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Alternative Transmission Patterns in Independently Acquired Nutritional Cosymbionts of Dictyopharidae Planthoppers

Sap-sucking hemipterans host specialized, heritable microorganisms that supplement their diet with essential nutrients. These microbes show unusual features that provide a unique perspective on the coevolution of host-symbiont systems but are still poorly understood. Here, we combine microscopy with...

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Autores principales: Michalik, Anna, Castillo Franco, Diego, Kobiałka, Michał, Szklarzewicz, Teresa, Stroiński, Adam, Łukasik, Piotr
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8406288/
https://www.ncbi.nlm.nih.gov/pubmed/34465022
http://dx.doi.org/10.1128/mBio.01228-21
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author Michalik, Anna
Castillo Franco, Diego
Kobiałka, Michał
Szklarzewicz, Teresa
Stroiński, Adam
Łukasik, Piotr
author_facet Michalik, Anna
Castillo Franco, Diego
Kobiałka, Michał
Szklarzewicz, Teresa
Stroiński, Adam
Łukasik, Piotr
author_sort Michalik, Anna
collection PubMed
description Sap-sucking hemipterans host specialized, heritable microorganisms that supplement their diet with essential nutrients. These microbes show unusual features that provide a unique perspective on the coevolution of host-symbiont systems but are still poorly understood. Here, we combine microscopy with high-throughput sequencing to revisit 80-year-old reports on the diversity of symbiont transmission modes in a broadly distributed planthopper family, Dictyopharidae. We show that in seven species examined, the ancestral nutritional symbionts Sulcia and Vidania producing essential amino acids are complemented by co-primary symbionts, either Arsenophonus or Sodalis, acquired several times independently by different host lineages and contributing to the biosynthesis of B vitamins. These symbionts reside within separate bacteriomes within the abdominal cavity, although in females Vidania also occupies bacteriocytes in the rectal organ. Notably, the symbionts are transovarially transmitted from mothers to offspring in two alternative ways. In most examined species, all nutritional symbionts simultaneously infect the posterior end of the full-grown oocytes and next gather in their perivitelline space. In contrast, in other species, Sodalis colonizes the cytoplasm of the anterior pole of young oocytes, forming a cluster separate from the “symbiont ball” formed by late-invading Sulcia and Vidania. Our results show how newly arriving microbes may utilize different strategies to establish long-term heritable symbiosis.
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spelling pubmed-84062882021-09-09 Alternative Transmission Patterns in Independently Acquired Nutritional Cosymbionts of Dictyopharidae Planthoppers Michalik, Anna Castillo Franco, Diego Kobiałka, Michał Szklarzewicz, Teresa Stroiński, Adam Łukasik, Piotr mBio Research Article Sap-sucking hemipterans host specialized, heritable microorganisms that supplement their diet with essential nutrients. These microbes show unusual features that provide a unique perspective on the coevolution of host-symbiont systems but are still poorly understood. Here, we combine microscopy with high-throughput sequencing to revisit 80-year-old reports on the diversity of symbiont transmission modes in a broadly distributed planthopper family, Dictyopharidae. We show that in seven species examined, the ancestral nutritional symbionts Sulcia and Vidania producing essential amino acids are complemented by co-primary symbionts, either Arsenophonus or Sodalis, acquired several times independently by different host lineages and contributing to the biosynthesis of B vitamins. These symbionts reside within separate bacteriomes within the abdominal cavity, although in females Vidania also occupies bacteriocytes in the rectal organ. Notably, the symbionts are transovarially transmitted from mothers to offspring in two alternative ways. In most examined species, all nutritional symbionts simultaneously infect the posterior end of the full-grown oocytes and next gather in their perivitelline space. In contrast, in other species, Sodalis colonizes the cytoplasm of the anterior pole of young oocytes, forming a cluster separate from the “symbiont ball” formed by late-invading Sulcia and Vidania. Our results show how newly arriving microbes may utilize different strategies to establish long-term heritable symbiosis. American Society for Microbiology 2021-08-31 /pmc/articles/PMC8406288/ /pubmed/34465022 http://dx.doi.org/10.1128/mBio.01228-21 Text en Copyright © 2021 Michalik et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Michalik, Anna
Castillo Franco, Diego
Kobiałka, Michał
Szklarzewicz, Teresa
Stroiński, Adam
Łukasik, Piotr
Alternative Transmission Patterns in Independently Acquired Nutritional Cosymbionts of Dictyopharidae Planthoppers
title Alternative Transmission Patterns in Independently Acquired Nutritional Cosymbionts of Dictyopharidae Planthoppers
title_full Alternative Transmission Patterns in Independently Acquired Nutritional Cosymbionts of Dictyopharidae Planthoppers
title_fullStr Alternative Transmission Patterns in Independently Acquired Nutritional Cosymbionts of Dictyopharidae Planthoppers
title_full_unstemmed Alternative Transmission Patterns in Independently Acquired Nutritional Cosymbionts of Dictyopharidae Planthoppers
title_short Alternative Transmission Patterns in Independently Acquired Nutritional Cosymbionts of Dictyopharidae Planthoppers
title_sort alternative transmission patterns in independently acquired nutritional cosymbionts of dictyopharidae planthoppers
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8406288/
https://www.ncbi.nlm.nih.gov/pubmed/34465022
http://dx.doi.org/10.1128/mBio.01228-21
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