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D种人类腺病毒中广泛的唾液酸使用情况。

Broad sialic acid usage amongst species D human adenovirus.

作者信息

Mundy Rosie M, Baker Alexander T, Bates Emily A, Cunliffe Tabitha G, Teijeira-Crespo Alicia, Moses Elise, Rizkallah Pierre J, Parker Alan L

机构信息

Division of Cancer & Genetics, Cardiff University School of Medicine, Cardiff, CF14 4XN UK.

Division of Infection & Immunity, Cardiff University School of Medicine, Cardiff, CF14 4XN UK.

出版信息

Npj Viruses. 2023;1(1):1. doi: 10.1038/s44298-023-00001-5. Epub 2023 Sep 26.

Abstract

Human adenoviruses (HAdV) are widespread pathogens causing usually mild infections. The Species D (HAdV-D) cause gastrointestinal tract infections and epidemic keratoconjunctivitis (EKC). Despite being significant pathogens, knowledge around HAdV-D mechanism of cell infection is lacking. Sialic acid (SA) usage has been proposed as a cell infection mechanism for EKC causing HAdV-D. Here we highlight an important role for SA engagement by many HAdV-D. We provide apo state crystal structures of 7 previously undetermined HAdV-D fiber-knob proteins, and structures of HAdV-D25, D29, D30 and D53 fiber-knob proteins in complex with SA. Biologically, we demonstrate that removal of cell surface SA reduced infectivity of HAdV-C5 vectors pseudotyped with HAdV-D fiber-knob proteins, whilst engagement of the classical HAdV receptor CAR was variable. Our data indicates variable usage of SA and CAR across HAdV-D. Better defining these interactions will enable improved development of antivirals and engineering of the viruses into refined therapeutic vectors.

摘要

人腺病毒(HAdV)是广泛传播的病原体,通常引起轻度感染。D种人腺病毒(HAdV-D)可导致胃肠道感染和流行性角结膜炎(EKC)。尽管HAdV-D是重要的病原体,但目前缺乏关于其细胞感染机制的了解。唾液酸(SA)的利用已被提出作为导致EKC的HAdV-D的一种细胞感染机制。在此,我们强调了许多HAdV-D与SA结合的重要作用。我们提供了7种先前未确定的HAdV-D纤维结蛋白的无配体状态晶体结构,以及与SA结合的HAdV-D25、D29、D30和D53纤维结蛋白的结构。从生物学角度来看,我们证明去除细胞表面的SA会降低用HAdV-D纤维结蛋白假型化的HAdV-C5载体的感染性,而经典HAdV受体柯萨奇病毒和腺病毒受体(CAR)的结合情况则各不相同。我们的数据表明,HAdV-D对SA和CAR的利用存在差异。更好地定义这些相互作用将有助于改进抗病毒药物的研发,并将病毒改造为更精确的治疗载体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a539/11721112/b6024deae4e0/44298_2023_1_Fig1_HTML.jpg

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