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. 2024 Mar 16;15:2379. doi: 10.1038/s41467-024-46648-3

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© The Author(s) 2024

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 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. 3 — a RSV-A phylogeny was reconstructed from 207 samples. b RSV-B phylogeny was reconstructed from 177 samples. At least 70% of the coding sequences were recovered from these samples. For infants with multiple samples collected, only the sample with the highest coverage was included. The trees were midpoint rooted. The sampling country of each strain is illustrated by tip colour. The scale bars represent the number of nucleotide substitutions per site. Human parechovirus A (HPeV-A) was not co-detected with any of the RSV-A strains; enterovirus B (EV-B) and human coronavirus 229E (HCoV-229E) were not co-detected with any of the RSV-B strains. Source data are provided as Source Data files. HAdV human adenovirus, HBoV human bocavirus, HCMV human cytomegalovirus, HHV-6 human herpesvirus 6, HPIV human parainfluenza virus, RSV respiratory syncytial virus, RV rhinovirus.