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一株表达血凝素蛋白的重组禽副黏病毒 3 型对鸡抵抗 H5N1 高致病性禽流感病毒攻击具有保护作用。

A recombinant avian paramyxovirus serotype 3 expressing the hemagglutinin protein protects chickens against H5N1 highly pathogenic avian influenza virus challenge.

机构信息

Virginia-Maryland College of Veterinary Medicine, University of Maryland, College Park, MD, USA.

出版信息

Sci Rep. 2020 Feb 10;10(1):2221. doi: 10.1038/s41598-020-59124-x.

DOI:10.1038/s41598-020-59124-x
PMID:32042001
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7010735/
Abstract

Highly pathogenic avian influenza (HPAI) is a devastating disease of poultry and a serious threat to public health. Vaccination with inactivated virus vaccines has been applied for several years as one of the major policies to control highly pathogenic avian influenza virus (HPAIV) infections in chickens. Viral-vectored HA protein vaccines are a desirable alternative for inactivated vaccines. However, each viral vector possesses its own advantages and disadvantages for the development of a HA-based vaccine against HPAIV. Recombinant Newcastle disease virus (rNDV) strain LaSota expressing HA protein vaccine has shown promising results against HPAIV; however, its replication is restricted only to the respiratory tract. Therefore, we thought to evaluate avian paramyxovirus serotype 3 (APMV-3) strain Netherlands as a safe vaccine vector against HPAIV, which has high efficiency replication in a greater range of host organs. In this study, we generated rAPMV-3 expressing the HA protein of H5N1 HPAIV using reverse genetics and evaluated the induction of neutralizing antibodies and protection by rAPMV3 and rNDV expressing the HA protein against HPAIV challenge in chickens. Our results showed that immunization of chickens with rAPMV-3 or rNDV expressing HA protein provided complete protection against HPAIV challenge. However, immunization of chickens with rAPMV-3 expressing HA protein induced higher level of neutralizing antibodies compared to that of rNDV expressing HA protein. These results suggest that a rAPMV-3 expressing HA protein might be a better vaccine for mass-vaccination of commercial chickens in field conditions.

摘要

高致病性禽流感(HPAI)是一种严重危害家禽的疾病,也是公共卫生的严重威胁。使用灭活病毒疫苗进行免疫接种已应用多年,是控制家禽高致病性禽流感病毒(HPAIV)感染的主要策略之一。基于病毒载体的 HA 蛋白疫苗是灭活疫苗的理想替代品。然而,每种病毒载体在开发针对 HPAIV 的基于 HA 的疫苗方面都有其自身的优势和劣势。表达 HA 蛋白的重组新城疫病毒(rNDV)株 LaSota 疫苗已显示出对抗 HPAIV 的有前途的结果;然而,其复制仅限于呼吸道。因此,我们认为评估禽副黏病毒血清型 3(APMV-3)株荷兰作为针对 HPAIV 的安全疫苗载体是可行的,因为它在更大范围的宿主器官中具有高效复制能力。在这项研究中,我们使用反向遗传学技术生成了表达 H5N1 HPAIV HA 蛋白的 rAPMV-3,并评估了 rAPMV3 和 rNDV 表达 HA 蛋白对 HPAIV 攻毒的中和抗体诱导和保护作用。我们的结果表明,用表达 HA 蛋白的 rAPMV-3 或 rNDV 免疫接种鸡可完全抵抗 HPAIV 攻毒。然而,与表达 HA 蛋白的 rNDV 相比,用表达 HA 蛋白的 rAPMV-3 免疫接种鸡诱导了更高水平的中和抗体。这些结果表明,表达 HA 蛋白的 rAPMV-3 可能是在田间条件下对商业鸡进行大规模免疫接种的更好疫苗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e26b/7010735/6363ab1d3235/41598_2020_59124_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e26b/7010735/b3ef153044c9/41598_2020_59124_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e26b/7010735/fc6400743f8e/41598_2020_59124_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e26b/7010735/da7dc4f11396/41598_2020_59124_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e26b/7010735/2e3bb4a18666/41598_2020_59124_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e26b/7010735/f4bde64f0e86/41598_2020_59124_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e26b/7010735/e60b27b2ac0d/41598_2020_59124_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e26b/7010735/1ba279666a4f/41598_2020_59124_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e26b/7010735/6363ab1d3235/41598_2020_59124_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e26b/7010735/b3ef153044c9/41598_2020_59124_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e26b/7010735/fc6400743f8e/41598_2020_59124_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e26b/7010735/da7dc4f11396/41598_2020_59124_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e26b/7010735/2e3bb4a18666/41598_2020_59124_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e26b/7010735/f4bde64f0e86/41598_2020_59124_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e26b/7010735/e60b27b2ac0d/41598_2020_59124_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e26b/7010735/1ba279666a4f/41598_2020_59124_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e26b/7010735/6363ab1d3235/41598_2020_59124_Fig8_HTML.jpg

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