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Effects of Experimental Sarcocystis neurona-Induced Infection on Immunity in an Equine Model

Sarcocystis neurona is the most common cause of Equine Protozoal Myeloencephalitis (EPM), affecting 0.5–1% horses in the United States during their lifetimes. The objective of this study was to evaluate the equine immune responses in an experimentally induced Sarcocystis neurona infection model. Neu...

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Detalles Bibliográficos
Autores principales: Lewis, S. Rochelle, Ellison, Siobhan P., Dascanio, John J., Lindsay, David S., Gogal, Robert M., Werre, Stephen R., Surendran, Naveen, Breen, Meghan E., Heid, Bettina M., Andrews, Frank M., Buechner-Maxwell, Virginia A., Witonsky, Sharon G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4590861/
https://www.ncbi.nlm.nih.gov/pubmed/26464923
http://dx.doi.org/10.1155/2014/239495
Descripción
Sumario:Sarcocystis neurona is the most common cause of Equine Protozoal Myeloencephalitis (EPM), affecting 0.5–1% horses in the United States during their lifetimes. The objective of this study was to evaluate the equine immune responses in an experimentally induced Sarcocystis neurona infection model. Neurologic parameters were recorded prior to and throughout the 70-day study by blinded investigators. Recombinant SnSAG1 ELISA for serum and CSF were used to confirm and track disease progression. All experimentally infected horses displayed neurologic signs after infection. Neutrophils, monocytes, and lymphocytes from infected horses displayed significantly delayed apoptosis at some time points. Cell proliferation was significantly increased in S. neurona-infected horses when stimulated nonspecifically with PMA/I but significantly decreased when stimulated with S. neurona compared to controls. Collectively, our results suggest that horses experimentally infected with S. neurona manifest impaired antigen specific response to S. neurona, which could be a function of altered antigen presentation, lack of antigen recognition, or both.