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低致病性禽流感 H13 和 H16 病毒的系统地理学和抗原多样性。

Phylogeography and Antigenic Diversity of Low-Pathogenic Avian Influenza H13 and H16 Viruses.

机构信息

Erasmus Medical Center, Department of Viroscience, Rotterdam, The Netherlands

Linnaeus University, Department of Biology and Environmental Science, Kalmar, Sweden.

出版信息

J Virol. 2020 Jun 16;94(13). doi: 10.1128/JVI.00537-20.

DOI:10.1128/JVI.00537-20
PMID:32321814
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7307148/
Abstract

Low-pathogenic avian influenza viruses (LPAIVs) are genetically highly variable and have diversified into multiple evolutionary lineages that are primarily associated with wild-bird reservoirs. Antigenic variation has been described for mammalian influenza viruses and for highly pathogenic avian influenza viruses that circulate in poultry, but much less is known about antigenic variation of LPAIVs. In this study, we focused on H13 and H16 LPAIVs that circulate globally in gulls. We investigated the evolutionary history and intercontinental gene flow based on the hemagglutinin (HA) gene and used representative viruses from genetically distinct lineages to determine their antigenic properties by hemagglutination inhibition assays. For H13, at least three distinct genetic clades were evident, while for H16, at least two distinct genetic clades were evident. Twenty and ten events of intercontinental gene flow were identified for H13 and H16 viruses, respectively. At least two antigenic variants of H13 and at least one antigenic variant of H16 were identified. Amino acid positions in the HA protein that may be involved in the antigenic variation were inferred, and some of the positions were located near the receptor binding site of the HA protein, as they are in the HA protein of mammalian influenza A viruses. These findings suggest independent circulation of H13 and H16 subtypes in gull populations, as antigenic patterns do not overlap, and they contribute to the understanding of the genetic and antigenic variation of LPAIVs naturally circulating in wild birds. Wild birds play a major role in the epidemiology of low-pathogenic avian influenza viruses (LPAIVs), which are occasionally transmitted-directly or indirectly-from them to other species, including domestic animals, wild mammals, and humans, where they can cause subclinical to fatal disease. Despite a multitude of genetic studies, the antigenic variation of LPAIVs in wild birds is poorly understood. Here, we investigated the evolutionary history, intercontinental gene flow, and antigenic variation among H13 and H16 LPAIVs. The circulation of subtypes H13 and H16 seems to be maintained by a narrower host range, in particular gulls, than the majority of LPAIV subtypes and may therefore serve as a model for evolution and epidemiology of H1 to H12 LPAIVs in wild birds. The findings suggest that H13 and H16 LPAIVs circulate independently of each other and emphasize the need to investigate within-clade antigenic variation of LPAIVs in wild birds.

摘要

低致病性禽流感病毒 (LPAIV) 在遗传上高度多变,并已分化为多个主要与野生鸟类宿主相关的进化谱系。哺乳动物流感病毒和在禽类中传播的高致病性禽流感病毒的抗原性变异已有描述,但对 LPAIV 的抗原性变异知之甚少。在这项研究中,我们专注于在全球海鸥中循环的 H13 和 H16 LPAIV。我们基于血凝素 (HA) 基因研究了进化历史和洲际基因流动,并使用遗传上不同谱系的代表性病毒通过血凝抑制试验来确定它们的抗原特性。对于 H13,至少有三个明显的遗传分支,而对于 H16,至少有两个明显的遗传分支。对于 H13 和 H16 病毒,分别确定了 20 次和 10 次洲际基因流动事件。至少鉴定出 H13 的两个抗原变体和 H16 的一个抗原变体。推断出 HA 蛋白中可能参与抗原变异的氨基酸位置,其中一些位置位于 HA 蛋白的受体结合位点附近,就像哺乳动物流感 A 病毒的 HA 蛋白一样。这些发现表明 H13 和 H16 亚型在海鸥群体中独立循环,因为抗原模式不重叠,这有助于了解野生鸟类中自然循环的 LPAIV 的遗传和抗原变异。野生鸟类在低致病性禽流感病毒 (LPAIV) 的流行病学中发挥着重要作用,它们偶尔会直接或间接地将病毒传播给其他物种,包括家畜、野生哺乳动物和人类,在这些物种中,它们会引起亚临床到致命的疾病。尽管进行了大量的遗传研究,但野生鸟类中 LPAIV 的抗原性变异仍知之甚少。在这里,我们研究了 H13 和 H16 LPAIV 的进化历史、洲际基因流动和抗原变异。与大多数 LPAIV 亚型相比,H13 和 H16 亚型的循环似乎受到更窄宿主范围的维持,特别是海鸥,因此可能成为野生鸟类中 H1 至 H12 LPAIV 进化和流行病学的模型。研究结果表明,H13 和 H16 LPAIV 相互独立循环,并强调需要调查野生鸟类中 LPAIV 的within-clade 抗原性变异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6391/7307148/52559d6d3a05/JVI.00537-20-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6391/7307148/94e0508f3d5a/JVI.00537-20-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6391/7307148/e8a02edb7a8b/JVI.00537-20-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6391/7307148/52559d6d3a05/JVI.00537-20-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6391/7307148/94e0508f3d5a/JVI.00537-20-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6391/7307148/e8a02edb7a8b/JVI.00537-20-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6391/7307148/52559d6d3a05/JVI.00537-20-f0003.jpg

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