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Reverse genetics based rgH5N2 vaccine provides protection against high dose challenge of H5N1 avian influenza virus in chicken

机译:基于反向遗传学的rgH5N2疫苗可抵抗鸡中H5N1禽流感病毒的高剂量攻击

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An inactivated vaccine was developed using the rgH5N2 virus (6 + 2 reassortant) generated by plasmid based reverse genetics system (RGS) with WSN/33/H1N1 as backbone virus. Following mutation of the basic amino acid cleavage site RRRKKR*GLF to IETR*GLF, the H5-HA (haemagglutinin) gene of the selected donor H5N1 virus (A/chicken/West Bengal/80995/2008) of antigenic Glade 2.2 was used along with the N2-NA gene from H9N2 field isolate (A/chicken/Uttar Pradesh/2543/2004) for generation of the rgH5N2 virus. A single dose (0.5 ml/bird) of the inactivated rgH5N2 vaccine protected 100% of the vaccinated chickens (n = 10) on 28th dpv (early challenge) and 90% of the vaccinated chickens (n = 10) on 200th dpv (late challenge) against high dose challenge with HPAI virus (10(9) EID50/bird). Challenge virus shedding via oropharynx and cloaca of the vaccinated chickens was detectable by realtime RT-PCR during 1-5 dpc and 1-9 days dpc in the early and the late challenge, respectively. The protective level of antibodies (mean HI titre > 128) was maintained without booster vaccination for 200 days. The present study provides the experimental evidence about the extent of protection provided by a reverse genetics based vaccine for Glade 2.2 H5N1 viruses against challenge with high dose of field virus at two different time points (28 dpv and 200 dpv). The challenge study is uniquely different from the previous similar experiments on account of 1000 times higher dose of challenge and protection at 200 dpv. The protection and virus shedding data of the study may be useful for countries planning to use H5 vaccine in poultry especially against the Glade 2.2 H5N1 viruses. (C) 2016 Elsevier Ltd. All rights reserved.
机译:使用rgH5N2病毒(6 + 2重配子)开发了一种灭活疫苗,该病毒是由基于质粒的逆向遗传系统(RGS)生成的,其中WSN / 33 / H1N1为骨干病毒。在将碱性氨基酸切割位点RRRKKK * GLF突变为IETR * GLF之后,使用了抗原性Glade 2.2的选定供体H5N1病毒(A /鸡/西孟加拉邦/ 80995/2008)的H5-HA(血凝素)基因用来自H9N2野外分离株(A / chicken /北方邦/ 2543/2004)的N2-NA基因产生rgH5N2病毒。一次灭活的rgH5N2疫苗单剂量(0.5 ml /只)在第28 dpv(早期攻击)时可保护100%的接种鸡(n = 10),在第200 dpv(晚期)可以保护90%的接种鸡(n = 10)。挑战),以高剂量挑战HPAI病毒(10(9)EID50 /只鸟)。通过实时RT-PCR在攻击的早期和晚期分别在1-5 dpc和1-9 dpc内通过实时RT-PCR检测到通过口咽和泄殖腔排出的攻击病毒。无需加强免疫即可维持抗体的保护水平(平均HI滴度> 128)达200天。本研究提供了关于基于逆向遗传学的疫苗对Glade 2.2 H5N1病毒在两个不同时间点(28 dpv和200 dpv)抵抗高剂量田间病毒攻击的保护程度的实验证据。由于200 dpv的挑战和保护剂量高出1000倍,因此挑战研究与之前的类似实验有独特的不同。该研究的保护和病毒清除数据可能对计划在禽类中使用H5疫苗,尤其是针对Glade 2.2 H5N1病毒的国家有用。 (C)2016 Elsevier Ltd.保留所有权利。

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