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Divergent evolutionary trajectories following speciation in two ectoparasitic honey bee mites

Multispecies host-parasite evolution is common, but how parasites evolve after speciating remains poorly understood. Shared evolutionary history and physiology may propel species along similar evolutionary trajectories whereas pursuing different strategies can reduce competition. We test these scena...

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Autores principales: Techer, Maeva A., Rane, Rahul V., Grau, Miguel L., Roberts, John M. K., Sullivan, Shawn T., Liachko, Ivan, Childers, Anna K., Evans, Jay D., Mikheyev, Alexander S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6773775/
https://www.ncbi.nlm.nih.gov/pubmed/31583288
http://dx.doi.org/10.1038/s42003-019-0606-0
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author Techer, Maeva A.
Rane, Rahul V.
Grau, Miguel L.
Roberts, John M. K.
Sullivan, Shawn T.
Liachko, Ivan
Childers, Anna K.
Evans, Jay D.
Mikheyev, Alexander S.
author_facet Techer, Maeva A.
Rane, Rahul V.
Grau, Miguel L.
Roberts, John M. K.
Sullivan, Shawn T.
Liachko, Ivan
Childers, Anna K.
Evans, Jay D.
Mikheyev, Alexander S.
author_sort Techer, Maeva A.
collection PubMed
description Multispecies host-parasite evolution is common, but how parasites evolve after speciating remains poorly understood. Shared evolutionary history and physiology may propel species along similar evolutionary trajectories whereas pursuing different strategies can reduce competition. We test these scenarios in the economically important association between honey bees and ectoparasitic mites by sequencing the genomes of the sister mite species Varroa destructor and Varroa jacobsoni. These genomes were closely related, with 99.7% sequence identity. Among the 9,628 orthologous genes, 4.8% showed signs of positive selection in at least one species. Divergent selective trajectories were discovered in conserved chemosensory gene families (IGR, SNMP), and Halloween genes (CYP) involved in moulting and reproduction. However, there was little overlap in these gene sets and associated GO terms, indicating different selective regimes operating on each of the parasites. Based on our findings, we suggest that species-specific strategies may be needed to combat evolving parasite communities.
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spelling pubmed-67737752019-10-03 Divergent evolutionary trajectories following speciation in two ectoparasitic honey bee mites Techer, Maeva A. Rane, Rahul V. Grau, Miguel L. Roberts, John M. K. Sullivan, Shawn T. Liachko, Ivan Childers, Anna K. Evans, Jay D. Mikheyev, Alexander S. Commun Biol Article Multispecies host-parasite evolution is common, but how parasites evolve after speciating remains poorly understood. Shared evolutionary history and physiology may propel species along similar evolutionary trajectories whereas pursuing different strategies can reduce competition. We test these scenarios in the economically important association between honey bees and ectoparasitic mites by sequencing the genomes of the sister mite species Varroa destructor and Varroa jacobsoni. These genomes were closely related, with 99.7% sequence identity. Among the 9,628 orthologous genes, 4.8% showed signs of positive selection in at least one species. Divergent selective trajectories were discovered in conserved chemosensory gene families (IGR, SNMP), and Halloween genes (CYP) involved in moulting and reproduction. However, there was little overlap in these gene sets and associated GO terms, indicating different selective regimes operating on each of the parasites. Based on our findings, we suggest that species-specific strategies may be needed to combat evolving parasite communities. Nature Publishing Group UK 2019-10-01 /pmc/articles/PMC6773775/ /pubmed/31583288 http://dx.doi.org/10.1038/s42003-019-0606-0 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
Techer, Maeva A.
Rane, Rahul V.
Grau, Miguel L.
Roberts, John M. K.
Sullivan, Shawn T.
Liachko, Ivan
Childers, Anna K.
Evans, Jay D.
Mikheyev, Alexander S.
Divergent evolutionary trajectories following speciation in two ectoparasitic honey bee mites
title Divergent evolutionary trajectories following speciation in two ectoparasitic honey bee mites
title_full Divergent evolutionary trajectories following speciation in two ectoparasitic honey bee mites
title_fullStr Divergent evolutionary trajectories following speciation in two ectoparasitic honey bee mites
title_full_unstemmed Divergent evolutionary trajectories following speciation in two ectoparasitic honey bee mites
title_short Divergent evolutionary trajectories following speciation in two ectoparasitic honey bee mites
title_sort divergent evolutionary trajectories following speciation in two ectoparasitic honey bee mites
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6773775/
https://www.ncbi.nlm.nih.gov/pubmed/31583288
http://dx.doi.org/10.1038/s42003-019-0606-0
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