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. 2019 Nov 21;10:5288. doi: 10.1038/s41467-019-13296-x

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© The Author(s) 2019

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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Fig. 5 — The role of the SOS response in MpaR activation. a qRT-PCR transcription analysis of SOS response representative genes (recA and umuD) in WT bacteria and bacteria harboring lexA3 mutation, with and without MC treatment at 30 ˚C. Transcription levels are presented as relative quantity (RQ), relative to their levels in untreated WT bacteria. The data represents three independent experiments. Error bars indicate a 95% confidence interval. b qRT-PCR transcription analysis of intact comK gene (attB site) in WT bacteria and bacteria harboring the lexA3 mutation upon MC treatment or during intracellular growth in macrophages (6 h post infection). attB levels are presented as relative quantity (RQ), relative to their levels in WT bacteria. The data represents three independent experiments. Error bars indicate a 95% confidence interval. Source data are provided as a Source Data file.