Publication:
Postnatal persistent infection with classical Swine Fever virus and its immunological implications.

cris.virtual.author-orcid0000-0001-8292-4634
cris.virtualsource.author-orcid14bcea6e-c224-4fc8-95a3-01d8aec94cb1
cris.virtualsource.author-orcide718d882-78c1-4668-960b-edb76ce64f3a
datacite.rightsopen.access
dc.contributor.authorMuñoz-González, Sara
dc.contributor.authorRuggli, Nicolas
dc.contributor.authorRosell, Rosa
dc.contributor.authorPérez, Lester Josué
dc.contributor.authorFrías-Leuporeau, Maria Teresa
dc.contributor.authorFraile, Lorenzo
dc.contributor.authorMontoya, Maria
dc.contributor.authorCordoba, Lorena
dc.contributor.authorDomingo, Mariano
dc.contributor.authorEhrensperger, Felix
dc.contributor.authorSummerfield, Artur
dc.contributor.authorGanges, Llilianne
dc.date.accessioned2025-01-08T20:00:27Z
dc.date.available2025-01-08T20:00:27Z
dc.date.issued2015
dc.description.abstractIt is well established that trans-placental transmission of classical swine fever virus (CSFV) during mid-gestation can lead to persistently infected offspring. The aim of the present study was to evaluate the ability of CSFV to induce viral persistence upon early postnatal infection. Two litters of 10 piglets each were infected intranasally on the day of birth with low and moderate virulence CSFV isolates, respectively. During six weeks after postnatal infection, most of the piglets remained clinically healthy, despite persistent high virus titres in the serum. Importantly, these animals were unable to mount any detectable humoral and cellular immune response. At necropsy, the most prominent gross pathological lesion was a severe thymus atrophy. Four weeks after infection, PBMCs from the persistently infected seronegative piglets were unresponsive to both, specific CSFV and non-specific PHA stimulation in terms of IFN-γ-producing cells. These results suggested the development of a state of immunosuppression in these postnatally persistently infected pigs. However, IL-10 was undetectable in the sera of the persistently infected animals. Interestingly, CSFV-stimulated PBMCs from the persistently infected piglets produced IL-10. Nevertheless, despite the addition of the anti-IL-10 antibody in the PBMC culture from persistently infected piglets, the response of the IFN-γ producing cells was not restored. Therefore, other factors than IL-10 may be involved in the general suppression of the T-cell responses upon CSFV and mitogen activation. Interestingly, bone marrow immature granulocytes were increased and targeted by the virus in persistently infected piglets. Taken together, we provided the first data demonstrating the feasibility of CSFV in generating a postnatal persistent disease, which has not been shown for other members of the Pestivirus genus yet. Since serological methods are routinely used in CSFV surveillance, persistently infected pigs might go unnoticed. In addition to the epidemiological and economic significance of persistent CSFV infection, this model could be useful for understanding the mechanisms of viral persistence.
dc.description.sponsorshipInstitut für Virologie und Immunologie (IVI)
dc.identifier.doi10.7892/boris.76069
dc.identifier.pmid25938664
dc.identifier.publisherDOI10.1371/journal.pone.0125692
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/198242
dc.language.isoen
dc.publisherPublic Library of Science
dc.relation.ispartofPLoS ONE
dc.relation.issn1932-6203
dc.relation.organizationDCD5A442C208E17DE0405C82790C4DE2
dc.relation.organizationDCD5A442C0BAE17DE0405C82790C4DE2
dc.relation.organizationDCD5A442C1CCE17DE0405C82790C4DE2
dc.subject.ddc600 - Technology::630 - Agriculture
dc.titlePostnatal persistent infection with classical Swine Fever virus and its immunological implications.
dc.typearticle
dspace.entity.typePublication
dspace.file.typetext
oaire.citation.issue5
oaire.citation.startPagee0125692
oaire.citation.volume10
oairecerif.author.affiliationInstitut für Virologie und Immunologie (IVI)
oairecerif.author.affiliationInstitut für Virologie und Immunologie (IVI)
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unibe.description.ispublishedpub
unibe.eprints.legacyId76069
unibe.journal.abbrevTitlePLOS ONE
unibe.refereedtrue
unibe.subtype.articlejournal

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