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. 2021 Jun 17;21:183. doi: 10.1186/s12866-021-02253-8

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© The Author(s) 2021

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. 3 — Structural comparison between L. paracasei LP10266 and five closely related strains (L. casei LC2W, L. casei LOCK919, L. paracasei N1115, L. paracasei TK1501, and L. paracasei TMW1.1434) at the genomic level. The rings (from outside to inside) represent CDS annotations on the positive strand, ORFs on the positive and negative strands, and CDS annotations on the negative strand, respectively. The red rings (from outside to inside) represent the BLAST results of L. paracasei TMW1.1434 (CP016355), L. paracasei TK1501 (CP017716), L. casei LC2W (CP002616), L. casei LOCK919 (CP005486), and L. paracasei N1115 (CP007122). The blue lines framed the prophage sequences at the nucleotide positions 575–618 and 1183–1227, respectively