A metabolic modeling-based framework for predicting trophic dependencies in native rhizobiomes of crop plants

The exchange of metabolites (i.e., metabolic interactions) between bacteria in the rhizosphere determines various plant-associated functions. Systematically understanding the metabolic interactions in the rhizosphere, as well as in other types of microbial communities, would open the door to the optimization of specific predefined functions of interest, and therefore to the harnessing of the functionality of various types of microbiomes. However, mechanistic knowledge regarding the gathering and interpretation of these interactions is limited. Here, we present a framework utilizing genomics and constraint-based modeling approaches, aiming to interpret the hierarchical trophic interactions in the soil environment. 243 genome scale metabolic models of bacteria associated with a specific disease-suppressive vs disease-conducive apple rhizospheres were drafted based on genome-resolved metagenomes, comprising an in silico native microbial community. Iteratively simulating microbial community members’ growth in a metabolomics-based apple root-like environment produced novel data on potential trophic successions, used to form a network of communal trophic dependencies. Network-based analyses have characterized interactions associated with beneficial vs non-beneficial microbiome functioning, pinpointing specific compounds and microbial species as potential disease supporting and suppressing agents. This framework provides a means for capturing trophic interactions and formulating a range of testable hypotheses regarding the metabolic capabilities of microbial communities within their natural environment. Essentially, it can be applied to different environments and biological landscapes, elucidating the conditions for the targeted manipulation of various microbiomes, and the execution of countless predefined functions.

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Publication Details

Journal
eLife
Published
2024-10-17
DOI
https://doi.org/10.7554/elife.94558.3
Citations
7
Primary Topic
Plant-Microbe Interactions and Immunity
Type
article
Field-Weighted Citation Impact
4.20

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article

A metabolic modeling-based framework for predicting trophic dependencies in native rhizobiomes of crop plants

Ofir Tal, Hanan Eizenberg, Mark Mazzola, Shiri Freilich et al.
7 citations
eLife
Plant-Microbe Interactions and Immunity
4.20
article

A metabolic modeling-based framework for predicting trophic dependencies in native rhizobiomes of crop plants

Ofir Tal, Hanan Eizenberg, Mark Mazzola, Shiri Freilich, Adi Faigenboim‐Doron, Maria Berihu, Alon Avraham Ginatt, Itai Sharon, Gon Carmi, Tracey Somera, Shlomit Medina, Einam Castel, Samir Droby
article en
7 citations

Abstract

The exchange of metabolites (i.e., metabolic interactions) between bacteria in the rhizosphere determines various plant-associated functions. Systematically understanding the metabolic interactions in the rhizosphere, as well as in other types of microbial communities, would open the door to the optimization of specific predefined functions of interest, and therefore to the harnessing of the functionality of various types of microbiomes. However, mechanistic knowledge regarding the gathering and interpretation of these interactions is limited. Here, we present a framework utilizing genomics and constraint-based modeling approaches, aiming to interpret the hierarchical trophic interactions in the soil environment. 243 genome scale metabolic models of bacteria associated with a specific disease-suppressive vs disease-conducive apple rhizospheres were drafted based on genome-resolved metagenomes, comprising an in silico native microbial community. Iteratively simulating microbial community members’ growth in a metabolomics-based apple root-like environment produced novel data on potential trophic successions, used to form a network of communal trophic dependencies. Network-based analyses have characterized interactions associated with beneficial vs non-beneficial microbiome functioning, pinpointing specific compounds and microbial species as potential disease supporting and suppressing agents. This framework provides a means for capturing trophic interactions and formulating a range of testable hypotheses regarding the metabolic capabilities of microbial communities within their natural environment. Essentially, it can be applied to different environments and biological landscapes, elucidating the conditions for the targeted manipulation of various microbiomes, and the execution of countless predefined functions.

eLifeVol. 13
Agricultural Research Service (US), United States Department of Agriculture (US), Hebrew University of Jerusalem (IL), Stellenbosch University (ZA), Western Galilee Hospital (IL), Agricultural Research Organization (IL), Israel Oceanographic and Limnological Research (IL), Tel Hai Academic College (IL)
United States - Israel Binational Agricultural Research and Development Fund
Life in Land
Openalex Percentile: Top 6%
Plant-Microbe Interactions and Immunity
4.20
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