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两剂免疫灭活重配 H5N2 病毒可保护鸡免受同源 2.3.2.1 分支和异源 2.2 分支高致病性禽流感 H5N1 病毒的致死性挑战。

A two dose immunization with an inactivated reassortant H5N2 virus protects chickens against lethal challenge with homologous 2.3.2.1 clade and heterologous 2.2 clade highly pathogenic avian influenza H5N1 viruses.

机构信息

ICAR- National Institute of High Security Animal Diseases, Bhopal, Madhya Pradesh, India; Immunology Section, ICAR - Indian Veterinary Research Institute, Izatnagar, Uttar Pradesh, India.

ICAR- National Institute of High Security Animal Diseases, Bhopal, Madhya Pradesh, India.

出版信息

Vet Microbiol. 2018 Apr;217:149-157. doi: 10.1016/j.vetmic.2018.03.004. Epub 2018 Mar 13.

Abstract

The present study was aimed at generating a reassortant vaccine candidate virus with clade 2.3.2.1 Hemagglutinin (HA) and its evaluation in a challenge study for protection against homologous (2.3.2.1 clade) and heterologous (2.2 clade) highly pathogenic avian influenza (HPAI) H5N1 viruses. Plasmid-based reverse genetics technique was used to rescue a 5 + 3 reassortant H5N2 strain containing the modified HA of H5N1 (clade 2.3.2.1), the Neuraminidase (NA) of H9N2, the Matrix (M) of H5N1 and the internal genes of A/WSN/33 H1N1. In addition, another 6 + 2 reassortant virus containing modified HA from H5N1 (clade 2.3.2.1), the NA from H9N2 and the internal genes of A/WSN/33 H1N1 was also rescued. The 5 + 3 reassortant H5N2 virus could grow to a higher titer in both MDCK cells and chicken eggs compared to the 6 + 2 reassortant H5N2 virus. The vaccine containing the inactivated 5 + 3 reassortant H5N2 virus was used in a two-dose immunization regime which protected specific pathogen free (SPF) chickens against two repeated challenges with homologous 2.3.2.1 clade and heterologous 2.2 clade HPAI H5N1 viruses. The 5 + 3 reassortant H5N2 virus based on clade 2.3.2.1 generated in this study can be effective in protecting chickens in the case of an outbreak caused by antigenically different clade 2.2 HPAI H5N1 viruses and opens the way to explore its applicability as potential vaccine candidate especially in the Asian countries reporting these clades frequently. The study also indicates that sequential immunization can broaden protection level against antigenically diverse strains of H5N1 viruses.

摘要

本研究旨在生成一种带有 2.3.2.1 分支血凝素(HA)的重组疫苗候选病毒,并在同源(2.3.2.1 分支)和异源(2.2 分支)高致病性禽流感(HPAI)H5N1 病毒的攻毒研究中对其进行评估。该研究采用基于质粒的反向遗传学技术拯救了一株 5+3 重配 H5N2 株,该株含有经过修饰的 H5N1(2.3.2.1 分支)HA、H9N2 的神经氨酸酶(NA)、H5N1 的基质(M)和 A/WSN/33 H1N1 的内部基因。此外,还拯救了另一株含有 H5N1(2.3.2.1 分支)修饰 HA、H9N2 NA 和 A/WSN/33 H1N1 内部基因的 6+2 重配病毒。与 6+2 重配 H5N2 病毒相比,5+3 重配 H5N2 病毒在 MDCK 细胞和鸡胚中均可达到更高的滴度。在两次免疫接种方案中,使用含有灭活的 5+3 重配 H5N2 病毒的疫苗可保护无特定病原体(SPF)鸡免受同源 2.3.2.1 分支和异源 2.2 分支 HPAI H5N1 病毒的两次重复攻毒。本研究中生成的基于 2.3.2.1 分支的 5+3 重配 H5N2 病毒可有效保护鸡群免受抗原不同的 2.2 分支 HPAI H5N1 病毒爆发的影响,并为探索其作为潜在疫苗候选物的适用性开辟了道路,特别是在经常报告这些分支的亚洲国家。该研究还表明,序贯免疫可以扩大对 H5N1 病毒抗原不同株的保护水平。

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