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首页> 外文期刊>Avian Pathology >Induction of cystic oviducts and protection against early challenge with infectious bronchitis virus serotype D388 (genotype QX) by maternally derived antibodies and by early vaccination
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Induction of cystic oviducts and protection against early challenge with infectious bronchitis virus serotype D388 (genotype QX) by maternally derived antibodies and by early vaccination

机译:母源抗体和早期疫苗接种可诱导囊性输卵管并预防传染性支气管炎病毒血清型D388(基因型QX)的早期攻击

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摘要

Since the end of 2003, strains of the D388 serotype (QX genotype) of infectious bronchitis virus (IBV) have caused considerable damage to the Dutch poultry industry. In order to better understand the pathogenesis of infection caused by this infectious bronchitis variant and to be able to support the poultry industry with substantiated advice to prevent or decrease the damage caused by the D388 strain, several vaccination and challenge experiments were performed in young specific pathogen free layers, young layers with maternally derived antibodies against the D388 strain and young commercial broiler breeders. The experiments confirmed the field observations that the D388 strain of the QX genotype is a very pathogenic strain that is able to cause cystic oviducts in a high percentage of birds, mortality due to nephritis and respiratory distress with complete tracheal ciliostasis and airsacculitis. Vaccination programmes using different combinations of heterologous live vaccines at day 0 or at days 0 and 14 induced a reasonable to high level of protection in the trachea, kidney, oviduct and air sacs against challenge with the D388 strain at 28 days of age. However, for very early protection, maternally-derived D388-neutralizing antibodies were shown to be very important. Titres of 9 to 10 log2 maternally-derived D388 virus-neutralizing antibodies, which provided partial protection against tracheal damage and a high protection against replication of D388 in the kidney after challenge at 6 or 10 days of age, could be achieved using a broad heterologous live priming and subsequent boosting using inactivated IBV vaccines containing two or three heterologous IBV antigens.
机译:自2003年底以来,传染性支气管炎病毒(IBV)的D388血清型(QX基因型)菌株对荷兰家禽业造成了相当大的破坏。为了更好地了解这种传染性支气管炎变体引起的感染的发病机制,并能够通过充分的建议来预防或减少D388菌株引起的损害,从而为家禽业提供支持,针对年轻的特定病原体进行了多次疫苗接种和攻毒实验自由层,带有抗D388品系的母源抗体的年轻层和年轻的商业肉鸡种鸡。实验证实了现场观察,QX基因型的D388菌株是一种致病性很强的菌株,能够在高比例的禽类中引起囊性输卵管,由于肾炎和呼吸窘迫而导致的死亡以及完全的气管切开和气管炎。在第0天或第0和14天使用不同组合的异源活疫苗进行的疫苗接种计划可在28天龄时对气管,肾脏,输卵管和气囊提供合理至高水平的保护,以抵抗D388菌株的攻击。然而,对于非常早期的保护,母源性D388中和抗体被证明非常重要。 9至10 log 2 母源D388病毒中和抗体的效价,在攻击6或10日龄后,对气管损伤提供部分保护,对肾脏中D388的复制提供高度保护。可以使用广泛的异源活启动和随后使用含有两种或三种异源IBV抗原的灭活IBV疫苗进行加强免疫来实现“免疫”。

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  • 来源
    《Avian Pathology》 |2011年第5期|p.463-471|共9页
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    GD (Animal Health Service), P.O. Box 9, 7400, AA, Deventer, The Netherlands;

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