Schalkoort R, Morgan D M, Spradbrow P B
Aust Vet J. 1982 Jun;58(6):260-3. doi: 10.1111/j.1751-0813.1982.tb00692.x.
Experiments were conducted with vaccines containing the V4 strain of Newcastle disease virus (NDV). Both living aqueous vaccines and vaccines consisting of virus incorporated oil emulsion were used. The calculated dose of virus contained in the oil emulsion vaccine was 10(8.7) 50% embryo infectious doses (EID50) per bird dose. Haemagglutinin inhibition (HI) antibody levels of 8 are presumed protective. One-day-old chicks with low levels of maternal antibody were vaccinated intraocularly with 10(6.3)EID50 ol live vaccine, and concurrently with oil emulsion vaccine. Presumed protective levels of antibody were present at two weeks post vaccination and were maintained for at least seven weeks longer. When adult birds 15 weeks old with no previous exposure to NDV were vaccinated intraocularly with 10(6.7)EID50 per bird, protective levels of antibody were produced within a week. Unvaccinated birds put in contact with the vaccinated birds produced similar antibody levels within 14 days. Revaccination with oil emulsion vaccine after antibody levels had fallen resulted in a rapid response with high levels of antibody. When antibody-free adult commercial birds with an unknown history of exposure to NDV were vaccinated intramuscularly with oil emulsion vaccine, high antibody levels were produced for at least 21 weeks. Concurrent intraocular inoculation with 10(7.0)EID50 live virus did not enhance the response. Natural infection of unvaccinated birds occurred during the experiment. This was detected by the presence of HI antibody levels of short duration. When antibody-free commercial birds were inoculated intramuscularly with oil emulsion vaccine containing 10(6.0), 10(7.0), or 10(8.0)EID50 per bird dose, 100% of birds inoculated with the highest dose produced presumed protective levels of antibody within two weeks, as compared with a 5-week delay when using the 10(7.0)EID50 per bird dose.
使用含有新城疫病毒(NDV)V4株的疫苗进行了实验。使用了活水性疫苗和由病毒掺入油乳剂组成的疫苗。油乳剂疫苗中所含病毒的计算剂量为每只鸡剂量10(8.7) 50%胚感染剂量(EID50)。血凝素抑制(HI)抗体水平为8被认为具有保护作用。母源抗体水平低的1日龄雏鸡通过眼内接种10(6.3)EID50的活疫苗,并同时接种油乳剂疫苗。接种后两周出现了推测的保护性抗体水平,并至少维持了七周以上。当15周龄未接触过NDV的成年鸡每只眼内接种10(6.7)EID50时,一周内产生了保护性抗体水平。未接种疫苗的鸡与接种疫苗的鸡接触后,在14天内产生了相似的抗体水平。抗体水平下降后用油乳剂疫苗再次接种导致抗体水平迅速升高。当无抗体的成年商业鸡,其接触NDV的历史不明,通过肌肉注射油乳剂疫苗时,高抗体水平至少维持了21周。同时眼内接种10(7.0)EID50的活病毒并未增强反应。实验期间未接种疫苗的鸡发生了自然感染。这通过短时间存在的HI抗体水平检测到。当无抗体的商业鸡通过肌肉注射每只鸡剂量含有10(6.0)、10(7.0)或10(8.0)EID50的油乳剂疫苗时,接种最高剂量的100%的鸡在两周内产生了推测的保护性抗体水平,而使用每只鸡剂量10(7.0)EID50时延迟了5周。