Abstract

Over the last century, leaps in technology for imaging, sampling, detection, high-throughput sequencing, and -omics analyses have revolutionized microbial ecology to enable rapid acquisition of extensive datasets for microbial communities across the ever-increasing temporal and spatial scales. The present challenge is capitalizing on our enhanced abilities of observation and integrating diverse data types from different scales, resolutions, and disciplines to reach a causal and mechanistic understanding of how microbial communities transform and respond to perturbations in the environment. This type of causal and mechanistic understanding will make predictions of microbial community behavior more robust and actionable in addressing microbially mediated global problems. To discern drivers of microbial community assembly and function, we recognize the need for a conceptual, quantitative framework that connects measurements of genomic potential, the environment, and ecological and physical forces to rates of microbial growth at specific locations. We describe the Framework for Integrated, Conceptual, and Systematic Microbial Ecology (FICSME), an experimental design framework for conducting process-focused microbial ecology studies that incorporates biological, chemical, and physical drivers of a microbial system into a conceptual model. Through iterative cycles that advance our understanding of the coupling across scales and processes, we can reliably predict how perturbations to microbial systems impact ecosystem-scale processes or vice versa. We describe an approach and potential applications for using the FICSME to elucidate the mechanisms of globally important ecological and physical processes, toward attaining the goal of predicting the structure and function of microbial communities in chemically complex natural environments.

Highlights

  • Microbial communities serve critical roles in all ecosystems and have a profound impact on human health, environmental health, and industrial capabilities

  • To provide a framework for conducting process-focused microbial ecology studies, we have incorporated biological, chemical, and physical processes of a microbial system into a conceptual model that tracks the abundance of a microbial strain over time at a given location based on intrinsic growth, metabolic capabilities, chemicals, and other microorganisms at the site (Figure 1 and Supplementary Table 1)

  • At the isolate and molecular levels, we have found that major selective pressures include concentration, heavy metals, nitrate, and low pH, which alter dissimilatory nitrate reduction (DNR) microbial growth (Carlson et al, 2019; Thorgersen et al, 2019)

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Summary

INTRODUCTION

Microbial communities serve critical roles in all ecosystems and have a profound impact on human health, environmental health, and industrial capabilities. To aid efforts that are building predictive understanding from genes to ecosystems, we have developed a conceptual modeling framework that models the composition, function, and ecological processes of microbial communities and environmental components at different scales (e.g., genes, individuals, populations, communities, and ecosystems) combined into an encompassing continuum between field and laboratory studies. Using a framework for experimental planning helps bridge theory and data for predictive and mechanistic understanding of biological processes (Lopatkin and Collins, 2020), which has come to the forefront as the field moves away from survey studies (Arkin and Schaffer, 2011; Widder et al, 2016; Prosser and Martiny, 2020) Combined utilization of this framework will overcome current barriers in microbial ecology, allowing for discovery and refinements phases to be iterated leading to a more process-focused predictive outcome

A CONCEPTUAL FRAMEWORK FOR PREDICTIVE MICROBIAL ECOLOGY STUDY DESIGN
DISCUSSION
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