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dc.contributor.authorDong, N
dc.contributor.authorNichols, H
dc.contributor.authorSun, Q
dc.contributor.authorChen, X
dc.contributor.authorZheng, J
dc.contributor.authorGuan, Z
dc.contributor.authorZhang, H
dc.contributor.authorDavison, A
dc.contributor.authorWezel, Y
dc.contributor.authorLi, Z
dc.contributor.authorLi, B
dc.contributor.authorLiu, K
dc.contributor.authorShao, D
dc.contributor.authorQiu, Y
dc.contributor.authorSun, J
dc.contributor.authorLi, X
dc.contributor.authorUpton, Mathew
dc.contributor.authorMa, Z
dc.contributor.authorJarvis, MA
dc.contributor.authorWei, J
dc.date.accessioned2023-06-08T21:38:20Z
dc.date.available2023-06-08T21:38:20Z
dc.date.issued2023-05-20
dc.identifier.issn2076-393X
dc.identifier.issn2076-393X
dc.identifier.other1004
dc.identifier.urihttps://pearl.plymouth.ac.uk/handle/10026.1/20965
dc.description.abstract

Streptococcus suis (S. suis) is a bacterial pathogen of pigs that has a major animal health and economic impact on the pig industry. Bovine herpesvirus-4 (BoHV-4) is a new virus-based vaccine vector that has been used for the immunogenic delivery of antigens from a variety of pathogens. In the present study, two recombinant BoHV-4-based vectors were evaluated for their ability to induce immunity and protection against S. suis in a rabbit model. The GMD protein is a fusion protein consisting of multiple dominant B-cell epitopes ((B-cell dominant epitopes of GAPDH, MRP, and DLDH antigens) (BoHV-4/GMD)) and the second suilysin (SLY) (BoHV-4/SLY) from S. suis serotype 2 (SS2). Both GMD and SLY delivered by the BoHV-4 vectors were recognized by sera from SS2-infected rabbits. The vaccination of rabbits with the BoHV-4 vectors induced antibodies against SS2, as well as against additional S. suis serotypes, SS7 and SS9. However, sera from BoHV-4/GMD-vaccinated animals promoted a significant level of phagocytic activity by pulmonary alveolar macrophages (PAMs) against SS2, SS7, and SS9. In contrast, sera from rabbits immunized with BoHV-4/SLY induced PAM phagocytic activity against only SS2. In addition, BoHV-4 vaccines differed in the associated level of protection against lethal SS2 challenge, which ranged from high (71.4%) to low (12.5%) for BoHV-4/GMD and BoHV-4/SLY, respectively. These data suggest BoHV-4/GMD as a promising vaccine candidate against S. suis disease.

dc.format.extent1004-1004
dc.format.mediumElectronic
dc.languageen
dc.publisherMDPI AG
dc.subjectStreptococcus suis
dc.subjectBoHV-4
dc.subjectGMD
dc.subjectsuilysin
dc.subjectserotype
dc.subjectvector-based vaccine
dc.subjectprotection
dc.titleBovine Herpesvirus-4 Based Vaccine Provides Protective Immunity against Streptococcus suis Disease in a Rabbit Model
dc.typejournal-article
dc.typeJournal Article
plymouth.author-urlhttps://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000997128900001&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=11bb513d99f797142bcfeffcc58ea008
plymouth.issue5
plymouth.volume11
plymouth.publication-statusPublished online
plymouth.journalVaccines
dc.identifier.doi10.3390/vaccines11051004
plymouth.organisational-group|Plymouth
plymouth.organisational-group|Plymouth|Research Groups
plymouth.organisational-group|Plymouth|Faculty of Health
plymouth.organisational-group|Plymouth|Research Groups|Institute of Translational and Stratified Medicine (ITSMED)
plymouth.organisational-group|Plymouth|Research Groups|Institute of Translational and Stratified Medicine (ITSMED)|CBR
plymouth.organisational-group|Plymouth|REF 2021 Researchers by UoA
plymouth.organisational-group|Plymouth|Users by role
plymouth.organisational-group|Plymouth|Users by role|Academics
plymouth.organisational-group|Plymouth|REF 2021 Researchers by UoA|UoA01 Clinical Medicine
plymouth.organisational-group|Plymouth|Faculty of Health|School of Biomedical Sciences
plymouth.organisational-group|Plymouth|Users by role|Researchers in ResearchFish submission
plymouth.organisational-group|Plymouth|Research Groups|Plymouth Institute of Health and Care Research (PIHR)
dc.publisher.placeSwitzerland
dcterms.dateAccepted2023-05-18
dc.date.updated2023-06-08T21:38:06Z
dc.rights.embargodate2023-6-10
dc.identifier.eissn2076-393X
dc.rights.embargoperiodforever
rioxxterms.versionofrecord10.3390/vaccines11051004


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