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Novel molecular approach to define pest species status and tritrophic interactions from historical Bemisia specimens

Museum specimens represent valuable genomic resources for understanding host-endosymbiont/parasitoid evolutionary relationships, resolving species complexes and nomenclatural problems. However, museum collections suffer DNA degradation, making them challenging for molecular-based studies. Here, the...

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Autores principales: Tay, W. T., Elfekih, S., Polaszek, A., Court, L. N., Evans, G. A., Gordon, K. H. J., De Barro, P. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5428565/
https://www.ncbi.nlm.nih.gov/pubmed/28348369
http://dx.doi.org/10.1038/s41598-017-00528-7
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author Tay, W. T.
Elfekih, S.
Polaszek, A.
Court, L. N.
Evans, G. A.
Gordon, K. H. J.
De Barro, P. J.
author_facet Tay, W. T.
Elfekih, S.
Polaszek, A.
Court, L. N.
Evans, G. A.
Gordon, K. H. J.
De Barro, P. J.
author_sort Tay, W. T.
collection PubMed
description Museum specimens represent valuable genomic resources for understanding host-endosymbiont/parasitoid evolutionary relationships, resolving species complexes and nomenclatural problems. However, museum collections suffer DNA degradation, making them challenging for molecular-based studies. Here, the mitogenomes of a single 1912 Sri Lankan Bemisia emiliae cotype puparium, and of a 1942 Japanese Bemisia puparium are characterised using a Next-Generation Sequencing approach. Whiteflies are small sap-sucking insects including B. tabaci pest species complex. Bemisia emiliae’s draft mitogenome showed a high degree of homology with published B. tabaci mitogenomes, and exhibited 98–100% partial mitochondrial DNA Cytochrome Oxidase I (mtCOI) gene identity with the B. tabaci species known as Asia II-7. The partial mtCOI gene of the Japanese specimen shared 99% sequence identity with the Bemisia ‘JpL’ genetic group. Metagenomic analysis identified bacterial sequences in both Bemisia specimens, while hymenopteran sequences were also identified in the Japanese Bemisia puparium, including complete mtCOI and rRNA genes, and various partial mtDNA genes. At 88–90% mtCOI sequence identity to Aphelinidae wasps, we concluded that the 1942 Bemisia nymph was parasitized by an Eretmocerus parasitoid wasp. Our approach enables the characterisation of genomes and associated metagenomic communities of museum specimens using 1.5 ng gDNA, and to infer historical tritrophic relationships in Bemisia whiteflies.
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spelling pubmed-54285652017-05-15 Novel molecular approach to define pest species status and tritrophic interactions from historical Bemisia specimens Tay, W. T. Elfekih, S. Polaszek, A. Court, L. N. Evans, G. A. Gordon, K. H. J. De Barro, P. J. Sci Rep Article Museum specimens represent valuable genomic resources for understanding host-endosymbiont/parasitoid evolutionary relationships, resolving species complexes and nomenclatural problems. However, museum collections suffer DNA degradation, making them challenging for molecular-based studies. Here, the mitogenomes of a single 1912 Sri Lankan Bemisia emiliae cotype puparium, and of a 1942 Japanese Bemisia puparium are characterised using a Next-Generation Sequencing approach. Whiteflies are small sap-sucking insects including B. tabaci pest species complex. Bemisia emiliae’s draft mitogenome showed a high degree of homology with published B. tabaci mitogenomes, and exhibited 98–100% partial mitochondrial DNA Cytochrome Oxidase I (mtCOI) gene identity with the B. tabaci species known as Asia II-7. The partial mtCOI gene of the Japanese specimen shared 99% sequence identity with the Bemisia ‘JpL’ genetic group. Metagenomic analysis identified bacterial sequences in both Bemisia specimens, while hymenopteran sequences were also identified in the Japanese Bemisia puparium, including complete mtCOI and rRNA genes, and various partial mtDNA genes. At 88–90% mtCOI sequence identity to Aphelinidae wasps, we concluded that the 1942 Bemisia nymph was parasitized by an Eretmocerus parasitoid wasp. Our approach enables the characterisation of genomes and associated metagenomic communities of museum specimens using 1.5 ng gDNA, and to infer historical tritrophic relationships in Bemisia whiteflies. Nature Publishing Group UK 2017-03-27 /pmc/articles/PMC5428565/ /pubmed/28348369 http://dx.doi.org/10.1038/s41598-017-00528-7 Text en © The Author(s) 2017 This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Tay, W. T.
Elfekih, S.
Polaszek, A.
Court, L. N.
Evans, G. A.
Gordon, K. H. J.
De Barro, P. J.
Novel molecular approach to define pest species status and tritrophic interactions from historical Bemisia specimens
title Novel molecular approach to define pest species status and tritrophic interactions from historical Bemisia specimens
title_full Novel molecular approach to define pest species status and tritrophic interactions from historical Bemisia specimens
title_fullStr Novel molecular approach to define pest species status and tritrophic interactions from historical Bemisia specimens
title_full_unstemmed Novel molecular approach to define pest species status and tritrophic interactions from historical Bemisia specimens
title_short Novel molecular approach to define pest species status and tritrophic interactions from historical Bemisia specimens
title_sort novel molecular approach to define pest species status and tritrophic interactions from historical bemisia specimens
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5428565/
https://www.ncbi.nlm.nih.gov/pubmed/28348369
http://dx.doi.org/10.1038/s41598-017-00528-7
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