Cargando…
Rapid brain development and reduced neuromodulator titres correlate with host shifts in Rhagoletis pomonella
Host shifts are considered a key generator of insect biodiversity. For insects, adaptation to new host plants often requires changes in larval/pupal development and adult behavioural preference toward new hosts. Neurochemicals play key roles in both development and behaviour and therefore provide a...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9449811/ https://www.ncbi.nlm.nih.gov/pubmed/36117862 http://dx.doi.org/10.1098/rsos.220962 |
_version_ | 1784784381872701440 |
---|---|
author | Kharva, Hinal Feder, Jeffrey L. Hahn, Daniel A. Olsson, Shannon B. |
author_facet | Kharva, Hinal Feder, Jeffrey L. Hahn, Daniel A. Olsson, Shannon B. |
author_sort | Kharva, Hinal |
collection | PubMed |
description | Host shifts are considered a key generator of insect biodiversity. For insects, adaptation to new host plants often requires changes in larval/pupal development and adult behavioural preference toward new hosts. Neurochemicals play key roles in both development and behaviour and therefore provide a potential source for such synchronization. Here, we correlated life-history timing, brain development and corresponding levels of 14 neurochemicals in Rhagoletis pomonella (Diptera: Tephritidae), a species undergoing ecological speciation through an ongoing host shift from hawthorn to apple fruit. These races exhibit differences in pupal diapause timing as well as adult behavioural preference with respect to their hosts. This difference in behavioural preference is coupled with differences in neurophysiological response to host volatiles. We found that apple race pupae exhibited adult brain morphogenesis three weeks faster after an identical simulated winter than the hawthorn race, which correlated with significantly lower titres of several neurochemicals. In some cases, particularly biogenic amines, differences in titres were reflected in the mature adult stage, when host preference is exhibited. In summary, life-history timing, neurochemical titre and brain development can be coupled in this speciating system, providing new hypotheses for the origins of new species through host shifts. |
format | Online Article Text |
id | pubmed-9449811 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-94498112022-09-15 Rapid brain development and reduced neuromodulator titres correlate with host shifts in Rhagoletis pomonella Kharva, Hinal Feder, Jeffrey L. Hahn, Daniel A. Olsson, Shannon B. R Soc Open Sci Organismal and Evolutionary Biology Host shifts are considered a key generator of insect biodiversity. For insects, adaptation to new host plants often requires changes in larval/pupal development and adult behavioural preference toward new hosts. Neurochemicals play key roles in both development and behaviour and therefore provide a potential source for such synchronization. Here, we correlated life-history timing, brain development and corresponding levels of 14 neurochemicals in Rhagoletis pomonella (Diptera: Tephritidae), a species undergoing ecological speciation through an ongoing host shift from hawthorn to apple fruit. These races exhibit differences in pupal diapause timing as well as adult behavioural preference with respect to their hosts. This difference in behavioural preference is coupled with differences in neurophysiological response to host volatiles. We found that apple race pupae exhibited adult brain morphogenesis three weeks faster after an identical simulated winter than the hawthorn race, which correlated with significantly lower titres of several neurochemicals. In some cases, particularly biogenic amines, differences in titres were reflected in the mature adult stage, when host preference is exhibited. In summary, life-history timing, neurochemical titre and brain development can be coupled in this speciating system, providing new hypotheses for the origins of new species through host shifts. The Royal Society 2022-09-07 /pmc/articles/PMC9449811/ /pubmed/36117862 http://dx.doi.org/10.1098/rsos.220962 Text en © 2022 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Organismal and Evolutionary Biology Kharva, Hinal Feder, Jeffrey L. Hahn, Daniel A. Olsson, Shannon B. Rapid brain development and reduced neuromodulator titres correlate with host shifts in Rhagoletis pomonella |
title | Rapid brain development and reduced neuromodulator titres correlate with host shifts in Rhagoletis pomonella |
title_full | Rapid brain development and reduced neuromodulator titres correlate with host shifts in Rhagoletis pomonella |
title_fullStr | Rapid brain development and reduced neuromodulator titres correlate with host shifts in Rhagoletis pomonella |
title_full_unstemmed | Rapid brain development and reduced neuromodulator titres correlate with host shifts in Rhagoletis pomonella |
title_short | Rapid brain development and reduced neuromodulator titres correlate with host shifts in Rhagoletis pomonella |
title_sort | rapid brain development and reduced neuromodulator titres correlate with host shifts in rhagoletis pomonella |
topic | Organismal and Evolutionary Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9449811/ https://www.ncbi.nlm.nih.gov/pubmed/36117862 http://dx.doi.org/10.1098/rsos.220962 |
work_keys_str_mv | AT kharvahinal rapidbraindevelopmentandreducedneuromodulatortitrescorrelatewithhostshiftsinrhagoletispomonella AT federjeffreyl rapidbraindevelopmentandreducedneuromodulatortitrescorrelatewithhostshiftsinrhagoletispomonella AT hahndaniela rapidbraindevelopmentandreducedneuromodulatortitrescorrelatewithhostshiftsinrhagoletispomonella AT olssonshannonb rapidbraindevelopmentandreducedneuromodulatortitrescorrelatewithhostshiftsinrhagoletispomonella |