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. 2021 May 6;14:239. doi: 10.1186/s13071-021-04744-z

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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. 2 — Specificity of UR-qPCR for detection of Coxiella burnetii. The specificity of UR-qPCR for the detection of C. burnetii was confirmed by the lack of amplification from the DNA templates of five other tick-borne pathogens (Anaplasma phagocytophilum, Ehrlichia chaffeensis, Ehrlichia canis, Toxoplasma gondii, Borrelia burgdorferi) and in the negative control, which lacked the DNA template. “P” is the positive control containing 10⁵ copies of C. burnetii recombinant DNA