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. 2017 Aug 21;7:9015. doi: 10.1038/s41598-017-09373-0

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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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Analysis of Bp_MARAN and Bp_{mouse-adapted} whole bacterial protein by 2-DE. The whole bacteria of Bp_MARAN (panel A) and Bp_{mouse-adapted} (panel B) grown to mid-logarithmic phase in LB medium were prepared using sonication method and analysed using 2-DE. A total of 450 μg of whole bacteria was separated on an IPG strip pH 3–10 in the first dimension, followed by the separation on SDS-12% PAGE for the second-dimension separation. The separated proteins were detected by CBB G-250 staining. Marked spots indicate proteins that were identified (red: up-regulated; and green: down-regulated). NS refers to spots that were not possibly identified by MALDI-TOF.