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The Functional Significance of Bacterial Predators
Predation structures food webs, influences energy flow, and alters rates and pathways of nutrient cycling through ecosystems, effects that are well documented for macroscopic predators. In the microbial world, predatory bacteria are common, yet little is known about their rates of growth and roles i...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8092244/ https://www.ncbi.nlm.nih.gov/pubmed/33906922 http://dx.doi.org/10.1128/mBio.00466-21 |
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author | Hungate, Bruce A. Marks, Jane C. Power, Mary E. Schwartz, Egbert van Groenigen, Kees Jan Blazewicz, Steven J. Chuckran, Peter Dijkstra, Paul Finley, Brianna K. Firestone, Mary K. Foley, Megan Greenlon, Alex Hayer, Michaela Hofmockel, Kirsten S. Koch, Benjamin J. Mack, Michelle C. Mau, Rebecca L. Miller, Samantha N. Morrissey, Ember M. Propster, Jeffrey R. Purcell, Alicia M. Sieradzki, Ella Starr, Evan P. Stone, Bram W. G. Terrer, César Pett-Ridge, Jennifer |
author_facet | Hungate, Bruce A. Marks, Jane C. Power, Mary E. Schwartz, Egbert van Groenigen, Kees Jan Blazewicz, Steven J. Chuckran, Peter Dijkstra, Paul Finley, Brianna K. Firestone, Mary K. Foley, Megan Greenlon, Alex Hayer, Michaela Hofmockel, Kirsten S. Koch, Benjamin J. Mack, Michelle C. Mau, Rebecca L. Miller, Samantha N. Morrissey, Ember M. Propster, Jeffrey R. Purcell, Alicia M. Sieradzki, Ella Starr, Evan P. Stone, Bram W. G. Terrer, César Pett-Ridge, Jennifer |
author_sort | Hungate, Bruce A. |
collection | PubMed |
description | Predation structures food webs, influences energy flow, and alters rates and pathways of nutrient cycling through ecosystems, effects that are well documented for macroscopic predators. In the microbial world, predatory bacteria are common, yet little is known about their rates of growth and roles in energy flows through microbial food webs, in part because these are difficult to quantify. Here, we show that growth and carbon uptake were higher in predatory bacteria compared to nonpredatory bacteria, a finding across 15 sites, synthesizing 82 experiments and over 100,000 taxon-specific measurements of element flow into newly synthesized bacterial DNA. Obligate predatory bacteria grew 36% faster and assimilated carbon at rates 211% higher than nonpredatory bacteria. These differences were less pronounced for facultative predators (6% higher growth rates, 17% higher carbon assimilation rates), though high growth and carbon assimilation rates were observed for some facultative predators, such as members of the genera Lysobacter and Cytophaga, both capable of gliding motility and wolf-pack hunting behavior. Added carbon substrates disproportionately stimulated growth of obligate predators, with responses 63% higher than those of nonpredators for the Bdellovibrionales and 81% higher for the Vampirovibrionales, whereas responses of facultative predators to substrate addition were no different from those of nonpredators. This finding supports the ecological theory that higher productivity increases predator control of lower trophic levels. These findings also indicate that the functional significance of bacterial predators increases with energy flow and that predatory bacteria influence element flow through microbial food webs. |
format | Online Article Text |
id | pubmed-8092244 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-80922442021-05-04 The Functional Significance of Bacterial Predators Hungate, Bruce A. Marks, Jane C. Power, Mary E. Schwartz, Egbert van Groenigen, Kees Jan Blazewicz, Steven J. Chuckran, Peter Dijkstra, Paul Finley, Brianna K. Firestone, Mary K. Foley, Megan Greenlon, Alex Hayer, Michaela Hofmockel, Kirsten S. Koch, Benjamin J. Mack, Michelle C. Mau, Rebecca L. Miller, Samantha N. Morrissey, Ember M. Propster, Jeffrey R. Purcell, Alicia M. Sieradzki, Ella Starr, Evan P. Stone, Bram W. G. Terrer, César Pett-Ridge, Jennifer mBio Research Article Predation structures food webs, influences energy flow, and alters rates and pathways of nutrient cycling through ecosystems, effects that are well documented for macroscopic predators. In the microbial world, predatory bacteria are common, yet little is known about their rates of growth and roles in energy flows through microbial food webs, in part because these are difficult to quantify. Here, we show that growth and carbon uptake were higher in predatory bacteria compared to nonpredatory bacteria, a finding across 15 sites, synthesizing 82 experiments and over 100,000 taxon-specific measurements of element flow into newly synthesized bacterial DNA. Obligate predatory bacteria grew 36% faster and assimilated carbon at rates 211% higher than nonpredatory bacteria. These differences were less pronounced for facultative predators (6% higher growth rates, 17% higher carbon assimilation rates), though high growth and carbon assimilation rates were observed for some facultative predators, such as members of the genera Lysobacter and Cytophaga, both capable of gliding motility and wolf-pack hunting behavior. Added carbon substrates disproportionately stimulated growth of obligate predators, with responses 63% higher than those of nonpredators for the Bdellovibrionales and 81% higher for the Vampirovibrionales, whereas responses of facultative predators to substrate addition were no different from those of nonpredators. This finding supports the ecological theory that higher productivity increases predator control of lower trophic levels. These findings also indicate that the functional significance of bacterial predators increases with energy flow and that predatory bacteria influence element flow through microbial food webs. American Society for Microbiology 2021-04-27 /pmc/articles/PMC8092244/ /pubmed/33906922 http://dx.doi.org/10.1128/mBio.00466-21 Text en Copyright © 2021 Hungate 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 Hungate, Bruce A. Marks, Jane C. Power, Mary E. Schwartz, Egbert van Groenigen, Kees Jan Blazewicz, Steven J. Chuckran, Peter Dijkstra, Paul Finley, Brianna K. Firestone, Mary K. Foley, Megan Greenlon, Alex Hayer, Michaela Hofmockel, Kirsten S. Koch, Benjamin J. Mack, Michelle C. Mau, Rebecca L. Miller, Samantha N. Morrissey, Ember M. Propster, Jeffrey R. Purcell, Alicia M. Sieradzki, Ella Starr, Evan P. Stone, Bram W. G. Terrer, César Pett-Ridge, Jennifer The Functional Significance of Bacterial Predators |
title | The Functional Significance of Bacterial Predators |
title_full | The Functional Significance of Bacterial Predators |
title_fullStr | The Functional Significance of Bacterial Predators |
title_full_unstemmed | The Functional Significance of Bacterial Predators |
title_short | The Functional Significance of Bacterial Predators |
title_sort | functional significance of bacterial predators |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8092244/ https://www.ncbi.nlm.nih.gov/pubmed/33906922 http://dx.doi.org/10.1128/mBio.00466-21 |
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