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Plant-associated fungi support bacterial resilience following water limitation

Drought disrupts soil microbial activity and many biogeochemical processes. Although plant-associated fungi can support plant performance and nutrient cycling during drought, their effects on nearby drought-exposed soil microbial communities are not well resolved. We used H(2)(18)O quantitative stab...

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Autores principales: Hestrin, Rachel, Kan, Megan, Lafler, Marissa, Wollard, Jessica, Kimbrel, Jeffrey A., Ray, Prasun, Blazewicz, Steven J., Stuart, Rhona, Craven, Kelly, Firestone, Mary, Nuccio, Erin E., Pett-Ridge, Jennifer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9666503/
https://www.ncbi.nlm.nih.gov/pubmed/36085516
http://dx.doi.org/10.1038/s41396-022-01308-6
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author Hestrin, Rachel
Kan, Megan
Lafler, Marissa
Wollard, Jessica
Kimbrel, Jeffrey A.
Ray, Prasun
Blazewicz, Steven J.
Stuart, Rhona
Craven, Kelly
Firestone, Mary
Nuccio, Erin E.
Pett-Ridge, Jennifer
author_facet Hestrin, Rachel
Kan, Megan
Lafler, Marissa
Wollard, Jessica
Kimbrel, Jeffrey A.
Ray, Prasun
Blazewicz, Steven J.
Stuart, Rhona
Craven, Kelly
Firestone, Mary
Nuccio, Erin E.
Pett-Ridge, Jennifer
author_sort Hestrin, Rachel
collection PubMed
description Drought disrupts soil microbial activity and many biogeochemical processes. Although plant-associated fungi can support plant performance and nutrient cycling during drought, their effects on nearby drought-exposed soil microbial communities are not well resolved. We used H(2)(18)O quantitative stable isotope probing (qSIP) and 16S rRNA gene profiling to investigate bacterial community dynamics following water limitation in the hyphospheres of two distinct fungal lineages (Rhizophagus irregularis and Serendipita bescii) grown with the bioenergy model grass Panicum hallii. In uninoculated soil, a history of water limitation resulted in significantly lower bacterial growth potential and growth efficiency, as well as lower diversity in the actively growing bacterial community. In contrast, both fungal lineages had a protective effect on hyphosphere bacterial communities exposed to water limitation: bacterial growth potential, growth efficiency, and the diversity of the actively growing bacterial community were not suppressed by a history of water limitation in soils inoculated with either fungus. Despite their similar effects at the community level, the two fungal lineages did elicit different taxon-specific responses, and bacterial growth potential was greater in R. irregularis compared to S. bescii-inoculated soils. Several of the bacterial taxa that responded positively to fungal inocula belong to lineages that are considered drought susceptible. Overall, H(2)(18)O qSIP highlighted treatment effects on bacterial community structure that were less pronounced using traditional 16S rRNA gene profiling. Together, these results indicate that fungal–bacterial synergies may support bacterial resilience to moisture limitation.
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spelling pubmed-96665032022-11-17 Plant-associated fungi support bacterial resilience following water limitation Hestrin, Rachel Kan, Megan Lafler, Marissa Wollard, Jessica Kimbrel, Jeffrey A. Ray, Prasun Blazewicz, Steven J. Stuart, Rhona Craven, Kelly Firestone, Mary Nuccio, Erin E. Pett-Ridge, Jennifer ISME J Article Drought disrupts soil microbial activity and many biogeochemical processes. Although plant-associated fungi can support plant performance and nutrient cycling during drought, their effects on nearby drought-exposed soil microbial communities are not well resolved. We used H(2)(18)O quantitative stable isotope probing (qSIP) and 16S rRNA gene profiling to investigate bacterial community dynamics following water limitation in the hyphospheres of two distinct fungal lineages (Rhizophagus irregularis and Serendipita bescii) grown with the bioenergy model grass Panicum hallii. In uninoculated soil, a history of water limitation resulted in significantly lower bacterial growth potential and growth efficiency, as well as lower diversity in the actively growing bacterial community. In contrast, both fungal lineages had a protective effect on hyphosphere bacterial communities exposed to water limitation: bacterial growth potential, growth efficiency, and the diversity of the actively growing bacterial community were not suppressed by a history of water limitation in soils inoculated with either fungus. Despite their similar effects at the community level, the two fungal lineages did elicit different taxon-specific responses, and bacterial growth potential was greater in R. irregularis compared to S. bescii-inoculated soils. Several of the bacterial taxa that responded positively to fungal inocula belong to lineages that are considered drought susceptible. Overall, H(2)(18)O qSIP highlighted treatment effects on bacterial community structure that were less pronounced using traditional 16S rRNA gene profiling. Together, these results indicate that fungal–bacterial synergies may support bacterial resilience to moisture limitation. Nature Publishing Group UK 2022-09-09 2022-12 /pmc/articles/PMC9666503/ /pubmed/36085516 http://dx.doi.org/10.1038/s41396-022-01308-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This 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/) .
spellingShingle Article
Hestrin, Rachel
Kan, Megan
Lafler, Marissa
Wollard, Jessica
Kimbrel, Jeffrey A.
Ray, Prasun
Blazewicz, Steven J.
Stuart, Rhona
Craven, Kelly
Firestone, Mary
Nuccio, Erin E.
Pett-Ridge, Jennifer
Plant-associated fungi support bacterial resilience following water limitation
title Plant-associated fungi support bacterial resilience following water limitation
title_full Plant-associated fungi support bacterial resilience following water limitation
title_fullStr Plant-associated fungi support bacterial resilience following water limitation
title_full_unstemmed Plant-associated fungi support bacterial resilience following water limitation
title_short Plant-associated fungi support bacterial resilience following water limitation
title_sort plant-associated fungi support bacterial resilience following water limitation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9666503/
https://www.ncbi.nlm.nih.gov/pubmed/36085516
http://dx.doi.org/10.1038/s41396-022-01308-6
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