In vivo transcriptomic profiling of colonic mucosa during Brachyspira hyodysenteriae infection in pigs
[EN] The little known pathophysiology of swine dysentery (SD) encourages novel studies to decipher the host response to this disease. The present study investigates the in vivo transcriptome of colonic mucosa, using RNA sequencing in 16 pigs experimentally infected with Brachyspira hyodysenteriae (B...
| Autores: | , , , , , , , , |
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| Tipo de recurso: | artículo |
| Estado: | Versión publicada |
| Fecha de publicación: | 2026 |
| País: | España |
| Institución: | Universidad de León |
| Repositorio: | BULERIA. Repositorio Institucional de la Universidad de León |
| OAI Identifier: | oai:buleria.unileon.es:10612/27611 |
| Acceso en línea: | https://hdl.handle.net/10612/27611 |
| Access Level: | acceso abierto |
| Palabra clave: | Sanidad animal Swine dysentery Intestine Spirochaetes Immunity RNA-seq 3109 Ciencias Veterinarias |
| Sumario: | [EN] The little known pathophysiology of swine dysentery (SD) encourages novel studies to decipher the host response to this disease. The present study investigates the in vivo transcriptome of colonic mucosa, using RNA sequencing in 16 pigs experimentally infected with Brachyspira hyodysenteriae (B. hyodysenteriae), at the onset of faecal shedding (Early_inf group, n = 8), and during the acute clinical disease, with mucohaemorrhagic diarrhoea (Acute_inf group, n = 8). No significant differences in gene expression were observed in Early_inf group, except for an overexpression of matrix metalloproteinases genes (MMPs), which may be associated with early ulceration of the colonic epithelium. The Acute_inf group showed a significant upregulation of the S100A8, S100A9 and S100A12 genes. However, most of the host biological processes were downregulated, particularly those related to the immune response, such as chemokines and cytokines signalling or immune cells chemotaxis and migration. Accordingly, the prediction of cell types associated with the detected transcripts revealed a depletion of immune cells, except neutrophils, and an enrichment of stromal cells in the Acute_inf group. Marked alterations in mucin gene expression were observed in this group, including overexpression of MUC5AC, MUC20, and GCNT3, a tendency in MUC2, and downregulation of MUC1 and MUC13. Although no significant changes were detected in the Early_inf group, a similar trend was observed. This study proposes several mechanisms associated with the pathophysiology of SD, revealing key aspects of host–pathogen interactions, particularly the host response to B. hyodysenteriae infection. |
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