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Infection and immune response to porcine hemagglutinating encephalomyelitis virus in grower pigs.

dc.contributor.authorMora-Díaz, Juan Carlos
dc.contributor.authorTemeeyasen, Gun
dc.contributor.authorMagtoto, Ronaldo
dc.contributor.authorRauh, Rolf
dc.contributor.authorNelson, William
dc.contributor.authorCarrillo-Ávila, José Antonio
dc.contributor.authorZimmerman, Jeffrey
dc.contributor.authorPiñeyro, Pablo
dc.contributor.authorGiménez-Lirola, Luis
dc.date.accessioned2023-02-09T10:38:59Z
dc.date.available2023-02-09T10:38:59Z
dc.date.issued2020-12-16
dc.description.abstractPorcine hemagglutinating encephalomyelitis virus (PHEV) is the cause of acute outbreaks of vomiting and wasting disease and/or encephalomyelitis in neonatal pigs, with naïve herds particularly vulnerable to clinical episodes. PHEV infections in older pigs are generally considered to be subclinical, but are poorly characterized in the refereed literature. In this study, twelve 7-week-old pigs were oronasally inoculated with 0.5 mL (1:128 HA titer) PHEV (Mengeling strain) and then followed through 42 days post inoculation (dpi). Fecal and oral fluid specimens were collected daily to evaluate viral shedding. Serum samples were tested for viremia, isotype-specific antibody responses, cytokine, and chemokine responses. Peripheral blood mononuclear cells were isolated to evaluate phenotype changes in immune cell subpopulations. No clinical signs were observed in PHEV inoculated pigs, but virus was detected in oral fluid (1-28 dpi) and feces (1-10 dpi). No viremia was detected, but a significant IFN-α response was observed in serum at 3 dpi, followed by the detection of IgM (dpi 7), and IgA/IgG (dpi 10). Flow cytometry revealed a one-off increase in cytotoxic T cells at 21 dpi. This study demonstrated that exposure of grower pigs to PHEV results in subclinical infection characterized by active viral replication and shedding followed by an active humoral and cell-mediated immune response that attenuates the course of the infection and results in viral clearance.
dc.identifier.doi10.1016/j.vetmic.2020.108958
dc.identifier.essn1873-2542
dc.identifier.pmid33387911
dc.identifier.unpaywallURLhttps://doi.org/10.1016/j.vetmic.2020.108958
dc.identifier.urihttp://hdl.handle.net/10668/16889
dc.journal.titleVeterinary microbiology
dc.journal.titleabbreviationVet Microbiol
dc.language.isoen
dc.organizationBiobanco del Sistema Sanitario Público de Andalucía
dc.organizationServicio Andaluz de Salud-SAS
dc.page.number108958
dc.pubmedtypeJournal Article
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectBetacoronavirus
dc.subjectCoronavirus
dc.subjectGrower-finisher pigs
dc.subjectImmune response
dc.subjectPorcine hemagglutinating encephalomyelitis virus
dc.subjectSubclinical infection
dc.subject.meshAnimals
dc.subject.meshAntibodies, Viral
dc.subject.meshBetacoronavirus 1
dc.subject.meshCoronavirus Infections
dc.subject.meshInterferon-alpha
dc.subject.meshSwine
dc.subject.meshSwine Diseases
dc.subject.meshViremia
dc.titleInfection and immune response to porcine hemagglutinating encephalomyelitis virus in grower pigs.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number253
dspace.entity.typePublication

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