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. 2022 Jul 8;53:57. doi: 10.1186/s13567-022-01073-6

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© The Author(s) 2022

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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Pathological evaluation of PPRV-induced lesions. A shows macroscopic lesions in digestive and respiratory tracts, while B, C and D depict histological scoring in lymphoid organs, respiratory and digestive tracts. E represents the accumulative macroscopic and histological scoring of suspected PPRV-induced post-mortem lesions. LN: lymph nodes. Single lines in each organ or group assessment represent the median. P-values were calculated using Tukey multiple comparison tests with individual variances computed for each comparison. Asterisks highlight the statistical differences observed between the infected or vaccinated groups and the mock-inoculated group. *P-values < 0.05; **P-values < 0.01; ***P-values < 0.001; ****P-values < 0.0001.