Animal influenza Laboratory of Ministry of Agriculture and State Key Laboratory of Veterinary Biotechnology, Harbin Veterinary Research Institute of CAAS, Harbin 150001, PR China.
Vet Microbiol. 2012 Dec 28;161(1-2):43-8. doi: 10.1016/j.vetmic.2012.07.005. Epub 2012 Jul 10.
The preparation of high-yield influenza H5N1 vaccine strains is challenging for researchers and manufacturers. Here, we used reverse genetics to generate a high-yield avian influenza vaccine strain based on a novel avian influenza virus. A high-yield attenuated recombinant H5N3 virus (rH5N3-DL) was prepared from the HA gene of A/Goose/Anhui/08 (H5N1), modified by deletion of the multiple basic amino acids at the cleavage site, the NA gene from A/Duck/Germany/1215/73 (H2N3), and the six internal genes from the high-yield A/Goose/Dalian/3/01 (H9N2) virus. rH5N3-DL grew to high HA titers (1:2048) in eggs, eight times those of the parental H5N1 virus, and four times higher than that of rH5N3-PR8 (six internal genes from the high-yield PR8). Infection tests demonstrated that rH5N3-DL was avirulent in chickens, chicken embryos, and mice. rH5N3-DL-vaccinated chickens were fully protected against the morbidity and mortality of a lethal challenge with homologous A/Goose/Anhui/08, but only 80% of chickens were protected after challenge with heterologous A/Goose/Guangdong/1/96. The N3 neuraminidase marker distinguishes rH5N3-DL-vaccinated from H5N1-infected animals. rH5N3-DL is thus a promising vaccine candidate to combat highly pathogenic avian influenza virus infections. The A/Goose/Dalian/3/01 virus could be a promising candidate as providing internal genes donors with high-yield properties in reverse-genetics system and might be applicable for future avian influenza vaccine development.
高产流感 H5N1 疫苗株的制备对研究人员和制造商来说是一个挑战。在这里,我们使用反向遗传学方法,基于新型禽流感病毒,生成了一种高产禽流感疫苗株。通过对 A/Goose/Anhui/08 (H5N1) 的 HA 基因进行修饰,删除了多个裂解位点的碱性氨基酸,使用 A/Duck/Germany/1215/73 (H2N3) 的 NA 基因和高产 A/Goose/Dalian/3/01 (H9N2) 病毒的六个内部基因,制备了高产减毒重组 H5N3 病毒 (rH5N3-DL)。rH5N3-DL 在鸡蛋中可达到高 HA 滴度 (1:2048),是亲本 H5N1 病毒的 8 倍,比 rH5N3-PR8 (高产 PR8 的六个内部基因)高 4 倍。感染试验表明,rH5N3-DL 在鸡、鸡胚和小鼠中均无致病性。rH5N3-DL 疫苗接种的鸡对同源 A/Goose/Anhui/08 的致死性攻毒具有完全保护作用,但对异源 A/Goose/Guangdong/1/96 的攻毒仅有 80%的鸡得到保护。N3 神经氨酸酶标记可区分 rH5N3-DL 疫苗接种动物和 H5N1 感染动物。因此,rH5N3-DL 是一种有前途的候选疫苗,可用于对抗高致病性禽流感病毒感染。A/Goose/Dalian/3/01 病毒可作为内部基因供体,在反向遗传学系统中具有高产特性,可能适用于未来的禽流感疫苗开发。