Wu Eugene Y, Robertson Alexander M, Zhu Hanglin Henry, Stasiak Corina, Murray-Nerger Laura A, Romanoff Emily, Woon Jesse, Bromme Beth A, Smith Jason G
Department of Biology, University of Richmond, Richmond, VA 23173, USA.
Department of Microbiology, University of Washington School of Medicine, Seattle, WA 98109, USA.
Viruses. 2024 Nov 25;16(12):1827. doi: 10.3390/v16121827.
Certain species D human adenoviruses (HAdV-D19, -D37, and -D64) are causative agents of epidemic keratoconjunctivitis. HAdV-D37 has previously been shown to bind CD46 (membrane cofactor protein) and sialic acid as adhesion receptors. HAdV-D64 is genetically highly similar to HAdV-D37, with an identical fiber protein sequence, but differs substantially in its penton base and hexon proteins, two other major capsid components, due to genetic recombination. Here, we demonstrate that, like HAdV-D37, HAdV-D64 virions bind directly to CD46 and that CD46 and sialic acid also function as receptors for HAdV-D64 on multiple cell types. Expression of CD46 on CD46-negative cells conferred susceptibility to HAdV-D64 entry. Specifically blocking HAdV-D64 binding to CD46 on the host cell surface strongly inhibits viral entry and gene delivery into multiple cell lines that represent target tissues. We show that CD46 is expressed on human conjunctival epithelial cells and directly binds to the HAdV-D64 virion. Our results suggest that HAdV-D64 may be used to deliver genes to target conjunctival cells and that interrupting HAdV-D64 entry through its interaction with CD46 may prevent or lessen adenovirus-associated ocular disease.
某些D种人类腺病毒(HAdV-D19、-D37和-D64)是流行性角结膜炎的病原体。先前已证明HAdV-D37可结合CD46(膜辅因子蛋白)和唾液酸作为粘附受体。HAdV-D64在基因上与HAdV-D37高度相似,纤维蛋白序列相同,但由于基因重组,其五邻体基座和六邻体蛋白(另外两个主要衣壳成分)有很大差异。在此,我们证明,与HAdV-D37一样,HAdV-D64病毒粒子直接结合CD46,并且CD46和唾液酸在多种细胞类型上也作为HAdV-D64的受体发挥作用。在CD46阴性细胞上表达CD46赋予细胞对HAdV-D64进入的敏感性。特异性阻断HAdV-D64与宿主细胞表面CD46的结合可强烈抑制病毒进入并将基因传递到代表靶组织的多种细胞系中。我们表明,CD46在人结膜上皮细胞上表达并直接结合HAdV-D64病毒粒子。我们的结果表明,HAdV-D64可用于将基因传递至靶结膜细胞,并且通过其与CD46的相互作用阻断HAdV-D64进入可能预防或减轻腺病毒相关的眼部疾病。