Cargando…

Cohabitation and roommate bias of symbiotic bacteria in insect hosts

Symbiotic interactions between insects and bacteria have long fascinated ecologists. Aphids have emerged as the model system on which to study the effect of endosymbiotic bacteria on their hosts. Aphid‐symbiont interactions are ecologically interesting as aphids host multiple secondary symbionts tha...

Descripción completa

Detalles Bibliográficos
Autor principal: Zytynska, Sharon E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6973153/
https://www.ncbi.nlm.nih.gov/pubmed/31758616
http://dx.doi.org/10.1111/mec.15295
_version_ 1783489987974529024
author Zytynska, Sharon E.
author_facet Zytynska, Sharon E.
author_sort Zytynska, Sharon E.
collection PubMed
description Symbiotic interactions between insects and bacteria have long fascinated ecologists. Aphids have emerged as the model system on which to study the effect of endosymbiotic bacteria on their hosts. Aphid‐symbiont interactions are ecologically interesting as aphids host multiple secondary symbionts that can provide broad benefits, such as protection against heat stress or specialist natural enemies (parasitic wasps and entomopathogenic fungi). There are nine common aphid secondary symbionts and individual aphids host on average 1–2 symbionts. A cost‐benefit trade‐off for hosting symbionts is thought to explain why not all aphids host every possible symbiont in a population. Both positive and negative associations between various symbionts occur, and this could happen due to increased costs when cohosting certain combinations or as a consequence of competitive interactions between the symbionts within a host. In this issue of Molecular Ecology, Mathé‐Hubert, Kaech, Hertaeg, Jaenike, and Vorburger (2019) use data on the symbiont status of field‐collected aphids to inform a model on the evolution of symbiont co‐occurrence. They vary the effective female population size as well as the rate of horizontal and maternal transmission to infer the relative impact of symbiont‐symbiont interactions versus random drift. Additional data analysis revisits an association between two symbionts in a fruit fly species using a long‐term data set to highlight that such interactions are not limited to aphids.
format Online
Article
Text
id pubmed-6973153
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-69731532020-01-27 Cohabitation and roommate bias of symbiotic bacteria in insect hosts Zytynska, Sharon E. Mol Ecol News and Views Symbiotic interactions between insects and bacteria have long fascinated ecologists. Aphids have emerged as the model system on which to study the effect of endosymbiotic bacteria on their hosts. Aphid‐symbiont interactions are ecologically interesting as aphids host multiple secondary symbionts that can provide broad benefits, such as protection against heat stress or specialist natural enemies (parasitic wasps and entomopathogenic fungi). There are nine common aphid secondary symbionts and individual aphids host on average 1–2 symbionts. A cost‐benefit trade‐off for hosting symbionts is thought to explain why not all aphids host every possible symbiont in a population. Both positive and negative associations between various symbionts occur, and this could happen due to increased costs when cohosting certain combinations or as a consequence of competitive interactions between the symbionts within a host. In this issue of Molecular Ecology, Mathé‐Hubert, Kaech, Hertaeg, Jaenike, and Vorburger (2019) use data on the symbiont status of field‐collected aphids to inform a model on the evolution of symbiont co‐occurrence. They vary the effective female population size as well as the rate of horizontal and maternal transmission to infer the relative impact of symbiont‐symbiont interactions versus random drift. Additional data analysis revisits an association between two symbionts in a fruit fly species using a long‐term data set to highlight that such interactions are not limited to aphids. John Wiley and Sons Inc. 2019-11-22 2019-12 /pmc/articles/PMC6973153/ /pubmed/31758616 http://dx.doi.org/10.1111/mec.15295 Text en © 2019 The Authors. Molecular Ecology published by John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle News and Views
Zytynska, Sharon E.
Cohabitation and roommate bias of symbiotic bacteria in insect hosts
title Cohabitation and roommate bias of symbiotic bacteria in insect hosts
title_full Cohabitation and roommate bias of symbiotic bacteria in insect hosts
title_fullStr Cohabitation and roommate bias of symbiotic bacteria in insect hosts
title_full_unstemmed Cohabitation and roommate bias of symbiotic bacteria in insect hosts
title_short Cohabitation and roommate bias of symbiotic bacteria in insect hosts
title_sort cohabitation and roommate bias of symbiotic bacteria in insect hosts
topic News and Views
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6973153/
https://www.ncbi.nlm.nih.gov/pubmed/31758616
http://dx.doi.org/10.1111/mec.15295
work_keys_str_mv AT zytynskasharone cohabitationandroommatebiasofsymbioticbacteriaininsecthosts