Department of Clinical Pathology, Faculty of Vet. Med., Menufiya University, El-Sadat Branch, Egypt.
Anaerobe. 2011 Dec;17(6):426-30. doi: 10.1016/j.anaerobe.2011.04.019. Epub 2011 Jun 1.
The present study was conducted to evaluate the efficacy and safety of three vaccination regimes of Clostridium perfringens (C. perfringens) type A, C and combined A&C toxoids based on their clinical signs and immunological effects. The vaccines were administered two times at two weeks interval (7 & 21 days old), then the birds were challenged (35 days old) with virulent strains of C. perfringens type A, C and combined A&C. Blood samples were taken one week after the first and second vaccination as well as after challenge. The evaluated parameters in this study included: clinical signs, gross intestinal lesions, complete blood count (CBC), serum protein, liver profiles, and enzyme-linked immunosorbent assay (ELISA) test for detecting serum antibody titers. The results revealed that immunization of broilers with C. perfringens type A, C and combined A&C toxoids resulted in a significant decrease in numbers of chickens with intestinal lesions particularly with the A&C toxoids vaccine. Results of the CBC values were significantly increased in all treated groups and challenged groups. Total leukocytic count decreased in challenged non vaccinated group while increased in challenged vaccinated birds. Results of biochemical assays implicated that there were a significant increase in serum protein and liver profiles. ELISA results explored a significant increase in antibody titers after immunization of broilers with C. perfringens type A, C and combined A&C toxoids particularly after the second dose of vaccination. We concluded that immunization of broilers with toxoid vaccines particularly the combined type A & C is safe, well-tolerated and can protect broiler chickens against necrotic enteritis particularly after the second booster dose of the vaccine.
本研究旨在评估三种产气荚膜梭菌(C. perfringens)A型、C 型和 A+C 联合类毒素疫苗的疗效和安全性,评估依据为临床症状和免疫效果。疫苗在两周(7 天和 21 天)的间隔内分两次接种,然后在 35 天用强毒型 A、C 和 A+C 产气荚膜梭菌对禽类进行攻毒。在第一次和第二次接种后以及攻毒后一周采集血液样本。本研究评估的参数包括:临床症状、肠道病变、全血细胞计数(CBC)、血清蛋白、肝功能和酶联免疫吸附试验(ELISA)检测血清抗体滴度。结果表明,用产气荚膜梭菌 A、C 和 A+C 联合类毒素免疫肉鸡可显著降低肠道病变鸡的数量,尤其是 A+C 联合类毒素疫苗。所有治疗组和攻毒组的 CBC 值均显著增加。白细胞总数在未接种攻毒组中减少,而在接种攻毒组中增加。生化分析结果表明,血清蛋白和肝功能均显著增加。ELISA 结果表明,用产气荚膜梭菌 A、C 和 A+C 联合类毒素免疫肉鸡后,抗体滴度显著增加,尤其是第二次接种后。综上所述,用类毒素疫苗免疫肉鸡,特别是 A+C 联合疫苗,安全、耐受良好,能有效保护肉鸡免受坏死性肠炎,尤其是在第二次加强剂量后。