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A Newcastle disease live virus vaccine is safe and efficacious at various storage conditions.
Huma, Iffat; Azeem, Shahan; Naz, Sarwat; Yaqub, Tahir; Mushtaq, Muhammad Hassan; Azam, Muhammad.
Afiliación
  • Huma I; Veterinary Research Institute, Lahore, Pakistan; Faculty of Veterinary Science, University of Veterinary and Animal Sciences, Lahore, Pakistan.
  • Azeem S; Faculty of Veterinary Science, University of Veterinary and Animal Sciences, Lahore, Pakistan. sazeem@uvas.edu.pk.
  • Naz S; Veterinary Research Institute, Lahore, Pakistan.
  • Yaqub T; Faculty of Veterinary Science, University of Veterinary and Animal Sciences, Lahore, Pakistan.
  • Mushtaq MH; Faculty of Veterinary Science, University of Veterinary and Animal Sciences, Lahore, Pakistan.
  • Azam M; Faculty of Livestock Business Management, University of Veterinary and Animal Sciences, Lahore, Pakistan.
Vet Ital ; 59(3)2024 Sep 18.
Article en En | MEDLINE | ID: mdl-39298117
ABSTRACT
Pure, potent and efficacious vaccines could help in the control of Newcastle disease (ND). The present study was designed to evaluate the thermo-stability of a live-attenuated ND virus vaccine containing the Mukteswar strain and to genetically characterize the seed virus. Moreover, the presence of extraneous agents (Fowl adenovirus, Mycoplasma, Salmonella Pullorum, and Salmonella Gallinarum) was assessed using polymerase chain reactions (PCR) optimized for detection in a panel. The vaccine was evaluated for its potency and efficacy after storage at 4°C, 25°C and 37°C for 36, 48, 96 and 144 hours. A total of 100 commercial broiler chickens were randomly divided into six groups and immunized with the vaccine stored at specified temperatures for the given times. Blood samples were collected on days 0, 7, 14, 21 and 28 post-vaccination, sera were separated and antibody titers were assessed using hemagglutination inhibition (HI) assay. The data were analyzed by two-way analysis of variance (ANOVA) and multivariate analysis of variance (MANOVA). Reverse-transcription  PCR targeting the F gene of Newcastle disease virus (NDV) and subsequent sequence analysis confirmed the presence of NDV in the vaccine seed (deposited to GenBank Acc. Nos. MK310260 and MK310261). Phylogenetic analysis revealed a close resemblance of the vaccine virus with other Avian Avulaviruses (NDV class II Genotype III viruses and more specifically with NDV Mukteswar vaccine strains), yet it was distinct from NDV class II Pakistani field isolates, which grouped into genotype XIII.2.1. The PCR testing confirmed that the vaccine was free from extraneous agents. The present study's findings propose an alternative rapid PCR-based method to evaluate the purity of NDV live vaccines. Together these data suggest that the tested vaccine is pure, potent and efficacious, yet continuous maintenance of the cold chain for vaccine storage is recommended to maintain its potency and efficacy.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Enfermedades de las Aves de Corral / Virus de la Enfermedad de Newcastle / Vacunas Atenuadas / Vacunas Virales / Pollos / Enfermedad de Newcastle Límite: Animals Idioma: En Revista: Vet Ital Año: 2024 Tipo del documento: Article País de afiliación: Pakistán

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Enfermedades de las Aves de Corral / Virus de la Enfermedad de Newcastle / Vacunas Atenuadas / Vacunas Virales / Pollos / Enfermedad de Newcastle Límite: Animals Idioma: En Revista: Vet Ital Año: 2024 Tipo del documento: Article País de afiliación: Pakistán