[Three-dimensional morphology of C6/36 cells infected by dengue virus: a study based on digital holographic microscopy].

Nan Fang Yi Ke Da Xue Xue Bao

Biosafety Level 3 Laboratory, School of Public Health, Southern Medical University, Guangzhou 510515, China.E-mail:

Published: March 2017

Objective: To monitor the 3-dimensional (3D) morphological changes of C6/36 cells during dengue virus (DENV) infection using a live-cell imaging technique based on digital holographic microscopy and provide clues for better understanding the mechanisms of DENV infection.

Methods: C6/36 cells were seeded in 6-well plates to determine the optimal imaging density under a holographic cell imager, and the morphological changes of the cells were recorded in response to a culture temperature change from 28 degrees celsius; to 37 degrees celsius; C6/36 cells were infected with 4 DENV strains with different serotypes at 28 degrees celsius; and incubated at 37 degrees celsius; for 24 h, and the 3D holograms and relevant morphological parameters were recorded at different time points using HoloMonitor M4 holographic cell imaging and analysis system.

Results: The holograms of C6/36 cells inoculated at the optimal density for imaging (4×10 per well) showed unified 3D morphologies of the single cells with minimal dispersions in the cell area, thickness and volume (P<0.05), which did not undergo obvious changes when the cells were incubated at 37 degrees celsius; for 24 h (P>0.05). The cell area and volume of the cells infected with the 4 DENV strains all increased and the cell thickness was reduced during incubation. Among the 4 strains, DENV-1 and DENV-2 caused reduced cell thickness while DENV-3 and DENV-4 increased the cell thickness, and the pattern and degree of such changes differ among the 4 strains.

Conclusions: Digital holographic microscopy allows monitoring of the complex morphological changes of cells during DENV infection. The 4 DENV strains with different serotypes causes characteristic cell damages during infection.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6780445PMC
http://dx.doi.org/10.3969/j.issn.1673-4254.2017.03.04DOI Listing

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