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. 2016 Jun 7;7:795. doi: 10.3389/fmicb.2016.00795

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Copyright © 2016 Gcebe, Michel, Gey van Pittius and Rutten.

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

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Alignment of EsxB aa sequences of M. fortuitum ATCC 6841 (M. fortuit), M. smegmatis MC² 155 (M. smegmat), M. malmesburii sp. nov (M. malmesb), M. komanii sp. nov., M. bovis, and M. tuberculosis (M. tubercu). ^*Represents identical sequences observed in all species, and >indicates presence of the same aa residue in at least one of the NTM species. Highly immunogenic epitopes of M. bovis as described by Vordermeier et al. (2000, 2003, 2007) are underlined.