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Dietary iron depletion at weaning imprints low microbiome diversity and this is not recovered with oral nano Fe(III)

Alterations in the gut microbiota have been recently linked to oral iron. We conducted two feeding studies including an initial diet-induced iron-depletion period followed by supplementation with nanoparticulate tartrate-modified ferrihydrite (Nano Fe(III): considered bioavailable to host but not ba...

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Autores principales: Pereira, Dora I A, Aslam, Mohamad F, Frazer, David M, Schmidt, Annemarie, Walton, Gemma E, McCartney, Anne L, Gibson, Glenn R, Anderson, Greg J, Powell, Jonathan J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BlackWell Publishing Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4335973/
https://www.ncbi.nlm.nih.gov/pubmed/25461615
http://dx.doi.org/10.1002/mbo3.213
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author Pereira, Dora I A
Aslam, Mohamad F
Frazer, David M
Schmidt, Annemarie
Walton, Gemma E
McCartney, Anne L
Gibson, Glenn R
Anderson, Greg J
Powell, Jonathan J
author_facet Pereira, Dora I A
Aslam, Mohamad F
Frazer, David M
Schmidt, Annemarie
Walton, Gemma E
McCartney, Anne L
Gibson, Glenn R
Anderson, Greg J
Powell, Jonathan J
author_sort Pereira, Dora I A
collection PubMed
description Alterations in the gut microbiota have been recently linked to oral iron. We conducted two feeding studies including an initial diet-induced iron-depletion period followed by supplementation with nanoparticulate tartrate-modified ferrihydrite (Nano Fe(III): considered bioavailable to host but not bacteria) or soluble ferrous sulfate (FeSO(4): considered bioavailable to both host and bacteria). We applied denaturing gradient gel electrophoresis and fluorescence in situ hybridization for study-1 and 454-pyrosequencing of fecal 16S rRNA in study-2. In study-1, the within-community microbial diversity increased with FeSO(4) (P = 0.0009) but not with Nano Fe(III) supplementation. This was confirmed in study-2, where we also showed that iron depletion at weaning imprinted significantly lower within- and between-community microbial diversity compared to mice weaned onto the iron-sufficient reference diet (P < 0.0001). Subsequent supplementation with FeSO(4) partially restored the within-community diversity (P = 0.006 in relation to the continuously iron-depleted group) but not the between-community diversity, whereas Nano Fe(III) had no effect. We conclude that (1) dietary iron depletion at weaning imprints low diversity in the microbiota that is not, subsequently, easily recovered; (2) in the absence of gastrointestinal disease iron supplementation does not negatively impact the microbiota; and (3) Nano Fe(III) is less available to the gut microbiota.
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spelling pubmed-43359732015-03-04 Dietary iron depletion at weaning imprints low microbiome diversity and this is not recovered with oral nano Fe(III) Pereira, Dora I A Aslam, Mohamad F Frazer, David M Schmidt, Annemarie Walton, Gemma E McCartney, Anne L Gibson, Glenn R Anderson, Greg J Powell, Jonathan J Microbiologyopen Original Research Alterations in the gut microbiota have been recently linked to oral iron. We conducted two feeding studies including an initial diet-induced iron-depletion period followed by supplementation with nanoparticulate tartrate-modified ferrihydrite (Nano Fe(III): considered bioavailable to host but not bacteria) or soluble ferrous sulfate (FeSO(4): considered bioavailable to both host and bacteria). We applied denaturing gradient gel electrophoresis and fluorescence in situ hybridization for study-1 and 454-pyrosequencing of fecal 16S rRNA in study-2. In study-1, the within-community microbial diversity increased with FeSO(4) (P = 0.0009) but not with Nano Fe(III) supplementation. This was confirmed in study-2, where we also showed that iron depletion at weaning imprinted significantly lower within- and between-community microbial diversity compared to mice weaned onto the iron-sufficient reference diet (P < 0.0001). Subsequent supplementation with FeSO(4) partially restored the within-community diversity (P = 0.006 in relation to the continuously iron-depleted group) but not the between-community diversity, whereas Nano Fe(III) had no effect. We conclude that (1) dietary iron depletion at weaning imprints low diversity in the microbiota that is not, subsequently, easily recovered; (2) in the absence of gastrointestinal disease iron supplementation does not negatively impact the microbiota; and (3) Nano Fe(III) is less available to the gut microbiota. BlackWell Publishing Ltd 2015-02 2014-12-02 /pmc/articles/PMC4335973/ /pubmed/25461615 http://dx.doi.org/10.1002/mbo3.213 Text en © 2014 Crown Copyright. MicrobiologyOpen published by John Wiley & Sons Ltd. http://creativecommons.org/licenses/by/3.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Pereira, Dora I A
Aslam, Mohamad F
Frazer, David M
Schmidt, Annemarie
Walton, Gemma E
McCartney, Anne L
Gibson, Glenn R
Anderson, Greg J
Powell, Jonathan J
Dietary iron depletion at weaning imprints low microbiome diversity and this is not recovered with oral nano Fe(III)
title Dietary iron depletion at weaning imprints low microbiome diversity and this is not recovered with oral nano Fe(III)
title_full Dietary iron depletion at weaning imprints low microbiome diversity and this is not recovered with oral nano Fe(III)
title_fullStr Dietary iron depletion at weaning imprints low microbiome diversity and this is not recovered with oral nano Fe(III)
title_full_unstemmed Dietary iron depletion at weaning imprints low microbiome diversity and this is not recovered with oral nano Fe(III)
title_short Dietary iron depletion at weaning imprints low microbiome diversity and this is not recovered with oral nano Fe(III)
title_sort dietary iron depletion at weaning imprints low microbiome diversity and this is not recovered with oral nano fe(iii)
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4335973/
https://www.ncbi.nlm.nih.gov/pubmed/25461615
http://dx.doi.org/10.1002/mbo3.213
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