Redig Patrick T, Tully Thomas N, Ritchie Branson W, Roy Alma F, Baudena M Alexandra, Chang Gwong-Jen J
Department of Clinical Sciences and The Raptor Center, College of Veterinary Medicine, University of Minnesota, Saint Paul, MN 55108, USA.
Am J Vet Res. 2011 Aug;72(8):1065-70. doi: 10.2460/ajvr.72.8.1065.
To evaluate the safety and efficacy of an experimental adjuvanted DNA-plasmid vaccine against West Nile virus (WNV) in red-tailed hawks (Buteo jamaicensis).
19 permanently disabled but otherwise healthy red-tailed hawks of mixed ages and both sexes without detectable serum antibodies against WNV.
Hawks were injected IM with an experimental WNV DNA-plasmid vaccine in an aluminum-phosphate adjuvant (n = 14) or with the adjuvant only (control group; 5). All birds received 2 injections at a 3-week interval. Blood samples for serologic evaluation were collected before the first injection and 4 weeks after the second injection (day 0). At day 0, hawks were injected SC with live WNV. Pre- and postchallenge blood samples were collected at intervals for 14 days for assessment of viremia and antibody determination; oropharyngeal and cloacal swabs were collected for assessment of viral shedding.
Vaccination was not associated with morbidity or deaths. Three of the vaccinated birds seroconverted after the second vaccine injection; all other birds seroconverted following the live virus injection. Vaccinated birds had significantly less severe viremia and shorter and less-intense shedding periods, compared with the control birds.
Use of the WNV DNA-plasmid vaccine in red-tailed hawks was safe, and vaccination attenuated but did not eliminate both the viremia and the intensity of postchallenge shedding following live virus exposure. Further research is warranted to conclusively determine the efficacy of this vaccine preparation for protection of red-tailed hawks and other avian species against WNV-induced disease.
评估一种实验性佐剂型DNA质粒疫苗对红尾鵟(Buteo jamaicensis)抗西尼罗河病毒(WNV)的安全性和有效性。
19只年龄和性别各异、永久性残疾但健康的红尾鵟,血清中未检测到抗WNV抗体。
给红尾鵟肌肉注射含磷酸铝佐剂的实验性WNV DNA质粒疫苗(n = 14),或仅注射佐剂(对照组;n = 5)。所有鸟类均间隔3周接受2次注射。在首次注射前和第二次注射后4周(第0天)采集血样进行血清学评估。在第0天,给红尾鵟皮下注射活WNV。在攻毒前后间隔14天采集血样以评估病毒血症并测定抗体;采集口咽和泄殖腔拭子以评估病毒脱落情况。
接种疫苗与发病或死亡无关。3只接种疫苗的鸟类在第二次疫苗注射后血清转化;所有其他鸟类在注射活病毒后血清转化。与对照鸟类相比,接种疫苗的鸟类病毒血症明显较轻,病毒脱落期更短且强度更低。
在红尾鵟中使用WNV DNA质粒疫苗是安全的,接种疫苗可减轻但不能消除活病毒暴露后的病毒血症和攻毒后脱落的强度。有必要进一步研究以最终确定这种疫苗制剂对保护红尾鵟和其他鸟类免受WNV诱导疾病的有效性。