Expression of influenza A virus glycan receptor candidates in mallard, chicken, and tufted duck.

IF 3.4 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Jonas Nilsson, Per Eriksson, Mahmoud M Naguib, Elinor Jax, Carina Sihlbom, Britt-Marie Olsson, Åke Lundkvist, Björn Olsen, Josef D Järhult, Göran Larson, Patrik Ellström
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引用次数: 0

Abstract

Influenza A virus (IAV) pandemics result from interspecies transmission events within the avian reservoir and further into mammals including humans. Receptor incompatibility due to differently expressed glycan structures between species has been suggested to limit zoonotic IAV transmission from the wild bird reservoir as well as between different bird species. Using glycoproteomics, we have studied the repertoires of expressed glycan structures with focus on putative sialic acid-containing glycan receptors for IAV in mallard, chicken and tufted duck; three bird species with different roles in the zoonotic ecology of IAV. The methodology used pinpoints specific glycan structures to specific glycosylation sites of identified glycoproteins and was also used to successfully discriminate α2-3- from α2-6-linked terminal sialic acids by careful analysis of oxonium ions released from glycopeptides in tandem MS/MS (MS2), and MS/MS/MS (MS3). Our analysis clearly demonstrated that all three bird species can produce complex N-glycans including α2-3-linked sialyl Lewis structures, as well as both N- and O- glycans terminated with both α2-3- and α2-6-linked Neu5Ac. We also found the recently identified putative IAV receptor structures, Man-6P N-glycopeptides, in all tissues of the three bird species. Furthermore, we found many similarities in the repertoires of expressed receptors both between the bird species investigated and to previously published data from pigs and humans. Our findings of sialylated glycan structures, previously anticipated to be mammalian specific, in all three bird species may have major implications for our understanding of the role of receptor incompatibility in interspecies transmission of IAV.

候选甲型流感病毒糖受体在野鸭、鸡和簇鸭中的表达。
甲型流感病毒(IAV)大流行源于禽类病毒库中的种间传播事件,并进一步传播到包括人类在内的哺乳动物体内。由于物种间表达的聚糖结构不同,导致受体不相容,这被认为限制了人畜共患的 IAV 从野生鸟类储库以及不同鸟类物种之间的传播。利用糖蛋白组学,我们研究了野鸭、鸡和簇鸭中表达的聚糖结构,重点研究了这三种在 IAV 人畜共患病生态学中扮演不同角色的鸟类的 IAV 假定含膳食纤维酸的聚糖受体。所使用的方法将特定的聚糖结构精确定位到已确定的糖蛋白的特定糖基化位点,并通过仔细分析串联质谱/质谱(MS 2)和质谱/质谱/质谱(MS 3)中从糖肽中释放的羰离子,成功地区分了α2-3-和α2-6-连接的末端sialic acids。我们的分析清楚地表明,所有这三种鸟类都能产生复杂的 N-聚糖,包括 α2-3-连接的 sialyl Lewis 结构,以及以 α2-3-连接的 Neu5Ac 和 α2-6-连接的 Neu5Ac 终止的 N-和 O-聚糖。我们还在三种鸟类的所有组织中发现了最近确定的 IAV 受体结构 Man-6P N-糖肽。此外,我们还发现所调查的鸟类物种之间表达的受体谱系有许多相似之处,而且与之前发表的猪和人的数据也有相似之处。我们在所有三个鸟类物种中发现了以前认为是哺乳动物特有的糖基化结构,这可能对我们理解受体不相容在 IAV 种间传播中的作用有重大影响。
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来源期刊
Glycobiology
Glycobiology 生物-生化与分子生物学
CiteScore
7.50
自引率
4.70%
发文量
73
审稿时长
3 months
期刊介绍: Established as the leading journal in the field, Glycobiology provides a unique forum dedicated to research into the biological functions of glycans, including glycoproteins, glycolipids, proteoglycans and free oligosaccharides, and on proteins that specifically interact with glycans (including lectins, glycosyltransferases, and glycosidases). Glycobiology is essential reading for researchers in biomedicine, basic science, and the biotechnology industries. By providing a single forum, the journal aims to improve communication between glycobiologists working in different disciplines and to increase the overall visibility of the field.
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