Abstract

Mounting evidence supports a connection between the composition of the infant gut microbiome and long-term health. In fact, aberrant microbiome compositions during key developmental windows in early life are associated with increased disease risk; therefore, making pertinent modifications to the microbiome during infancy offers significant promise to improve human health. There is growing support for integrating the concept of ecosystem services (the provision of benefits from ecosystems to humans) in linking specific microbiome functions to human well-being. This framework is widely applied in conservation efforts of macro-ecosystems and offers a systematic approach to guide restoration actions aimed to recover critical ecological functions. The aim of this work is to apply the ecosystem services framework to integrate recent studies demonstrating stable alteration of the gut microbiome of breastfed infants when Bifidobacterium longum subsp. infantis EVC001, a gut symbiont capable of efficiently utilizing human milk oligosaccharides into organic acids that are beneficial for the infant and lower intestinal pH, is reintroduced. Additionally, using examples from the literature we illustrate how the absence of B. infantis results in diminished ecosystem services, which may be associated with health consequences related to immune and metabolic disorders. Finally, we propose a model by which infant gut dysbiosis can be defined as a reduction in ecosystem services supplied to the host by the gut microbiome rather than merely changes in diversity or taxonomic composition. Given the increased interest in targeted microbiome modification therapies to decrease acute and chronic disease risk, the model presented here provides a framework to assess the effectiveness of such strategies from a host-centered perspective.

Highlights

  • Disruption to the composition and function of the early life gut microbiome is recognized for its role in irregular immune development [1, 2], metabolic disorders [3] and inflammation [4, 5]

  • If pandemic non-communicable diseases such as type 1 diabetes, obesity, allergy, and asthma are associated with impaired microbiomes during infancy, as suggested by emerging evidence [3, 10,11,12,13,14,15], relevant modulation of the microbiome in early life provides a compelling solution for addressing the increasing public health burden associated with these diseases

  • We propose a model in which the absence of these beneficial functions and the consequential reduction in one or more ecosystem services can be defined as dysbiosis

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Summary

Frontiers in Nutrition

Mounting evidence supports a connection between the composition of the infant gut microbiome and long-term health. Aberrant microbiome compositions during key developmental windows in early life are associated with increased disease risk; making pertinent modifications to the microbiome during infancy offers significant promise to improve human health. There is growing support for integrating the concept of ecosystem services (the provision of benefits from ecosystems to humans) in linking specific microbiome functions to human well-being. This framework is widely applied in conservation efforts of macro-ecosystems and offers a systematic approach to guide restoration actions aimed to recover critical ecological functions.

INTRODUCTION
BIOLOGICAL CONSIDERATIONS IN DEFINING A HEALTHY INFANT GUT MICROBIOME
SUPPORTING AND PROVISIONING SERVICES OF THE GUT MICROBIOME IN EARLY LIFE
Uses and limitations of diversity in microbial ecology
Basic ecosystem processes that maintain the generation of all other services
Ecosystem stability index Mucosal and epithelial barrier integrity Fecal pH
INTEGRATING ECOSYSTEM SERVICES IN THE EVALUATION OF THE INFANT GUT MICROBIOME
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