The haemagglutinin gene of bovine-origin H5N1 influenza viruses currently retains receptor-binding and pH-fusion characteristics of avian host phenotype.

IF 8.4 2区 医学 Q1 IMMUNOLOGY Emerging Microbes & Infections Pub Date : 2025-12-01 Epub Date: 2025-01-27 DOI:10.1080/22221751.2025.2451052
Jiayun Yang, Mehnaz Qureshi, Reddy Kolli, Thomas P Peacock, Jean-Remy Sadeyen, Toby Carter, Samuel Richardson, Rebecca Daines, Wendy S Barclay, Ian H Brown, Munir Iqbal
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Abstract

Clade 2.3.4.4b H5N1 high pathogenicity avian influenza virus (HPAIV) has caused a panzootic affecting all continents except Australia, expanding its host range to several mammalian species. In March 2024, H5N1 HPAIV was first detected in dairy cattle and goats in the United States. Over 891 dairy farms across 16 states have tested positive until 25 December 2024, with zoonotic infections reported among dairy workers. This raises concerns about the virus undergoing evolutionary changes in cattle that could enhance its zoonotic potential. The Influenza glycoprotein haemagglutinin (HA) facilitates entry into host cells through receptor binding and pH-induced fusion with cellular membranes. Adaptive changes in HA modulate virus-host cell interactions. This study compared the HA genes of cattle and goat H5N1 viruses with the dominant avian-origin clade 2.3.4.4b H5N1 in the United Kingdom, focusing on receptor binding, pH fusion, and thermostability. All the tested H5N1 viruses showed binding exclusively to avian-like receptors, with a pH fusion of 5.9, outside the pH range associated with efficient human airborne transmissibility (pH 5.0-5.5). We further investigated the impact of emerging HA substitutions seen in the ongoing cattle outbreaks, but saw little phenotypic difference, with continued exclusive binding to avian-like receptor analogues and pHs of fusion above 5.8. This suggests that the HA genes from the cattle and goat outbreaks do not pose an enhanced threat compared to circulating avian viruses. However, given the rapid evolution of H5 viruses, continuous monitoring and updated risk assessments remain essential to understanding virus zoonotic and pandemic risks.

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牛源H5N1流感病毒血凝素基因目前保留了鸟类宿主表型的受体结合和ph融合特征。
支系 2.3.4.4b H5N1 高致病性禽流感病毒(HPAIV)已造成泛流行,影响到除澳大利亚以外的所有大陆,并将其宿主范围扩大到多个哺乳动物物种。2024 年 3 月,美国首次在奶牛和山羊中检测到 H5N1 高致病性禽流感病毒。截至 2024 年 12 月 25 日,16 个州超过 891 个奶牛场的检测结果呈阳性,据报告,奶牛场工人中出现了人畜共患感染。这引发了人们对该病毒在牛体内发生进化变化的担忧,进而可能增强其人畜共患病的可能性。流感糖蛋白血凝素(HA)通过受体结合和 pH 值诱导与细胞膜融合,促进病毒进入宿主细胞。HA 的适应性变化可调节病毒与宿主细胞的相互作用。本研究比较了牛和山羊 H5N1 病毒的 HA 基因与英国主要禽源支系 2.3.4.4b H5N1 病毒的 HA 基因,重点关注受体结合、pH 融合和热稳定性。所有测试的 H5N1 病毒都显示只与禽类类受体结合,pH 值融合度为 5.9,超出了与人类通过空气有效传播相关的 pH 值范围(pH 值为 5.0 至 5.5)。我们进一步研究了正在爆发的牛疫情中新出现的 HA 替代的影响,但发现表型差异不大,仍然只与类禽受体类似物结合,融合 pH 值高于 5.8。这表明,与流行的禽类病毒相比,牛和山羊疫情中的 HA 基因不会造成更大的威胁。不过,鉴于 H5 病毒的快速进化,持续监测和更新风险评估对于了解病毒的人畜共患和大流行风险仍然至关重要。
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来源期刊
Emerging Microbes & Infections
Emerging Microbes & Infections IMMUNOLOGY-MICROBIOLOGY
CiteScore
26.20
自引率
2.30%
发文量
276
审稿时长
20 weeks
期刊介绍: Emerging Microbes & Infections is a peer-reviewed, open-access journal dedicated to publishing research at the intersection of emerging immunology and microbiology viruses. The journal's mission is to share information on microbes and infections, particularly those gaining significance in both biological and clinical realms due to increased pathogenic frequency. Emerging Microbes & Infections is committed to bridging the scientific gap between developed and developing countries. This journal addresses topics of critical biological and clinical importance, including but not limited to: - Epidemic surveillance - Clinical manifestations - Diagnosis and management - Cellular and molecular pathogenesis - Innate and acquired immune responses between emerging microbes and their hosts - Drug discovery - Vaccine development research Emerging Microbes & Infections invites submissions of original research articles, review articles, letters, and commentaries, fostering a platform for the dissemination of impactful research in the field.
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