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Global prevalence and distribution of genes and microorganisms involved in mercury methylation
Mercury (Hg) methylation produces the neurotoxic, highly bioaccumulative methylmercury (MeHg). The highly conserved nature of the recently identified Hg methylation genes hgcAB provides a foundation for broadly evaluating spatial and niche-specific patterns of microbial Hg methylation potential in n...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4646819/ https://www.ncbi.nlm.nih.gov/pubmed/26601305 http://dx.doi.org/10.1126/sciadv.1500675 |
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author | Podar, Mircea Gilmour, Cynthia C. Brandt, Craig C. Soren, Allyson Brown, Steven D. Crable, Bryan R. Palumbo, Anthony V. Somenahally, Anil C. Elias, Dwayne A. |
author_facet | Podar, Mircea Gilmour, Cynthia C. Brandt, Craig C. Soren, Allyson Brown, Steven D. Crable, Bryan R. Palumbo, Anthony V. Somenahally, Anil C. Elias, Dwayne A. |
author_sort | Podar, Mircea |
collection | PubMed |
description | Mercury (Hg) methylation produces the neurotoxic, highly bioaccumulative methylmercury (MeHg). The highly conserved nature of the recently identified Hg methylation genes hgcAB provides a foundation for broadly evaluating spatial and niche-specific patterns of microbial Hg methylation potential in nature. We queried hgcAB diversity and distribution in >3500 publicly available microbial metagenomes, encompassing a broad range of environments and generating a new global view of Hg methylation potential. The hgcAB genes were found in nearly all anaerobic (but not aerobic) environments, including oxygenated layers of the open ocean. Critically, hgcAB was effectively absent in ~1500 human and mammalian microbiomes, suggesting a low risk of endogenous MeHg production. New potential methylation habitats were identified, including invertebrate digestive tracts, thawing permafrost soils, coastal “dead zones,” soils, sediments, and extreme environments, suggesting multiple routes for MeHg entry into food webs. Several new taxonomic groups capable of methylating Hg emerged, including lineages having no cultured representatives. Phylogenetic analysis points to an evolutionary relationship between hgcA and genes encoding corrinoid iron-sulfur proteins functioning in the ancient Wood-Ljungdahl carbon fixation pathway, suggesting that methanogenic Archaea may have been the first to perform these biotransformations. |
format | Online Article Text |
id | pubmed-4646819 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-46468192015-11-23 Global prevalence and distribution of genes and microorganisms involved in mercury methylation Podar, Mircea Gilmour, Cynthia C. Brandt, Craig C. Soren, Allyson Brown, Steven D. Crable, Bryan R. Palumbo, Anthony V. Somenahally, Anil C. Elias, Dwayne A. Sci Adv Research Articles Mercury (Hg) methylation produces the neurotoxic, highly bioaccumulative methylmercury (MeHg). The highly conserved nature of the recently identified Hg methylation genes hgcAB provides a foundation for broadly evaluating spatial and niche-specific patterns of microbial Hg methylation potential in nature. We queried hgcAB diversity and distribution in >3500 publicly available microbial metagenomes, encompassing a broad range of environments and generating a new global view of Hg methylation potential. The hgcAB genes were found in nearly all anaerobic (but not aerobic) environments, including oxygenated layers of the open ocean. Critically, hgcAB was effectively absent in ~1500 human and mammalian microbiomes, suggesting a low risk of endogenous MeHg production. New potential methylation habitats were identified, including invertebrate digestive tracts, thawing permafrost soils, coastal “dead zones,” soils, sediments, and extreme environments, suggesting multiple routes for MeHg entry into food webs. Several new taxonomic groups capable of methylating Hg emerged, including lineages having no cultured representatives. Phylogenetic analysis points to an evolutionary relationship between hgcA and genes encoding corrinoid iron-sulfur proteins functioning in the ancient Wood-Ljungdahl carbon fixation pathway, suggesting that methanogenic Archaea may have been the first to perform these biotransformations. American Association for the Advancement of Science 2015-10-09 /pmc/articles/PMC4646819/ /pubmed/26601305 http://dx.doi.org/10.1126/sciadv.1500675 Text en Copyright © 2015, The Authors http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (http://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Research Articles Podar, Mircea Gilmour, Cynthia C. Brandt, Craig C. Soren, Allyson Brown, Steven D. Crable, Bryan R. Palumbo, Anthony V. Somenahally, Anil C. Elias, Dwayne A. Global prevalence and distribution of genes and microorganisms involved in mercury methylation |
title | Global prevalence and distribution of genes and microorganisms involved in mercury methylation |
title_full | Global prevalence and distribution of genes and microorganisms involved in mercury methylation |
title_fullStr | Global prevalence and distribution of genes and microorganisms involved in mercury methylation |
title_full_unstemmed | Global prevalence and distribution of genes and microorganisms involved in mercury methylation |
title_short | Global prevalence and distribution of genes and microorganisms involved in mercury methylation |
title_sort | global prevalence and distribution of genes and microorganisms involved in mercury methylation |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4646819/ https://www.ncbi.nlm.nih.gov/pubmed/26601305 http://dx.doi.org/10.1126/sciadv.1500675 |
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