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. 2017 Feb 23;13:1176934317691269. doi: 10.1177/1176934317691269

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© The Author(s) 2017

This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 License (http://www.creativecommons.org/licenses/by-nc/3.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page(https://us.sagepub.com/en-us/nam/open-access-at-sage).

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Figure 6. — Analysis of Castlerea virus (CsV) replication in C6/36 and RML-12 cells. Immunofluorescent staining (green fluorescence) of double-stranded RNA (dsRNA) replicative intermediates produced by CsV infection in (A) C6/36 cells and (B) RML-12 cells. Main images were taken at ×40 magnification, whereas inset shows ×63 magnification. The log of average titre per millilitre harvested at each of these time points is shown as in white text in each panel. (C) Comparison of cytopathic effect production by CsV in C6/36 and RML-12 cell lines at 72 hours post infection (hpi).