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. 2020 Apr 29;51:58. doi: 10.1186/s13567-020-00781-1

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© The Author(s) 2020

Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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PUCV protein expression profiling. SDS-PAGE of proteins expressed in PUCV-infected BHK-BSR cells detected by pulse radiolabelling of proteins with L[³⁵S]-methionine and L[³⁵S]-cysteine for 1 h at various times post-infection (left panel); or by immunoblotting using PUCV-specific mouse immune ascites fluid at various times post-infection (right panel). Bands corresponding approximately in size to the estimated molecular masses of the major viral structural proteins (L, G, N, P and M) and the non-structural glycoprotein (G_NS) are indicated. Other bands that appear to be induced or were detected by immunoblotting in infected cells but not mock-infected cells are also indicated with arrowheads.