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Two-tiered mutualism improves survival and competitiveness of cross-feeding soil bacteria

Metabolic cross-feeding is a pervasive microbial interaction type that affects community stability and functioning and directs carbon and energy flows. The mechanisms that underlie these interactions and their association with metal/metalloid biogeochemistry, however, remain poorly understood. Here,...

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Autores principales: Ge, Zhan-Biao, Zhai, Zhi-Qiang, Xie, Wan-Ying, Dai, Jun, Huang, Ke, Johnson, David R., Zhao, Fang-Jie, Wang, Peng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10579247/
https://www.ncbi.nlm.nih.gov/pubmed/37737252
http://dx.doi.org/10.1038/s41396-023-01519-5
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author Ge, Zhan-Biao
Zhai, Zhi-Qiang
Xie, Wan-Ying
Dai, Jun
Huang, Ke
Johnson, David R.
Zhao, Fang-Jie
Wang, Peng
author_facet Ge, Zhan-Biao
Zhai, Zhi-Qiang
Xie, Wan-Ying
Dai, Jun
Huang, Ke
Johnson, David R.
Zhao, Fang-Jie
Wang, Peng
author_sort Ge, Zhan-Biao
collection PubMed
description Metabolic cross-feeding is a pervasive microbial interaction type that affects community stability and functioning and directs carbon and energy flows. The mechanisms that underlie these interactions and their association with metal/metalloid biogeochemistry, however, remain poorly understood. Here, we identified two soil bacteria, Bacillus sp. BP-3 and Delftia sp. DT-2, that engage in a two-tiered mutualism. Strain BP-3 has low utilization ability of pyruvic acid while strain DT-2 lacks hexokinase, lacks a phosphotransferase system, and is defective in glucose utilization. When strain BP-3 is grown in isolation with glucose, it releases pyruvic acid to the environment resulting in acidification and eventual self-killing. However, when strain BP-3 is grown together with strain DT-2, strain DT-2 utilizes the released pyruvic acid to meet its energy requirements, consequently rescuing strain BP-3 from pyruvic acid-induced growth inhibition. The two bacteria further enhance their collective competitiveness against other microbes by using arsenic as a weapon. Strain DT-2 reduces relatively non-toxic methylarsenate [MAs(V)] to highly toxic methylarsenite [MAs(III)], which kills or suppresses competitors, while strain BP-3 detoxifies MAs(III) by methylation to non-toxic dimethylarsenate [DMAs(V)]. These two arsenic transformations are enhanced when strains DT-2 and BP-3 are grown together. The two strains, along with their close relatives, widely co-occur in soils and their abundances increase with the soil arsenic concentration. Our results reveal that these bacterial types employ a two-tiered mutualism to ensure their collective metabolic activity and maintain their ecological competitive against other soil microbes. These findings shed light on the intricateness of bacterial interactions and their roles in ecosystem functioning.
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spelling pubmed-105792472023-10-18 Two-tiered mutualism improves survival and competitiveness of cross-feeding soil bacteria Ge, Zhan-Biao Zhai, Zhi-Qiang Xie, Wan-Ying Dai, Jun Huang, Ke Johnson, David R. Zhao, Fang-Jie Wang, Peng ISME J Article Metabolic cross-feeding is a pervasive microbial interaction type that affects community stability and functioning and directs carbon and energy flows. The mechanisms that underlie these interactions and their association with metal/metalloid biogeochemistry, however, remain poorly understood. Here, we identified two soil bacteria, Bacillus sp. BP-3 and Delftia sp. DT-2, that engage in a two-tiered mutualism. Strain BP-3 has low utilization ability of pyruvic acid while strain DT-2 lacks hexokinase, lacks a phosphotransferase system, and is defective in glucose utilization. When strain BP-3 is grown in isolation with glucose, it releases pyruvic acid to the environment resulting in acidification and eventual self-killing. However, when strain BP-3 is grown together with strain DT-2, strain DT-2 utilizes the released pyruvic acid to meet its energy requirements, consequently rescuing strain BP-3 from pyruvic acid-induced growth inhibition. The two bacteria further enhance their collective competitiveness against other microbes by using arsenic as a weapon. Strain DT-2 reduces relatively non-toxic methylarsenate [MAs(V)] to highly toxic methylarsenite [MAs(III)], which kills or suppresses competitors, while strain BP-3 detoxifies MAs(III) by methylation to non-toxic dimethylarsenate [DMAs(V)]. These two arsenic transformations are enhanced when strains DT-2 and BP-3 are grown together. The two strains, along with their close relatives, widely co-occur in soils and their abundances increase with the soil arsenic concentration. Our results reveal that these bacterial types employ a two-tiered mutualism to ensure their collective metabolic activity and maintain their ecological competitive against other soil microbes. These findings shed light on the intricateness of bacterial interactions and their roles in ecosystem functioning. Nature Publishing Group UK 2023-09-22 2023-11 /pmc/articles/PMC10579247/ /pubmed/37737252 http://dx.doi.org/10.1038/s41396-023-01519-5 Text en © The Author(s) 2023 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
Ge, Zhan-Biao
Zhai, Zhi-Qiang
Xie, Wan-Ying
Dai, Jun
Huang, Ke
Johnson, David R.
Zhao, Fang-Jie
Wang, Peng
Two-tiered mutualism improves survival and competitiveness of cross-feeding soil bacteria
title Two-tiered mutualism improves survival and competitiveness of cross-feeding soil bacteria
title_full Two-tiered mutualism improves survival and competitiveness of cross-feeding soil bacteria
title_fullStr Two-tiered mutualism improves survival and competitiveness of cross-feeding soil bacteria
title_full_unstemmed Two-tiered mutualism improves survival and competitiveness of cross-feeding soil bacteria
title_short Two-tiered mutualism improves survival and competitiveness of cross-feeding soil bacteria
title_sort two-tiered mutualism improves survival and competitiveness of cross-feeding soil bacteria
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10579247/
https://www.ncbi.nlm.nih.gov/pubmed/37737252
http://dx.doi.org/10.1038/s41396-023-01519-5
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