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. 2022 Aug 24;19:19. doi: 10.1186/s12977-022-00598-0

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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 — Comparison of replication competitive advantages between ALV-A and ALV-K based on RCASBP. a, c The replication capacities of RCASBP(A) and RCASBP(K) were observed by fluorescence microscopy. b, d The percentages of GFP/mCherry-positive DF-1 cells transfected with RCASBP(A)-EGFP and RCASBP(K)-EGFP were determined by flow cytometry. Three independent experiments were performed, and the data are shown as the means of triplicate samples