动物甲型流感病毒对人唾液酸受体的逐渐适应

IF 5.7 2区 医学 Q1 VIROLOGY
Mengying Liu, Frank JM van Kuppeveld, Cornelis AM de Haan, Erik de Vries
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引用次数: 0

摘要

源自动物宿主的甲型流感病毒(IAV)对人类健康构成持续威胁,西班牙流感大流行证明了这一点。感染始于与宿主受体的附着,这是免疫、预防和治疗干预的关键步骤。病毒血凝素与宿主特异性受体库结合的微调需要与破坏受体的神经氨酸酶(NA)活性保持平衡,这是宿主适应的关键步骤。它决定了NA依赖性病毒的运动性,使IAV能够穿过粘液层,与上皮细胞表面结合并迁移到上皮细胞表面,到达支持内吞摄取的位置。增强人型受体结合的地方病/人畜共患IAV的典型适应是众所周知的,但其选择所需的背景和时间跨度提出了许多问题。我们讨论了最近的进展,重点是IAV与人类和潜在中间宿主中存在的异质受体库相互作用的动力学性质。将讨论中间宿主对人型受体结合的潜在预适应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Gradual adaptation of animal influenza A viruses to human-type sialic acid receptors

Influenza A viruses (IAVs) originating from animal reservoirs pose continuous threats to human health as demonstrated by the Spanish flu pandemic. Infection starts by attachment to host receptors, a crucial step that is targeted by immunological, prophylactic, and therapeutic intervention. Fine-tuning of virus hemagglutinin binding to host-specific receptor repertoires needs to remain balanced to receptor-destroying neuraminidase (NA) activity and is a key step in host adaptation. It determines NA-dependent virus motility, enabling IAVs to traverse the mucus layer and to bind to, and migrate over, the epithelial cell surface for reaching a location supporting endocytic uptake. Canonical adaptations in enzootic/zoonotic IAVs enhancing human-type receptor binding are well-known, but the context and timespan required for their selection pose many questions. We discuss recent developments, focusing on the dynamic nature of interactions of IAV with the heterogeneous receptor repertoires present in humans and potential intermediate hosts. Potential pre-adaption toward human-type receptor binding in intermediate hosts will be discussed.

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来源期刊
CiteScore
11.80
自引率
5.10%
发文量
76
审稿时长
83 days
期刊介绍: Current Opinion in Virology (COVIRO) is a systematic review journal that aims to provide specialists with a unique and educational platform to keep up to date with the expanding volume of information published in the field of virology. It publishes 6 issues per year covering the following 11 sections, each of which is reviewed once a year: Emerging viruses: interspecies transmission; Viral immunology; Viral pathogenesis; Preventive and therapeutic vaccines; Antiviral strategies; Virus structure and expression; Animal models for viral diseases; Engineering for viral resistance; Viruses and cancer; Virus vector interactions. There is also a section that changes every year to reflect hot topics in the field.
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