Classical Swine Fever Virus vs. Classical Swine Fever Virus

Two groups with three wild boars each were used: Group A (animals 1 to 3) served as the control, and Group B (animals 4 to 6) was postnatally persistently infected with the Cat01 strain of CSFV (primary virus). The animals, six weeks old and clinically healthy, were inoculated with the virulent stra...

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Autores: Muñoz González, Sara, Pérez-Simó, Marta, Colom Cadena, Andreu|||0000-0003-0983-2412, Cabezón Ponsoda, Óscar|||0000-0001-7543-8371, Bohórquez Garzón, José Alejandro|||0000-0002-6715-1757, Rosell, Rosa|||0000-0002-8294-1159, Pérez, Lester Josue|||0000-0002-5717-5181, Marco, Ignasi|||0000-0001-7479-3419, Lavín González, Santiago|||0000-0001-5655-588X, Domingo, Mariano|||0000-0002-9623-4826, Ganges, Llilianne|||0000-0002-8644-3560
Tipo de recurso: artículo
Fecha de publicación:2016
País:España
Institución:Universitat Autònoma de Barcelona
Repositorio:Dipòsit Digital de Documents de la UAB
Idioma:inglés
OAI Identifier:oai:ddd.uab.cat:170615
Acceso en línea:https://ddd.uab.cat/record/170615
https://dx.doi.org/urn:doi:10.1371/journal.pone.0149469
Access Level:acceso abierto
Palabra clave:RNA extraction
Swine
Superinfection
Enzyme-linked immunoassays
Sequence analysis
Viral persistence and latency
Immune response
RNA viruses
Descripción
Sumario:Two groups with three wild boars each were used: Group A (animals 1 to 3) served as the control, and Group B (animals 4 to 6) was postnatally persistently infected with the Cat01 strain of CSFV (primary virus). The animals, six weeks old and clinically healthy, were inoculated with the virulent strain Margarita (secondary virus). For exclusive detection of the Margarita strain, a specific qRT-PCR assay was designed, which proved not to have cross-reactivity with the Cat01 strain. The wild boars persistently infected with CSFV were protected from superinfection by the virulent CSFV Margarita strain, as evidenced by the absence of clinical signs and the absence of Margarita RNA detection in serum, swabs and tissue samples. Additionally, in PBMCs, a well-known target for CSFV viral replication, only the primary infecting virus RNA (Cat01 strain) could be detected, even after the isolation in ST cells, demonstrating SIE at the tissue level in vivo. Furthermore, the data analysis of the Margarita qRT-PCR, by means of calculated ΔCt values, supported that PBMCs from persistently infected animals were substantially protected from superinfection after in vitro inoculation with the Margarita virus strain, while this virus was able to infect naive PBMCs efficiently. In parallel, IFN-α values were undetectable in the sera from animals in Group B after inoculation with the CSFV Margarita strain. Furthermore, these animals were unable to elicit adaptive humoral (no E2-specific or neutralising antibodies) or cellular immune responses (in terms of IFN-γ-producing cells) after inoculation with the second virus. Finally, a sequence analysis could not detect CSFV Margarita RNA in the samples tested from Group B. Our results suggested that the SIE phenomenon might be involved in the evolution and phylogeny of the virus, as well as in CSFV control by vaccination. To the best of our knowledge, this study was one of the first showing efficient suppression of superinfection in animals, especially in the absence of IFN-α, which might be associated with the lack of innate immune mechanisms.