No abstract

The diagnosis of brucellosis is mainly based on the detection of anti-LPS antibodies. High temperature kills Brucella cells by causing lysis of the membrane, so the phenol-heat killed brucella antigen may lake specificity as a result of destruction the majority of proteins in the cell wall. Accordingly, attention was directed to produce antigen using binary ethylene imine as an inactivator. The produced antigen showed high specificity in detecting Brucella abortus and Brucella melitensis-infected animals, but sensitivity was not affected in comparison with the standard Rose Bengal antigen. In Enzyme immunotransfer blot (EITB), phenol-heat killed brucella cells showed only 3 bands (37.375, 23.47 and 7.83 kDa) that denotes denaturation for at least 6 bands whereas binary inactivated brucella cells showed similarity with non-treated ones.

This study was conducted to evaluate the protective effect of Brucella melitensis Rev.1 and the use of BCG vaccine as immunostimulant by subcutaneous injection in Guinea pigs. Lab. animals were divided into 8 groups: Combined Rev.1 and BCG vaccines injected in the1 st group & both vaccines were injected simultaneously in the 2 nd group. Three groups sensitized with BCG vaccine then injected with Rev.1 vaccine one week, two week & three weeks intervals respectively. Other two groups were injected with BCG and Rev.1 vaccine individually. The last one was unvaccinated control. All injected animals showed resistance to infection with 16 M strain (90 %, 80 %, 80, 60 %, 70 %, 0 % and 70 % respectively).Thus animals vaccinated with bivalent Rev.1 and BCG vaccines (in one shot) showed the best protective level to infection.