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. 2022 Jul 11;51(1):265–270. doi: 10.1007/s15010-022-01874-z

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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/.

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Fig. 4 — Maximum-likelihood tree based on selection of full genome sequences of MPXV. Genome sequence of MPXV-IMBmuc1 was obtained from direct sequencing of clinical material using Illumina-short read technology and subsequent de-novo assembly. A selection of full genomes of MPXV classified as West-African-clade as well as isolate Zaire-96-I-16 were used for alignment of this new sequence with phylogenetic grouping. The calculated tree was rooted at the separation between the Central and West African clades. German patient sequence marked with a green dot