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重组禽流感病毒 A 型 H5N8 系 2.3.4.4b 在 Madin-Darby 犬肾细胞中的差异复制特征。

Differential replication characteristic of reassortant avian influenza A viruses H5N8 clade 2.3.4.4b in Madin-Darby canine kidney cell.

机构信息

Reference Laboratory for Veterinary Quality Control on Poultry Production (RLQP), Animal Health Research Institute, Agriculture Research Center (ARC), Giza, 12618, Egypt.

Department of Medical Microbiology and Parasitology, Faculty of Medicine, University of Jeddah, Jeddah, Saudi Arabia.

出版信息

Poult Sci. 2023 Jul;102(7):102685. doi: 10.1016/j.psj.2023.102685. Epub 2023 Mar 29.

Abstract

Late in 2016, multiple reassortant highly pathogenic (HP) avian influenza virus (AIVs) H5N8 was detected. AIVs infect different isolated hosts with a specific viral tropism. In the current study, the whole genome of the Egyptian A/chicken/NZ/2022 was genetically characterized. The H5N8-A/Common-coot/Egypt/CA285/2016, A/duck/Egypt/SS19/2017 previously isolated in Egypt, and the recently circulating A/chicken/Egypt/NZ/2022 reassortant viruses' replication, pathogenicity, and viral load in comparison to the H5N1-Clade 2.2.1.2 were investigated on Madin-Darby canine kidney cell (MDCK), by using the cytopathic effect (CPE) percent and matrix-gene reverse transcription quantitative real-time polymerase chain reaction to compute the virus titer at various points in time. The A/chicken/Egypt/NZ/2022 virus was similar to the reassortant strain clade 2.3.4.4b discovered in farms in 2016. The 2 sub-groupings of hemagglutinin (HA) and neuraminidase (NA) genes were identified (I and II); the A/chicken/Egypt/NZ/2022 HA and NA genes were associated with subgroup II. The subgroup II of the HA gene was further divided into A and B owing to acquired specific mutations. The A/chicken/Egypt/NZ/2022 in our study was associated with subgroup B. The M, NS, PB1, and PB2 genes were shown to be clustered into clade 2.3.4.4b by full genome sequence analysis; however, the PA and NP genes were found to be associated with H6N2 viruses, which had particular mutations that improved viral virulence and mammalian transmission. The current results showed that the circulating H5N8 viruses were more variable than previous viruses analyzed in 2016 and 2017. Compared to other reassortant HPAI H5N8, and HPAI H5N1, the growth kinetics of A/chicken/Egypt/NZ/2022 had a high CPE without the addition of trypsin and the most viral copies with a significant difference (P < 0.01) in comparison to HPAI H5N8 and HPAI H5N1 reassortant viruses. Accordingly, the effective viral replication of A/chicken/Egypt/NZ/2022 in the MDCK than other viruses may play a factor in the spread and maintenance of specific reassortant H5N8 influenza virus in the field.

摘要

2016 年末,检测到多种重配高致病性(HP)禽流感病毒(AIV)H5N8。AIV 以特定的病毒嗜性感染不同的隔离宿主。在本研究中,对从埃及分离的 A/鸡/新西兰/2022 进行了全基因组遗传特征分析。之前在埃及分离的 H5N8-A/普通潜鸭/埃及/CA285/2016 和 A/鸭/埃及/SS19/2017,以及最近流行的 A/鸡/埃及/新西兰/2022 重配病毒,与 H5N1-Clade 2.2.1.2 相比,在 Madin-Darby 犬肾细胞(MDCK)上的复制、致病性和病毒载量进行了研究,使用细胞病变效应(CPE)百分比和基质基因反转录定量实时聚合酶链反应来计算不同时间点的病毒滴度。A/鸡/埃及/新西兰/2022 病毒与 2016 年在农场发现的重配株 2.3.4.4b 类似。鉴定了血凝素(HA)和神经氨酸酶(NA)基因的 2 个亚群(I 和 II);A/鸡/埃及/新西兰/2022 的 HA 和 NA 基因与亚群 II 相关。由于获得了特定的突变,HA 基因的亚群 II 进一步分为 A 和 B。在本研究中,A/鸡/埃及/新西兰/2022 与亚群 B 相关。全基因组序列分析表明,M、NS、PB1 和 PB2 基因聚类为 2.3.4.4b 分支;然而,PA 和 NP 基因与 H6N2 病毒有关,这些病毒具有特定的突变,提高了病毒的毒力和哺乳动物的传播能力。目前的结果表明,与 2016 年和 2017 年分析的以前的病毒相比,循环的 H5N8 病毒具有更高的变异性。与其他重配的高致病性禽流感 H5N8 和高致病性禽流感 H5N1 相比,A/鸡/埃及/新西兰/2022 的生长动力学具有高 CPE,无需添加胰酶,并且与高致病性禽流感 H5N8 和高致病性禽流感 H5N1 重配病毒相比,具有最显著的差异(P < 0.01)。因此,A/鸡/埃及/新西兰/2022 在 MDCK 中的有效病毒复制可能比其他病毒更能在现场传播和维持特定的重配 H5N8 流感病毒。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/97cf/10245327/881bc4a61304/gr1a.jpg

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