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Investigating the microbial community of Cacopsylla spp. as potential factor in vector competence of phytoplasma
Phytoplasmas are obligatory intracellular bacteria that colonize the phloem of many plant species and cause hundreds of plant diseases worldwide. In nature, phytoplasmas are primarily transmitted by hemipteran vectors. While all phloem‐feeding insects could in principle transmit phytoplasmas, only a...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9804460/ https://www.ncbi.nlm.nih.gov/pubmed/35876309 http://dx.doi.org/10.1111/1462-2920.16138 |
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author | Schuler, Hannes Dittmer, Jessica Borruso, Luigimaria Galli, Jonas Fischnaller, Stefanie Anfora, Gianfranco Rota‐Stabelli, Omar Weil, Tobias Janik, Katrin |
author_facet | Schuler, Hannes Dittmer, Jessica Borruso, Luigimaria Galli, Jonas Fischnaller, Stefanie Anfora, Gianfranco Rota‐Stabelli, Omar Weil, Tobias Janik, Katrin |
author_sort | Schuler, Hannes |
collection | PubMed |
description | Phytoplasmas are obligatory intracellular bacteria that colonize the phloem of many plant species and cause hundreds of plant diseases worldwide. In nature, phytoplasmas are primarily transmitted by hemipteran vectors. While all phloem‐feeding insects could in principle transmit phytoplasmas, only a limited number of species have been confirmed as vectors. Knowledge about factors that might determine the vector capacity is currently scarce. Here, we characterized the microbiomes of vector and non‐vector species of apple proliferation (AP) phytoplasma ‘Candidatus Phytoplasma mali’ to investigate their potential role in the vector capacity of the host. We performed high‐throughput 16S rRNA metabarcoding of the two principal AP‐vectors Cacopsylla picta and Cacopsylla melanoneura and eight Cacopsylla species, which are not AP‐vectors but co‐occur in apple orchards. The microbiomes of all species are dominated by Carsonella, the primary endosymbiont of psyllids and a second uncharacterized Enterobacteriaceae endosymbiont. Each Cacopsylla species harboured a species‐specific phylotype of both symbionts. Moreover, we investigated differences between the microbiomes of AP‐vector versus non‐vector species and identified the predominant endosymbionts but also Wolbachia and several minor taxa as potential indicator species. Our study highlights the importance of considering the microbiome in future investigations of potential factors influencing host vector competence. We investigated the potential role of symbiotic bacteria in the acquisition and transmission of phytoplasma. By comparing the two main psyillid vector species of Apple proliferation (AP) phytoplasma and eight co‐occurring species, which are not able to vector AP‐phytoplasma, we found differences in the microbial communities of AP‐vector and non‐vector species, which appear to be driven by the predominant symbionts in both vector species and Wolbachia and several minor taxa in the non‐vector species. In contrast, infection with AP‐phytoplasma did not affect microbiome composition in both vector species. Our study provides new insights into the endosymbiont diversity of Cacopsylla spp. and highlights the importance of considering the microbiome when investigating potential factors influencing host vector competence. |
format | Online Article Text |
id | pubmed-9804460 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98044602023-01-03 Investigating the microbial community of Cacopsylla spp. as potential factor in vector competence of phytoplasma Schuler, Hannes Dittmer, Jessica Borruso, Luigimaria Galli, Jonas Fischnaller, Stefanie Anfora, Gianfranco Rota‐Stabelli, Omar Weil, Tobias Janik, Katrin Environ Microbiol Research Articles Phytoplasmas are obligatory intracellular bacteria that colonize the phloem of many plant species and cause hundreds of plant diseases worldwide. In nature, phytoplasmas are primarily transmitted by hemipteran vectors. While all phloem‐feeding insects could in principle transmit phytoplasmas, only a limited number of species have been confirmed as vectors. Knowledge about factors that might determine the vector capacity is currently scarce. Here, we characterized the microbiomes of vector and non‐vector species of apple proliferation (AP) phytoplasma ‘Candidatus Phytoplasma mali’ to investigate their potential role in the vector capacity of the host. We performed high‐throughput 16S rRNA metabarcoding of the two principal AP‐vectors Cacopsylla picta and Cacopsylla melanoneura and eight Cacopsylla species, which are not AP‐vectors but co‐occur in apple orchards. The microbiomes of all species are dominated by Carsonella, the primary endosymbiont of psyllids and a second uncharacterized Enterobacteriaceae endosymbiont. Each Cacopsylla species harboured a species‐specific phylotype of both symbionts. Moreover, we investigated differences between the microbiomes of AP‐vector versus non‐vector species and identified the predominant endosymbionts but also Wolbachia and several minor taxa as potential indicator species. Our study highlights the importance of considering the microbiome in future investigations of potential factors influencing host vector competence. We investigated the potential role of symbiotic bacteria in the acquisition and transmission of phytoplasma. By comparing the two main psyillid vector species of Apple proliferation (AP) phytoplasma and eight co‐occurring species, which are not able to vector AP‐phytoplasma, we found differences in the microbial communities of AP‐vector and non‐vector species, which appear to be driven by the predominant symbionts in both vector species and Wolbachia and several minor taxa in the non‐vector species. In contrast, infection with AP‐phytoplasma did not affect microbiome composition in both vector species. Our study provides new insights into the endosymbiont diversity of Cacopsylla spp. and highlights the importance of considering the microbiome when investigating potential factors influencing host vector competence. John Wiley & Sons, Inc. 2022-08-04 2022-10 /pmc/articles/PMC9804460/ /pubmed/35876309 http://dx.doi.org/10.1111/1462-2920.16138 Text en © 2022 The Authors. Environmental Microbiology published by Society for Applied Microbiology and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Schuler, Hannes Dittmer, Jessica Borruso, Luigimaria Galli, Jonas Fischnaller, Stefanie Anfora, Gianfranco Rota‐Stabelli, Omar Weil, Tobias Janik, Katrin Investigating the microbial community of Cacopsylla spp. as potential factor in vector competence of phytoplasma |
title | Investigating the microbial community of Cacopsylla spp. as potential factor in vector competence of phytoplasma |
title_full | Investigating the microbial community of Cacopsylla spp. as potential factor in vector competence of phytoplasma |
title_fullStr | Investigating the microbial community of Cacopsylla spp. as potential factor in vector competence of phytoplasma |
title_full_unstemmed | Investigating the microbial community of Cacopsylla spp. as potential factor in vector competence of phytoplasma |
title_short | Investigating the microbial community of Cacopsylla spp. as potential factor in vector competence of phytoplasma |
title_sort | investigating the microbial community of cacopsylla spp. as potential factor in vector competence of phytoplasma |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9804460/ https://www.ncbi.nlm.nih.gov/pubmed/35876309 http://dx.doi.org/10.1111/1462-2920.16138 |
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