Life history strategies among soil bacteria-dichotomy for few, continuum for many.

Bram W G Stone, Paul Dijkstra, Brianna K Finley, Raina Fitzpatrick, Megan M Foley, Michaela Hayer, Kirsten S Hofmockel, Benjamin J Koch, Junhui Li, Xiao Jun A Liu, Ayla Martinez, Rebecca L Mau, Jane Marks, Victoria Monsaint-Queeney, Ember M Morrissey, Jeffrey Propster, Jennifer Pett-Ridge, Alicia M Purcell, Egbert Schwartz, Bruce A Hungate

Journal: The ISME journal 2023;17(4):611-619

PMID: 36732614

Abstract

Study of life history strategies may help predict the performance of microorganisms in nature by organizing the complexity of microbial communities into groups of organisms with similar strategies. Here, we tested the extent that one common application of life history theory, the copiotroph-oligotroph framework, could predict the relative population growth rate of bacterial taxa in soils from four different ecosystems. We measured the change of in situ relative growth rate to added glucose and ammonium using both O-HO and C quantitative stable isotope probing to test whether bacterial taxa sorted into copiotrophic and oligotrophic groups. We saw considerable overlap in nutrient responses across most bacteria regardless of phyla, with many taxa growing slowly and few taxa that grew quickly. To define plausible life history boundaries based on in situ relative growth rates, we applied Gaussian mixture models to organisms' joint O-C signatures and found that across experimental replicates, few taxa could consistently be assigned as copiotrophs, despite their potential for fast growth. When life history classifications were assigned based on average relative growth rate at varying taxonomic levels, finer resolutions (e.g., genus level) were significantly more effective in capturing changes in nutrient response than broad taxonomic resolution (e.g., phylum level). Our results demonstrate the difficulty in generalizing bacterial life history strategies to broad lineages, and even to single organisms across a range of soils and experimental conditions. We conclude that there is a continued need for the direct measurement of microbial communities in soil to advance ecologically realistic frameworks.

© 2023. Battelle Memorial Institute.

Address: Earth and Biological Sciences Directorate, Pacific Northwest National Lab, Richland, WA, USA. [email protected].; Center for Ecosystem Science and Society, Northern Arizona University, Flagstaff, AZ, USA. [email protected].; Center for Ecosystem Science and Society, Northern Arizona University, Flagstaff, AZ, USA.; Department of Biological Sciences, Northern Arizona University, Flagstaff, AZ, USA.; Department of Ecology and Evolutionary Biology, University of California, Irvine, CA, USA.; Center for Ecosystem Science and Society, Northern Arizona University, Flagstaff, AZ, USA.; Earth and Biological Sciences Directorate, Pacific Northwest National Lab, Richland, WA, USA.; Department of Agronomy, Iowa State University, Ames, IA, USA.; Center for Ecosystem Science and Society, Northern Arizona University, Flagstaff, AZ, USA.; APC Microbiome Ireland and School of Microbiology, University College Cork, Cork, Ireland.; Institute for Environmental Genomics, Department of Microbiology and Plant Biology, University of Oklahoma, Norman, OK, USA.; Division of Plant and Soil Sciences, West Virginia University, Morgantown, WV, USA.; Physical and Life Sciences Directorate, Lawrence Livermore National Lab, Livermore, CA, USA.; Life and Environmental Sciences Department, University of California Merced, Merced, CA, USA.; Center for Ecosystem Science and Society, Northern Arizona University, Flagstaff, AZ, USA.; Department of Biological Sciences, Northern Arizona University, Flagstaff, AZ, USA.; Department of Biological Sciences, Texas Tech University, Lubbock, TX, USA.
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