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利用单基因重配病毒研究甲型禽流感病毒基因在野生型甲型人流感病毒对松鼠猴和成年人类志愿者减毒过程中的作用。

Use of single-gene reassortant viruses to study the role of avian influenza A virus genes in attenuation of wild-type human influenza A virus for squirrel monkeys and adult human volunteers.

作者信息

Clements M L, Subbarao E K, Fries L F, Karron R A, London W T, Murphy B R

机构信息

Department of International Health, Johns Hopkins University School of Hygiene and Public Health, Baltimore, Maryland.

出版信息

J Clin Microbiol. 1992 Mar;30(3):655-62. doi: 10.1128/jcm.30.3.655-662.1992.

Abstract

The transfer of six internal RNA segments from the avian influenza A/Mallard/New York/6750/78 (H2N2) virus reproducibly attenuates human influenza A viruses for squirrel monkeys and adult humans. To identify the avian influenza A virus genes that specify the attenuation and host range restriction of avian-human (ah) influenza A reassortant viruses (referred to as ah reassortants), we isolated six single-gene reassortant viruses (SGRs), each having a single internal RNA segment of the influenza A/Mallard/New York/6750/78 virus and seven RNA segments from the human influenza A/Los Angeles/2/87 (H3N2) wild-type virus. To assess the level of attenuation, we compared each SGR with the A/Los Angeles/2/87 wild-type virus and a 6-2 gene ah reassortant (having six internal RNA segments from the avian influenza A virus parent and two genes encoding the hemagglutinin and neuraminidase glycoproteins from the wild-type human influenza A virus) for the ability to replicate in seronegative squirrel monkeys and adult human volunteers. In monkeys and humans, replication of the 6-2 gene ah reassortant was highly restricted. In humans, the NS, M, PB2, and PB1 SGRs each replicated significantly less efficiently (P less than 0.05) than the wild-type human influenza A virus parent, suggesting that each of these genes contributes to the attenuation phenotype. In monkeys, only the NP, PB2, and possibly the M genes contributed to the attenuation phenotype. These discordant observations, particularly with regard to the NP SGR, indicate that not all genetic determinants of attenuation of influenza A viruses for humans can be identified during studies of SGRs conducted with monkeys. The PB2 and M SGRs that were attenuated in humans each exhibited a new phenotype that was not observed for either parental virus. Thus, it was not possible to determine whether avian influenza virus PB2 or M gene itself or a specific constellation of avian and human influenza A virus specified restriction of virus replication in humans.

摘要

将来自甲型禽流感病毒A/绿头鸭/纽约/6750/78(H2N2)的6个内部RNA片段进行转移,可重复性地使甲型人流感病毒对松鼠猴和成年人减毒。为了鉴定决定禽-人(ah)甲型流感重配病毒(称为ah重配体)减毒和宿主范围限制的甲型禽流感病毒基因,我们分离出6种单基因重配病毒(SGR),每种病毒都有甲型禽流感病毒A/绿头鸭/纽约/6750/78的一个单一内部RNA片段以及来自甲型人流感病毒A/洛杉矶/2/87(H3N2)野生型病毒的7个RNA片段。为了评估减毒水平,我们将每种SGR与A/洛杉矶/2/87野生型病毒以及一种6-2基因ah重配体(具有来自甲型禽流感病毒亲本的6个内部RNA片段以及来自野生型甲型人流感病毒的两个编码血凝素和神经氨酸酶糖蛋白的基因)进行比较,以确定它们在血清阴性的松鼠猴和成年人类志愿者体内的复制能力。在猴和人身上,6-2基因ah重配体的复制受到高度限制。在人类中,NS、M、PB2和PB1 SGR的复制效率均显著低于野生型甲型人流感病毒亲本(P小于0.05),这表明这些基因中的每一个都对减毒表型有贡献。在猴中,只有NP、PB2以及可能的M基因对减毒表型有贡献。这些不一致的观察结果,特别是关于NP SGR的观察结果,表明并非所有甲型流感病毒对人类减毒的遗传决定因素都能在对猴进行的SGR研究中被识别出来。在人类中减毒的PB2和M SGR各自表现出一种新的表型,这在两种亲本病毒中均未观察到。因此,不可能确定甲型禽流感病毒PB2或M基因本身,或者禽和甲型人流感病毒的特定组合是否规定了病毒在人类中的复制限制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4843/265127/631475f569bc/jcm00027-0134-a.jpg

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