Author/Authors :
Aghayian, Leila Department of Microbiology and Immunology - Faculty of Veterinary Medicin - University of Tehran - Tehran, Iran , Ghalyanchilangeroudi, Arash Department of Microbiology and Immunology - Faculty of Veterinary Medicin - University of Tehran - Tehran, Iran , Hamedi, Mona Department of Microbiology and Immunology - Faculty of Veterinary Medicin - University of Tehran - Tehran, Iran , Ziafati Kafi, Zahara Department of Microbiology and Immunology - Faculty of Veterinary Medicin - University of Tehran - Tehran, Iran , FallahMehrabadi, Mohammad Hossein Department of Poultry Diseases - RAZI Vaccine and Serum Research Institute - Agricultural Research - Education and Extension Organization (AREEO) - Tehran, Iran , Ghafouri, Ali Department of Clinical Sciences - Faculty of Veterinary Medicine - Ferdowsi University of Mashhad , Hosseini, Hossein Department of Clinical Sciences - Faculty of Veterinary Medicine - Islamic Azad University - Karaj Branch, Karaj, Iran , khaltabadi Farahani, Reza Iranian Veterinary Organization - Tehran, Iran , Maghsoudloo, Hossein Iranian Veterinary Organization - Tehran, Iran , Abdollahi, Hamed Iranian Veterinary Organization - Tehran, Iran
Abstract :
Infectious bronchitis is an economically important disease,
especially in chickens. It causes disorders in the respiratory tract, kidney and reproductive
tract of affected birds. The annual losses imposed by the disease are significant in the Iranian
poultry industry. The Infectious bronchitis virus has many different serotypes and mutations
in its RNA results in the virus variation which makes the control of IB more difficult. The
control strategy of IB is based on vaccination and it has been used live and inactivated
vaccines. Vaccines against different strains of the virus have been used. Vaccines should be
against specific strains in each area. The application of an appropriate ELISA kit which can
detect the level of antibody response leads to choosing an effective vaccine.
Materials and Methods: The current study compared antibody response after four
vaccination approach and then compared 3 ELISA kits for the detection of antibody rising. A
total of 100 SPF chickens were divided into 5 groups. The first group considered as the
control and H120-H120, H120-1/96, H120-4/91, and H120-IB88 protocols were conducted
for the 2nd, 3rd, 4th, and 5th groups, respectively. The validation of the Proflok, BioChek
and IDEXX ELISA kits were evaluated after vaccination.
Results: Significant differences in titers between four vaccination approaches were shown
better by Biochek, Idexx and Proflok kits respectively. Also, the highest antibody titration
belonged to the 4th group and the highest titration detected by the Proflok kit which had the
most sensitivity.
Conclusions: According to our results, it is important to use endemic strains of the IBV for
vaccination to have better cross-protection. In this study, as the 3 studied kits had different
sensitivity and specificity, different antibody rising was detected.
Keywords :
Vaccination protocol , Iran , Infectious bronchitis , ELISA kit