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Monitoring correlates of SARS-CoV-2 infection in cell culture using a two-photon-active calcium-sensitive dye.
Máthé, Domokos; Szalay, Gergely; Cseri, Levente; Kis, Zoltán; Pályi, Bernadett; Földes, Gábor; Kovács, Noémi; Fülöp, Anna; Szepesi, Áron; Hajdrik, Polett; Csomos, Attila; Zsembery, Ákos; Kádár, Kristóf; Katona, Gergely; Mucsi, Zoltán; Rózsa, Balázs József; Kovács, Ervin.
Afiliación
  • Máthé D; Department of Biophysics and Radiation Biology, Semmelweis University, Tuzoltó utca 37-47, 1094, Budapest, Hungary. mathe.domokos@med.semmelweis-univ.hu.
  • Szalay G; In Vivo Imaging Advanced Core Facility, Hungarian Centre of Excellence for Molecular Medicine, Tuzoltó utca 37-47, 1094, Budapest, Hungary. mathe.domokos@med.semmelweis-univ.hu.
  • Cseri L; HUN-REN Physical Virology Research Group, Semmelweis University, Tuzoltó utca 37-47, 1094, Budapest, Hungary. mathe.domokos@med.semmelweis-univ.hu.
  • Kis Z; Laboratory of 3D Functional Network and Dendritic Imaging, HUN-REN Institute of Experimental Medicine, Szigony utca 43, 1083, Budapest, Hungary.
  • Pályi B; BrainVisionCenter, Liliom utca 43-45, 1094, Budapest, Hungary.
  • Földes G; BrainVisionCenter, Liliom utca 43-45, 1094, Budapest, Hungary.
  • Kovács N; Femtonics Ltd., Tuzoltó utca 59, 1094, Budapest, Hungary.
  • Fülöp A; National Center for Public Health, Albert Flórián út 2-6, 1097, Budapest, Hungary.
  • Szepesi Á; National Center for Public Health, Albert Flórián út 2-6, 1097, Budapest, Hungary.
  • Hajdrik P; National Heart and Lung Institute, Imperial College London, Du Cane Road, London, W12 0NN, UK.
  • Csomos A; Heart and Vascular Center, Semmelweis University, Városmajor utca. 68, 1122, Budapest, Hungary.
  • Zsembery Á; In Vivo Imaging Advanced Core Facility, Hungarian Centre of Excellence for Molecular Medicine, Tuzoltó utca 37-47, 1094, Budapest, Hungary.
  • Kádár K; Femtonics Ltd., Tuzoltó utca 59, 1094, Budapest, Hungary.
  • Katona G; Laboratory of 3D Functional Network and Dendritic Imaging, HUN-REN Institute of Experimental Medicine, Szigony utca 43, 1083, Budapest, Hungary.
  • Mucsi Z; BrainVisionCenter, Liliom utca 43-45, 1094, Budapest, Hungary.
  • Rózsa BJ; Department of Biophysics and Radiation Biology, Semmelweis University, Tuzoltó utca 37-47, 1094, Budapest, Hungary.
  • Kovács E; Femtonics Ltd., Tuzoltó utca 59, 1094, Budapest, Hungary.
Cell Mol Biol Lett ; 29(1): 105, 2024 Jul 19.
Article en En | MEDLINE | ID: mdl-39030477
ABSTRACT

BACKGROUND:

The organism-wide effects of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) viral infection are well studied, but little is known about the dynamics of how the infection spreads in time among or within cells due to the scarcity of suitable high-resolution experimental systems. It has been reported that SARS-CoV-2 infection pathways converge at calcium influx and subcellular calcium distribution changes. Imaging combined with a proper staining technique is an effective tool for studying subcellular calcium-related infection and replication mechanisms at such resolutions.

METHODS:

Using two-photon (2P) fluorescence imaging with our novel Ca-selective dye, automated image analysis and clustering analysis were applied to reveal titer and variant effects on SARS-CoV-2-infected Vero E6 cells.

RESULTS:

The application of a new calcium sensor molecule is shown, combined with a high-end 2P technique for imaging and identifying the patterns associated with cellular infection damage within cells. Vero E6 cells infected with SARS-CoV-2 variants, D614G or B.1.1.7, exhibit elevated cytosolic calcium levels, allowing infection monitoring by tracking the cellular changes in calcium level by the internalized calcium sensor. The imaging provides valuable information on how the level and intracellular distribution of calcium are perturbed during the infection. Moreover, two-photon calcium sensing allowed the distinction of infections by two studied viral variants via cluster analysis of the image parameters. This approach will facilitate the study of cellular correlates of infection and their quantification depending on viral variants and viral load.

CONCLUSIONS:

We propose a new two-photon microscopy-based method combined with a cell-internalized sensor to quantify the level of SARS-CoV-2 infection. We optimized the applied dye concentrations to not interfere with viral fusion and viral replication events. The presented method ensured the proper monitoring of viral infection, replication, and cell fate. It also enabled distinguishing intracellular details of cell damage, such as vacuole and apoptotic body formation. Using clustering analysis, 2P microscopy calcium fluorescence images were suitable to distinguish two different viral variants in cell cultures. Cellular harm levels read out by calcium imaging were quantitatively related to the initial viral multiplicity of infection numbers. Thus, 2P quantitative calcium imaging might be used as a correlate of infection or a correlate of activity in cellular antiviral studies.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Calcio / Colorantes Fluorescentes / SARS-CoV-2 / COVID-19 Límite: Animals / Humans Idioma: En Revista: Cell Mol Biol Lett Asunto de la revista: BIOLOGIA MOLECULAR Año: 2024 Tipo del documento: Article País de afiliación: Hungria Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Calcio / Colorantes Fluorescentes / SARS-CoV-2 / COVID-19 Límite: Animals / Humans Idioma: En Revista: Cell Mol Biol Lett Asunto de la revista: BIOLOGIA MOLECULAR Año: 2024 Tipo del documento: Article País de afiliación: Hungria Pais de publicación: Reino Unido