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. 2022 Mar 9;19:41. doi: 10.1186/s12985-022-01769-3

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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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Fig. 1 — Proposed categorization of GB viruses.Maximum likelihood tree (Tamura 3-parameter nucleotide model and gamma distribution, T92 + G) depicting phylogenetic relationship of Human Pegiviruses with other main members of Flaviviridea family. The phylogenetic tree was constructed based on the complete coding sequence (CDS) of these viruses. The values at the tree branches are the bootstrap support values calculated from 1000 replicates. Scale bar indicates an evolutionary distance of 0.5 substitutions per position in the sequence. GB virus type A, B, C, D (GBV-A, GBV-B, GBV-C, GBV-D), simian Pegivirus(SPgV), human Pegivirus(HPgV), Bat Pegivirus(BPgV), CPZ: chimpanzees