Abstract

Gut microbiomes perform essential services for their hosts, including helping them to digest food and manage pathogens and parasites. Performing these services requires a diverse and constantly changing set of metabolic functions from the bacteria in the microbiome. The metabolic repertoire of the microbiome is ultimately dependent on the outcomes of the ecological interactions of its member microbes, as these interactions in part determine the taxonomic composition of the microbiome. The ecological processes that underpin the microbiome's ability to handle a variety of metabolic challenges might involve rapid turnover of the gut microbiome in response to new metabolic challenges, or it might entail maintaining sufficient diversity in the microbiome that any new metabolic demands can be met from an existing set of bacteria. To differentiate between these scenarios, we examine the gut bacteria and resident eukaryotes of two generalist‐insectivore lizards, while simultaneously identifying the arthropod prey each lizard was digesting at the time of sampling. We find that the cohorts of bacteria that occur significantly more or less often than expected with arthropod diet items or eukaryotes include bacterial species that are highly similar to each other metabolically. This pattern in the bacterial microbiome could represent an early step in the taxonomic shifts in bacterial microbiome that occur when host lineages change their diet niche over evolutionary timescales.

Highlights

  • The ecological community of bacteria that composes vertebrate gut microbiomes performs a set of metabolic functions (Coyte, Schluter, & Foster, 2015; Douglas & Werren, 2016), some of which benefit their host (Foster, Schluter, Coyte, & Rakoff‐Nahoum, 2017; Hanning & Diaz‐Sanchez, 2015)

  • Using community ecol‐ ogy analyses, we identify ecological interactions between all taxa, and test whether bacteria that interact with a diet item or eukary‐ ote have a consistent metabolic profile (Kanehisa, Sato, Kawashima, Furumichi, & Tanabe, 2016)

  • We considered the functional profiles of bacterial OTUs that oc‐ curred more or less frequently than expected with eukaryotic mi‐ crobes and diet items

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Summary

| INTRODUCTION

The ecological community of bacteria that composes vertebrate gut microbiomes performs a set of metabolic functions (Coyte, Schluter, & Foster, 2015; Douglas & Werren, 2016), some of which benefit their host (Foster, Schluter, Coyte, & Rakoff‐Nahoum, 2017; Hanning & Diaz‐Sanchez, 2015). | 12472 framework for how vertebrates interact with their environment (Alberdi, Aizpurua, Bohmann, Zepeda‐Mendoza, & Gilbert, 2016) Through their interaction with their hosts, microbiome function can affect entire ecological communities. We test hypotheses about the ecological interactions that underpin functional profile in the gut microbiomes of two lizard host species Both species are generalist insectivores that reproduce oviparously. A subset of the bacteria (OTUs) in the microbiome could react to the diet item or eukaryote in a consistent and predictable manner From this background, we predict how the host‐microbiome system evolves in response to both ongoing and novel interactions with the host's wider biotic community

| METHODS
| DISCUSSION
Findings
CONFLICT OF INTEREST
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