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A transcriptome-based phylogenetic study of hard ticks (Ixodidae)

Hard ticks are widely distributed across temperate regions, show strong variation in host associations, and are potential vectors of a diversity of medically important zoonoses, such as Lyme disease. To address unresolved issues with respect to the evolutionary relationships among certain species or...

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Autores principales: Charrier, N. Pierre, Hermouet, Axelle, Hervet, Caroline, Agoulon, Albert, Barker, Stephen C., Heylen, Dieter, Toty, Céline, McCoy, Karen D., Plantard, Olivier, Rispe, Claude
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6733903/
https://www.ncbi.nlm.nih.gov/pubmed/31501478
http://dx.doi.org/10.1038/s41598-019-49641-9
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author Charrier, N. Pierre
Hermouet, Axelle
Hervet, Caroline
Agoulon, Albert
Barker, Stephen C.
Heylen, Dieter
Toty, Céline
McCoy, Karen D.
Plantard, Olivier
Rispe, Claude
author_facet Charrier, N. Pierre
Hermouet, Axelle
Hervet, Caroline
Agoulon, Albert
Barker, Stephen C.
Heylen, Dieter
Toty, Céline
McCoy, Karen D.
Plantard, Olivier
Rispe, Claude
author_sort Charrier, N. Pierre
collection PubMed
description Hard ticks are widely distributed across temperate regions, show strong variation in host associations, and are potential vectors of a diversity of medically important zoonoses, such as Lyme disease. To address unresolved issues with respect to the evolutionary relationships among certain species or genera, we produced novel RNA-Seq data sets for nine different Ixodes species. We combined this new data with 18 data sets obtained from public databases, both for Ixodes and non-Ixodes hard tick species, using soft ticks as an outgroup. We assembled transcriptomes (for 27 species in total), predicted coding sequences and identified single copy orthologues (SCO). Using Maximum-likelihood and Bayesian frameworks, we reconstructed a hard tick phylogeny for the nuclear genome. We also obtained a mitochondrial DNA-based phylogeny using published genome sequences and mitochondrial sequences derived from the new transcriptomes. Our results confirm previous studies showing that the Ixodes genus is monophyletic and clarify the relationships among Ixodes sub-genera. This work provides a baseline for studying the evolutionary history of ticks: we indeed found an unexpected acceleration of substitutions for mitochondrial sequences of Prostriata, and for nuclear and mitochondrial genes of two species of Rhipicephalus, which we relate with patterns of genome architecture and changes of life-cycle, respectively.
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spelling pubmed-67339032019-09-20 A transcriptome-based phylogenetic study of hard ticks (Ixodidae) Charrier, N. Pierre Hermouet, Axelle Hervet, Caroline Agoulon, Albert Barker, Stephen C. Heylen, Dieter Toty, Céline McCoy, Karen D. Plantard, Olivier Rispe, Claude Sci Rep Article Hard ticks are widely distributed across temperate regions, show strong variation in host associations, and are potential vectors of a diversity of medically important zoonoses, such as Lyme disease. To address unresolved issues with respect to the evolutionary relationships among certain species or genera, we produced novel RNA-Seq data sets for nine different Ixodes species. We combined this new data with 18 data sets obtained from public databases, both for Ixodes and non-Ixodes hard tick species, using soft ticks as an outgroup. We assembled transcriptomes (for 27 species in total), predicted coding sequences and identified single copy orthologues (SCO). Using Maximum-likelihood and Bayesian frameworks, we reconstructed a hard tick phylogeny for the nuclear genome. We also obtained a mitochondrial DNA-based phylogeny using published genome sequences and mitochondrial sequences derived from the new transcriptomes. Our results confirm previous studies showing that the Ixodes genus is monophyletic and clarify the relationships among Ixodes sub-genera. This work provides a baseline for studying the evolutionary history of ticks: we indeed found an unexpected acceleration of substitutions for mitochondrial sequences of Prostriata, and for nuclear and mitochondrial genes of two species of Rhipicephalus, which we relate with patterns of genome architecture and changes of life-cycle, respectively. Nature Publishing Group UK 2019-09-09 /pmc/articles/PMC6733903/ /pubmed/31501478 http://dx.doi.org/10.1038/s41598-019-49641-9 Text en © The Author(s) 2019 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Charrier, N. Pierre
Hermouet, Axelle
Hervet, Caroline
Agoulon, Albert
Barker, Stephen C.
Heylen, Dieter
Toty, Céline
McCoy, Karen D.
Plantard, Olivier
Rispe, Claude
A transcriptome-based phylogenetic study of hard ticks (Ixodidae)
title A transcriptome-based phylogenetic study of hard ticks (Ixodidae)
title_full A transcriptome-based phylogenetic study of hard ticks (Ixodidae)
title_fullStr A transcriptome-based phylogenetic study of hard ticks (Ixodidae)
title_full_unstemmed A transcriptome-based phylogenetic study of hard ticks (Ixodidae)
title_short A transcriptome-based phylogenetic study of hard ticks (Ixodidae)
title_sort transcriptome-based phylogenetic study of hard ticks (ixodidae)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6733903/
https://www.ncbi.nlm.nih.gov/pubmed/31501478
http://dx.doi.org/10.1038/s41598-019-49641-9
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