Heavy metal exposure causes changes in the metabolic health-associated gut microbiome and metabolites

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Heavy metal exposure causes changes in the metabolic health-associated gut microbiome and metabolites. / Li, Xuan Ji; Brejnrod, Asker Daniel; Ernst, Madeleine; Rykær, Martin; Herschend, Jakob; Olsen, Nanna Mee Coops; Dorrestein, Pieter C.; Rensing, Christopher; Sørensen, Søren Johannes.

I: Environment International, Bind 126, 2019, s. 454-467.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Li, XJ, Brejnrod, AD, Ernst, M, Rykær, M, Herschend, J, Olsen, NMC, Dorrestein, PC, Rensing, C & Sørensen, SJ 2019, 'Heavy metal exposure causes changes in the metabolic health-associated gut microbiome and metabolites', Environment International, bind 126, s. 454-467. https://doi.org/10.1016/j.envint.2019.02.048

APA

Li, X. J., Brejnrod, A. D., Ernst, M., Rykær, M., Herschend, J., Olsen, N. M. C., Dorrestein, P. C., Rensing, C., & Sørensen, S. J. (2019). Heavy metal exposure causes changes in the metabolic health-associated gut microbiome and metabolites. Environment International, 126, 454-467. https://doi.org/10.1016/j.envint.2019.02.048

Vancouver

Li XJ, Brejnrod AD, Ernst M, Rykær M, Herschend J, Olsen NMC o.a. Heavy metal exposure causes changes in the metabolic health-associated gut microbiome and metabolites. Environment International. 2019;126:454-467. https://doi.org/10.1016/j.envint.2019.02.048

Author

Li, Xuan Ji ; Brejnrod, Asker Daniel ; Ernst, Madeleine ; Rykær, Martin ; Herschend, Jakob ; Olsen, Nanna Mee Coops ; Dorrestein, Pieter C. ; Rensing, Christopher ; Sørensen, Søren Johannes. / Heavy metal exposure causes changes in the metabolic health-associated gut microbiome and metabolites. I: Environment International. 2019 ; Bind 126. s. 454-467.

Bibtex

@article{67986378246944f3bbf7532d951b3482,
title = "Heavy metal exposure causes changes in the metabolic health-associated gut microbiome and metabolites",
abstract = "BACKGROUND: Exposure to arsenic and cadmium is common. Epidemiological and animal studies have suggested that exposure to these two heavy metals can cause metabolic health problems, including type 2 diabetes (T2DM). It has been hypothesized that T2DM could be mediated through the gut microbiome and the metabolites it produces. Although many studies have investigated the association between the gut microbiome and T2DM, few have focused on the connection to arsenic and cadmium.RESULTS: We applied 16S rRNA gene amplicon sequencing and untargeted LC-MS/MS metabolomics to examine the changes in the gut microbiome and metabolite profiles of exposed mice to relevant levels of cadmium and arsenic in the drinking water over two weeks. Cadmium chloride (Cd) exposure significantly changed the mice gut microbiome and resulted in a significantly lower microbial diversity whereas sodium arsenite (As) caused a non-significant decrease in microbial diversity. For Cd and As treatment respectively, we identified 5 and 2 phyla with significant changes and 42 and 24 genera. Bacterial genera that were observed to decline upon both treatments, included several butyrate-producers. Both As and Cd treatment perturbed the metabolome significantly, with 50 ppm Cd compound exposure having the greatest effect when compared to 50 ppm As compound exposure. Two unidentified features were differentially abundant in the As group, while 33 features changed in the Cd group. Differential abundance analysis of all bile acid associated molecular components showed differences under both treatments. Finally, integrative network analysis via bipartite correlation networks suggested that several genera, including the metabolically important Blautia, Eisenbergiella, Clostridium_XlVa, etc. declined in numbers of metabolite interactions.CONCLUSIONS: These results demonstrated that As and Cd exposure caused significant changes to the gut microbiome and metabolome by affecting bile acids, amino acids and taxa associated with metabolic health.",
author = "Li, {Xuan Ji} and Brejnrod, {Asker Daniel} and Madeleine Ernst and Martin Ryk{\ae}r and Jakob Herschend and Olsen, {Nanna Mee Coops} and Dorrestein, {Pieter C.} and Christopher Rensing and S{\o}rensen, {S{\o}ren Johannes}",
note = "Copyright {\textcopyright} 2019. Published by Elsevier Ltd.",
year = "2019",
doi = "10.1016/j.envint.2019.02.048",
language = "English",
volume = "126",
pages = "454--467",
journal = "Environment international",
issn = "0160-4120",
publisher = "Pergamon Press",

}

RIS

TY - JOUR

T1 - Heavy metal exposure causes changes in the metabolic health-associated gut microbiome and metabolites

AU - Li, Xuan Ji

AU - Brejnrod, Asker Daniel

AU - Ernst, Madeleine

AU - Rykær, Martin

AU - Herschend, Jakob

AU - Olsen, Nanna Mee Coops

AU - Dorrestein, Pieter C.

