Genomics reveal local skin immune response key to control sarcoptic mange in Iberian ibex (Capra pyrenaica)

[EN] Background: Sarcoptic mange is an emerging and neglected contagious skin disease caused by the mite Sarcoptes scabiei, affecting humans, domestic animals, and wildlife. Mange is the main disease and a major concern for the management and conservation of populations of Iberian ibex (Capra pyrena...

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Detalles Bibliográficos
Autores: Ráez Bravo, Arián, Granados, José Enrique, Espinosa Cerrato, José, Nonell, Lara, Serrano, Emmanuel, Puigdecanet, Eulàlia, Bódalo, Marta, Pérez, Jesús M., Soriguer, Ramón C., Cano Manuel, Francisco Javier, Fandos, Paulino, López Olvera, Jorge Ramón
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2024
País:España
Institución:Universidad de León
Repositorio:BULERIA. Repositorio Institucional de la Universidad de León
OAI Identifier:oai:buleria.unileon.es:10612/25941
Acceso en línea:https://bmcgenomics.biomedcentral.com/articles/10.1186/s12864-024-10999-4
https://hdl.handle.net/10612/25941
Access Level:acceso abierto
Palabra clave:Sanidad animal
Veterinaria
Gene expession
Gene set enrichment analysis
Genomic response
Immune response
Microarray
Sarcoptes scabiei
3109 Ciencias Veterinarias
3109.02 Genética
3109.03 Inmunología
Descripción
Sumario:[EN] Background: Sarcoptic mange is an emerging and neglected contagious skin disease caused by the mite Sarcoptes scabiei, affecting humans, domestic animals, and wildlife. Mange is the main disease and a major concern for the management and conservation of populations of Iberian ibex (Capra pyrenaica), a medium-sized mountain ungulate endemic to the Iberian Peninsula and Northern Pyrenees. Differences in host-parasite interaction and host immune response determine mange clinical outcome, but little is known about the related differences in gene expression. This study determined blood and skin gene expressions in S. scabiei-experimentally infested Iberian ibexes. Results: Infestation with S. scabiei promoted immune and inflammatory genomic responses both in skin and blood, with two different clinical outcomes: either severe infestation or recovery. Sarcoptes scabiei induced local skin immunosuppression to favour its multiplication and establishment of the infestation in the host. Skin gene expression was mostly inflammatory and inefficient to control mange in the severely infected ibexes. Conversely, the immune skin response of the recovered ibexes effectively recognised S. scabiei and activated T-cells, limiting the infestation. Consequently, inflammation-related genes were more expressed in the blood of the severely infested ibexes than in those that recovered. Conclusions: The results demonstrate that skin local cellular immune response is key to control sarcoptic mange and prevent the systemic spread of the disease and the associated inflammatory response. These results will be useful to understand the pathogenesis and drivers of the differential outcome of mange at individual scale, and the population and ecological consequences of such variability in Iberian ibex, as well as in other wildlife species, domestic animals, and humans