Kurukulsuriya Shanika, Ahmed Khawaja Ashfaque, Ojkic Davor, Gunawardana Thushari, Gupta Ashish, Goonewardene Kalhari, Karunaratne Ruwani, Popowich Shelly, Willson Philip, Tikoo Suresh K, Gomis Susantha
Department of Veterinary Pathology, Western College of Veterinary Medicine, University of Saskatchewan, Saskatoon, S7N 5B4, SK, Canada.
Animal Health Laboratory, University of Guelph, P.O. Box 3612, Guelph, ON N1H 6R8, Canada.
Res Vet Sci. 2016 Oct;108:54-9. doi: 10.1016/j.rvsc.2016.08.002. Epub 2016 Aug 4.
Antibiotic-free and safe animal products are most desirable among consumers. However, ensuring safe poultry products is a challenging task when the chicken immune system is compromised. Infectious bursal disease virus (IBDV) causes immunosuppression and predisposes chickens to secondary infections. Breeder vaccination against IBDV is routinely practiced for producing chicks with maternally-derived antibody (MAb) to prevent infection in newly hatched chicks. The majority of IBDV circulating in Canadian farms are variant strains (vIBDV). Whether circulating vIBDV strains are immunosuppressive in chicks or are amenable to current vaccine regimens has not previously been tested through challenge studies. In this study, one-day-old broiler chicks (n=240) carrying MAb were obtained from broiler breeders vaccinated with commercial IBDV vaccines. In the first set of experiments (n=40/group), at six days post-hatch, one group was challenged with a Canadian field isolate, vIBDV (strain-SK09) (3×10(3) EID50). The second and the third groups (controls) were inoculated with non-immunosuppressive IBDV D-78 (10×10(3) TCID50) and saline, respectively. Histopathological examination on days 14 and 30 post-challenge revealed that despite the high level of MAb, vIBDV (SK09) caused severe bursal damage in chicks. Another set of experiments with treatment groups as above, demonstrated that pre-exposure of chicks with vIBDV (SK09) caused immunosuppression resulting in significantly higher mortality and disease severity in chicks challenged with a virulent strain of Escherichia coli (E. coli). Our data provide evidence that IBDV strains circulating in Canada are immunosuppressive, not amenable to current anti-IBDV vaccination strategy, and a potential threat to antibiotic-free chicken farming.
无抗生素且安全的动物产品在消费者中最为理想。然而,当鸡的免疫系统受损时,确保家禽产品安全是一项具有挑战性的任务。传染性法氏囊病病毒(IBDV)会导致免疫抑制,并使鸡易患继发性感染。为了使雏鸡产生母源抗体(MAb)以预防新孵出雏鸡的感染,常规做法是对种鸡进行IBDV疫苗接种。在加拿大农场中传播的大多数IBDV是变异株(vIBDV)。此前尚未通过攻毒研究来测试循环中的vIBDV毒株在雏鸡中是否具有免疫抑制作用,或者是否适用于当前的疫苗接种方案。在本研究中,从接种了商用IBDV疫苗的肉鸡种鸡中获得了携带MAb的1日龄肉鸡雏鸡(n = 240)。在第一组实验(每组n = 40)中,在孵化后第6天,一组用加拿大田间分离株vIBDV(SK09株)(3×10³ EID50)进行攻毒。第二组和第三组(对照组)分别接种非免疫抑制性IBDV D - 78(10×10³ TCID50)和生理盐水。攻毒后第14天和第30天的组织病理学检查显示,尽管MAb水平很高,但vIBDV(SK09)仍在雏鸡中引起了严重的法氏囊损伤。另一组与上述处理组相同的实验表明,用vIBDV(SK09)预先感染雏鸡会导致免疫抑制,从而使受到致病性大肠杆菌(E. coli)攻击的雏鸡死亡率显著升高且疾病严重程度增加。我们的数据提供了证据,表明在加拿大传播的IBDV毒株具有免疫抑制作用,不适用于当前的抗IBDV疫苗接种策略,并且对无抗生素养鸡业构成潜在威胁。