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. 2023 Jan 10;17(3):417–431. doi: 10.1038/s41396-023-01357-5

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© The Author(s) 2023

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. 4 — A Swimming (left, 0.3% agar) and surface motility (right, 0.5% agar) abilities on the TY plate with Congo red. *, notable cracks in colonies of the exoQ, exoF, and exoP mutants. B, C Diameter of colonies under swimming (B) and surface motility (C) conditions as shown in (A). D Fluorescence stereo microscopy pictures of surface motility ability of the fadL mutant (red) and the exoF mutant (red) compared to the wild-type SF2 (WT; green) in an inoculant mixture (mixed in different ratios as follows: 1:9, 3:7, 5:5, 7:3, and 9:1). B, C Different letters indicate significant difference between means (±SEM; ANOVA followed by Duncan’s test, alpha = 0.05; three independent experiments).