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Assessment of Mycoplasma gallisepticum vaccine efficacy in a co-infection challenge model with QX-like infectious bronchitis virus.
Bwala, Dauda G; Solomon, Ponman; Duncan, Neil; Wandrag, Daniel B R; Abolnik, Celia.
Afiliação
  • Bwala DG; a Poultry Section, Department of Production Animal Studies, Faculty of Veterinary Science , University of Pretoria , Onderstepoort , South Africa.
  • Solomon P; b National Veterinary Research Institute , Vom , Nigeria.
  • Duncan N; a Poultry Section, Department of Production Animal Studies, Faculty of Veterinary Science , University of Pretoria , Onderstepoort , South Africa.
  • Wandrag DBR; b National Veterinary Research Institute , Vom , Nigeria.
  • Abolnik C; c Pathology Section, Department of Paraclinical Science, Faculty of Veterinary Science , University of Pretoria , Onderstepoort , South Africa.
Avian Pathol ; 47(3): 261-270, 2018 Jun.
Article em En | MEDLINE | ID: mdl-29451010
ABSTRACT
Mycoplasma 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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças das Aves Domésticas / Vacinas Bacterianas / Galinhas / Vírus da Bronquite Infecciosa / Mycoplasma gallisepticum / Infecções por Mycoplasma Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças das Aves Domésticas / Vacinas Bacterianas / Galinhas / Vírus da Bronquite Infecciosa / Mycoplasma gallisepticum / Infecções por Mycoplasma Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2018 Tipo de documento: Article