Abstract

Rat is a widely used mammalian model for gut microbiota research. However, due to the difficulties of individual in vitro culture of many of the gut bacteria, much information about the microbial behaviors in the rat gut remains largely unknown. Here, to characterize the in situ growth and division of rat gut bacteria, we apply a chemical strategy that integrates the use of sequential tagging with D-amino acid-based metabolic probes (STAMP) with fluorescence in situ hybridization (FISH) to rat gut microbiota. Following sequential gavages of two different fluorescent D-amino acid probes to rats, the resulting dually labeled gut bacteria provides chronological information of their in situ cell wall synthesis. After taxonomical labeling with FISH probes, most of which are newly designed in this study, we successfully identify the growth patterns of 15 bacterial species, including two that have not been cultured separately in the laboratory. Furthermore, using our labeling protocol, we record Butyrivibrio fibrisolvens cells growing at different growth stages of a complete cell division cycle, which offers a new scope for understanding basic microbial activities in the gut of mammalian hosts.

Highlights

  • The compositions and activities of the microbial community in the gut reflect the co-evolution between the host and gut microbes (Marchesi et al, 2016)

  • After taxonomical labeling with fluorescence in situ hybridization (FISH) probes, most of which are newly designed in this study, we successfully identify the growth patterns of 15 bacterial species, including two that have not been cultured separately in the laboratory

  • After sequentially administered two fluorescent D-amino acid-based probes (FDAA) containing different fluorophores to SD rats by gavages, we identified a panel of bacterial species by FISH staining, and imaged their in situ growth and multiplication processes using their FDAA labeling signals

Read more

Summary

INTRODUCTION

The compositions and activities of the microbial community in the gut reflect the co-evolution between the host and gut microbes (Marchesi et al, 2016). After sequentially administered two fluorescent D-amino acid-based probes (FDAA) containing different fluorophores to SD rats by gavages, we identified a panel of bacterial species by FISH staining, and imaged their in situ growth and multiplication processes using their FDAA labeling signals. It presents an easy-to-operate and efficient approach to address basic microbiology questions of gut “dark matter” in rat, showcasing the applicability of this integrative protocol in studying the gut microbiotas in different mammalian hosts

RESULTS
DISCUSSION
METHODS AND MATERIALS
DATA AVAILABILITY STATEMENT
ETHICS STATEMENT
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call