# Challenge Dose Titration in a Mycobacterium bovis Infection Model in Goats

**Authors:** Elisabeth M. Liebler-Tenorio, Nadine Wedlich, Julia Figl, Heike Köhler, Reiner Ulrich, Charlotte Schröder, Melanie Rissmann, Leander Grode, Stefan H. E. Kaufmann, Christian Menge

PMC · DOI: 10.3390/ijms25189799 · International Journal of Molecular Sciences · 2024-09-10

## TL;DR

This study establishes a reproducible goat model for Mycobacterium bovis infection, showing dose-dependent lesion differences useful for vaccine testing.

## Contribution

The study introduces a reproducible M. bovis challenge model in goats with dose-dependent lesion outcomes.

## Key findings

- Infected goats did not show clinical signs but had M. bovis in feces.
- Dose-dependent effects were observed in lesion size and early generalization.
- All infected goats developed paucibacillary granulomas in lungs and lymph nodes.

## Abstract

Goats are natural hosts of Mycobacterium (M.) bovis, and affected herds can be the cause of significant economic losses. Similarites in disease course and lesions of M. bovis infections in goats and M. tuberculosis in humans make goats good models for human tuberculosis. The aim of this investigation was to characterize M. bovis challenge models in goats. For this, goats were endobronchially inoculated with three doses of M. bovis or culture medium. Clinical signs, shedding, and immune responses were monitored until 146 days post inoculation (dpi). At necropsy, lesions were examined by computed tomography, histology, and bacteriological culture. Infected goats did not develop clinical signs. M. bovis was cultured from feces, but never from nasal swabs. IGRAs were positive from 28 dpi onwards, antibodies at 140 dpi, and SICCT at 146 dpi. The increase in CD25+, IFN-γ+, and IFN-γ-releasing T-cell subpopulations was time-related, but not dose-dependent. All infected goats developed paucibacillary granulomas in the lungs and regional lymph nodes. M. bovis was regularly cultured. Dose-dependent effects included the size of pulmonary lesions, caverns, intestinal lesions, and early generalization in the high-dose group. In summary, reproducible challenge models with dose-dependent differences in lesions were established, which may serve for testing vaccines for veterinary or medical use.

## Linked entities

- **Diseases:** tuberculosis (MONDO:0018076)

## Full-text entities

- **Genes:** IFN-gamma [NCBI Gene 100860815]
- **Diseases:** Infected (MESH:D007239), tuberculosis (MESH:D014376), caverns (MESH:D020786), intestinal lesions (MESH:D007410), granulomas (MESH:D006099), pulmonary lesions (MESH:D008171), Mycobacterium bovis Infection (MESH:D009164)
- **Species:** Capra hircus (domestic goat, species) [taxon 9925], Homo sapiens (human, species) [taxon 9606], Mycobacterium tuberculosis (species) [taxon 1773]

## Full text

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## Figures

13 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11431947/full.md

## References

83 references — full list in the complete paper: https://tomesphere.com/paper/PMC11431947/full.md

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Source: https://tomesphere.com/paper/PMC11431947