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. 2017 Dec 12;7:17388. doi: 10.1038/s41598-017-17689-0

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© The Author(s) 2017

Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.

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Ectopic expression of DUSP1 inhibits JNK and p38 phosphorylation elicited by SeV and RSV infections. A549 cells were transfected with an empty- or DUSP1-encoding plasmid before infection with SeV at 40 HAU/10⁶ cells (A,B) or RSV at a MOI of 3 (C) for the indicated times. Levels of DUSP1, phosphorylated JNK (JNK-P), total JNK, phosphorylated p38 (p38-P), total p38, SeV N and RSV N protein levels were monitored by immunoblot. Equal loading was verified using anti-tubulin antibodies. The data are representative of at least three independent experiments. Samples that are compared derive from the same experiment and blots were processed in parallel. Full-length blots are presented in Supplementary Figure 5. NS: non-specific.