The Development of 3D Bovine Intestinal Organoid Derived Models to Investigate Mycobacterium Avium ssp

Rosemary Blake1, Kirsty Jensen1, Neil Mabbott1

  • 1The Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh, Edinburgh, United Kingdom.

Insights

New bovine intestinal models allow researchers to study Mycobacterium avium subspecies paratuberculosis (MAP) infection in vitro. These models show promise for developing diagnostics and vaccines for Johne's Disease in cattle.

Area of Science:

  • Veterinary microbiology
  • Animal science
  • Infectious disease research

Background:

  • Mycobacterium avium subspecies paratuberculosis (MAP) causes Johne's Disease, a costly enteritis in ruminants.
  • Current understanding of MAP-host interactions is limited, hindering diagnostic and vaccine development.
  • Existing research models do not fully replicate the bovine intestinal environment for studying MAP.

Purpose of the Study:

  • To characterize and validate novel in vitro bovine intestinal models for MAP infection studies.
  • To compare the invasiveness of different MAP strains in these new models.
  • To establish a more relevant system for investigating early MAP pathogenesis and reducing animal use.

Main Methods:

  • Development and characterization of three bovine intestinal in vitro models: 2D monolayers, 3D basal-out enteroids, and 3D apical-out organoids.
  • Cell type validation using RT-qPCR for gene expression and confocal microscopy for protein expression.
  • Infection assays with MAP strains K10 and C49, followed by confocal microscopy and genome copy number quantification.

Main Results:

  • All three models successfully represented the cell types of the original bovine intestinal tissue.
  • Intracellular MAP was observed in all models upon exposure to MAP strains K10 and C49.
  • MAP strain C49 demonstrated higher invasiveness than K10 in the early stages of infection across all models.

Conclusions:

  • Bovine enteroid-based models are suitable for studying MAP infection in a physiologically relevant in vitro setting.
  • These models provide a valuable platform for investigating early MAP pathogenesis.
  • The developed models contribute to reducing animal use in scientific research for Johne's Disease studies.

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