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. 2021 Jan 14;14:12. doi: 10.1186/s12284-021-00453-4

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© The Author(s) 2021

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/.

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Fig. 4 — OsCOX11 functions as a negative regulator of basal resistance against M. oryzae. a Disease symptoms of P_Ubi::OsCOX11 and WT plants in response to M. oryzae isolate 10–441. The inoculated leaves were photographed at 12 dpi. b Lesion area was measured with ImageJ software. Data are shown as the mean ± SD (**P < 0.01, n > 12). c Fungal biomass in inoculated leaves, as quantified by qPCR comparing the DNA amounts of the fungal gene MoPot2 and the rice gene OsUbq. Data are shown as mean ± SD (**P < 0.01, n > 12). d Disease symptoms of oscox11/OsCOX11 and WT plants inoculated with M. oryzae isolate 13–219. The leaves were photographed at 12 dpi. e Lesion area was measured with ImageJ software. Data are shown as mean ± standard error (SD) (**P < 0.01, n > 12). f Relative fungal biomass on M. oryzae-inoculated leaves, as measured by qPCR. Data are shown as mean ± SD (**P < 0.01, n > 12)