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Multi-environment ecogenomics analysis of the cosmopolitan phylum Gemmatimonadota

Gemmatimonadota is a diverse bacterial phylum commonly found in environments such as soils, rhizospheres, fresh waters, and sediments. So far, the phylum contains just six cultured species (five of them sequenced), which limits our understanding of their diversity and metabolism. Therefore, we analy...

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Autores principales: Mujakić, Izabela, Cabello-Yeves, Pedro J., Villena-Alemany, Cristian, Piwosz, Kasia, Rodriguez-Valera, Francisco, Picazo, Antonio, Camacho, Antonio, Koblížek, Michal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10581226/
https://www.ncbi.nlm.nih.gov/pubmed/37732776
http://dx.doi.org/10.1128/spectrum.01112-23
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author Mujakić, Izabela
Cabello-Yeves, Pedro J.
Villena-Alemany, Cristian
Piwosz, Kasia
Rodriguez-Valera, Francisco
Picazo, Antonio
Camacho, Antonio
Koblížek, Michal
author_facet Mujakić, Izabela
Cabello-Yeves, Pedro J.
Villena-Alemany, Cristian
Piwosz, Kasia
Rodriguez-Valera, Francisco
Picazo, Antonio
Camacho, Antonio
Koblížek, Michal
author_sort Mujakić, Izabela
collection PubMed
description Gemmatimonadota is a diverse bacterial phylum commonly found in environments such as soils, rhizospheres, fresh waters, and sediments. So far, the phylum contains just six cultured species (five of them sequenced), which limits our understanding of their diversity and metabolism. Therefore, we analyzed over 400 metagenome-assembled genomes (MAGs) and 5 culture-derived genomes representing Gemmatimonadota from various aquatic environments, hydrothermal vents, sediments, soils, and host-associated (with marine sponges and coral) species. The principal coordinate analysis based on the presence/absence of genes in Gemmatimonadota genomes and phylogenomic analysis documented that marine and host-associated Gemmatimonadota were the most distant from freshwater and wastewater species. A smaller genome size and coding sequences (CDS) number reduction were observed in marine MAGs, pointing to an oligotrophic environmental adaptation. Several metabolic pathways are restricted to specific environments. For example, genes for anoxygenic phototrophy were found only in freshwater, wastewater, and soda lake sediment genomes. There were several genomes from soda lake sediments and wastewater containing type IC/ID ribulose-1,5-bisphosphate carboxylase/oxygenase (RuBisCO). Various genomes from wastewater harbored bacterial type II RuBisCO, whereas RuBisCO-like protein was found in genomes from fresh waters, soil, host-associated, and marine sediments. Gemmatimonadota does not contain nitrogen fixation genes; however, the nosZ gene, involved in the reduction of N(2)O, was present in genomes from most environments, missing only in marine water and host-associated Gemmatimonadota. The presented data suggest that Gemmatimonadota evolved as an organotrophic species relying on aerobic respiration and then remodeled its genome inventory when adapting to particular environments. IMPORTANCE: Gemmatimonadota is a rarely studied bacterial phylum consisting of a handful of cultured species. Recent culture-independent studies documented that these organisms are distributed in many environments, including soil, marine, fresh, and waste waters. However, due to the lack of cultured species, information about their metabolic potential and environmental role is scarce. Therefore, we collected Gemmatimonadota metagenome-assembled genomes (MAGs) from different habitats and performed a systematic analysis of their genomic characteristics and metabolic potential. Our results show how Gemmatimonadota have adapted their genomes to different environments.
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spelling pubmed-105812262023-10-18 Multi-environment ecogenomics analysis of the cosmopolitan phylum Gemmatimonadota Mujakić, Izabela Cabello-Yeves, Pedro J. Villena-Alemany, Cristian Piwosz, Kasia Rodriguez-Valera, Francisco Picazo, Antonio Camacho, Antonio Koblížek, Michal Microbiol Spectr Research Article Gemmatimonadota is a diverse bacterial phylum commonly found in environments such as soils, rhizospheres, fresh waters, and sediments. So far, the phylum contains just six cultured species (five of them sequenced), which limits our understanding of their diversity and metabolism. Therefore, we analyzed over 400 metagenome-assembled genomes (MAGs) and 5 culture-derived genomes representing Gemmatimonadota from various aquatic environments, hydrothermal vents, sediments, soils, and host-associated (with marine sponges and coral) species. The principal coordinate analysis based on the presence/absence of genes in Gemmatimonadota genomes and phylogenomic analysis documented that marine and host-associated Gemmatimonadota were the most distant from freshwater and wastewater species. A smaller genome size and coding sequences (CDS) number reduction were observed in marine MAGs, pointing to an oligotrophic environmental adaptation. Several metabolic pathways are restricted to specific environments. For example, genes for anoxygenic phototrophy were found only in freshwater, wastewater, and soda lake sediment genomes. There were several genomes from soda lake sediments and wastewater containing type IC/ID ribulose-1,5-bisphosphate carboxylase/oxygenase (RuBisCO). Various genomes from wastewater harbored bacterial type II RuBisCO, whereas RuBisCO-like protein was found in genomes from fresh waters, soil, host-associated, and marine sediments. Gemmatimonadota does not contain nitrogen fixation genes; however, the nosZ gene, involved in the reduction of N(2)O, was present in genomes from most environments, missing only in marine water and host-associated Gemmatimonadota. The presented data suggest that Gemmatimonadota evolved as an organotrophic species relying on aerobic respiration and then remodeled its genome inventory when adapting to particular environments. IMPORTANCE: Gemmatimonadota is a rarely studied bacterial phylum consisting of a handful of cultured species. Recent culture-independent studies documented that these organisms are distributed in many environments, including soil, marine, fresh, and waste waters. However, due to the lack of cultured species, information about their metabolic potential and environmental role is scarce. Therefore, we collected Gemmatimonadota metagenome-assembled genomes (MAGs) from different habitats and performed a systematic analysis of their genomic characteristics and metabolic potential. Our results show how Gemmatimonadota have adapted their genomes to different environments. American Society for Microbiology 2023-09-21 /pmc/articles/PMC10581226/ /pubmed/37732776 http://dx.doi.org/10.1128/spectrum.01112-23 Text en Copyright © 2023 Mujakic et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Mujakić, Izabela
Cabello-Yeves, Pedro J.
Villena-Alemany, Cristian
Piwosz, Kasia
Rodriguez-Valera, Francisco
Picazo, Antonio
Camacho, Antonio
Koblížek, Michal
Multi-environment ecogenomics analysis of the cosmopolitan phylum Gemmatimonadota
title Multi-environment ecogenomics analysis of the cosmopolitan phylum Gemmatimonadota
title_full Multi-environment ecogenomics analysis of the cosmopolitan phylum Gemmatimonadota
title_fullStr Multi-environment ecogenomics analysis of the cosmopolitan phylum Gemmatimonadota
title_full_unstemmed Multi-environment ecogenomics analysis of the cosmopolitan phylum Gemmatimonadota
title_short Multi-environment ecogenomics analysis of the cosmopolitan phylum Gemmatimonadota
title_sort multi-environment ecogenomics analysis of the cosmopolitan phylum gemmatimonadota
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10581226/
https://www.ncbi.nlm.nih.gov/pubmed/37732776
http://dx.doi.org/10.1128/spectrum.01112-23
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