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. 2020 Sep 7;13:452. doi: 10.1186/s13071-020-04322-9

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© The Author(s) 2020

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. 6 — Overall allele frequency from field samples, Muguga, Kiambu and Serengeti (together referred to Muguga cocktail), Chitongo, Gikongoro and Nyakizu vaccine isolates showing 41, 10, 8 and 6 unique alleles from Rwanda field samples, Chitongo, Gikongoro and Nyakizu vaccine isolates, respectively. A higher proportion of unique alleles is observed as compared to shared alleles. Predominant alleles were calculated as proportions of the total of each satellite marker and histograms were generated from the multi-locus genotype. The numbers on the x-axis represent the allele sizes in base pairs observed on each locus