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. 2024 Jan 30;17(2):e14330. doi: 10.1111/1751-7915.14330

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© 2023 The Authors. Microbial Biotechnology published by Applied Microbiology International and John Wiley & Sons Ltd.

This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.

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(A) Bubble plot showing the relative abundance of each bacterial endophyte strain (y‐axis) used in vitro co‐spotting growth experiments after 24 h, as obtained from 16S rRNA gene sequencing analysis. The samples are arranged and subplot according to each specific consortium (i.e. Consortium A, B, C, D, E, F) (x‐axis). (B) Bubble plot showing the relative abundance of each bacterial endophyte strain (y‐axis) used in planta compatibility growth experiments after 15 dpi. The seed inoculation method has been used in this compatibility growth experiments of 5‐bacterial‐strain‐consortia. The samples are arranged and subplot according to each specific consortium (i.e. Consortium A, B, C, D, E, F) (x‐axis). Control denotes samples collected immediately after co‐inoculum setup. The size of the bubble represents the relative abundance and the median of the percentage of at least three replicates, and colours indicate each bacterial strain used in this experiment.