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评估重组喙羽病病毒衣壳蛋白作为鹦鹉喙羽病疫苗的效果。

Assessment of recombinant beak and feather disease virus capsid protein as a vaccine for psittacine beak and feather disease.

作者信息

Bonne Nicolai, Shearer Patrick, Sharp Margaret, Clark Phillip, Raidal Shane

机构信息

School of Veterinary and Biomedical Sciences, Murdoch University, Murdoch, WA 6150, Australia.

School of Agricultural and Veterinary Sciences, Charles Sturt University, Wagga Wagga, NSW 2678, Australia.

出版信息

J Gen Virol. 2009 Mar;90(Pt 3):640-647. doi: 10.1099/vir.0.006932-0.

Abstract

Beak and feather disease virus (BFDV) is a significant pathogen of wild Australasian and African psittacine birds. We assessed the immunogenicity of recombinant BFDV capsid (recBFDVcap) to protect against the development of psittacine beak and feather disease (PBFD). Long-billed corellas (Cacatua tenuirostris) (n=13) received (by injection) 1 ml vaccine containing 10 microg recBFDVcap on day 0 and 0.4 ml vaccine containing 66.8 microg recBFDVcap on day 11. All vaccinated corellas and five non-vaccinated control corellas were given 0.4 ml BFDV suspension [titre=log(2) 12 haemagglutination units (HAU) 50 microl(-1)] intramuscularly and 0.1 ml orally 16 days after booster vaccination. Blood was collected during the vaccination period and blood and feathers were collected after BFDV administration. Testing of blood samples included BFDV DNA detection by PCR and quantitative PCR (qPCR) as well as antibody detection by haemagglutination inhibition (HI) and on feather samples, BFDV DNA and antigen was detected by haemagglutination (HA) and qPCR. Four of 97 blood samples collected from vaccinated birds after virus challenge tested positive by PCR, whereas 17 of 35 samples taken from non-vaccinated control corellas tested positive. Vaccinated birds did not develop feather lesions, had only transient PCR-detectable viraemia and had no evidence of persistent infection 270 days post-challenge using PCR, histopathology and immunohistochemistry. Non-vaccinated control corellas developed transient feather lesions and had PCR, HI and HA test results consistent with PBFD. They were BFDV PCR-positive for up to 41 days post-challenge and qPCR demonstrated reduced virus replication in vaccinated birds compared with non-vaccinated control birds.

摘要

喙羽病病毒(BFDV)是澳大利亚和非洲野生鹦鹉科鸟类的一种重要病原体。我们评估了重组BFDV衣壳(recBFDVcap)预防鹦鹉喙羽病(PBFD)发生的免疫原性。13只长喙凤头鹦鹉(Cacatua tenuirostris)在第0天接受(注射)1毫升含10微克recBFDVcap的疫苗,在第11天接受0.4毫升含66.8微克recBFDVcap的疫苗。在加强免疫接种16天后,给所有接种疫苗的凤头鹦鹉和5只未接种疫苗的对照凤头鹦鹉肌肉注射0.4毫升BFDV悬液[滴度=log(2) 12血凝单位(HAU)50微升-1],并口服0.1毫升。在疫苗接种期间采集血液,在给予BFDV后采集血液和羽毛。血液样本检测包括通过PCR和定量PCR(qPCR)检测BFDV DNA以及通过血凝抑制(HI)检测抗体,对于羽毛样本,通过血凝(HA)和qPCR检测BFDV DNA和抗原。病毒攻击后从接种疫苗的鸟类采集的97份血液样本中有4份通过PCR检测呈阳性,而从未接种疫苗的对照凤头鹦鹉采集的35份样本中有17份检测呈阳性。接种疫苗的鸟类未出现羽毛病变,仅有短暂的可通过PCR检测到的病毒血症,并且在攻击后270天使用PCR、组织病理学和免疫组织化学均未发现持续感染的证据。未接种疫苗的对照凤头鹦鹉出现短暂的羽毛病变,其PCR、HI和HA检测结果与PBFD一致。它们在攻击后长达41天BFDV PCR呈阳性,并且qPCR显示与未接种疫苗的对照鸟类相比,接种疫苗的鸟类病毒复制减少。

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