Efficacy of two commercial ready-to-use PCV2 and mycoplasma hyopneumoniae vaccines under field conditions

dc.contributor.affiliationUniversidade de Santiago de Compostela. Departamento de Patoloxía Animalgl
dc.contributor.authorLópez-Lorenzo, Gonzalo
dc.contributor.authorPrieto Lago, Alberto
dc.contributor.authorLópez Novo, Cynthia
dc.contributor.authorDíaz Fernández, Pablo
dc.contributor.authorLópez Sández, Ceferino Manuel
dc.contributor.authorMorrondo Pelayo, María Patrocinio
dc.contributor.authorFernández Rodríguez, Gonzalo
dc.contributor.authorDíaz Cao, José Manuel
dc.date.accessioned2021-12-20T09:02:39Z
dc.date.available2021-12-20T09:02:39Z
dc.date.issued2021
dc.description.abstractPorcine Circovirus Type 2 (PCV2) and Mycoplasma hyopneumoniae are economically important pathogens in swine farms. Vaccination is the main preventive measure for both infections. In order to test two ready-to-use bivalent vaccines, 646 piglets from a herd actively infected with both pathogens were stratified according to the sow parity number and randomly assigned to three groups: A and B were vaccinated with two different vaccines, respectively, while C remained as the unvaccinated control. Vaccine efficacy was assessed based on the weight, average daily weight gai (ADWG), degree of lung lesions, presence of PCV2 viremia by qPCR and presence of PCV2 and M. hyopneumoniae antibody levels by ELISA. Our data revealed that the sow parity did not influence the vaccine outcomes. Good results for most of the analyzed parameters were observed in both vaccinated groups. ADGW and final weight were higher and lung lesions were less evident in both vaccinated groups than in the control one, but only Group A showed a significant improvement. PCV2 viremia was not detected in Group A, but it did appear in Group B coinciding with its peak in Group C. Finally, both the PCV2 and M. hyopneumoniae serological patterns differed depending on the employed vaccinegl
dc.description.peerreviewedSIgl
dc.identifier.citationAnimals 2021, 11(6), 1553gl
dc.identifier.doi10.3390/ani11061553
dc.identifier.issn2076-2615
dc.identifier.urihttp://hdl.handle.net/10347/27250
dc.language.isoenggl
dc.publisherMDPIgl
dc.relation.publisherversionhttps://doi.org/10.3390/ani11061553gl
dc.rights© 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https:// creativecommons.org/licenses/by/ 4.0/).gl
dc.rightsAtribución 4.0 Internacional
dc.rights.accessRightsopen accessgl
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectPCV2gl
dc.subjectMycoplasma hyopneumoniaegl
dc.subjectReady-to-usegl
dc.subjectVaccinationgl
dc.subjectSow paritygl
dc.subjectField trialgl
dc.titleEfficacy of two commercial ready-to-use PCV2 and mycoplasma hyopneumoniae vaccines under field conditionsgl
dc.typejournal articlegl
dc.type.hasVersionVoRgl
dspace.entity.typePublication
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