Cargando…
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...
Autores principales: | , , , , , |
---|---|
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 |
_version_ | 1783746490101923840 |
---|---|
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. |
format | Online Article Text |
id | pubmed-8406288 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT michalikanna alternativetransmissionpatternsinindependentlyacquirednutritionalcosymbiontsofdictyopharidaeplanthoppers AT castillofrancodiego alternativetransmissionpatternsinindependentlyacquirednutritionalcosymbiontsofdictyopharidaeplanthoppers AT kobiałkamichał alternativetransmissionpatternsinindependentlyacquirednutritionalcosymbiontsofdictyopharidaeplanthoppers AT szklarzewiczteresa alternativetransmissionpatternsinindependentlyacquirednutritionalcosymbiontsofdictyopharidaeplanthoppers AT stroinskiadam alternativetransmissionpatternsinindependentlyacquirednutritionalcosymbiontsofdictyopharidaeplanthoppers AT łukasikpiotr alternativetransmissionpatternsinindependentlyacquirednutritionalcosymbiontsofdictyopharidaeplanthoppers |