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First report on the seroprevalence of avian encephalomyelitis virus antibody in Sonali (cross-bred) chickens in Bogura, Bangladesh.
Ali, Md Zulfekar; Shaon, Md Taohid Wasim; Moula, Mohammad Moktader; Bary, Md Akramul; Al Momen Sabuj, Abdullah; Khaled, Shamsul Arefin; Bhuiyan, Zafar Ahmed; Giasuddin, Md.
Afiliação
  • Ali MZ; Animal Health Research Division, Bangladesh Livestock Research Institute, Dhaka, Bangladesh.
  • Shaon MTW; Central Poultry Laboratory, Nourish Poultry and Hatchery Ltd., Dhaka, Bangladesh.
  • Moula MM; Central Poultry Laboratory, Nourish Poultry and Hatchery Ltd., Dhaka, Bangladesh.
  • Bary MA; Central Poultry Laboratory, Nourish Poultry and Hatchery Ltd., Dhaka, Bangladesh.
  • Al Momen Sabuj A; Central Poultry Laboratory, Nourish Poultry and Hatchery Ltd., Dhaka, Bangladesh.
  • Khaled SA; Central Poultry Laboratory, Nourish Poultry and Hatchery Ltd., Dhaka, Bangladesh.
  • Bhuiyan ZA; Central Poultry Laboratory, Nourish Poultry and Hatchery Ltd., Dhaka, Bangladesh.
  • Giasuddin M; Animal Health Research Division, Bangladesh Livestock Research Institute, Dhaka, Bangladesh.
J Adv Vet Anim Res ; 8(1): 78-83, 2021 Mar.
Article em En | MEDLINE | ID: mdl-33860016
OBJECTIVES: The study intended to detect the presence and distribution of avian encephalomyelitis virus (AEV)-specific antibodies in Sonali (cross-bred) parent chickens regarding farm location, flock size, and age in Bogura district of Bangladesh, a Sonali chicken belt. MATERIALS AND METHODS: A total of 275 Sonali parent chickens' blood samples were collected randomly from 39 flocks during laying age with a healthy and non-vaccination history against AEV. Blood samples were collected aseptically from the wing veins of chickens using 3-ml syringes and sera were separated. Then, the sera were transferred to the laboratory by maintaining a cool chain. Indirect enzyme-linked immunosorbent assay was used to detect the specific antibodies against AEV present in the sera samples. RESULTS: Overall, 70.18% of the chickens were found seropositive for AEV antibodies. Based on the location, the highest seropositivity was recorded in Bogura Sadar [91.30%, confidence intervals (CI) 79.21%-97.58%], and the lowest was in the Adomdighi sub-district (45.45%, CI 29.49%-63.08%). For flock size, AEV seropositivity was significantly (p < 0.05) higher in the large flock (82.22%, CI 72.74%-89.48%). Regarding age groups, the seropositivity of AEV was significantly (p < 0.05) increased with chickens' age. Higher seropositivity was noted in chickens aged >51 weeks (89.32%, CI 81.69%-94.55%). CONCLUSION: The results indicate that AEV is circulating in the environment, and chickens were exposed to the field strain of AEV. To the best of our knowledge, this is the first report on AEV in chickens in Bangladesh. Proper vaccination and standard farm biosecurity practice could minimize AEV infection in chickens. A detailed epidemiology study, detection, and characterization of the AEV would be essential for effective AEV infection control.
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Texto completo: 1 Bases de dados: MEDLINE Idioma: En Revista: J Adv Vet Anim Res Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Bangladesh

Texto completo: 1 Bases de dados: MEDLINE Idioma: En Revista: J Adv Vet Anim Res Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Bangladesh