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. 2024 Oct 27;14:25608. doi: 10.1038/s41598-024-76479-7

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© The Author(s) 2024

Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, 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 you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. 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-nc-nd/4.0/.

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Fig. 1 — (A) Alignment of nucleotide sequence for target Pvmdr 1 gene (Accession number AY571984.1). Arrows indicate sequences of designed F3, B3, FIP and BIP primers used in the study for LAMP assay. Point mutation highlighted by yellow (T958M → ACG-ATG) was inserted at 3’ end of FIP in mutation specific primers. (B) Schematic representation of designed LAMP primers F3, B3, FIP (F1c + F2) and BIP (B1c + B2) specific for amplifying wild types (T958) and for mutation (958 M). F1c and B1c sequences are complementary to F1 and B1.