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      Phylogeography and population differentiation in Hepatozoon canis (Apicomplexa: Hepatozoidae) reveal expansion and gene flow in world populations

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          Abstract

          Background

          Hepatozoon canis is a protozoan transmitted to dogs and other wild carnivores by the ingestion of ticks containing mature oocysts and is considered the principal cause of canine hepatozoonosis in the world. Here, we examined ribosomal RNA 18S gene sequence variation to determine the genetic differences and phylogeographic diversity of H. canis from various geographical areas around the world.

          Methods

          We used 550 publicly available sequences of H. canis from 46 countries to assess haplotype relationships, geographical structure, genetic diversity indices, and relationships among populations. We performed neutrality tests and pairwise comparisons of fixation index ( F ST) values between groups and pairwise comparisons of F ST values between populations. To determine whether populations are structured, analyses of molecular variance (AMOVAs) and spatial analysis of molecular variance (SAMOVA) were performed.

          Results

          The dataset of H. canis yielded 76 haplotypes. Differentiation among populations indicated that there is no phylogeographical structure ( G ST = 0.302 ± 0.0475). Moreover, when samples were grouped by continents a significant F ST was obtained, meaning that populations were genetically differentiated. The AMOVA showed that 57.4% of the genetic variation was explained by differences within populations when all locations were treated as a single group and revealed that there is no population structure when populations are grouped into two, three, and four groups ( F CT, p > 0.05), suggesting that dispersal between populations is high. SAMOVA revealed significant F CT values for groups K = 5. The Tajima’s D and Fu’s Fs show that populations have undergone recent expansion, and the mismatch distribution analysis showed population expansion (multimodal distribution).

          Conclusions

          The current molecular data confirmed that H. canis does not show phylogeographic or population structure. The haplotypes exhibit low genetic differentiation, suggesting a recent expansion due to gene flow among populations. These results provide pivotal information required for future detailed population genetic analysis or to establish control strategies of this parasite.

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          Supplementary Information

          The online version contains supplementary material available at 10.1186/s13071-021-04924-x.

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          Most cited references65

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          Posterior Summarization in Bayesian Phylogenetics Using Tracer 1.7

          Abstract Bayesian inference of phylogeny using Markov chain Monte Carlo (MCMC) plays a central role in understanding evolutionary history from molecular sequence data. Visualizing and analyzing the MCMC-generated samples from the posterior distribution is a key step in any non-trivial Bayesian inference. We present the software package Tracer (version 1.7) for visualizing and analyzing the MCMC trace files generated through Bayesian phylogenetic inference. Tracer provides kernel density estimation, multivariate visualization, demographic trajectory reconstruction, conditional posterior distribution summary, and more. Tracer is open-source and available at http://beast.community/tracer.
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            jModelTest 2: more models, new heuristics and parallel computing.

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              Clustal W and Clustal X version 2.0.

              The Clustal W and Clustal X multiple sequence alignment programs have been completely rewritten in C++. This will facilitate the further development of the alignment algorithms in the future and has allowed proper porting of the programs to the latest versions of Linux, Macintosh and Windows operating systems. The programs can be run on-line from the EBI web server: http://www.ebi.ac.uk/tools/clustalw2. The source code and executables for Windows, Linux and Macintosh computers are available from the EBI ftp site ftp://ftp.ebi.ac.uk/pub/software/clustalw2/
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                Author and article information

                Contributors
                acini.vasquez@inecol.mx
                arturo.barbachano-guerrero@colorado.edu
                diangulo@gmail.com
                VictorHugo.JarquinDiaz@mdc-berin.de
                Journal
                Parasit Vectors
                Parasit Vectors
                Parasites & Vectors
                BioMed Central (London )
                1756-3305
                14 September 2021
                14 September 2021
                2021
                : 14
                : 467
                Affiliations
                [1 ]GRID grid.452507.1, ISNI 0000 0004 1798 0367, Red de Biología Evolutiva, , Instituto de Ecología, ; 91073 Xalapa, Veracruz Mexico
                [2 ]GRID grid.42707.36, ISNI 0000 0004 1766 9560, Centro de Investigaciones Tropicales, , Universidad Veracruzana, ; Xalapa, Veracruz 91000 México
                [3 ]GRID grid.266190.a, ISNI 0000000096214564, BioFrontiers Institute, , University of Colorado Boulder, ; Boulder, CO 80303 USA
                [4 ]GRID grid.6363.0, ISNI 0000 0001 2218 4662, Experimental and Clinical Research Center, , A Cooperation Between the Max-Delbrück-Center for Molecular Medicine in the Helmholtz Association and the Charité-Universitätsmedizin Berlin, ; Berlin, Germany
                [5 ]GRID grid.419491.0, ISNI 0000 0001 1014 0849, Charité-Universitätsmedizin Berlin, , Corporate Member of Freie Universität Berlin and Humboldt-Universität Zu Berlin, Experimental and Clinical Research Center, ; Lindenberger Weg 80, 13125 Berlin, Germany
                [6 ]GRID grid.419491.0, ISNI 0000 0001 1014 0849, Max-Delbrück-Center for Molecular Medicine in the Helmholtz Association (MDC), ; Berlin, Germany
                Author information
                http://orcid.org/0000-0003-3758-1091
                Article
                4924
                10.1186/s13071-021-04924-x
                8439048
                34521451
                4bdf3b82-faa4-4ca3-9f57-437488431d0f
                © 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.

                History
                : 14 April 2021
                : 3 August 2021
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100001656, Helmholtz-Gemeinschaft;
                Funded by: Max-Delbrück-Centrum für Molekulare Medizin in der Helmholtz-Gemeinschaft (MDC) (4219)
                Categories
                Research
                Custom metadata
                © The Author(s) 2021

                Parasitology
                dog parasites,hemoparasites,tick-borne pathogens,18s rrna gene,ticks
                Parasitology
                dog parasites, hemoparasites, tick-borne pathogens, 18s rrna gene, ticks

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