4.8 Article

Dual-Fluorescence Labeling Pseudovirus for Real-Time Imaging of Single SARS-CoV-2 Entry in Respiratory Epithelial Cells

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 13, 期 21, 页码 24477-24486

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.1c03897

关键词

pseudo-SARS-CoV-2 virus; single-virus imaging; endocytic entry; dual fluorescence; respiratory epithelial cells

资金

  1. National Key Research and Development Program of China [2017YFA0205503]
  2. National Natural Science Foundation [21890743]
  3. Strategic Priority Research Program of the Chinese Academy of Sciences, China [XDB29050100]
  4. Youth Innovation Promotion Association CAS [2021359]
  5. Natural Science Foundation of Guangdong [2018B030306046]
  6. China Postdoctoral Science Foundation [2019M663154]

向作者/读者索取更多资源

The study created a dual color pseudo-SARS-CoV-2 virus using a pseudovirus strategy, allowing tracking of virus movement and fate of labeled components. Pseudo-SARS-CoV-2 mainly entered host cells through endocytosis, with infection efficiency correlated to the expression of ACE2 receptor on host cell surface. The dual-color fluorescently labeled pseudovirus system is believed to be a useful tool for various purposes in SARS-CoV-2/COVID-19 research.
The pseudovirus strategy makes studies of highly pathogenic viruses feasible without the restriction of high-level biosafety facility, thus greatly contributing to virology and is used in the research studies of SARS-CoV-2. Here, we generated a dual color pseudo-SARS-CoV-2 virus using a human immunodeficiency virus-1 pseudovirus production system and the SARS-CoV-2 spike (S) glycoprotein, of which the membrane was labeled with a lipophilic dye (DiO) and the genomic RNA-related viral protein R (Vpr) of the viral core was fused with mCherry. With this dual-color labeling strategy, not only the movement of the whole virus but also the fate of the labeled components can be traced. The pseudovirions were applied to track the viral entry at a single-particle level in four types of the human respiratory cells: nasal epithelial cells (HNEpC), pulmonary alveolar epithelial cells (HPAEpiC), bronchial epithelial cells (BEP-2D), and oral epithelial cells (HOEC). Pseudo-SARS-CoV-2 entered into the host cell and released the viral core into the cytoplasm, which clearly indicates that the host entry mainly occurred through endocytosis. The infection efficiency was found to be correlated with the expression of the known receptor of SARS-CoV-2, angiotensin-converting 2 (ACE2) on the host cell surface. We believe that the dual-color fluorescently labeled pseudovirus system created in this study can be applied as a useful tool for many purposes in SARS-CoV-2/COVID-19.

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