, Marcel R. M., Xavier, Joao B., Taur, Ying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6704593/
https://www.ncbi.nlm.nih.gov/pubmed/31262981
http://dx.doi.org/10.1128/IAI.00206-19
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author Morjaria, Sejal
Schluter, Jonas
Taylor, Bradford P.
Littmann, Eric R.
Carter, Rebecca A.
Fontana, Emily
Peled, Jonathan U.
van den Brink, Marcel R. M.
Xavier, Joao B.
Taur, Ying
author_facet Morjaria, Sejal
Schluter, Jonas
Taylor, Bradford P.
Littmann, Eric R.
Carter, Rebecca A.
Fontana, Emily
Peled, Jonathan U.
van den Brink, Marcel R. M.
Xavier, Joao B.
Taur, Ying
author_sort Morjaria, Sejal
collection PubMed
description Dramatic microbiota changes and loss of commensal anaerobic bacteria are associated with adverse outcomes in hematopoietic cell transplantation (HCT) recipients. In this study, we demonstrate these dynamic changes at high resolution through daily stool sampling and assess the impact of individual antibiotics on those changes. We collected 272 longitudinal stool samples (with mostly daily frequency) from 18 patients undergoing HCT and determined their composition by multiparallel 16S rRNA gene sequencing as well as the density of bacteria in stool by quantitative PCR (qPCR). We calculated microbiota volatility to quantify rapid shifts and developed a new dynamic systems inference method to assess the specific impact of antibiotics. The greatest shifts in microbiota composition occurred between stem cell infusion and reconstitution of healthy immune cells. Piperacillin-tazobactam caused the most severe declines among obligate anaerobes. Our approach of daily sampling, bacterial density determination, and dynamic systems modeling allowed us to infer the independent effects of specific antibiotics on the microbiota of HCT patients.
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spelling pubmed-67045932019-08-29 Antibiotic-Induced Shifts in Fecal Microbiota Density and Composition during Hematopoietic Stem Cell Transplantation Morjaria, Sejal Schluter, Jonas Taylor, Bradford P. Littmann, Eric R. Carter, Rebecca A. Fontana, Emily Peled, Jonathan U. van den Brink, Marcel R. M. Xavier, Joao B. Taur, Ying Infect Immun Host-Associated Microbial Communities Dramatic microbiota changes and loss of commensal anaerobic bacteria are associated with adverse outcomes in hematopoietic cell transplantation (HCT) recipients. In this study, we demonstrate these dynamic changes at high resolution through daily stool sampling and assess the impact of individual antibiotics on those changes. We collected 272 longitudinal stool samples (with mostly daily frequency) from 18 patients undergoing HCT and determined their composition by multiparallel 16S rRNA gene sequencing as well as the density of bacteria in stool by quantitative PCR (qPCR). We calculated microbiota volatility to quantify rapid shifts and developed a new dynamic systems inference method to assess the specific impact of antibiotics. The greatest shifts in microbiota composition occurred between stem cell infusion and reconstitution of healthy immune cells. Piperacillin-tazobactam caused the most severe declines among obligate anaerobes. Our approach of daily sampling, bacterial density determination, and dynamic systems modeling allowed us to infer the independent effects of specific antibiotics on the microbiota of HCT patients. American Society for Microbiology 2019-08-21 /pmc/articles/PMC6704593/ /pubmed/31262981 http://dx.doi.org/10.1128/IAI.00206-19 Text en Copyright © 2019 Morjaria et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Host-Associated Microbial Communities
Morjaria, Sejal
Schluter, Jonas
Taylor, Bradford P.
Littmann, Eric R.
Carter, Rebecca A.
Fontana, Emily
Peled, Jonathan U.
van den Brink, Marcel R. M.
Xavier, Joao B.
Taur, Ying
Antibiotic-Induced Shifts in Fecal Microbiota Density and Composition during Hematopoietic Stem Cell Transplantation
title Antibiotic-Induced Shifts in Fecal Microbiota Density and Composition during Hematopoietic Stem Cell Transplantation
title_full Antibiotic-Induced Shifts in Fecal Microbiota Density and Composition during Hematopoietic Stem Cell Transplantation
title_fullStr Antibiotic-Induced Shifts in Fecal Microbiota Density and Composition during Hematopoietic Stem Cell Transplantation
title_full_unstemmed Antibiotic-Induced Shifts in Fecal Microbiota Density and Composition during Hematopoietic Stem Cell Transplantation
title_short Antibiotic-Induced Shifts in Fecal Microbiota Density and Composition during Hematopoietic Stem Cell Transplantation
title_sort antibiotic-induced shifts in fecal microbiota density and composition during hematopoietic stem cell transplantation
topic Host-Associated Microbial Communities
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6704593/
https://www.ncbi.nlm.nih.gov/pubmed/31262981
http://dx.doi.org/10.1128/IAI.00206-19
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