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| DOI | 10.1016/J.VETMIC.2023.109921 | ||||
| Año | 2023 | ||||
| Tipo | artículo de investigación |
Citas Totales
Autores Afiliación Chile
Instituciones Chile
% Participación
Internacional
Autores
Afiliación Extranjera
Instituciones
Extranjeras
Mycoplasma synoviae is a pathogen of poultry that causes upper respiratory tract disease. MS-H is a live attenuated temperature-sensitive vaccine that effectively control M. synoviae infection in chickens. However, the mechanisms underpinning protection have not been described previously. In this study, specific-pathogen-free chickens were vaccinated at 3 weeks of age with MS-H vaccine and challenged with field strain M. synoviae 94011/v-18d at 6 weeks of age. Tracheal mucosal inflammation was characterised by the assessment of thickness, histopathological lesions, cellular infiltrates and cytokine transcription. Tracheal lesion scores of unvaccinated-challenged (-V+C) birds were higher than that of vaccinated-challenged (+V+C) birds. +V+C birds displayed early upregulation of IL-4, consistent with a Th-2-skewed response, followed by a later increase in IFN-γ transcription, indicating transition to a Th-1-skewed response. -V+C birds displayed a concurrent early Th-2 and Th-17 response characterised by increase expression of IL-4 and IL-17A respectively, and late T regulatory response characterised by increased IL-10 transcription. +V+C chickens had more cytotoxic T cells (CD8+ T cells) at 7- and 21 days post-challenge (dpc), while -V+C chickens had higher numbers of infiltrating CD4+CD25+ at 7 and 21 dpc. Overall, these observations suggest that the immune response in +V+C chickens had an inflammation characterised by an early Th-2 skewed response followed closely by a Th-1 response and infiltration of cytotoxic T cells, while the response in -V+C chickens was an early Th-2/Th-17-skewed response closely followed by a T regulatory response.
| Ord. | Autor | Género | Institución - País |
|---|---|---|---|
| 1 | Omotainse, Oluwadamilola S. | - |
Asia Pacific Centre for Animal Health - Australia
Univ Melbourne - Australia |
| 2 | Wawegama, Nadeeka K. | - |
Asia Pacific Centre for Animal Health - Australia
Univ Melbourne - Australia |
| 3 | Kulappu Arachchige, Sathya N. | - |
Asia Pacific Centre for Animal Health - Australia
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| 3 | Arachchige, Sathya N. Kulappu | - |
Univ Melbourne - Australia
Asia Pacific Centre for Animal Health - Australia |
| 4 | Coppo, Mauricio C. | - |
Asia Pacific Centre for Animal Health - Australia
Universidad Nacional Andrés Bello - Chile Univ Melbourne - Australia |
| 5 | Vaz, Paola K. | Mujer |
Asia Pacific Centre for Animal Health - Australia
Univ Melbourne - Australia |
| 6 | Saliha, Uneeb | - |
Asia Pacific Centre for Animal Health - Australia
Univ Melbourne - Australia |
| 7 | Bogeski, Mirjana | Mujer |
Faculty of Veterinary and Agricultural Sciences - Australia
Univ Melbourne - Australia |
| 8 | Noormohammadi, Amir H. | Hombre |
Asia Pacific Centre for Animal Health - Australia
Univ Melbourne - Australia |
| 9 | Stent, Andrew W. | Hombre |
Asia Pacific Centre for Animal Health - Australia
Univ Melbourne - Australia |
| Fuente |
|---|
| University of Melbourne |
| Melbourne International Fee Remission Scholarship |
| Melbourne Research Scholarship |
| Agradecimiento |
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| OSO was supported by Melbourne International Fee Remission and Melbourne Research Scholarships. The authors acknowledge the assistance of Dr Pollob Shil, Ms June Daly and Ms Angela Chircop (staff of APCAH Animal house facility, the University of Melbourne) for caring for the animals. Drs Allison van de Meene and Gabriela Segal for training in acquisition of fluorescent images at the Biological Optical Microscopy Platform, the University of Melbourne. |
| OSO was supported by Melbourne International Fee Remission and Melbourne Research Scholarships. The authors acknowledge the assistance of Dr Pollob Shil, Ms June Daly and Ms Angela Chircop (staff of APCAH Animal house facility, the University of Melbourne) for caring for the animals. Drs Allison van de Meene and Gabriela Segal for training in acquisition of fluorescent images at the Biological Optical Microscopy Platform, the University of Melbourne. |