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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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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. |
format | Online Article Text |
id | pubmed-6773775 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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