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. 2017 Aug 29;7:9659. doi: 10.1038/s41598-017-09260-8

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© The Author(s) 2017

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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.

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Gene expression during in-vitro seed colonization of Aspergillus flavus in groundnut. (a) Temporal distribution of relative abundance in expressed genes at different stages of fungal infection. The relative expression is found to be higher in infected samples of J 11 (J11-I) as compared to their control counter parts (J11-C) at 2^nd day after inoculation (2DAI). The expression level of infected samples of JL 24 (JL24-I) was higher as compared to JL24-C. (b) Relative abundance of all the genes expressed during in-vitro seed colonization across subgenomes of groundnut progenitors. The relative abundance in terms of FPKM values were mapped onto A10 and B07 of A and B subgenomes, respectively. (c) Number of differentially expressed genes-DEGs (induced and repressed) during in-vitro seed colonization. The highest number of DEGs were mapped onto A03 and B03 of A and B subgenomes, respectively.