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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...

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Autores principales: Schuler, Hannes, Dittmer, Jessica, Borruso, Luigimaria, Galli, Jonas, Fischnaller, Stefanie, Anfora, Gianfranco, Rota‐Stabelli, Omar, Weil, Tobias, Janik, Katrin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2022
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.
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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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