Microbiome Methods in Experimental Autoimmune Encephalomyelitis

David P Daberkow1, Kristina Hoffman1, Hannah M Kohl1

  • 1Department of Biology, Eastern Washington University, Cheney, Washington.

Current Protocols
|December 6, 2021
PubMed

Insights

Investigating the gut microbiome in experimental autoimmune encephalomyelitis (EAE) models reveals that environmental conditions, such as animal facility origin, significantly impact disease induction. Consistent housing is crucial for reliable EAE studies in multiple sclerosis research.

Area of Science:

  • Neuroimmunology
  • Microbiome Research
  • Animal Models of Disease

Background:

  • The gut microbiome plays a crucial role in modulating immune responses.
  • Experimental autoimmune encephalomyelitis (EAE) is a key animal model for studying multiple sclerosis (MS), a human neuroinflammatory demyelinating disease.
  • Understanding the gut-microbiome-brain axis (GMBA) is vital for neuroinflammation research.

Purpose of the Study:

  • To establish a protocol for analyzing gut microbiome composition changes in EAE mice.
  • To assess the influence of different animal facility environments on EAE induction.
  • To explore GMBA regulators in neuroinflammation and demyelination.

Main Methods:

  • Gut microbiome profiling before and after EAE induction in mice.
  • DNA extraction and microbiome analysis techniques.
  • Comparative analysis of EAE induction in mice from distinct facilities.

Main Results:

  • Significant differences in EAE induction levels were observed in mice from different animal facilities.
  • Gut microbiome composition varies based on environmental conditions.
  • Environmental consistency is critical for reproducible EAE model outcomes.

Conclusions:

  • Animal facility conditions significantly affect EAE induction, highlighting the need for standardized environments.
  • Microbiome analysis provides insights into disease modulation in neuroinflammatory conditions.
  • Consistent environmental controls are essential for the validity of EAE and other animal disease models.

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