| 壳聚糖/pcDNA-DPV-gC基因在雏鸭体内的抗原表达和分布 |
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| 引用本文： | 沈福晓,蒋金凤,程安春,汪铭书,路立婷,贾仁勇,朱德康,陈孝跃,孙涛. 壳聚糖/pcDNA-DPV-gC基因在雏鸭体内的抗原表达和分布[J]. 中国农业科学, 2011, 44(18): 3909-3917. DOI: 10.3864/j.issn.0578-1752.2011.18.023 |
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| 作者姓名： | 沈福晓 蒋金凤 程安春 汪铭书 路立婷 贾仁勇 朱德康 陈孝跃 孙涛 |
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| 作者单位： | 1.四川农业大学预防兽医研究所;2.四川农业大学动物医学院禽病防治研究中心;3.四川农业大学动物疫病与人类健康四川省重点实验室;4.山东省出入境检验检疫局技术中心 |
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| 基金项目： | 教育部“长江学者和创新团队发展计划”创新团队项目(IRT0848); 现代农业产业技术体系建设专项基金(CARS-43-8); 国家“973”课题(2011CB111606) |
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| 摘 要： | 【目的】以DPV gC基因疫苗（pcDNA-DPV-gC）为模型，采用复凝法制备壳聚糖/pcDNA-DPV-gC纳米微球，对其在雏鸭体内的抗原表达和分布进行初步研究。【方法】将壳聚糖/pcDNA-DPV-gC基因疫苗以肌注、滴鼻和口服3种途径免疫20日龄雏鸭，于免疫后不同时间点（4h、12h、1d、3d、5d、7d、2 w、4 w、6 w和10 w）分别随机宰杀2只雏鸭，采集肝、脾、肺、肾、胰、脑、胸腺、哈氏腺、法氏囊、食道、十二指肠、盲肠和直肠，应用间接免疫组化检测DPV gC基因在雏鸭体内的抗原表达和分布。【结果】①肌注组免疫雏鸭1 d，肝脏、法氏囊、十二指肠、盲肠和直肠检测到DPV gC蛋白；滴鼻组免疫雏鸭12 h，肺脏出现阳性信号，1 d哈氏腺和法氏囊检测到DPV gC蛋白；口服组免疫雏鸭12 h，食道出现中等强度的阳性信号，1 d法氏囊、十二指肠、盲肠和直肠检测到DPV gC蛋白；②在3种免疫途径中，肝脏、肺脏、法氏囊、哈氏腺、食道、十二指肠、盲肠和直肠是DPV gC抗原表达的主要器官；阳性信号主要在肝细胞、肺上皮细胞、法氏囊和哈氏腺淋巴细胞、食道上皮细胞和肠道粘膜上皮细胞及固有层细胞等部位；③不同免疫途径免疫的壳聚糖/pcDNA-DPV-gC基因疫苗在雏鸭体内的抗原表达量和持续时间的总体表达规律为：肌注组＞滴鼻组＞口服组。【结论】壳聚糖能促进DPV gC基因在雏鸭体内的表达和分布，肌肉注射是壳聚糖/pcDNA-DPV-gC基因疫苗首选的免疫方式。
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| 关 键 词： | 壳聚糖 壳聚糖/pcDNA-DPV-gC基因 抗原表达 分布 |
| 收稿时间： | 2011-11-30 |
Antigenic Expression and Distribution of Chitosan/pcDNADPV-gC Gene in the Vaccinated Ducklings |
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| SHEN Fu-xiaot,JIANG Jin-feng,CHENG An-chun,WANG Ming-shu,LU Li-ting,JIA Ren-yong,ZHU De-kang,CHEN Xiao-yue,SUN Tao. Antigenic Expression and Distribution of Chitosan/pcDNADPV-gC Gene in the Vaccinated Ducklings[J]. Scientia Agricultura Sinica, 2011, 44(18): 3909-3917. DOI: 10.3864/j.issn.0578-1752.2011.18.023 |
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| Authors: | SHEN Fu-xiaot JIANG Jin-feng CHENG An-chun WANG Ming-shu LU Li-ting JIA Ren-yong ZHU De-kang CHEN Xiao-yue SUN Tao |
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| Affiliation: | SHEN Fu-xiao1,3,JIANG Jin-feng1,CHENG An-chun1,2,WANG Ming-shu1,LU Li-ting1,JIA Ren-yong1,ZHU De-kang2,CHEN Xiao-yue2,SUN Tao1,4(1Institute of Preventive Veterinary Medicine,Sichuan Agricultural University,Chengdu 611130,2Avian Disease Research Center,College of Veterinary Medicine,Ya'an 625014,Sichuan,3Key Laboratory of Animal Disease and Human Health of Sichuan Province,4Shandong Entry-Exit Inspection and Quarantine Bureau,Qingdao 266002,Sha... |
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| Abstract: | 【Objective】 DNA-chitosan nanoparticles carrying duck plague virus (DPV) gC gene were constructed by using complex coacervation process to investigate its antigenic expression and distribution in the vaccinated ducklings. 【Method】 The 20-day-old DPV-free ducklings were respectively immunized with chitosan/pcDNA-DPV-gC gene vaccine via intramuscular injection, nasal administration and oral administration. At intervals of 4 h, 12 h, 1 d, 3 d, 5 d, 7 d, 2 w, 4 w, 6 w and 10 w post-vaccination (p.v.), two ducklings were randomly euthanatized and their organs (liver, spleen, lung, kidney, pancreas, brain, thymus, Harderian gland, bursa of Fabricius, esophagus, duodenum, caecum, and rectum) were collected. Meanwhile, an indirect immunohistochemical staining (IHC) was developed to detect antigenic expression and distribution of DPV gC antigens in the vaccinated ducklings. 【Result】 The DPV gC proteins were found in the liver, bursa of Fabricius, duodenum, caecum and rectum in the intramuscular injection group at 1 d post-vaccination (p.v.); Moreover, the immunogenicity were firstly found in the lung at 12 h p.v., and the DPV gC proteins were observed in the bursa of Fabricius and Harderian gland in the nasal administration group at 1 d p.v. Furthermore, the positive signals were firstly found in the esophagus at 12 h p.v., and the DPV gC proteins were observed in the bursa of Fabricius, duodenum, caecum and rectum in the oral administration group at 1 d p.v.. The DPV gC proteins were distributed in the liver, lung, bursa of Fabricius, Harderian gland, esophagus, duodenum, caecum and rectum, which were served as the principal sites for DPV gC antigens localization. The positive immunogenicity was mainly distributed in the parenchymal hepatic cells, epithelial cells of lung, lymphocytes of Harderian gland and bursa of Fabricius, epithelial cells of esophagus, epithelial cells and lamina propria mucosae cells of intestinal tract. According to the immunogenicity intensity and duration time via different immunization routes, the positive staining in all tissues was in the order of intramuscular injection group＞nasal administration group＞oral administration group. 【Conclusion】 The results demonstrated that chitosan as a polycationic gene carrier could promote the expression efficiency of DPV gC antigens in the vaccinated ducklings. Intramuscular injection was considered to be the best immunization routes to inoculated chitosan/pcDNA- DPV-gC gene vaccine. |
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| Keywords: | chitosan chitosan/pcDNA-DPV-gC gene antigenic expression distribution |
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