Cargando…

Rapid remodeling of the soil lipidome in response to a drying-rewetting event

BACKGROUND: Microbiomes contribute to multiple ecosystem services by transforming organic matter in the soil. Extreme shifts in the environment, such as drying-rewetting cycles during drought, can impact the microbial metabolism of organic matter by altering microbial physiology and function. These...

Descripción completa

Detalles Bibliográficos
Autores principales: Couvillion, Sneha P., Danczak, Robert E., Naylor, Dan, Smith, Montana L., Stratton, Kelly G., Paurus, Vanessa L., Bloodsworth, Kent J., Farris, Yuliya, Schmidt, Darren J., Richardson, Rachel E., Bramer, Lisa M., Fansler, Sarah J., Nakayasu, Ernesto S., McDermott, Jason E., Metz, Thomas O., Lipton, Mary S., Jansson, Janet K., Hofmockel, Kirsten S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9969633/
https://www.ncbi.nlm.nih.gov/pubmed/36849975
http://dx.doi.org/10.1186/s40168-022-01427-4
_version_ 1784897773025361920
author Couvillion, Sneha P.
Danczak, Robert E.
Naylor, Dan
Smith, Montana L.
Stratton, Kelly G.
Paurus, Vanessa L.
Bloodsworth, Kent J.
Farris, Yuliya
Schmidt, Darren J.
Richardson, Rachel E.
Bramer, Lisa M.
Fansler, Sarah J.
Nakayasu, Ernesto S.
McDermott, Jason E.
Metz, Thomas O.
Lipton, Mary S.
Jansson, Janet K.
Hofmockel, Kirsten S.
author_facet Couvillion, Sneha P.
Danczak, Robert E.
Naylor, Dan
Smith, Montana L.
Stratton, Kelly G.
Paurus, Vanessa L.
Bloodsworth, Kent J.
Farris, Yuliya
Schmidt, Darren J.
Richardson, Rachel E.
Bramer, Lisa M.
Fansler, Sarah J.
Nakayasu, Ernesto S.
McDermott, Jason E.
Metz, Thomas O.
Lipton, Mary S.
Jansson, Janet K.
Hofmockel, Kirsten S.
author_sort Couvillion, Sneha P.
collection PubMed
description BACKGROUND: Microbiomes contribute to multiple ecosystem services by transforming organic matter in the soil. Extreme shifts in the environment, such as drying-rewetting cycles during drought, can impact the microbial metabolism of organic matter by altering microbial physiology and function. These physiological responses are mediated in part by lipids that are responsible for regulating interactions between cells and the environment. Despite this critical role in regulating the microbial response to stress, little is known about microbial lipids and metabolites in the soil or how they influence phenotypes that are expressed under drying-rewetting cycles. To address this knowledge gap, we conducted a soil incubation experiment to simulate soil drying during a summer drought of an arid grassland, then measured the response of the soil lipidome and metabolome during the first 3 h after wet-up. RESULTS: Reduced nutrient access during soil drying incurred a replacement of membrane phospholipids, resulting in a diminished abundance of multiple phosphorus-rich membrane lipids. The hot and dry conditions increased the prevalence of sphingolipids and lipids containing long-chain polyunsaturated fatty acids, both of which are associated with heat and osmotic stress-mitigating properties in fungi. This novel finding suggests that lipids commonly present in eukaryotes such as fungi may play a significant role in supporting community resilience displayed by arid land soil microbiomes during drought. As early as 10 min after rewetting dry soil, distinct changes were observed in several lipids that had bacterial signatures including a rapid increase in the abundance of glycerophospholipids with saturated and short fatty acid chains, prototypical of bacterial membrane lipids. Polar metabolites including disaccharides, nucleic acids, organic acids, inositols, and amino acids also increased in abundance upon rewetting. This rapid metabolic reactivation and growth after rewetting coincided with an increase in the relative abundance of firmicutes, suggesting that members of this phylum were positively impacted by rewetting. CONCLUSIONS: Our study revealed specific changes in lipids and metabolites that are indicative of stress adaptation, substrate use, and cellular recovery during soil drying and subsequent rewetting. The drought-induced nutrient limitation was reflected in the lipidome and polar metabolome, both of which rapidly shifted (within hours) upon rewet. Reduced nutrient access in dry soil caused the replacement of glycerophospholipids with phosphorus-free lipids and impeded resource-expensive osmolyte accumulation. Elevated levels of ceramides and lipids with long-chain polyunsaturated fatty acids in dry soil suggest that lipids likely play an important role in the drought tolerance of microbial taxa capable of synthesizing these lipids. An increasing abundance of bacterial glycerophospholipids and triacylglycerols with fatty acids typical of bacteria and polar metabolites suggest a metabolic recovery in representative bacteria once the environmental conditions are conducive for growth. These results underscore the importance of the soil lipidome as a robust indicator of microbial community responses, especially at the short time scales of cell-environment reactions. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-022-01427-4.
