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[H5N1禽流感血凝素包被的假型病毒的特性研究]

[Characterization of pseudotyped viruses coated with hemagglutinin of H5N1 avian influenza].

作者信息

Zhang Yu-song, Wang Da-yan, Gao Rong-bao, Dong Jie, Li Zi, Zhang Ye, Bai Tian, Wang Min, Wen Le-ying, Shu Yue-long

机构信息

State Key Laboratory for Viral Genetic Engineering, Institute for Viral Disease Control and Prevention, Chinese Center for Disease Control and Prevention, Beijing, China.

出版信息

Zhonghua Shi Yan He Lin Chuang Bing Du Xue Za Zhi. 2009 Dec;23(6):401-4.

Abstract

OBJECTIVE

To construct pseudovirus bearing H5N1 HA based on a lentivirus vector system. Then we study the biological feature of the pseudovirus. With the newly established viral particles, we performed the serological tests.

METHODS

H5N1 avian influenza virus that isolated from human case was cloned to construct pLP-HA, then pLP-HA co-transfected with lentivirus vector plasmids pLP1, pLP2 and pEmGFP into 293T cells. The supernatant was harvested 48h post-transfection. Concentrated by super centrifuge, the pseudotyped viruses were analyzed by infection test, HA test and micro-neutralization test. At the same time, optimized HA gene and a Vietnam H5N1 HA gene were used to construct pseudotyped virus for comparison.

RESULTS

Pseudotyped virus particles can be observed with electronic microscope. Western-blot revealed that HA glycoprotein can be expressed in the virions. Our neutralization assay by using the pseudoviruses was comparable with the conventional microneutralization assay with wild-type viruses. A high degree of correlation was detected.

CONCLUSION

Pseudotyped Viruses coated with HA of H5N1 High Pathogenic Avian Influenza were successfully constructed; it can be used to for the microneutralization assay. The HA gene from different sources affect the efficiency of the packaging of the pseudovirus. But the optimized HA gene can not obviously improve packaging efficiency of the pseudovirus.

摘要

目的

构建基于慢病毒载体系统携带H5N1血凝素(HA)的假病毒。然后研究该假病毒的生物学特性。利用新构建的病毒颗粒进行血清学检测。

方法

将从人类病例中分离的H5N1禽流感病毒进行克隆构建pLP-HA,然后将pLP-HA与慢病毒载体质粒pLP1、pLP2和pEmGFP共转染至293T细胞。转染后48小时收集上清液。通过超速离心浓缩,对假型病毒进行感染试验、血凝试验和微量中和试验分析。同时,使用优化的HA基因和越南H5N1 HA基因构建假型病毒进行比较。

结果

通过电子显微镜可观察到假型病毒颗粒。蛋白质免疫印迹法显示HA糖蛋白可在病毒粒子中表达。我们使用假病毒进行的中和试验与使用野生型病毒的传统微量中和试验相当。检测到高度相关性。

结论

成功构建了包被H5N1高致病性禽流感HA的假型病毒;可用于微量中和试验。不同来源的HA基因影响假病毒的包装效率。但优化的HA基因不能明显提高假病毒的包装效率。

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