AU - Rensing, Christopher

AU - Sørensen, Søren Johannes

N1 - Copyright © 2019. Published by Elsevier Ltd.

PY - 2019

Y1 - 2019

N2 - BACKGROUND: Exposure to arsenic and cadmium is common. Epidemiological and animal studies have suggested that exposure to these two heavy metals can cause metabolic health problems, including type 2 diabetes (T2DM). It has been hypothesized that T2DM could be mediated through the gut microbiome and the metabolites it produces. Although many studies have investigated the association between the gut microbiome and T2DM, few have focused on the connection to arsenic and cadmium.RESULTS: We applied 16S rRNA gene amplicon sequencing and untargeted LC-MS/MS metabolomics to examine the changes in the gut microbiome and metabolite profiles of exposed mice to relevant levels of cadmium and arsenic in the drinking water over two weeks. Cadmium chloride (Cd) exposure significantly changed the mice gut microbiome and resulted in a significantly lower microbial diversity whereas sodium arsenite (As) caused a non-significant decrease in microbial diversity. For Cd and As treatment respectively, we identified 5 and 2 phyla with significant changes and 42 and 24 genera. Bacterial genera that were observed to decline upon both treatments, included several butyrate-producers. Both As and Cd treatment perturbed the metabolome significantly, with 50 ppm Cd compound exposure having the greatest effect when compared to 50 ppm As compound exposure. Two unidentified features were differentially abundant in the As group, while 33 features changed in the Cd group. Differential abundance analysis of all bile acid associated molecular components showed differences under both treatments. Finally, integrative network analysis via bipartite correlation networks suggested that several genera, including the metabolically important Blautia, Eisenbergiella, Clostridium_XlVa, etc. declined in numbers of metabolite interactions.CONCLUSIONS: These results demonstrated that As and Cd exposure caused significant changes to the gut microbiome and metabolome by affecting bile acids, amino acids and taxa associated with metabolic health.

AB - BACKGROUND: Exposure to arsenic and cadmium is common. Epidemiological and animal studies have suggested that exposure to these two heavy metals can cause metabolic health problems, including type 2 diabetes (T2DM). It has been hypothesized that T2DM could be mediated through the gut microbiome and the metabolites it produces. Although many studies have investigated the association between the gut microbiome and T2DM, few have focused on the connection to arsenic and cadmium.RESULTS: We applied 16S rRNA gene amplicon sequencing and untargeted LC-MS/MS metabolomics to examine the changes in the gut microbiome and metabolite profiles of exposed mice to relevant levels of cadmium and arsenic in the drinking water over two weeks. Cadmium chloride (Cd) exposure significantly changed the mice gut microbiome and resulted in a significantly lower microbial diversity whereas sodium arsenite (As) caused a non-significant decrease in microbial diversity. For Cd and As treatment respectively, we identified 5 and 2 phyla with significant changes and 42 and 24 genera. Bacterial genera that were observed to decline upon both treatments, included several butyrate-producers. Both As and Cd treatment perturbed the metabolome significantly, with 50 ppm Cd compound exposure having the greatest effect when compared to 50 ppm As compound exposure. Two unidentified features were differentially abundant in the As group, while 33 features changed in the Cd group. Differential abundance analysis of all bile acid associated molecular components showed differences under both treatments. Finally, integrative network analysis via bipartite correlation networks suggested that several genera, including the metabolically important Blautia, Eisenbergiella, Clostridium_XlVa, etc. declined in numbers of metabolite interactions.CONCLUSIONS: These results demonstrated that As and Cd exposure caused significant changes to the gut microbiome and metabolome by affecting bile acids, amino acids and taxa associated with metabolic health.

U2 - 10.1016/j.envint.2019.02.048

DO - 10.1016/j.envint.2019.02.048

M3 - Journal article

C2 - 30844581

VL - 126

SP - 454

EP - 467

JO - Environment international

JF - Environment international

SN - 0160-4120

ER -

ID: 214682982