细胞糖萼包裹呼吸道合胞病毒(RSV)颗粒的证据,这些颗粒形成于RSV感染的人气道细胞表面

IF 2.4 3区 医学 Q3 VIROLOGY Virology Pub Date : 2025-03-01 Epub Date: 2025-01-18 DOI:10.1016/j.virol.2025.110415
Soak Kuan Lai , Zhi Qi Lee , Trina Isabel Tan , Boon Huan Tan , Richard J. Sugrue
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引用次数: 0

摘要

我们研究了呼吸道合胞病毒(RSV)颗粒如何绕过病毒感染的A549细胞上的糖萼。采用凝集素WGA-AL488探针和分别检测硫酸肝素(HS)和syndecan-4蛋白(SYND4)的anti-HS和anti-syndecan-4抗体检测糖环。rsv感染细胞的成像提供了证据,证明糖萼在病毒细丝形成时包裹着病毒细丝,并且糖萼的HS部分和SYND4等成分显示在成熟病毒细丝的表面。G蛋白在这些细胞中的重组表达表明,G蛋白被运输到具有明确糖萼的预先存在的丝状细胞结构中,进一步表明糖萼维持在病毒颗粒组装的位置。这些数据提供证据表明,在RSV颗粒组装过程中,病毒细丝被糖萼包裹,糖萼应被视为病毒细丝的一个结构组成部分。
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Evidence that the cell glycocalyx envelops respiratory syncytial virus (RSV) particles that form on the surface of RSV-infected human airway cells
We examined how respiratory syncytial virus (RSV) particles circumvent the overlying glycocalyx on virus-infected A549 cells. The glycocalyx was detected using the lectin WGA-AL488 probe, and the antibodies anti-HS and anti-syndecan-4 that detect heparin sulphate (HS) and the syndecan-4 protein (SYND4) respectively. Imaging of RSV-infected cells provided evidence that the glycocalyx envelopes the virus filaments as they form, and that components of the glycocalyx such as HS moieties and SYND4 are displayed on the surface of the mature virus filaments. Recombinant expression of the G protein in these cells suggested that the G protein was trafficked into pre-existing filamentous cellular structures with a well-defined glycocalyx, further suggesting that the glycocalyx is maintained at the site of virus particle assembly. These data provide evidence that during RSV particle assembly the virus filaments become enveloped by the glycocalyx, and that the glycocalyx should be considered as a structural component of virus filaments.
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来源期刊
Virology
Virology 医学-病毒学
CiteScore
6.00
自引率
0.00%
发文量
157
审稿时长
50 days
期刊介绍: Launched in 1955, Virology is a broad and inclusive journal that welcomes submissions on all aspects of virology including plant, animal, microbial and human viruses. The journal publishes basic research as well as pre-clinical and clinical studies of vaccines, anti-viral drugs and their development, anti-viral therapies, and computational studies of virus infections. Any submission that is of broad interest to the community of virologists/vaccinologists and reporting scientifically accurate and valuable research will be considered for publication, including negative findings and multidisciplinary work.Virology is open to reviews, research manuscripts, short communication, registered reports as well as follow-up manuscripts.
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