氨基肽酶N冠状病毒受体在家养和野生偶蹄动物和食肉动物呼吸道和消化道的分布。

IF 3.6 4区 医学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Fabian Z X Lean, Giulia Gallo, Joseph Newman, Stuart Ackroyd, Simon Spiro, Ruth Cox, Ingebjørg Helena Nymo, Caroline Bröjer, Aleksija Neimanis, Alejandro Suárez-Bonnet, Simon L Priestnall, Holly Everest, Sarah Keep, Dalan Bailey, Richard J Delahay, Amanda H Seekings, Lorraine M McElhinney, Sharon M Brookes, Alejandro Núñez
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引用次数: 0

摘要

氨基肽酶 N(APN)是一种跨膜蛋白,它能介导几种临床上重要的冠状病毒(CoV)的尖峰蛋白附着,这些冠状病毒是动物和人类呼吸道和肠道疾病的罪魁祸首。为了评估 APN 介导的病毒滋养潜能,我们使用免疫组化方法鉴定了 APN 受体在各种半齿兽(颈鹿、牛、骆驼和麂类)和食肉兽(犬科、猫科、鼬科和狮科)呼吸道和肠道组织中的分布情况。在肺部,APN 的表达仅限于偶蹄类动物,在支气管上皮中的表达较强,而在肺细胞中的表达较弱。鼻甲和气管样本(如果有的话)显示,节肢动物的 APN 表达强于食肉动物。在多个类群的小肠中,肠细胞的微绒毛上都能持续检测到 APN,而在结肠中的存在则变化较大。在受检动物中,猪和羊驼在上呼吸道和下呼吸道中始终表达最丰富的 APN。对来自人类、偶蹄类动物和食肉类动物的 APN 同源物序列进行的硅学评估发现了不同的进化关系。进一步对羊驼α-冠状病毒和人类冠状病毒 229E 与同源和异源羊驼和人类 APN 的结合进行了硅学预测,发现了大量重叠的结合足迹,氨基酸残基高度保守,这表明 229E 类似病毒或祖先病毒在非人类动物宿主体内发生了进化分化和随后的适应。这种将解剖学和硅学相结合的方法加深了人们对依赖 APN 的 CoVs 的宿主易感性、组织滋养性和病毒传播机制的了解,并有可能为未来的疾病建模、监测和控制策略提供信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Distribution of aminopeptidase N coronavirus receptors in the respiratory and digestive tracts of domestic and wild artiodactyls and carnivores.

Aminopeptidase N (APN) is a transmembrane protein that mediates the attachment of the spike protein of several clinically important coronaviruses (CoVs) responsible for respiratory and intestinal diseases in animals and humans. To assess the potential for APN-mediated viral tropism, we characterized APN receptor distribution in the respiratory and intestinal tissues of various artiodactyls (cervids, bovids, camelids and suids) and carnivores (canids, felids, mustelids and phocids) using immunohistochemistry. In the lungs, APN expression was limited to artiodactyls, with strong expression in the bronchiolar epithelium and weaker expression in pneumocytes. Nasal turbinate and tracheal samples, where available, showed stronger APN expression in artiodactyls over carnivores. APN was consistently detected on the microvilli of enterocytes in the small intestine across multiple taxa, while the presence in the colon was more variable. Of the animals examined, pig and alpaca consistently expressed the most abundant APN in the upper and lower respiratory tract. In silico evaluation of APN orthologue sequences from humans, artiodactyls and carnivores identified distinct evolutionary relationships. Further in silico binding predictions for alpaca alphacoronavirus and human coronavirus 229E with cognate and heterologous alpaca and human APN revealed substantial overlapping binding footprints with high conservation of amino acid residues, suggesting an evolutionary divergence and subsequent adaptation of a 229E-like or ancestral virus within a non-human animal host. This combined anatomical and in silico approach enhances understanding of host susceptibility, tissue tropism and viral transmission mechanisms in APN-dependent CoVs and has the potential to inform future strategies for disease modelling, surveillance and control.

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来源期刊
Journal of General Virology
Journal of General Virology 医学-病毒学
CiteScore
7.70
自引率
2.60%
发文量
91
审稿时长
3 months
期刊介绍: JOURNAL OF GENERAL VIROLOGY (JGV), a journal of the Society for General Microbiology (SGM), publishes high-calibre research papers with high production standards, giving the journal a worldwide reputation for excellence and attracting an eminent audience.
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