Guelph Research and Development Centre, Agriculture and Agri-Food Canada, Guelph, Ontario N1G 5C9, Canada.
Department of Pathobiology, University of Guelph, Guelph, Ontario N1G 2W1, Canada.
Vet Microbiol. 2019 Mar;230:7-13. doi: 10.1016/j.vetmic.2019.01.005. Epub 2019 Jan 7.
Necrotic enteritis (NE) is an economically important disease of broiler chickens that is caused primarily by Clostridium perfringens strains that produce the NetB toxin. It is controlled in North America principally through the application of in-feed antimicrobials, but alternative control methods, such as vaccination, are urgently needed. We previously identified a cluster of C. perfringens genes prevalent in disease-causing strains, denominated VR-10B, that is predicted to encode a pilus. The current study evaluated the ability of three predicted pilin structural subunits (CnaA, FimA, FimB) to protect against NE in two immunization studies. In the first study, young broiler chickens were immunized twice intramuscularly (i.m.) with CnaA or FimA, which resulted in only a weak serum antibody response, and no reduction in the severity of intestinal lesions following experimental challenge with C. perfringens strain CP1. In the second study, chickens were injected subcutaneously (s.c.) with CnaA, FimB, or a combination of all three proteins, on days 7, 14 and 19, which resulted in a marked antibody response specific to each antigen. Chickens immunized with either CnaA or FimB had significantly reduced NE lesion severity, whereas immunization with all three proteins in combination did not provide protection. Western blot experiments using serum from immunized birds were also performed, providing the first experimental evidence to suggest that this locus may in fact encode a functional pilus structure.
坏死性肠炎(NE)是一种对肉鸡具有重要经济意义的疾病,主要由产生 NetB 毒素的产气荚膜梭菌菌株引起。在北美,主要通过应用饲料中的抗菌药物来控制该病,但迫切需要替代控制方法,例如疫苗接种。我们之前确定了一组在致病菌株中普遍存在的产气荚膜梭菌基因簇,称为 VR-10B,该基因簇预测编码一种菌毛。本研究在两项免疫研究中评估了三种预测的菌毛结构亚基(CnaA、FimA、FimB)预防 NE 的能力。在第一项研究中,年轻的肉鸡通过肌肉内(i.m.)免疫两次接种 CnaA 或 FimA,仅导致微弱的血清抗体反应,并且在实验性挑战 CP1 型产气荚膜梭菌后,肠道病变的严重程度没有降低。在第二项研究中,鸡在第 7、14 和 19 天通过皮下(s.c.)注射 CnaA、FimB 或三种蛋白的组合,导致针对每种抗原的明显抗体反应。用 CnaA 或 FimB 免疫的鸡的 NE 病变严重程度显著降低,而联合使用三种蛋白则不能提供保护。用免疫鸡的血清进行的 Western blot 实验也提供了第一个实验证据,表明该基因座实际上可能编码一种功能性菌毛结构。