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. 2022 Nov 30;613(7945):721–728. doi: 10.1038/s41586-022-05569-1

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© The Author(s) 2022

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 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/.

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Extended Data Fig. 4 — (a and b): Alkaline growth of Δvca0040 V. cholerae bearing pBAD18 vectors expressing (a) SAOUHSC_00846 from S. aureus or (b) HVO_RS12060 from H. volcanii. (c-e): Composition and crosslinking analysis in the indicated V. cholerae strains at the indicated pH in M63 media. Suppressor: Δvca0040/ΔsecDF1. (f and g): Same as c-e for S. aureus grown in the indicated conditions. a, b: representative data from n = 3 cultures per strain/condition. c-g: mean ± SD from n = 3 cultures per strain/condition. Statistical analysis was performed with one-way ANOVAs with Tukey’s multiple comparison tests (c-e) or unpaired student’s two-tailed t-tests (f, g).