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. 2023 Jan 27;15:4. doi: 10.1186/s13099-022-00528-7

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© The Author(s) 2023

Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 4 — S. warneri invades both intestinal and nonintestinal cells using actin-dependent mechanisms. A Quantification of the intracellular bacteria in T84 cells after growth in the stationary (stat.) or exponential (expo.) phases (% of inoculum) (mean ± s.e.m.; n = 6; *P < 0.05; **P < 0.01; two-tailed Mann‒Whitney test). B Quantification of the intracellular bacteria in HeLa cells (% of inoculum) (mean ± s.e.m.; n = 7; *P < 0.05; two-tailed Wilcoxon test). C Quantification of bacterial internalisation by Caco2 cells pretreated or not with Cytochalasin D (CytD), expressed as a percentage of the control conditions (no CytD) (mean ± s.e.m.; n = 6; *P < 0.05; two-tailed Wilcoxon test)