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Trial for preparation and evaluation of inactivated multicomponent vaccine containing BVD, IBR, PI-3 viruses, Salmonella typhimurium and Salmonella dublin for calves [electronic resource].

By:

Ghattas, W. M

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Language: English Summary language: Arabic Description: p.45-56Other title:

محاولة تحضير ومعايرة لقاح جامع مثبط يحتوى على فيروسات مرض الأسهال البقرى الفيروسى ومرض ألتهاب القصبة الهوائية الرغامى المعدى وفيروس البارا أنفلونزا-3 وبكتيريا السالمونيلا تيفيميوريوم والسالمونيلا دبلن فى العجول [Added title page title]

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Zagazig veterinary journal, 2009 v. 37 (3) [electronic resource].

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In: Zagazig Veterinary Journal 2009.v.37(3)Summary: An inactivated multicomponent vaccine adjuvanted with aluminum hydroxide gel against Bovine Viral Diarrhea (BVD), Infectious Bovine Rhinotracheits (IPR), and Para influenza-3 (PI3) viruses with S. typhimurium and S. dublin bacteria was prepared. The vaccine was pure and safe. Potency evaluation was applied on 12 adult apparently healthy calves divided into 4 groups 3 animals for each. The immune responses were monitored using serum neutralization, agglutination and mouse protection tests. The results revealed a lack of interaction and antagonistic effect among the component of the prepared vaccine. The humeral immune responses gave antibody titers over the permissible limit of protective level and persist for 24 weeks post vaccination (period of study).

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An inactivated multicomponent vaccine adjuvanted with aluminum hydroxide gel against Bovine Viral Diarrhea (BVD), Infectious Bovine Rhinotracheits (IPR), and Para influenza-3 (PI3) viruses with S. typhimurium and S. dublin bacteria was prepared. The vaccine was pure and safe. Potency evaluation was applied on 12 adult apparently healthy calves divided into 4 groups 3 animals for each. The immune responses were monitored using serum neutralization, agglutination and mouse protection tests. The results revealed a lack of interaction and antagonistic effect among the component of the prepared vaccine. The humeral immune responses gave antibody titers over the permissible limit of protective level and persist for 24 weeks post vaccination (period of study).

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