Assessment of Mycoplasma gallisepticum vaccine efficacy in a co-infection challenge model with QX-like infectious bronchitis virus

dc.contributor.authorBwala, Dauda Garba
dc.contributor.authorSolomon, Ponman
dc.contributor.authorDuncan, N.M. (Neil)
dc.contributor.authorWandrag, D.B.R. (Daniel)
dc.contributor.authorAbolnik, Celia
dc.date.accessioned2018-05-23T11:20:09Z
dc.date.issued2018
dc.description.abstractMycoplasma gallisepticum (MG) is the primary cause of chronic respiratory disease in poultry. We investigated the protective efficacy of the live-attenuated ts-11 and 6/85 MG vaccines against a local MG strain and, in order to enhance signs and mimic a typical field situation, we co-infected birds with a virulent strain of QX-like infectious bronchitis virus (IBV). Both vaccines showed similar ability to protect infected chickens from clinical signs, although ts-11 performed slightly better. Despite the lower protection against clinical disease, 6/85-vaccinated birds had significantly (P ≤ 0.05) lower tracheal lesion scores and mucosal thickness at day 28 post-vaccination (7 days post-challenge [dpc] with MG, 2 dpc IBV) and day 31 post-vaccination (10 dpc MG challenge, 5 dpc IBV) compared to ts-11 vaccinated birds, but these difference was not significant at day 33 (12 dpc MG, 7 dpc IBV). Pathogen infection and replication was assessed by qPCR, and the 6/85 vaccine produced a more significant (P ≤ 0.05) reduction in MG replication in the lungs, kidneys and livers but enhanced late replication in bursae and caecal tonsils. In contrast, the ts-11 vaccine had a more pronounced reductive effect on replication in tracheas, air sacs, bursae and heart at days 28 and 31, yet increased replication in lungs. Interestingly, both vaccines provided non-specific protection against IBV challenge. The co-challenge model provided useful data on vaccine efficacy, especially on days 31 and 33, and tracheas, lungs, air sacs, kidneys, liver and caecal tonsils were the best organs to assess.en_ZA
dc.description.departmentParaclinical Sciencesen_ZA
dc.description.departmentProduction Animal Studiesen_ZA
dc.description.embargo2019-03-14
dc.description.librarianhj2018en_ZA
dc.description.librarianes2025en
dc.description.sdgSDG-02: Zero hungeren
dc.description.sdgSDG-03: Good health and well-beingen
dc.description.sdgSDG-12: Responsible consumption and productionen
dc.description.sdgSDG-17: Partnerships for the goalsen
dc.description.sponsorshipDGB was a recipient of a University of Pretoria scholarship.en_ZA
dc.description.urihttp://www.tandfonline.com/loi/cavp20en_ZA
dc.identifier.citationDauda G. Bwala, Ponman Solomon, Neil Duncan, Daniel B.R. Wandrag & Celia Abolnik (2018) Assessment of Mycoplasma gallisepticum vaccine efficacy in a co-infection challenge model with QX-like infectious bronchitis virus, Avian Pathology, 47:3, 261-270, DOI: 10.1080/03079457.2018.1440064.en_ZA
dc.identifier.issn0307-9457 (print)
dc.identifier.issn1465-3338 (online)
dc.identifier.other10.1080/03079457.2018.1440064
dc.identifier.urihttp://hdl.handle.net/2263/64992
dc.language.isoenen_ZA
dc.publisherTaylor and Francisen_ZA
dc.rights© 2018 Houghton Trust Ltd. This is an electronic version of an article published in Avian Pathology, vol. 47, no. 3, pp. 261-270, 2018. doi : 10.1080/03079457.2018.1440064. Avian Pathology is available online at : http://www.tandfonline.com/loi/cavp20.en_ZA
dc.subjectMycoplasma gallisepticum (MG)en_ZA
dc.subjectQX-like infectious bronchitis virusen_ZA
dc.subjectInfectious bronchitis virus (IBV)en_ZA
dc.subjectqPCRen_ZA
dc.subjectPoultryen_ZA
dc.subjectProtectionen_ZA
dc.subjectChicken tracheaen_ZA
dc.subjectImmune responseen_ZA
dc.subjectVirulenceen_ZA
dc.subjectCo-infection modelen_ZA
dc.subjectChallengesen_ZA
dc.subjectVaccinesen_ZA
dc.subjectRespiratory tracten_ZA
dc.subject.otherVeterinary science articles SDG-02en
dc.subject.otherVeterinary science articles SDG-03en
dc.subject.otherVeterinary science articles SDG-12en
dc.subject.otherVeterinary science articles SDG-17en
dc.titleAssessment of Mycoplasma gallisepticum vaccine efficacy in a co-infection challenge model with QX-like infectious bronchitis virusen_ZA
dc.typePostprint Articleen_ZA

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