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Comparative SARS-CoV-2 Omicron BA.5 variant and D614G-Wuhan strain infections in ferrets: insights into attenuation and disease progression during subclinical to mild COVID-19

dc.contributor.authorBarroso Arévalo, Sandra
dc.contributor.authorSánchez Morales, Lidia
dc.contributor.authorPorras González, Néstor
dc.contributor.authorDíaz Frutos, Marta
dc.contributor.authorBarasona García-Arévalo, José Ángel
dc.contributor.authorIsla, Julio
dc.contributor.authorLópez, Débora
dc.contributor.authorGortázar, Christian
dc.contributor.authorDomínguez Rodríguez, Lucas José
dc.contributor.authorSánchez-Vizcaíno Rodríguez, José Manuel
dc.date.accessioned2024-09-05T15:52:12Z
dc.date.available2024-09-05T15:52:12Z
dc.date.issued2024-08-15
dc.description.abstractIntroduction: As the SARS-CoV-2 virus continues to evolve and new variants emerge, it becomes crucial to understand the comparative pathological and immunological responses elicited by different strains. This study focuses on the original Wuhan strain and the Omicron variant, which have demonstrated significant differences in clinical outcomes and immune responses. Methods: We employed ferrets as an experimental model to assess the D614G variant (a derivative of the Wuhan strain) and the Omicron BA.5 variant. Each variant was inoculated into separate groups of ferrets to compare disease severity, viral dissemination, and immune responses. Results: The D614G variant induced more severe disease and greater viral spread than the Omicron variant. Notably, ferrets infected with the D614G variant exhibited a robust neutralizing antibody response, whereas those infected with the Omicron variant failed to produce a detectable neutralizing antibody response. Despite the clearance of the virus from nearly all tissues by 7 days post-infection, an increase in pathological lesions was observed from 14 to 21 days, particularly in those infected with the D614G variant, suggesting a sustained immune response even after viral clearance. Discussion: These findings underscore the adaptability of SARS-CoV-2 and illuminate how susceptibility and clinical manifestations vary across different strains and species. The results emphasize the necessity of considering both the direct effects of viral infection and the indirect, often prolonged, impacts of the immune response in evaluating the outcomes of SARS-CoV-2 infections.en
dc.description.departmentDepto. de Sanidad Animal
dc.description.facultyFac. de Veterinaria
dc.description.facultyCentro de Vigilancia Sanitaria Veterinaria (VISAVET)
dc.description.refereedTRUE
dc.description.sponsorshipComunidad de Madrid
dc.description.sponsorshipEuropean Union
dc.description.sponsorshipMinisterio de Ciencia, Innovación y Universidades (España)
dc.description.statuspub
dc.identifier.citationBarroso-Arévalo S, Sánchez-Morales L, Porras N, Díaz-Frutos M, Barasona JA, Isla J, López D, Gortázar C, Domínguez L and Sánchez-Vizcaíno JM (2024) Comparative SARS-CoV-2 Omicron BA.5 variant and D614G-Wuhan strain infections in ferrets: insights into attenuation and disease progression during subclinical to mild COVID-19. Front. Vet. Sci. 11:1435464. doi: 10.3389/fvets.2024.1435464
dc.identifier.doi10.3389/fvets.2024.1435464
dc.identifier.essn2297-1769
dc.identifier.officialurlhttps://doi.org/10.3389/fvets.2024.1435464
dc.identifier.pmid39211479
dc.identifier.urihttps://hdl.handle.net/20.500.14352/107979
dc.journal.titleFrontiers in Veterinary Science
dc.language.isoeng
dc.page.final18
dc.page.initial1
dc.publisherFrontiers
dc.rightsAttribution 4.0 Internationalen
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subject.cdu363.09
dc.subject.cdu636.09
dc.subject.keywordSARS-CoV-2
dc.subject.keywordExperimental model
dc.subject.keywordPathogenesis
dc.subject.keywordOmicron
dc.subject.keywordFerrets
dc.subject.keywordAttenuation
dc.subject.ucmVeterinaria
dc.subject.unesco3109 Ciencias Veterinarias
dc.titleComparative SARS-CoV-2 Omicron BA.5 variant and D614G-Wuhan strain infections in ferrets: insights into attenuation and disease progression during subclinical to mild COVID-19en
dc.typejournal article
dc.type.hasVersionVoR
dc.volume.number11
dspace.entity.typePublication
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