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. 2022 Nov 8;18:392. doi: 10.1186/s12917-022-03481-4

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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. 2 — Molecular characterization of the emergent PEDV strains. a Alignment of partial S protein sequences of 7 S-INDEL like strains in this study and the prototype S-INDEL strains in the United States (OH851 and Minnesota58), South Korea (KNU-1406-1), and China (ZL29). b Locations of unique amino acid (aa) insertions identified in the 91 detected sequences. The symbol “-” indicates an aa deletion. Unique variations of aa are labelled with yellow