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Foot-and-mouth disease virus infection of dendritic cells triggers phosphorylation of ERK1/2 inducing class I presentation and apoptosis

Foot-and-mouth disease (FMD) is a highly contagious viral disease of cloven-hoofed animals. This pathology is caused by foot-and-mouth disease virus (FMDV). Over time, the development of vaccines to prevent the spread of this illness became essential. Vaccines currently used contain the inactivated...

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Main Authors: Langellotti, Cecilia Ana, Cesar, Gonzalo, Soria, Ivana, Quattrocchi, Valeria, Jancic, Carolina Cristina, Zamorano, Patricia Ines, Vermeulen, Elba Monica
Format: info:ar-repo/semantics/artículo
Language:Inglés
Published: Elsevier 2019
Subjects:
Aphthovirus
Phosphorylation
Cytotoxicity
Virus Fiebre Aftosa
Fosforilación
Citotoxicidad
Foot and Mouth Disease Virus
Caspase-9
Inactive Viral Particles
ERK1/2 MAPK
Células Dendríticas
Online Access:http://hdl.handle.net/20.500.12123/4535
https://www.sciencedirect.com/science/article/pii/S0264410X15009858?via%3Dihub
https://doi.org/10.1016/j.vaccine.2015.07.038
Summary:Foot-and-mouth disease (FMD) is a highly contagious viral disease of cloven-hoofed animals. This pathology is caused by foot-and-mouth disease virus (FMDV). Over time, the development of vaccines to prevent the spread of this illness became essential. Vaccines currently used contain the inactivated form of the virus. However, vaccination generates an immune response different to that induced by the infection. We investigated whether these differences are related to intracellular mechanisms on dendritic cells (DCs). As a result, we demonstrated that the internalization of infective virus triggered the phosphorylation of ERK1/2, which was involved in the activation of caspase-9, the intrinsic pathway of apoptosis and the delivery of viral peptides on MHC class I molecules. While, inactivated virus (iFMDV) did not affect this pathway or any function mediated by its activation. As described, infectious virus in DCs was also associated to autophagy LC3 protein and was associated to lysosomal protein Lamp-2; contrary to observe for the iFMDV. Strikingly, the processing of viral antigens to accommodate in class I molecules does not appear to involve the proteasome. Finally, this increased presentation promotes a specific cytotoxic response against infectious virus.

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