| Autor: |
Galvão CC; Instituto de Medicina Veterinária, Universidade Federal do Pará, Castanhal, Pará CEP 68740-970, Brazil., Barbosa JD; Instituto de Medicina Veterinária, Universidade Federal do Pará, Castanhal, Pará CEP 68740-970, Brazil., Oliveira CMC; Instituto de Medicina Veterinária, Universidade Federal do Pará, Castanhal, Pará CEP 68740-970, Brazil., Otaka DY; Instituto de Medicina Veterinária, Universidade Federal do Pará, Castanhal, Pará CEP 68740-970, Brazil., Silva PRO; Instituto de Medicina Veterinária, Universidade Federal do Pará, Castanhal, Pará CEP 68740-970, Brazil., Ferreira MRA; Centro de Desenvolvimento Tecnológico, Núcleo de Biotecnologia, Universidade Federal de Pelotas, Pelotas, Rio Grande do Sul CEP 96160-000, Brazil., Moreira Júnior C; Centro de Desenvolvimento Tecnológico, Núcleo de Biotecnologia, Universidade Federal de Pelotas, Pelotas, Rio Grande do Sul CEP 96160-000, Brazil., Conceição FR; Centro de Desenvolvimento Tecnológico, Núcleo de Biotecnologia, Universidade Federal de Pelotas, Pelotas, Rio Grande do Sul CEP 96160-000, Brazil., Salvarani FM; Instituto de Medicina Veterinária, Universidade Federal do Pará, Castanhal, Pará CEP 68740-970, Brazil. |
| Abstrakt: |
The alpha (CPA), beta (CPB) and epsilon (ETX) toxins of Clostridium perfringens are responsible for causing diseases that are difficult to eradicate and have lethal potential in production animals. Vaccination of herds is still the best control strategy. Recombinant clostridial vaccines have shown good success at inducing neutralizing antibody titers and appear to be a viable alternative to the conventional production of commercial clostridial toxoids. Research is still needed on the longevity of the humoral immune response induced by recombinant proteins in immunized animals, preferably in target species. The objective of this study was to measure the humoral immune response of cattle immunized with trivalent vaccines containing the recombinant proteins alpha (rCPA), beta (rCPB) and epsilon (rETX) of C. perfringens produced in Escherichia coli at three different concentrations (100, 200, and 400 µg) of each protein for 12 months. The recombinant vaccines containing 200 (RV2) and 400 µg (RV3) yielded statistically similar results at 56 days. They performed better throughout the study period because they induced higher neutralizing antibody titers and were detectable for up to 150 and 180 days, respectively. Regarding industrial-scale production, RV2 would be the most economical and viable formulation as it achieved results similar to RV3 at half the concentration of recombinant proteins in its formulation. However, none of the vaccines tested induced the production of detectable antibody titers on day 365 of the experiment, the time of revaccination typically recommended in vaccination protocols. Thus, reiterating the need for research in the field of vaccinology to achieve greater longevity of the humoral immune response against these clostridial toxins in animals, in addition to the need to discuss the vaccine schedules and protocols adopted in cattle production. |
