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Characterizing the microbiome of ectoparasitic louse flies feeding on migratory raptors

Louse flies (Diptera: Hippoboscidae) are obligate ectoparasites that often cause behavioral, pathogenic, and evolutionary effects on their hosts. Interactions between ectoparasites and avian hosts, especially migrating taxa, may influence avian pathogen spread in tropical and temperate ecosystems an...

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Autores principales: McCabe, Rebecca A., Receveur, Joseph P., Houtz, Jennifer L., Thomas, Kayli L., Benbow, M. Eric, Pechal, Jennifer L., Wallace, John R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7271990/
https://www.ncbi.nlm.nih.gov/pubmed/32497084
http://dx.doi.org/10.1371/journal.pone.0234050
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author McCabe, Rebecca A.
Receveur, Joseph P.
Houtz, Jennifer L.
Thomas, Kayli L.
Benbow, M. Eric
Pechal, Jennifer L.
Wallace, John R.
author_facet McCabe, Rebecca A.
Receveur, Joseph P.
Houtz, Jennifer L.
Thomas, Kayli L.
Benbow, M. Eric
Pechal, Jennifer L.
Wallace, John R.
author_sort McCabe, Rebecca A.
collection PubMed
description Louse flies (Diptera: Hippoboscidae) are obligate ectoparasites that often cause behavioral, pathogenic, and evolutionary effects on their hosts. Interactions between ectoparasites and avian hosts, especially migrating taxa, may influence avian pathogen spread in tropical and temperate ecosystems and affect long-term survival, fitness and reproductive success. The purpose of this study was to characterize the vector-associated microbiome of ectoparasitic louse flies feeding on migrating raptors over the fall migration period. Surveys for louse flies occurred during fall migration (2015–2016) at a banding station in Pennsylvania, United States; flies were collected from seven species of migrating raptors, and we sequenced their microbial (bacteria and archaea) composition using high-throughput targeted amplicon sequencing of the 16S rRNA gene (V4 region). All louse flies collected belonged to the same species, Icosta americana. Our analysis revealed no difference in bacterial communities of louse flies retrieved from different avian host species. The louse fly microbiome was dominated by a primary endosymbiont, suggesting that louse flies maintain a core microbial structure despite receiving blood meals from different host species. Thus, our findings highlight the importance of characterizing both beneficial and potentially pathogenic endosymbionts when interpreting how vector-associated microbiomes may impact insect vectors and their avian hosts.
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spelling pubmed-72719902020-06-12 Characterizing the microbiome of ectoparasitic louse flies feeding on migratory raptors McCabe, Rebecca A. Receveur, Joseph P. Houtz, Jennifer L. Thomas, Kayli L. Benbow, M. Eric Pechal, Jennifer L. Wallace, John R. PLoS One Research Article Louse flies (Diptera: Hippoboscidae) are obligate ectoparasites that often cause behavioral, pathogenic, and evolutionary effects on their hosts. Interactions between ectoparasites and avian hosts, especially migrating taxa, may influence avian pathogen spread in tropical and temperate ecosystems and affect long-term survival, fitness and reproductive success. The purpose of this study was to characterize the vector-associated microbiome of ectoparasitic louse flies feeding on migrating raptors over the fall migration period. Surveys for louse flies occurred during fall migration (2015–2016) at a banding station in Pennsylvania, United States; flies were collected from seven species of migrating raptors, and we sequenced their microbial (bacteria and archaea) composition using high-throughput targeted amplicon sequencing of the 16S rRNA gene (V4 region). All louse flies collected belonged to the same species, Icosta americana. Our analysis revealed no difference in bacterial communities of louse flies retrieved from different avian host species. The louse fly microbiome was dominated by a primary endosymbiont, suggesting that louse flies maintain a core microbial structure despite receiving blood meals from different host species. Thus, our findings highlight the importance of characterizing both beneficial and potentially pathogenic endosymbionts when interpreting how vector-associated microbiomes may impact insect vectors and their avian hosts. Public Library of Science 2020-06-04 /pmc/articles/PMC7271990/ /pubmed/32497084 http://dx.doi.org/10.1371/journal.pone.0234050 Text en © 2020 McCabe et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
McCabe, Rebecca A.
Receveur, Joseph P.
Houtz, Jennifer L.
Thomas, Kayli L.
Benbow, M. Eric
Pechal, Jennifer L.
Wallace, John R.
Characterizing the microbiome of ectoparasitic louse flies feeding on migratory raptors
title Characterizing the microbiome of ectoparasitic louse flies feeding on migratory raptors
title_full Characterizing the microbiome of ectoparasitic louse flies feeding on migratory raptors
title_fullStr Characterizing the microbiome of ectoparasitic louse flies feeding on migratory raptors
title_full_unstemmed Characterizing the microbiome of ectoparasitic louse flies feeding on migratory raptors
title_short Characterizing the microbiome of ectoparasitic louse flies feeding on migratory raptors
title_sort characterizing the microbiome of ectoparasitic louse flies feeding on migratory raptors
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7271990/
https://www.ncbi.nlm.nih.gov/pubmed/32497084
http://dx.doi.org/10.1371/journal.pone.0234050
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