Evaluation of global distribution, genetic evolution, and mammalian infectivity and pathogenicity of H13 and H16 avian influenza viruses.

IF 7.5 2区 医学 Q1 IMMUNOLOGY
Emerging Microbes & Infections Pub Date : 2025-12-01 Epub Date: 2025-03-28 DOI:10.1080/22221751.2025.2482695
Xiang Li, Ao Li, Fengyi Qu, Yi Li, Fangyuan Chen, Xinru Lv, Qing An, Mengdan Fei, Hongyu Chen, Hongrui Liang, Xiaotian Zhang, Jinghao Li, Mingyuan Yu, Siyuan Qin, Linhong Xie, Shenglai Yin, Zheng Huang, Siyuan Yang, Heting Sun, Xiang Li, Hongliang Chai
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引用次数: 0

Abstract

H13 and H16 subtype avian influenza viruses (AIVs) typically infect Charadriiformes, are widely distributed throughout coastal regions worldwide, and pose a risk of spill-over to mammals. Systematic research on the epidemiology, transmission dynamics, and biological characteristics of these subtypes remains limited. To address this gap, we analyzed 20 years of wild bird influenza surveillance data from China integrated with global influenza database information to reconstruct the global spatiotemporal distribution, transmission dynamics and public health implications of H13 and H16. During influenza surveillance, 28 H13 and 19 H16 viruses were isolated. The phylogenetic trees for the H13 and H16 viruses revealed that both subtypes could be classified into three distinct groups. Viruses from H13 Group A, H13 Group C, and H16 Group C demonstrated frequent genetic exchanges and intercontinental transmission on a global scale. Mapping host migration revealed overlap between virus spread and host migration pathways. Our results suggest that host migration is a key driver of widespread distribution, cross-regional spread, and gene exchange for some H13 and H16 lineages. Virus isolates exhibit high genetic diversity with rich genotypic variation. Most isolates carry mammalian-adaptive mutations, such as the G228S mutation in the HA protein. H13 and H16 isolates of multiple genotypes infected mice without prior adaptation and exhibited varying tissue tropism. In summary, these findings indicate that host migration patterns are closely associated with the evolution of H13 and H16 AIVs. The potential risk of mammalian infection is highlighted, as viruses carrying mammalian-adaptive mutations may lead to new infection cases.

H13和H16禽流感病毒全球分布、遗传进化、哺乳动物传染性和致病性的评估。
摘要/ abstract摘要:th13和H16亚型禽流感病毒(aiv)主要感染翼形虫,广泛分布于全球沿海地区,对哺乳动物具有外溢性风险。对这些亚型的流行病学、传播动力学和生物学特性的系统研究仍然有限。为了弥补这一空白,我们结合全球流感数据库信息,分析了中国20年的野生禽流感监测数据,重建了H13和H16的全球时空分布、传播动态和公共卫生影响。在流感监测期间,分离出28株H13和19株H16病毒。H13和H16病毒的系统发育树显示,这两种亚型可以分为三个不同的组。H13 A群、H13 C群和H16 C群病毒在全球范围内表现出频繁的基因交换和洲际传播。宿主迁移映射揭示了病毒传播和宿主迁移途径之间的重叠。我们的研究结果表明,宿主迁移是H13和H16谱系广泛分布、跨区域传播和基因交换的关键驱动因素。病毒分离株具有较高的遗传多样性和丰富的基因型变异。大多数分离株携带哺乳动物适应性突变,如血凝素蛋白中的G228S突变。多种基因型的H13和H16分离株感染小鼠没有事先适应,并表现出不同的组织趋向性。综上所述,这些发现表明宿主迁移模式与H13和H16 aiv的进化密切相关。由于携带哺乳动物适应性突变的病毒可能导致新的感染病例,因此强调了哺乳动物感染的潜在风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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