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. 2018 Nov 16;12(2):555–564. doi: 10.1038/s41385-018-0109-1

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© The Author(s) 2018

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 — BCG-immunised mice are protected against M. tb infection 26 weeks post-immunisation. IN or ID BCG-immunised mice were challenged 26 weeks later with M. tb via aerosol. Four weeks post-challenge, CFU were enumerated in lung and spleens. Individual log₁₀ CFU values are shown with bars indicating mean ± SEM (n ≥ 5). One-way ANOVA with Tukey’s post-test for significance; ****P < 0.0001; **P < 0.01