Cargando…

Morphological adaptation for ectosymbiont maintenance and transmission during metamorphosis in Lagria beetles

The diversity and success of holometabolous insects is partly driven by metamorphosis, which allows for the exploitation of different niches and decouples growth and tissue differentiation from reproduction. Despite its benefits, metamorphosis comes with the cost of temporal vulnerability during pup...

Descripción completa

Detalles Bibliográficos
Autores principales: Janke, Rebekka S., Moog, Safira, Weiss, Benjamin, Kaltenpoth, Martin, Flórez, Laura V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9468232/
https://www.ncbi.nlm.nih.gov/pubmed/36111144
http://dx.doi.org/10.3389/fphys.2022.979200
_version_ 1784788365018660864
author Janke, Rebekka S.
Moog, Safira
Weiss, Benjamin
Kaltenpoth, Martin
Flórez, Laura V.
author_facet Janke, Rebekka S.
Moog, Safira
Weiss, Benjamin
Kaltenpoth, Martin
Flórez, Laura V.
author_sort Janke, Rebekka S.
collection PubMed
description The diversity and success of holometabolous insects is partly driven by metamorphosis, which allows for the exploitation of different niches and decouples growth and tissue differentiation from reproduction. Despite its benefits, metamorphosis comes with the cost of temporal vulnerability during pupation and challenges associated with tissue reorganizations. These rearrangements can also affect the presence, abundance, and localization of beneficial microbes in the host. However, how symbionts are maintained or translocated during metamorphosis and which adaptations are necessary from each partner during this process remains unknown for the vast majority of symbiotic systems. Here, we show that Lagria beetles circumvent the constraints of metamorphosis by maintaining defensive symbionts on the surface in specialized cuticular structures. The symbionts are present in both sexes throughout larval development and during the pupal phase, in line with a protective role during the beetle’s immature stages. By comparing symbiont titer and morphology of the cuticular structures between sexes using qPCR, fluorescence in situ hybridization, and micro-computed tomography, we found that the organs likely play an important role as a symbiont reservoir for transmission to female adults, since symbiont titers and structures are reduced in male pupae. Using symbiont-sized fluorescent beads, we demonstrate transfer from the region of the dorsal symbiont-housing organs to the opening of the reproductive tract of adult females, suggesting that symbiont relocation on the outer surface is possible, even without specialized symbiont adaptations or motility. Our results illustrate a strategy for holometabolous insects to cope with the challenge of symbiont maintenance during metamorphosis via an external route, circumventing problems associated with internal tissue reorganization. Thereby, Lagria beetles keep a tight relationship with their beneficial partners during growth and metamorphosis.
format Online
Article
Text
id pubmed-9468232
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-94682322022-09-14 Morphological adaptation for ectosymbiont maintenance and transmission during metamorphosis in Lagria beetles Janke, Rebekka S. Moog, Safira Weiss, Benjamin Kaltenpoth, Martin Flórez, Laura V. Front Physiol Physiology The diversity and success of holometabolous insects is partly driven by metamorphosis, which allows for the exploitation of different niches and decouples growth and tissue differentiation from reproduction. Despite its benefits, metamorphosis comes with the cost of temporal vulnerability during pupation and challenges associated with tissue reorganizations. These rearrangements can also affect the presence, abundance, and localization of beneficial microbes in the host. However, how symbionts are maintained or translocated during metamorphosis and which adaptations are necessary from each partner during this process remains unknown for the vast majority of symbiotic systems. Here, we show that Lagria beetles circumvent the constraints of metamorphosis by maintaining defensive symbionts on the surface in specialized cuticular structures. The symbionts are present in both sexes throughout larval development and during the pupal phase, in line with a protective role during the beetle’s immature stages. By comparing symbiont titer and morphology of the cuticular structures between sexes using qPCR, fluorescence in situ hybridization, and micro-computed tomography, we found that the organs likely play an important role as a symbiont reservoir for transmission to female adults, since symbiont titers and structures are reduced in male pupae. Using symbiont-sized fluorescent beads, we demonstrate transfer from the region of the dorsal symbiont-housing organs to the opening of the reproductive tract of adult females, suggesting that symbiont relocation on the outer surface is possible, even without specialized symbiont adaptations or motility. Our results illustrate a strategy for holometabolous insects to cope with the challenge of symbiont maintenance during metamorphosis via an external route, circumventing problems associated with internal tissue reorganization. Thereby, Lagria beetles keep a tight relationship with their beneficial partners during growth and metamorphosis. Frontiers Media S.A. 2022-08-30 /pmc/articles/PMC9468232/ /pubmed/36111144 http://dx.doi.org/10.3389/fphys.2022.979200 Text en Copyright © 2022 Janke, Moog, Weiss, Kaltenpoth and Flórez. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Janke, Rebekka S.
Moog, Safira
Weiss, Benjamin
Kaltenpoth, Martin
Flórez, Laura V.
Morphological adaptation for ectosymbiont maintenance and transmission during metamorphosis in Lagria beetles
title Morphological adaptation for ectosymbiont maintenance and transmission during metamorphosis in Lagria beetles
title_full Morphological adaptation for ectosymbiont maintenance and transmission during metamorphosis in Lagria beetles
title_fullStr Morphological adaptation for ectosymbiont maintenance and transmission during metamorphosis in Lagria beetles
title_full_unstemmed Morphological adaptation for ectosymbiont maintenance and transmission during metamorphosis in Lagria beetles
title_short Morphological adaptation for ectosymbiont maintenance and transmission during metamorphosis in Lagria beetles
title_sort morphological adaptation for ectosymbiont maintenance and transmission during metamorphosis in lagria beetles
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9468232/
https://www.ncbi.nlm.nih.gov/pubmed/36111144
http://dx.doi.org/10.3389/fphys.2022.979200
work_keys_str_mv AT jankerebekkas morphologicaladaptationforectosymbiontmaintenanceandtransmissionduringmetamorphosisinlagriabeetles
AT moogsafira morphologicaladaptationforectosymbiontmaintenanceandtransmissionduringmetamorphosisinlagriabeetles
AT weissbenjamin morphologicaladaptationforectosymbiontmaintenanceandtransmissionduringmetamorphosisinlagriabeetles
AT kaltenpothmartin morphologicaladaptationforectosymbiontmaintenanceandtransmissionduringmetamorphosisinlagriabeetles
AT florezlaurav morphologicaladaptationforectosymbiontmaintenanceandtransmissionduringmetamorphosisinlagriabeetles