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. 2020 Oct 11;8:146. doi: 10.1186/s40168-020-00921-x

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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. 5 — The neighbour-joining tree of microbiome Bray-Curtis dissimilarities for 93 Triatoma early instar individuals, showing microbiome species specificity is determined by host phylogeny and geographic origin. The nodes are coloured according to host phylogeny. The simplified phylogenetic scheme for the five Triatoma species is based on Georgieva et al. [5] and Ibarra-Cerdeña et al. [82]. The dashed line reflects the uncertain position of T. rubida. Sample geographic origin is designated as follows: SA (TX) San Antonio, Texas; Ch (TX) Chaparral, Texas; Tu (AZ) University of Arizona Desert Station, Tucson, Arizona; LC (AZ) Las Cienegas National Conservation Area, Arizona