format Online
Article
Text
id pubmed-9969633
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-99696332023-02-28 Rapid remodeling of the soil lipidome in response to a drying-rewetting event Couvillion, Sneha P. Danczak, Robert E. Naylor, Dan Smith, Montana L. Stratton, Kelly G. Paurus, Vanessa L. Bloodsworth, Kent J. Farris, Yuliya Schmidt, Darren J. Richardson, Rachel E. Bramer, Lisa M. Fansler, Sarah J. Nakayasu, Ernesto S. McDermott, Jason E. Metz, Thomas O. Lipton, Mary S. Jansson, Janet K. Hofmockel, Kirsten S. Microbiome Research BACKGROUND: Microbiomes contribute to multiple ecosystem services by transforming organic matter in the soil. Extreme shifts in the environment, such as drying-rewetting cycles during drought, can impact the microbial metabolism of organic matter by altering microbial physiology and function. These physiological responses are mediated in part by lipids that are responsible for regulating interactions between cells and the environment. Despite this critical role in regulating the microbial response to stress, little is known about microbial lipids and metabolites in the soil or how they influence phenotypes that are expressed under drying-rewetting cycles. To address this knowledge gap, we conducted a soil incubation experiment to simulate soil drying during a summer drought of an arid grassland, then measured the response of the soil lipidome and metabolome during the first 3 h after wet-up. RESULTS: Reduced nutrient access during soil drying incurred a replacement of membrane phospholipids, resulting in a diminished abundance of multiple phosphorus-rich membrane lipids. The hot and dry conditions increased the prevalence of sphingolipids and lipids containing long-chain polyunsaturated fatty acids, both of which are associated with heat and osmotic stress-mitigating properties in fungi. This novel finding suggests that lipids commonly present in eukaryotes such as fungi may play a significant role in supporting community resilience displayed by arid land soil microbiomes during drought. As early as 10 min after rewetting dry soil, distinct changes were observed in several lipids that had bacterial signatures including a rapid increase in the abundance of glycerophospholipids with saturated and short fatty acid chains, prototypical of bacterial membrane lipids. Polar metabolites including disaccharides, nucleic acids, organic acids, inositols, and amino acids also increased in abundance upon rewetting. This rapid metabolic reactivation and growth after rewetting coincided with an increase in the relative abundance of firmicutes, suggesting that members of this phylum were positively impacted by rewetting. CONCLUSIONS: Our study revealed specific changes in lipids and metabolites that are indicative of stress adaptation, substrate use, and cellular recovery during soil drying and subsequent rewetting. The drought-induced nutrient limitation was reflected in the lipidome and polar metabolome, both of which rapidly shifted (within hours) upon rewet. Reduced nutrient access in dry soil caused the replacement of glycerophospholipids with phosphorus-free lipids and impeded resource-expensive osmolyte accumulation. Elevated levels of ceramides and lipids with long-chain polyunsaturated fatty acids in dry soil suggest that lipids likely play an important role in the drought tolerance of microbial taxa capable of synthesizing these lipids. An increasing abundance of bacterial glycerophospholipids and triacylglycerols with fatty acids typical of bacteria and polar metabolites suggest a metabolic recovery in representative bacteria once the environmental conditions are conducive for growth. These results underscore the importance of the soil lipidome as a robust indicator of microbial community responses, especially at the short time scales of cell-environment reactions. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-022-01427-4. BioMed Central 2023-02-27 /pmc/articles/PMC9969633/ /pubmed/36849975 http://dx.doi.org/10.1186/s40168-022-01427-4 Text en © © Battelle Memorial Institute 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Couvillion, Sneha P.
