Brucellosis 2003 proceedings - PHIDIAS
Brucellosis 2003 proceedings - PHIDIAS
Brucellosis 2003 proceedings - PHIDIAS
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Poster Session<br />
melitensis wild type virulent strain 16M. Four weeks after inoculation, strain WRSPA<br />
completely cleared from spleens. These results indicate that strain WRSPA is not as<br />
virulent as strain 16M and not as attenuated as strain WRRP1. The recombinant<br />
strains WR201PA and WRSPA have potential as vaccine candidates against anthrax<br />
and brucellosis in humans.<br />
92- EVALUATION OF B. abortus M1luc AND I2 AS VACCINES AGAINST BOVINE<br />
BRUCELOSIS.<br />
E. Campos 1 , S. Cravero 1 , A. Fiorentino 2 , A. Arese 1 , F. Paolicci 2 , C. Campero 2 , O. Rossetti 1 . (1) Inst.<br />
de Biotecnología. CICVyA. Argentina. (2) EEA Balcarce. INTA. Buenos Aires. Argentina.<br />
B. abortus M1luc is a mutant strain derived from S19 in which most of bp26<br />
sequence has been replaced by the luc gene. I2 is a double mutant in which, apart<br />
from bp26 mutation, most of omp19 has been deleted. In BALB/c mice, M1luc<br />
behaved as S19. I2 was more attenuated than S19 but conferred the same level of<br />
protection against challenge with S2308. The objective was to obtain strains that<br />
could be easily distinguished from field strains (by use of the luc marker) and that<br />
had an associated diagnostic test (using BP26 antigen). In I2, the objective was to<br />
generate a strain that would also have less residual virulence than S19, retaining its<br />
protection capacity. For evaluation in the natural host, groups of 5-month old heifers<br />
were either not vaccinated or vaccinated with 2x10 10 CFU of S19, M1luc or I2 (N=15,<br />
each). All vaccines generated equal humoral immune response against LPS. Animals<br />
were inseminated and then challenged, in the third trimester of pregnancy, with<br />
3x10 7 CFU of S2308. The protection levels against abortion were 78.6% for S19,<br />
81.8% for M1luc and 45.5% for I2. From the non-vaccinated group, 25% did not<br />
abort. These results indicate that Omp19 is necessary for S19 full protection<br />
capacity. The BP26-i ELISA was highly specific for animals vaccinated with M1luc or<br />
I2. S19 vaccinated animals developed anti-BP26 antibodies after 6 months of<br />
vaccination. The control group did not present antibodies against BP26 at any time.<br />
However, sensitivity after the experimental challenge was much lower than the one<br />
obtained for naturally infected cattle.<br />
93- EVALUATION OF NOVEL Brucella abortus AND Brucella melitensis<br />
DELETION MUTANTS AS POTENTIAL VACCINE CANDIDATES IN THE MOUSE<br />
AND GOAT MODELS OF BRUCELLOSIS.<br />
M. Kahl 1 , P. H. Elzer 2 , S. D. Hagius 2 , D. S. Davis 1 , A. Den-Hartigh 3 , R. Tsolis 3 and T. A. Ficht 1 . (1)<br />
Veterinary Pathobiology, Texas A&M University and Texas Agricultural Experiment Station, College<br />
Station, TX 77843-4467. USA. (2) Department of Veterinary Science, LSU AgCenter, Baton Rouge,<br />
LA. USA. (3) Microbiology and Immunology, Texas A&M Health Science Center, College Station, TX.<br />
USA.<br />
Using in vivo screening of signature tagged mutant banks, we have identified<br />
several B. abortus genes that are attenuated in virulence due to a reduced ability to<br />
either establish or maintain a successful infection in the mouse model. Based on the<br />
ability of selected mutants to stimulate a protective immune response in the mouse,<br />
we hypothesized that one or more deletion mutants may prove to be superior to<br />
currently available vaccines in large animals. The creation of unmarked deletion<br />
142<br />
<strong>Brucellosis</strong> <strong>2003</strong> International Research Conference