Yang Jiayun, Qureshi Mehnaz, Kolli Reddy, Peacock Thomas P, Sadeyen Jean-Remy, Carter Toby, Richardson Samuel, Daines Rebecca, Barclay Wendy S, Brown Ian H, Iqbal Munir
The Pirbright Institute, Pirbright, UK.
Department of Infectious Disease, Imperial College London, London, UK.
Emerg Microbes Infect. 2025 Dec;14(1):2451052. doi: 10.1080/22221751.2025.2451052. Epub 2025 Jan 27.
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.
2.3.4.4b分支H5N1高致病性禽流感病毒(HPAIV)已引发一场除澳大利亚外影响各大洲的大流行,并将其宿主范围扩大到几种哺乳动物。2024年3月,H5N1 HPAIV首次在美国的奶牛和山羊中被检测到。截至2024年12月25日,美国16个州的891多个奶牛场检测呈阳性,并有报道称奶牛场工人出现人畜共患感染。这引发了人们对该病毒在牛群中发生进化变化从而增强其人畜共患潜力的担忧。流感糖蛋白血凝素(HA)通过受体结合以及pH值诱导的与细胞膜融合来促进进入宿主细胞。HA的适应性变化调节病毒与宿主细胞的相互作用。本研究将牛和山羊H5N1病毒的HA基因与英国占主导地位的禽源2.3.4.4b分支H5N1进行了比较,重点关注受体结合、pH值融合和热稳定性。所有测试的H5N1病毒均仅与禽源样受体结合,pH值融合为5.9,不在与高效人际空气传播相关的pH值范围(pH 5.0 - 5.5)内。我们进一步研究了在当前牛群疫情中出现的HA替代的影响,但几乎没有发现表型差异,仍继续仅与禽源样受体类似物结合,融合pH值高于5.8。这表明与正在传播的禽病毒相比,来自牛和山羊疫情的HA基因并未构成更大威胁。然而,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人畜共患和大流行风险仍然至关重要。