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细菌体诱导兔唇袋狸体液免疫应答表达兔 zona pellucida 3 蛋白。

Humoral immune responses in brushtail possums (Trichosurus vulpecula) induced by bacterial ghosts expressing possum zona pellucida 3 protein.

机构信息

National Research Centre for Possum Biocontrol at Landcare Research, PO Box 40, Lincoln 7640, New Zealand.

出版信息

Vaccine. 2010 Jun 11;28(26):4268-74. doi: 10.1016/j.vaccine.2010.04.032. Epub 2010 Apr 29.

Abstract

The introduced common brushtail possum (Trichosurus vulpecula) is a major pest in New Zealand and immunocontraceptive vaccines are being developed for biocontrol of possum populations, with bacterial ghosts (BGs) being evaluated as a means of oral delivery. Recombinant BGs expressing possum zona pellucida 3 protein (ZP3) as an L' membrane-anchored protein (ZP3-L') or as an S-layer SbsA-fusion protein (MBP-SbsA-ZP3) were produced by the expression of the cloned bacteriophage phiX174 lysis gene E in E. coli NM522. The humoral immune responses of possums immunised with BGs expressing possum ZP3 were investigated following oral, intranasal/conjunctival, parenteral, and intraduodenal administration to evaluate the BG-ZP3 system for possum fertility control. Antibodies to possum ZP3 were detected in the serum, oviduct secretions, and follicular fluid of immunised animals. Intranasal/conjunctival immunisation elicited reliable antibody immune response in serum and at a key effector site, the ovarian follicular fluid. Intraduodenal administration of possum ZP3 BG vaccine as a priming immunisation elicited significant systemic immune responses, but oral immunisation did not, indicating that protection of BG vaccines from degradation by gastric acidity would enhance the effectiveness of orally delivered vaccines. The detection of antibodies at elevated levels at target sites in the reproductive tract following mucosal delivery demonstrates, for the first time, the potential of BGs as an effective system for vaccine delivery to wild animals, and intranasal/conjunctival immunisation as a promising means for delivery of immunocontraceptive vaccines to wild animals.

摘要

引入的普通帚尾袋貂(Trichosurus vulpecula)是新西兰的主要害虫,正在开发免疫避孕疫苗来控制袋貂种群,细菌噬菌体(BGs)被评估为口服递送的一种方法。通过在大肠杆菌 NM522 中表达克隆的噬菌体 phiX174 裂解基因 E,生产了表达袋貂透明带 3 蛋白(ZP3)作为 L'膜锚定蛋白(ZP3-L')或 S 层 SbsA 融合蛋白(MBP-SbsA-ZP3)的重组 BGs。通过口服、鼻内/结膜、肠胃外和十二指肠内给药,研究了免疫 BGs 表达的袋貂的体液免疫反应,以评估 BG-ZP3 系统在控制袋貂生育力方面的应用。在免疫动物的血清、输卵管分泌物和卵泡液中检测到针对袋貂 ZP3 的抗体。鼻内/结膜免疫在血清和关键效应部位——卵巢卵泡液中引起了可靠的抗体免疫反应。作为初次免疫,十二指肠内给予袋貂 ZP3 BG 疫苗引起了显著的全身免疫反应,但口服免疫则没有,这表明保护 BG 疫苗免受胃酸降解将提高口服疫苗的有效性。在生殖道靶部位检测到抗体水平升高,这首次证明了 BGs 作为一种将疫苗递送到野生动物的有效系统的潜力,以及鼻内/结膜免疫作为向野生动物递送免疫避孕疫苗的一种有前途的手段。

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