Pathological and immunohistochemical assessment of the impact of three different strains of swine enteric coronaviruses in the intestinal barrier

[EN]Swine enteric coronaviruses, such as porcine epidemic diarrhea virus (PEDV) or transmissible gastroenteritis virus (TGEV), have risen concern for the porcine industry and research community due to the increase in their virulence, their potential recombination capacity and the emergence of new va...

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Detalles Bibliográficos
Autores: Ruedas Torres, Inés, Puente Fernández, Héctor, Fristikova, Karola, Argüello Rodríguez, Héctor, Salguero, Francisco Javier, Carvajal Urueña, Ana María, Gómez Laguna, Jaime
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:10612/26162
Acceso en línea:https://www.sciencedirect.com/science/article/pii/S0378113523003103?via%3Dihub
https://hdl.handle.net/10612/26162
Access Level:acceso abierto
Palabra clave:Inmunología
Sanidad animal
Veterinaria
PEDV
SeCoV
Intestine
Intestinal barrier
Cellular death
FoxP3
3109 Ciencias Veterinarias
3109.03 Inmunología
3109.11 Virología
3104.08 Porcinos
Descripción
Sumario:[EN]Swine enteric coronaviruses, such as porcine epidemic diarrhea virus (PEDV) or transmissible gastroenteritis virus (TGEV), have risen concern for the porcine industry and research community due to the increase in their virulence, their potential recombination capacity and the emergence of new variants. This in vivo study aims to compare the impact of three different strains of swine enteric coronaviruses [(two G1b (S-INDEL) PEDV strains and a recombinant TGEV-PEDV or Swine enteric coronavirus (SeCoV)] in the intestine of 3-weeks-old infected piglets, focusing on the pathology and main components of the intestinal barrier, including the number of goblet cells, and the expression of IgA as well as FoxP3, a regulatory T cell marker. Severity of lesions was evidenced in the three infected groups and was highly correlated with the viral load in feces and the frequency of viral antigen-positive cells. Furthermore, higher cellular death together with an increase in the expression of the FoxP3 marker was detected in the duodenum and jejunum of infected animals at 3 days post-infection. Our results highlight a recruitment of FoxP3+ cells in the small intestine of infected animals which may represent a response to the tissue damage caused by viral replication and cell death. Further studies should be addressed to determine the potential role of these cells during swine enteric coronavirus infections.