Danczak, Robert E.
Naylor, Dan
Smith, Montana L.
Stratton, Kelly G.
Paurus, Vanessa L.
Bloodsworth, Kent J.
Farris, Yuliya
Schmidt, Darren J.
Richardson, Rachel E.
Bramer, Lisa M.
Fansler, Sarah J.
Nakayasu, Ernesto S.
McDermott, Jason E.
Metz, Thomas O.
Lipton, Mary S.
Jansson, Janet K.
Hofmockel, Kirsten S.
Rapid remodeling of the soil lipidome in response to a drying-rewetting event
title Rapid remodeling of the soil lipidome in response to a drying-rewetting event
title_full Rapid remodeling of the soil lipidome in response to a drying-rewetting event
title_fullStr Rapid remodeling of the soil lipidome in response to a drying-rewetting event
title_full_unstemmed Rapid remodeling of the soil lipidome in response to a drying-rewetting event
title_short Rapid remodeling of the soil lipidome in response to a drying-rewetting event
title_sort rapid remodeling of the soil lipidome in response to a drying-rewetting event
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9969633/
https://www.ncbi.nlm.nih.gov/pubmed/36849975
http://dx.doi.org/10.1186/s40168-022-01427-4
work_keys_str_mv AT couvillionsnehap rapidremodelingofthesoillipidomeinresponsetoadryingrewettingevent
AT danczakroberte rapidremodelingofthesoillipidomeinresponsetoadryingrewettingevent
AT naylordan rapidremodelingofthesoillipidomeinresponsetoadryingrewettingevent
AT smithmontanal rapidremodelingofthesoillipidomeinresponsetoadryingrewettingevent
AT strattonkellyg rapidremodelingofthesoillipidomeinresponsetoadryingrewettingevent
AT paurusvanessal rapidremodelingofthesoillipidomeinresponsetoadryingrewettingevent
AT bloodsworthkentj rapidremodelingofthesoillipidomeinresponsetoadryingrewettingevent
AT farrisyuliya rapidremodelingofthesoillipidomeinresponsetoadryingrewettingevent
AT schmidtdarrenj rapidremodelingofthesoillipidomeinresponsetoadryingrewettingevent
AT richardsonrachele rapidremodelingofthesoillipidomeinresponsetoadryingrewettingevent
AT bramerlisam rapidremodelingofthesoillipidomeinresponsetoadryingrewettingevent
AT fanslersarahj rapidremodelingofthesoillipidomeinresponsetoadryingrewettingevent
AT nakayasuernestos rapidremodelingofthesoillipidomeinresponsetoadryingrewettingevent
AT mcdermottjasone rapidremodelingofthesoillipidomeinresponsetoadryingrewettingevent
AT metzthomaso rapidremodelingofthesoillipidomeinresponsetoadryingrewettingevent
AT liptonmarys rapidremodelingofthesoillipidomeinresponsetoadryingrewettingevent
AT janssonjanetk rapidremodelingofthesoillipidomeinresponsetoadryingrewettingevent
AT hofmockelkirstens rapidremodelingofthesoillipidomeinresponsetoadryingrewettingevent