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Responses of Coastal Marine Microbiomes Exposed to Anthropogenic Dissolved Organic Carbon

[Image: see text] Coastal seawaters receive thousands of organic pollutants. However, we have little understanding of the response of microbiomes to this pool of anthropogenic dissolved organic carbon (ADOC). In this study, coastal microbial communities were challenged with ADOC at environmentally r...

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Autores principales: Cerro-Gálvez, Elena, Dachs, Jordi, Lundin, Daniel, Fernández-Pinos, María-Carmen, Sebastián, Marta, Vila-Costa, Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8491159/
https://www.ncbi.nlm.nih.gov/pubmed/33606522
http://dx.doi.org/10.1021/acs.est.0c07262
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author Cerro-Gálvez, Elena
Dachs, Jordi
Lundin, Daniel
Fernández-Pinos, María-Carmen
Sebastián, Marta
Vila-Costa, Maria
author_facet Cerro-Gálvez, Elena
Dachs, Jordi
Lundin, Daniel
Fernández-Pinos, María-Carmen
Sebastián, Marta
Vila-Costa, Maria
author_sort Cerro-Gálvez, Elena
collection PubMed
description [Image: see text] Coastal seawaters receive thousands of organic pollutants. However, we have little understanding of the response of microbiomes to this pool of anthropogenic dissolved organic carbon (ADOC). In this study, coastal microbial communities were challenged with ADOC at environmentally relevant concentrations. Experiments were performed at two Mediterranean sites with different impact by pollutants and nutrients: off the Barcelona harbor (“BCN”), and at the Blanes Bay (“BL”). ADOC additions stimulated prokaryotic leucine incorporation rates at both sites, indicating the use of ADOC as growth substrate. The percentage of “membrane-compromised” cells increased with increasing ADOC, indicating concurrent toxic effects of ADOC. Metagenomic analysis of the BCN community challenged with ADOC showed a significant growth of Methylophaga and other gammaproteobacterial taxa belonging to the rare biosphere. Gene expression profiles showed a taxon-dependent response, with significantly enrichments of transcripts from SAR11 and Glaciecola spp. in BCN and BL, respectively. Further, the relative abundance of transposon-related genes (in BCN) and transcripts (in BL) correlated with the number of differentially abundant genes (in BCN) and transcripts (in BLA), suggesting that microbial responses to pollution may be related to pre-exposure to pollutants, with transposons playing a role in adaptation to ADOC. Our results point to a taxon-specific response to low concentrations of ADOC that impact the functionality, structure and plasticity of the communities in coastal seawaters. This work contributes to address the influence of pollutants on microbiomes and their perturbation to ecosystem services and ocean health.
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spelling pubmed-84911592021-10-05 Responses of Coastal Marine Microbiomes Exposed to Anthropogenic Dissolved Organic Carbon Cerro-Gálvez, Elena Dachs, Jordi Lundin, Daniel Fernández-Pinos, María-Carmen Sebastián, Marta Vila-Costa, Maria Environ Sci Technol [Image: see text] Coastal seawaters receive thousands of organic pollutants. However, we have little understanding of the response of microbiomes to this pool of anthropogenic dissolved organic carbon (ADOC). In this study, coastal microbial communities were challenged with ADOC at environmentally relevant concentrations. Experiments were performed at two Mediterranean sites with different impact by pollutants and nutrients: off the Barcelona harbor (“BCN”), and at the Blanes Bay (“BL”). ADOC additions stimulated prokaryotic leucine incorporation rates at both sites, indicating the use of ADOC as growth substrate. The percentage of “membrane-compromised” cells increased with increasing ADOC, indicating concurrent toxic effects of ADOC. Metagenomic analysis of the BCN community challenged with ADOC showed a significant growth of Methylophaga and other gammaproteobacterial taxa belonging to the rare biosphere. Gene expression profiles showed a taxon-dependent response, with significantly enrichments of transcripts from SAR11 and Glaciecola spp. in BCN and BL, respectively. Further, the relative abundance of transposon-related genes (in BCN) and transcripts (in BL) correlated with the number of differentially abundant genes (in BCN) and transcripts (in BLA), suggesting that microbial responses to pollution may be related to pre-exposure to pollutants, with transposons playing a role in adaptation to ADOC. Our results point to a taxon-specific response to low concentrations of ADOC that impact the functionality, structure and plasticity of the communities in coastal seawaters. This work contributes to address the influence of pollutants on microbiomes and their perturbation to ecosystem services and ocean health. American Chemical Society 2021-02-19 2021-07-20 /pmc/articles/PMC8491159/ /pubmed/33606522 http://dx.doi.org/10.1021/acs.est.0c07262 Text en © 2021 American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Cerro-Gálvez, Elena
Dachs, Jordi
Lundin, Daniel
Fernández-Pinos, María-Carmen
Sebastián, Marta
Vila-Costa, Maria
Responses of Coastal Marine Microbiomes Exposed to Anthropogenic Dissolved Organic Carbon
title Responses of Coastal Marine Microbiomes Exposed to Anthropogenic Dissolved Organic Carbon
title_full Responses of Coastal Marine Microbiomes Exposed to Anthropogenic Dissolved Organic Carbon
title_fullStr Responses of Coastal Marine Microbiomes Exposed to Anthropogenic Dissolved Organic Carbon
title_full_unstemmed Responses of Coastal Marine Microbiomes Exposed to Anthropogenic Dissolved Organic Carbon
title_short Responses of Coastal Marine Microbiomes Exposed to Anthropogenic Dissolved Organic Carbon
title_sort responses of coastal marine microbiomes exposed to anthropogenic dissolved organic carbon
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8491159/
https://www.ncbi.nlm.nih.gov/pubmed/33606522
http://dx.doi.org/10.1021/acs.est.0c07262
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