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DNA-mediated vaccination conferring protection against infectious bursal disease in broiler chickens in the presence of maternal antibody

机译:DNA介导的疫苗接种可在存在母源抗体的情况下保护肉鸡免受传染性法氏囊病

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摘要

The objective of the present study was to determine if a DNA vaccine carrying large segment gene of infectious bursal disease virus (IBDV) could confer protection against infectious bursal disease (IBD) in broiler chickens in the presence of maternal antibody. Broiler chickens with maternal antibody titers to IBDV were intramuscularly injected with a DNA plasmid coding for VP2, VP3, and VP4 genes of IBDV strain variant E (VE) (P/VP243/E) at 1-day, 1-week, and/or 2 weeks old. The dose of P/VP243/E used ranging from 400 mu g to 10 mg. Broiler chickens at 3 weeks old were orally challenged with IBDV strain (VE) and observed for 10 days. Only broiler chickens vaccinated with 7.5 or 10 mg of P/VP243/E 3 times had 90 or 100% protection against challenge by IBDV strain VE and protected broiler chickens had significantly higher (P< 0.05) bursa weight/body weight (B/B) ratios, significantly lower (P< 0.05) bursal lesion scores, and the absence of IBDV antigens in bursae determined by immunofluorescent antibody assay (IFA). Antibody titers to IBDV as determined by enzyme-linked immunosorbent assay (ELISA) or virus neutralization (VN) assay in chickens of each group in each trial were gradually decreased prior to challenge. There was no significant difference (P> 0.05) in ELISA or VN titers to IBDV among all groups of broiler chickens or among the groups of broiler chickens vaccinated with various dose of P/VP243/E before challenge. Broiler chickens in the groups receiving 7.5 or 10 mg of P/VP243/E had significantly lower (P< 0.05) DIM or VN titers to IBDV than those in the challenge control (CC) groups or the other groups vaccinated with various dose of P/VP243/E after challenge. Broiler chickens in the groups vaccinated with 10 mg of P/VP243/E 3 times had significantly higher (P <0.05) stimulation indices for IBDV-stimulated lymphocyte proliferation response than those in the vector control (VC) or CC group at 14, 21, 24, or 31 days after first DNA vaccination. The results indicated that DNA vaccination with DNA encoding large segment gene of IBDV confers protection against challenge by IBDV in broiler chickens with maternal antibody to IBDV.
机译:本研究的目的是确定带有母鸡传染性法氏囊病病毒(IBDV)大片段基因的DNA疫苗能否在母鸡抗体存在的情况下为肉鸡提供针对鸡传染性法氏囊病(IBD)的保护。在1天,1周和/或在肌肉注射IBDV母源抗体滴度的肉鸡,将其编码IBDV株E(VE)(P / VP243 / E)VP2,VP3和VP4基因的DNA质粒肌肉注射。或2周大。 P / VP243 / E的剂量范围为400μg至10mg。用IBDV毒株(VE)对3周龄的肉鸡进行口服攻击,并观察10天。仅接种了7.5或10 mg P / VP243 / E 3次的肉鸡对IBDV株VE的攻击具有90%或100%的保护,而受保护的肉鸡的法氏囊体重/体重(B / B)明显更高(P <0.05)比率,明显降低(P <0.05)的法氏囊病变评分以及通过免疫荧光抗体测定(IFA)确定的法氏囊中没有IBDV抗原。通过酶联免疫吸附测定(ELISA)或病毒中和(VN)测定确定的每项试验中每组鸡的IBDV抗体滴度在攻击前逐渐降低。在各组肉鸡或接种不同剂量P / VP243 / E的肉鸡组之间,ELISA或IBDV的VN滴度对IBDV均无显着差异(P> 0.05)。接受7.5或10 mg P / VP243 / E的肉鸡对IBDV的DIM或VN滴度明显低于挑战对照组(CC)或接种了不同剂量P的其他组的IBDV(P <0.05) / VP243 / E挑战后。接种10 mg P / VP243 / E 3次的组中的肉鸡对IBDV刺激的淋巴细胞增殖反应的刺激指数显着高于载体对照组(VC)或CC组在14、21时的刺激指数(P <0.05)第一次DNA疫苗接种后24天或31天。结果表明,用IBDV大片段基因编码的DNA进行的DNA疫苗接种可在具有IBDV母源抗体的肉鸡中提供针对IBDV攻击的保护。

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