Abstract

The host microbiome plays an essential role in health and disease. Microbiome modification by pathogens or probiotics has been poorly explored especially in the case of probiotic yeasts. Next-generation sequencing currently provides the best tools for their characterization. Debaryomyces hansenii 97 (D. hansenii 97) and Yarrowia lipolytica 242 (Y. lipolytica 242) are yeasts that protect wildtype zebrafish (Danio rerio) larvae against a Vibrio anguillarum (V. anguillarum) infection, increasing their survival rate. We investigate the effect of these microorganisms on the microbiome and neutrophil response (inflammation) in zebrafish larvae line Tg(Bacmpx:GFP)i114. We postulated that preinoculation of larvae with yeasts would attenuate the intestinal neutrophil response and prevent modification of the larval microbiome induced by the pathogen. Microbiome study was performed by sequencing the V3-V4 region of the 16S rRNA gene and prediction of metabolic pathways by Piphillin in conventionally raised larvae. Survival and the neutrophil response were both evaluated in conventional and germ-free conditions. V. anguillarum infection resulted in higher neutrophil number in the intestinal area compared to non-infected larvae in both conditions. In germ-free conditions, infected larvae pre-inoculated with yeasts showed fewer neutrophil numbers than infected larvae. In both conditions, only D. hansenii 97 increased the survival of infected larvae. Beta diversity of the microbiota was modified by V. anguillarum and both yeasts, compared to non-inoculated larvae. At 3 days post-infection, V. anguillarum modified the relative abundance of 10 genera, and pre-inoculation with D. hansenii 97 and Y. lipolytica 242 prevented the modification of 5 and 6 of these genera, respectively. Both yeasts prevent the increase of Ensifer and Vogesella identified as negative predictors for larval survival (accounting for 40 and 27 of the variance, respectively). In addition, yeast pre-inoculation prevents changes in some metabolic pathways altered by V. anguillarum’s infection. These results suggest that both yeasts and V. anguillarum can shape the larval microbiota configuration in the early developmental stage of D. rerio. Moreover, modulation of key taxa or metabolic pathways of the larval microbiome by yeasts can be associated with the survival of infected larvae. This study contributes to the understanding of yeast–pathogen–microbiome interactions, although further studies are needed to elucidate the mechanisms involved.

Highlights

  • The host microbiota participates in several physiological processes such as development, digestion, metabolism, immune stimulation, and neurological functions

  • We investigated whether probiotic yeasts D. hansenii 97 and Y. lipolytica 242 can affect neutrophil recruitment to the intestine, one of the entry points of V. anguillarum

  • We evaluated the effect of V. anguillarum infection and pre-inoculation of both yeasts on the survival rate of Tg(Bacmpx:GFP)i114 larvae (Figure 1A)

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Summary

INTRODUCTION

The host microbiota participates in several physiological processes such as development, digestion, metabolism, immune stimulation, and neurological functions. These yeast strains have the potential for application in the aquaculture sector, considering their fish origin and the health benefits reported in the zebrafish model They protected conventionally raised and germ-free wild type (Tab 5) zebrafish larvae against a Vibrio anguillarum infection by increasing their survival (Caruffo et al, 2015). Both yeast strains reduced the pathogen concentration in the host and prevented the up-regulation of inflammatory cytokines (il1b, tnfa, c3, mpx) (Caruffo et al, 2016). The transgenic zebrafish line Tg(Bacmpx:GFP)i114 was used to investigate the effect of two potential probiotic yeasts and the pathogen V. anguillarum on the microbiome composition and neutrophil response. We postulated that the pre-inoculation of larvae with each yeast would attenuate the neutrophil response and prevent modification of the larval microbiome induced by the pathogen

MATERIALS AND METHODS
RESULTS
Membrane transport information processing
DISCUSSION
ETHICS STATEMENT
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