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. 2018 Dec 18;8:17947. doi: 10.1038/s41598-018-36779-1

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© The Author(s) 2018

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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Effect of elimination of ¹O₂, ONOO⁻, and ONOOH by radical scavengers on viral titer of FCV during operation of the DBD plasma torch. The indicated concentrations of radical scavengers for ¹O₂ (NaN₃) (a), ONOO⁻ (uric acid) (b), and ONOOH (ascorbic acid) (c) were added to FCV-infected cell lysate. Samples were then exposed to the DBD plasma torch for 2 min, and the viral titer of FCV (TCID₅₀) was determined. Zero viral titer means below the detection limit. Differences with **p < 0.01 versus the control (0 mM for NaN₃ and ascorbic acid; 0 µM for uric acid) were considered significant.