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Laboulbeniales hyperparasites (Fungi, Ascomycota) of bat flies: Independent origins and host associations
The aim of this study was to explore the diversity of ectoparasitic fungi (Ascomycota, Laboulbeniales) that use bat flies (Diptera, Hippoboscoidea) as hosts. Bat flies themselves live as ectoparasites on the fur and wing membranes of bats (Mammalia, Chiroptera); hence this is a tripartite parasite s...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6145224/ https://www.ncbi.nlm.nih.gov/pubmed/30250711 http://dx.doi.org/10.1002/ece3.4359 |
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author | Haelewaters, Danny Page, Rachel A. Pfister, Donald H. |
author_facet | Haelewaters, Danny Page, Rachel A. Pfister, Donald H. |
author_sort | Haelewaters, Danny |
collection | PubMed |
description | The aim of this study was to explore the diversity of ectoparasitic fungi (Ascomycota, Laboulbeniales) that use bat flies (Diptera, Hippoboscoidea) as hosts. Bat flies themselves live as ectoparasites on the fur and wing membranes of bats (Mammalia, Chiroptera); hence this is a tripartite parasite system. Here, we collected bats, bat flies, and Laboulbeniales, and conducted phylogenetic analyses of Laboulbeniales to contrast morphology with ribosomal sequence data. Parasitism of bat flies by Laboulbeniales arose at least three times independently, once in the Eastern Hemisphere (Arthrorhynchus) and twice in the Western Hemisphere (Gloeandromyces, Nycteromyces). We hypothesize that the genera Arthrorhynchus and Nycteromyces evolved independently from lineages of ectoparasites of true bugs (Hemiptera). We assessed phylogenetic diversity of the genus Gloeandromyces by considering the LSU rDNA region. Phenotypic plasticity and position‐induced morphological adaptations go hand in hand. Different morphotypes belong to the same phylogenetic species. Two species, G. pageanus and G. streblae, show divergence by host utilization. In our assessment of coevolution, we only observe congruence between the Old World clades of bat flies and Laboulbeniales. The other associations are the result of the roosting ecology of the bat hosts. This study has considerably increased our knowledge about bats and their associated ectoparasites and shown the necessity of including molecular data in Laboulbeniales taxonomy. |
format | Online Article Text |
id | pubmed-6145224 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-61452242018-09-24 Laboulbeniales hyperparasites (Fungi, Ascomycota) of bat flies: Independent origins and host associations Haelewaters, Danny Page, Rachel A. Pfister, Donald H. Ecol Evol Original Research The aim of this study was to explore the diversity of ectoparasitic fungi (Ascomycota, Laboulbeniales) that use bat flies (Diptera, Hippoboscoidea) as hosts. Bat flies themselves live as ectoparasites on the fur and wing membranes of bats (Mammalia, Chiroptera); hence this is a tripartite parasite system. Here, we collected bats, bat flies, and Laboulbeniales, and conducted phylogenetic analyses of Laboulbeniales to contrast morphology with ribosomal sequence data. Parasitism of bat flies by Laboulbeniales arose at least three times independently, once in the Eastern Hemisphere (Arthrorhynchus) and twice in the Western Hemisphere (Gloeandromyces, Nycteromyces). We hypothesize that the genera Arthrorhynchus and Nycteromyces evolved independently from lineages of ectoparasites of true bugs (Hemiptera). We assessed phylogenetic diversity of the genus Gloeandromyces by considering the LSU rDNA region. Phenotypic plasticity and position‐induced morphological adaptations go hand in hand. Different morphotypes belong to the same phylogenetic species. Two species, G. pageanus and G. streblae, show divergence by host utilization. In our assessment of coevolution, we only observe congruence between the Old World clades of bat flies and Laboulbeniales. The other associations are the result of the roosting ecology of the bat hosts. This study has considerably increased our knowledge about bats and their associated ectoparasites and shown the necessity of including molecular data in Laboulbeniales taxonomy. John Wiley and Sons Inc. 2018-07-24 /pmc/articles/PMC6145224/ /pubmed/30250711 http://dx.doi.org/10.1002/ece3.4359 Text en © 2018 The Authors. Ecology and Evolution published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Haelewaters, Danny Page, Rachel A. Pfister, Donald H. Laboulbeniales hyperparasites (Fungi, Ascomycota) of bat flies: Independent origins and host associations |
title | Laboulbeniales hyperparasites (Fungi, Ascomycota) of bat flies: Independent origins and host associations |
title_full | Laboulbeniales hyperparasites (Fungi, Ascomycota) of bat flies: Independent origins and host associations |
title_fullStr | Laboulbeniales hyperparasites (Fungi, Ascomycota) of bat flies: Independent origins and host associations |
title_full_unstemmed | Laboulbeniales hyperparasites (Fungi, Ascomycota) of bat flies: Independent origins and host associations |
title_short | Laboulbeniales hyperparasites (Fungi, Ascomycota) of bat flies: Independent origins and host associations |
title_sort | laboulbeniales hyperparasites (fungi, ascomycota) of bat flies: independent origins and host associations |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6145224/ https://www.ncbi.nlm.nih.gov/pubmed/30250711 http://dx.doi.org/10.1002/ece3.4359 |
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