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Genomic and Transcriptomic Changes That Mediate Increased Platinum Resistance in Cupriavidus metallidurans

The extensive anthropogenic use of platinum, a rare element found in low natural abundance in the Earth’s continental crust and one of the critical raw materials in the EU innovation partnership framework, has resulted in increased concentrations in surface environments. To minimize its spread and i...

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Autores principales: Ali, Md Muntasir, Provoost, Ann, Maertens, Laurens, Leys, Natalie, Monsieurs, Pieter, Charlier, Daniel, Van Houdt, Rob
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6357080/
https://www.ncbi.nlm.nih.gov/pubmed/30669395
http://dx.doi.org/10.3390/genes10010063
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author Ali, Md Muntasir
Provoost, Ann
Maertens, Laurens
Leys, Natalie
Monsieurs, Pieter
Charlier, Daniel
Van Houdt, Rob
author_facet Ali, Md Muntasir
Provoost, Ann
Maertens, Laurens
Leys, Natalie
Monsieurs, Pieter
Charlier, Daniel
Van Houdt, Rob
author_sort Ali, Md Muntasir
collection PubMed
description The extensive anthropogenic use of platinum, a rare element found in low natural abundance in the Earth’s continental crust and one of the critical raw materials in the EU innovation partnership framework, has resulted in increased concentrations in surface environments. To minimize its spread and increase its recovery from the environment, biological recovery via different microbial systems is explored. In contrast, studies focusing on the effects of prolonged exposure to Pt are limited. In this study, we used the metal-resistant Cupriavidus metallidurans NA4 strain to explore the adaptation of environmental bacteria to platinum exposure. We used a combined Nanopore–Illumina sequencing approach to fully resolve all six replicons of the C. metallidurans NA4 genome, and compared them with the C. metallidurans CH34 genome, revealing an important role in metal resistance for its chromid rather than its megaplasmids. In addition, we identified the genomic and transcriptomic changes in a laboratory-evolved strain, displaying resistance to 160 µM Pt(4+). The latter carried 20 mutations, including a large 69.9 kb deletion in its plasmid pNA4_D (89.6 kb in size), and 226 differentially-expressed genes compared to its parental strain. Many membrane-related processes were affected, including up-regulation of cytochrome c and a lytic transglycosylase, down-regulation of flagellar and pili-related genes, and loss of the pNA4_D conjugative machinery, pointing towards a significant role in the adaptation to platinum.
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spelling pubmed-63570802019-02-04 Genomic and Transcriptomic Changes That Mediate Increased Platinum Resistance in Cupriavidus metallidurans Ali, Md Muntasir Provoost, Ann Maertens, Laurens Leys, Natalie Monsieurs, Pieter Charlier, Daniel Van Houdt, Rob Genes (Basel) Article The extensive anthropogenic use of platinum, a rare element found in low natural abundance in the Earth’s continental crust and one of the critical raw materials in the EU innovation partnership framework, has resulted in increased concentrations in surface environments. To minimize its spread and increase its recovery from the environment, biological recovery via different microbial systems is explored. In contrast, studies focusing on the effects of prolonged exposure to Pt are limited. In this study, we used the metal-resistant Cupriavidus metallidurans NA4 strain to explore the adaptation of environmental bacteria to platinum exposure. We used a combined Nanopore–Illumina sequencing approach to fully resolve all six replicons of the C. metallidurans NA4 genome, and compared them with the C. metallidurans CH34 genome, revealing an important role in metal resistance for its chromid rather than its megaplasmids. In addition, we identified the genomic and transcriptomic changes in a laboratory-evolved strain, displaying resistance to 160 µM Pt(4+). The latter carried 20 mutations, including a large 69.9 kb deletion in its plasmid pNA4_D (89.6 kb in size), and 226 differentially-expressed genes compared to its parental strain. Many membrane-related processes were affected, including up-regulation of cytochrome c and a lytic transglycosylase, down-regulation of flagellar and pili-related genes, and loss of the pNA4_D conjugative machinery, pointing towards a significant role in the adaptation to platinum. MDPI 2019-01-18 /pmc/articles/PMC6357080/ /pubmed/30669395 http://dx.doi.org/10.3390/genes10010063 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Ali, Md Muntasir
Provoost, Ann
Maertens, Laurens
Leys, Natalie
Monsieurs, Pieter
Charlier, Daniel
Van Houdt, Rob
Genomic and Transcriptomic Changes That Mediate Increased Platinum Resistance in Cupriavidus metallidurans
title Genomic and Transcriptomic Changes That Mediate Increased Platinum Resistance in Cupriavidus metallidurans
title_full Genomic and Transcriptomic Changes That Mediate Increased Platinum Resistance in Cupriavidus metallidurans
title_fullStr Genomic and Transcriptomic Changes That Mediate Increased Platinum Resistance in Cupriavidus metallidurans
title_full_unstemmed Genomic and Transcriptomic Changes That Mediate Increased Platinum Resistance in Cupriavidus metallidurans
title_short Genomic and Transcriptomic Changes That Mediate Increased Platinum Resistance in Cupriavidus metallidurans
title_sort genomic and transcriptomic changes that mediate increased platinum resistance in cupriavidus metallidurans
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6357080/
https://www.ncbi.nlm.nih.gov/pubmed/30669395
http://dx.doi.org/10.3390/genes10010063
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