Cargando…

Genome-resolved metagenomics reveals novel archaeal and bacterial genomes from Amazonian forest and pasture soils

Amazonian soil microbial communities are known to be affected by the forest-to-pasture conversion, but the identity and metabolic potential of most of their organisms remain poorly characterized. To contribute to the understanding of these communities, here we describe metagenome-assembled genomes (...

Descripción completa

Detalles Bibliográficos
Autores principales: Venturini, Andressa M., Gontijo, Júlia B., Mandro, Jéssica A., Paula, Fabiana S., Yoshiura, Caio A., da França, Aline G., Tsai, Siu M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Microbiology Society 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9455692/
https://www.ncbi.nlm.nih.gov/pubmed/35894927
http://dx.doi.org/10.1099/mgen.0.000853
_version_ 1784785633944797184
author Venturini, Andressa M.
Gontijo, Júlia B.
Mandro, Jéssica A.
Paula, Fabiana S.
Yoshiura, Caio A.
da França, Aline G.
Tsai, Siu M.
author_facet Venturini, Andressa M.
Gontijo, Júlia B.
Mandro, Jéssica A.
Paula, Fabiana S.
Yoshiura, Caio A.
da França, Aline G.
Tsai, Siu M.
author_sort Venturini, Andressa M.
collection PubMed
description Amazonian soil microbial communities are known to be affected by the forest-to-pasture conversion, but the identity and metabolic potential of most of their organisms remain poorly characterized. To contribute to the understanding of these communities, here we describe metagenome-assembled genomes (MAGs) recovered from 12 forest and pasture soil metagenomes of the Brazilian Eastern Amazon. We obtained 11 forest and 30 pasture MAGs (≥50% of completeness and ≤10 % of contamination), distributed among two archaeal and 11 bacterial phyla. The taxonomic classification results suggest that most MAGs may represent potential novel microbial taxa. MAGs selected for further evaluation included members of Acidobacteriota , Actinobacteriota , Desulfobacterota_B, Desulfobacterota_F, Dormibacterota, Eremiobacterota , Halobacteriota, Proteobacteria , and Thermoproteota , thus revealing their roles in carbohydrate degradation and mercury detoxification as well as in the sulphur, nitrogen, and methane cycles. A methane-producing Archaea of the genus Methanosarcina was almost exclusively recovered from pasture soils, which can be linked to a sink-to-source shift after the forest-to-pasture conversion. The novel MAGs constitute an important resource to help us unravel the yet-unknown microbial diversity in Amazonian soils and its functional potential and, consequently, the responses of these microorganisms to land-use change.
format Online
Article
Text
id pubmed-9455692
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Microbiology Society
record_format MEDLINE/PubMed
spelling pubmed-94556922022-09-09 Genome-resolved metagenomics reveals novel archaeal and bacterial genomes from Amazonian forest and pasture soils Venturini, Andressa M. Gontijo, Júlia B. Mandro, Jéssica A. Paula, Fabiana S. Yoshiura, Caio A. da França, Aline G. Tsai, Siu M. Microb Genom Short Communications Amazonian soil microbial communities are known to be affected by the forest-to-pasture conversion, but the identity and metabolic potential of most of their organisms remain poorly characterized. To contribute to the understanding of these communities, here we describe metagenome-assembled genomes (MAGs) recovered from 12 forest and pasture soil metagenomes of the Brazilian Eastern Amazon. We obtained 11 forest and 30 pasture MAGs (≥50% of completeness and ≤10 % of contamination), distributed among two archaeal and 11 bacterial phyla. The taxonomic classification results suggest that most MAGs may represent potential novel microbial taxa. MAGs selected for further evaluation included members of Acidobacteriota , Actinobacteriota , Desulfobacterota_B, Desulfobacterota_F, Dormibacterota, Eremiobacterota , Halobacteriota, Proteobacteria , and Thermoproteota , thus revealing their roles in carbohydrate degradation and mercury detoxification as well as in the sulphur, nitrogen, and methane cycles. A methane-producing Archaea of the genus Methanosarcina was almost exclusively recovered from pasture soils, which can be linked to a sink-to-source shift after the forest-to-pasture conversion. The novel MAGs constitute an important resource to help us unravel the yet-unknown microbial diversity in Amazonian soils and its functional potential and, consequently, the responses of these microorganisms to land-use change. Microbiology Society 2022-07-27 /pmc/articles/PMC9455692/ /pubmed/35894927 http://dx.doi.org/10.1099/mgen.0.000853 Text en © 2022 The Authors https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License.
spellingShingle Short Communications
Venturini, Andressa M.
Gontijo, Júlia B.
Mandro, Jéssica A.
Paula, Fabiana S.
Yoshiura, Caio A.
da França, Aline G.
Tsai, Siu M.
Genome-resolved metagenomics reveals novel archaeal and bacterial genomes from Amazonian forest and pasture soils
title Genome-resolved metagenomics reveals novel archaeal and bacterial genomes from Amazonian forest and pasture soils
title_full Genome-resolved metagenomics reveals novel archaeal and bacterial genomes from Amazonian forest and pasture soils
title_fullStr Genome-resolved metagenomics reveals novel archaeal and bacterial genomes from Amazonian forest and pasture soils
title_full_unstemmed Genome-resolved metagenomics reveals novel archaeal and bacterial genomes from Amazonian forest and pasture soils
title_short Genome-resolved metagenomics reveals novel archaeal and bacterial genomes from Amazonian forest and pasture soils
title_sort genome-resolved metagenomics reveals novel archaeal and bacterial genomes from amazonian forest and pasture soils
topic Short Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9455692/
https://www.ncbi.nlm.nih.gov/pubmed/35894927
http://dx.doi.org/10.1099/mgen.0.000853
work_keys_str_mv AT venturiniandressam genomeresolvedmetagenomicsrevealsnovelarchaealandbacterialgenomesfromamazonianforestandpasturesoils
AT gontijojuliab genomeresolvedmetagenomicsrevealsnovelarchaealandbacterialgenomesfromamazonianforestandpasturesoils
AT mandrojessicaa genomeresolvedmetagenomicsrevealsnovelarchaealandbacterialgenomesfromamazonianforestandpasturesoils
AT paulafabianas genomeresolvedmetagenomicsrevealsnovelarchaealandbacterialgenomesfromamazonianforestandpasturesoils
AT yoshiuracaioa genomeresolvedmetagenomicsrevealsnovelarchaealandbacterialgenomesfromamazonianforestandpasturesoils
AT dafrancaalineg genomeresolvedmetagenomicsrevealsnovelarchaealandbacterialgenomesfromamazonianforestandpasturesoils
AT tsaisium genomeresolvedmetagenomicsrevealsnovelarchaealandbacterialgenomesfromamazonianforestandpasturesoils