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Updated: Sep 4, 2025

Author Spotlight: Development and Characterization of 2D Intestinal Monolayer Models from Bovine Organoids for Pathogen Interaction Studies
Published on: June 14, 2024
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.
Abstract:
Mycobacterium avium subspecies paratuberculosis (MAP) is the etiological agent of Johne's Disease, a chronic enteritis of ruminants prevalent across the world. It is estimated that approximately 50% of UK dairy herds are infected with MAP, but this is likely an underestimate of the true prevalence. Infection can result in reduced milk yield, infertility and premature culling of the animal, leading to significant losses to the farming economy and negatively affecting animal welfare. Understanding the initial interaction between MAP and the host is critical to develop improved diagnostic tools and novel vaccines. Here we describe the characterisation of three different multicellular in vitro models derived from bovine intestinal tissue, and their use for the study of cellular interactions with MAP. In addition to the previously described basal-out 3D bovine enteroids, we have established viable 2D monolayers and 3D apical-out organoids. The apical-out enteroids differ from previously described bovine enteroids as the apical surface is exposed on the exterior surface of the 3D structure, enabling study of host-pathogen interactions at the epithelial surface without the need for microinjection. We have characterised the cell types present in each model system using RT-qPCR to detect predicted cell type-specific gene expression, and confocal microscopy for cell type-specific protein expression. Each model contained the cells present in the original bovine intestinal tissue, confirming they were representative of the bovine gut. Exposure of the three model systems to the K10 reference strain of MAP K10, and a recent Scottish isolate referred to as C49, led to the observation of intracellular bacteria by confocal microscopy. Enumeration of the bacteria by quantification of genome copy number, indicated that K10 was less invasive than C49 at early time points in infection in all model systems. This study shows that bovine enteroid-based models are permissive to infection with MAP and that these models may be useful in investigating early stages of MAP pathogenesis in a physiologically relevant in vitro system, whilst reducing the use of animals in scientific research. Bos taurus: urn:lsid:zoobank.org:act:4C90C4FA-6296-4972-BE6A-5EF578677D64.
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.

