Abstract

ABSTRACTAnimal hosts must co-exist with beneficial microbes while simultaneously being able to mount rapid, non-specific, innate immune responses to pathogenic microbes. How this balance is achieved is not fully understood, and disruption of this relationship can lead to disease. Excessive inflammatory responses to resident microbes are characteristic of certain gastrointestinal pathologies such as inflammatory bowel disease (IBD). The immune dysregulation of IBD has complex genetic underpinnings that cannot be fully recapitulated with single-gene-knockout models. A deeper understanding of the genetic regulation of innate immune responses to resident microbes requires the ability to measure immune responses in the presence and absence of the microbiota using vertebrate models with complex genetic variation. Here, we describe a new gnotobiotic vertebrate model to explore the natural genetic variation that contributes to differences in innate immune responses to microbiota. Threespine stickleback, Gasterosteus aculeatus, has been used to study the developmental genetics of complex traits during the repeated evolution from ancestral oceanic to derived freshwater forms. We established methods to rear germ-free stickleback larvae and gnotobiotic animals monoassociated with single bacterial isolates. We characterized the innate immune response of these fish to resident gut microbes by quantifying the neutrophil cells in conventionally reared monoassociated or germ-free stickleback from both oceanic and freshwater populations grown in a common intermediate salinity environment. We found that oceanic and freshwater fish in the wild and in the laboratory share many intestinal microbial community members. However, oceanic fish mount a strong immune response to residential microbiota, whereas freshwater fish frequently do not. A strong innate immune response was uniformly observed across oceanic families, but this response varied among families of freshwater fish. The gnotobiotic stickleback model that we have developed therefore provides a platform for future studies mapping the natural genetic basis of the variation in immune response to microbes.

Highlights

  • Animals and their associated microbial communities co-exist in dynamic relationships involving complex networks of interactions and signals (McFall-Ngai et al, 2013)

  • We established methods to rear germ-free stickleback larvae and gnotobiotic animals mono-associated with single bacterial isolates

  • A strong innate immune response was uniformly observed across oceanic families, but this response varied among families of freshwater fish

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Summary

Introduction

Animals and their associated microbial communities co-exist in dynamic relationships involving complex networks of interactions and signals (McFall-Ngai et al, 2013). These resident microbes provide important services to the host such as nutrient acquisition and pathogen exclusion (Khosravi and Mazmanian, 2013; Tremaroli and Bäckhed, 2012). Even as the immune system protects the host from pathogens, it must maintain a homeostatic relationship with, or tolerance of, the beneficial resident microbial community Loss of this immune tolerance is a characteristic of inflammatory bowel diseases (IBD) (Graham and Xavier, 2013). The normal range of innate immune responses to resident microbiota that occurs within populations of healthy individuals has not been extensively explored

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