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. 2020 Jun 15;11:62. doi: 10.1186/s40104-020-00468-9

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© The Author(s) 2020

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. 2 — The protective effects of TTO on bovine mammary epithelial cells (BMECs). (a) Evaluation of proliferative effects of TTO on BMECs. The BMECs were incubated with 0 (control group), 0.0125%, 0.025%, 0.05%, or 0.1% TTO for 6 h. (b) Viability of BMECs exposed to S. aureus with or without TTO treatment. BMECs were cultured in the absence of S. aureus and TTO (control group), in the presence of S. aureus and absence of TTO (S. aureus group), and in the presence of S. aureus and 0.0125%, 0.025%, 0.05%, or 0.1% TTO (TTO-treated groups) for 6 h. Data are presented as the means ± SEM (n = 4). Means at the different concentration of TTO with different letters (a-d) differ significantly for treatment effect