Abstract

Laboratory animals with human microbiome have increasingly been used to study the role of bacteria and host interaction. Drosophila melanogaster, as a model of microbiota-host interaction with high reproductive efficiency and high availability, has always been lacking studies of interaction with human gut microbiome. In this study, we attempted to use antibiotic therapy and human fecal exposure strategy to transfer the human microbiome to the drosophila. The method includes depleting the original intestinal bacteria using a broad-spectrum antibiotic and then introducing human microorganisms by a diet supplemented with donor’s fecal samples. The sequencing results showed that 80–87.5% of the OTUs (Operational Taxonomic Units) from donor feces were adopted by the recipient drosophila following 30 days of observation. In comparison to females, the male recipient drosophila inherited more microbiota from the donor feces and had significantly increased lifespan as well as improved vertical climbing ability. Furthermore, distinctly differential expression patterns for age and insulin-like signaling-related genes were obtained for the male vs. female recipients. Only the male drosophila offspring acquired the characteristics of the donor fecal microbiota.

Highlights

  • The intestinal bacteria comprise the microbial community that resides in the human intestine

  • We attempted to develop a convenient and anthropomorphic drosophila model of human intestinal bacteria that can be used for scientific research. To establish such a model, we first transfer human microbiota to drosophila by using antibiotic therapy and human fecal microbiota exposure, and we investigated the stability of the intestinal bacteria and its heritability of passage through the analysis of 16S rDNA sequencing results

  • The sequencing analysis showed that 80–87.5% of OTUs that had belonged to the donor feces were adopted by the recipient drosophila during the 30 days of observation (Figure S1)

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Summary

Introduction

The intestinal bacteria comprise the microbial community that resides in the human intestine. The number of bacteria in the human intestine is approximately 100 trillion, with the corresponding total number of genes approximately 150 times the number of human genes. Intestinal bacteria are known as the “second genome” of the human body [1]. It has been confirmed that intestinal bacteria play a key role in most metabolic processes and are associated with many diseases [2–4]

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