Characterization of Fetal Brain Damage in Early Abortions of Ovine Toxoplasmosis

[EN]There is an unacknowledged clinical presentation of ovine toxoplasmosis characterized by early abortions and lesions of fetal leukoencephalomalacia. To investigate the pathogenesis of this condition, the extent and distribution of leukomalacia and the variations in the cell populations associate...

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Detalles Bibliográficos
Autores: Gutiérrez Expósito, Daniel, Arteche Villasol, Noive, Vallejo García, Raquel, Ferreras Estrada, María del Carmen, Ferre, Ignacio, Sánchez Sánchez, Roberto, Ortega Mora, Luis Miguel, Pérez Pérez, Valentín, Benavides Silván, Julio
Tipo de recurso: artículo
Estado:Versión enviada para evaluación y publicación
Fecha de publicación:2020
País:España
Institución:Universidad de León
Repositorio:BULERIA. Repositorio Institucional de la Universidad de León
OAI Identifier:oai:buleria.unileon.es:10612/26445
Acceso en línea:https://journals.sagepub.com/doi/10.1177/0300985820921539
https://hdl.handle.net/10612/26445
Access Level:acceso abierto
Palabra clave:Sanidad animal
Veterinaria
βAPP
Brain
Early abortions
Immunohistochemistry
Leukomalacia
Necrosis
Sheep
Toxoplasmosis
3109.07 Patología
2401.12 Parasitología Animal
3109.05 Microbiología
Descripción
Sumario:[EN]There is an unacknowledged clinical presentation of ovine toxoplasmosis characterized by early abortions and lesions of fetal leukoencephalomalacia. To investigate the pathogenesis of this condition, the extent and distribution of leukomalacia and the variations in the cell populations associated with it were characterized in 32 fetal brains from 2 previously published experimental studies of Toxoplasma gondii infection in pregnant sheep. Immunohistochemical labeling of βAPP allowed for the detection of leukomalacia in 100/110 (91%) studied samples. There was no clear influence of the challenge dose or the area of the brain (frontal lobe, corpus callosum, midbrain, and cerebellum). In tissues with leukomalacia, there was loss of oligodendrocytes and increased number of astrocytes and microglia both in the areas of necrosis but also in the surrounding area. These findings were similar to those described in ovine experimental models (inflammation syndrome and hypoxic models) of periventricular leukomalacia in humans. Thus, a fetal inflammatory syndrome may be involved in the pathogenesis of early abortion in ovine toxoplasmosis. However, further studies are needed to determine the pathogenesis of this clinical presentation because placental thrombosis and resulting hypoxia could also be responsible for the leukomalacia.