Cargando…
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...
Autores principales: | , , , , , , , , , |
---|---|
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 |
_version_ | 1783445533560406016 |
---|---|
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. |
format | Online Article Text |
id | pubmed-6704593 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT morjariasejal antibioticinducedshiftsinfecalmicrobiotadensityandcompositionduringhematopoieticstemcelltransplantation AT schluterjonas antibioticinducedshiftsinfecalmicrobiotadensityandcompositionduringhematopoieticstemcelltransplantation AT taylorbradfordp antibioticinducedshiftsinfecalmicrobiotadensityandcompositionduringhematopoieticstemcelltransplantation AT littmannericr antibioticinducedshiftsinfecalmicrobiotadensityandcompositionduringhematopoieticstemcelltransplantation AT carterrebeccaa antibioticinducedshiftsinfecalmicrobiotadensityandcompositionduringhematopoieticstemcelltransplantation AT fontanaemily antibioticinducedshiftsinfecalmicrobiotadensityandcompositionduringhematopoieticstemcelltransplantation AT peledjonathanu antibioticinducedshiftsinfecalmicrobiotadensityandcompositionduringhematopoieticstemcelltransplantation AT vandenbrinkmarcelrm antibioticinducedshiftsinfecalmicrobiotadensityandcompositionduringhematopoieticstemcelltransplantation AT xavierjoaob antibioticinducedshiftsinfecalmicrobiotadensityandcompositionduringhematopoieticstemcelltransplantation AT taurying antibioticinducedshiftsinfecalmicrobiotadensityandcompositionduringhematopoieticstemcelltransplantation |