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. 2021 Jan 9;11:16. doi: 10.1186/s13568-020-01177-2

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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 — Changes to fungal DNA (28S rDNA) of A. brasiliensis spotted onto an aluminium plate following APDBD treatment. The level of intact 28S rDNA from A. brasiliensis spotted onto an aluminium plate was quantified by real-time PCR. The level of the corresponding amplified product for the 0 min sample was assigned a value of 100%. Differences where p < 0.05(*) and p < 0.01(**) versus Control (0 min) were considered significant when verified by the non-repeated measured ANOVA followed by the Bonferroni correction. NS means no significant difference compared to Control (0 min)