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Título

Characterization of thymus atrophy in calves with subclinical BVD challenged with BHV-1

AutorRomero-Palomo, F.; Risalde, María Ángeles; Gómez-Villamandos, J. C.
Palabras claveBovine herpesvirus type 1 (BHV-1)
Thymus atrophy
Apoptosis
Immunohistochemistry
Bovine viral diarrhea virus (BVDV)
Fecha de publicación2015
EditorElsevier
CitaciónVeterinary Microbiology 177(1-2): 32-42 (2015)
ResumenSince the thymus is a target organ for the bovine viral diarrhea virus (BVDV), our experiment aimed to understand its relationship with the immunosuppressive effect by studying the consequences of a previous infection with BVDV on the thymus of calves challenged with bovine herpesvirus 1.1 (BHV-1). For this purpose, 12 animals were inoculated intranasally with non-cytopathic BVDV-1; 12 days later, 10 of them were coinfected intranasally with BHV-1. These animals were euthanized in batches of two at 0, 1, 2, 4, 7 or 14. dpi with BHV-1. Another 10 calves were inoculated solely with BHV-1 and euthanized in batches of two at 1, 2, 4, 7 or 14. dpi with BHV-1; two uninoculated calves were used as negative controls. Thymus samples from these animals were processed for viral detection and histopathological, immunohistochemical, and ultrastructural studies focused on BVDV/BHV-1 antigens, cortex:medulla ratio, apoptosis (TUNEL and caspase-3), collagen deposition, and factor VIII endothelial detection. Our study revealed the immunohistochemical presence of BVDV antigen in all animals in the BVDV-infected group, unlike BHV-1 detection, which was observed in animals in both infection groups only by molecular techniques. BVDV-preinfected animals showed severe atrophic changes associated with reduced cortex:medulla ratio, higher presence of cortical apoptosis, and increased collagen deposition and vascularization. However, calves solely infected with BHV-1 did not show atrophic changes. These findings could affect not only the numbers of circulating and local mature T cells but also the T cell-mediated immunity, which seems to be impaired during infections with this virus, thus favoring pathogenic effects during secondary infections.
URIhttp://hdl.handle.net/10261/141783
DOI10.1016/j.vetmic.2015.02.018
Identificadoresdoi: 10.1016/j.vetmic.2015.02.018
e-issn: 1873-2542
issn: 0378-1135
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