Cargando…

Transcriptomic and life history responses of the mayfly Neocloeon triangulifer to chronic diel thermal challenge

To better understand the effects of transient thermal stress in an aquatic insect, we first identified static temperatures associated with fitness deficits, and then reared larvae from egg hatch to adulthood under diurnally variable regimens including daily forays into deleterious temperatures. We s...

Descripción completa

Detalles Bibliográficos
Autores principales: Chou, Hsuan, Jima, Dereje D., Funk, David H., Jackson, John K., Sweeney, Bernard W., Buchwalter, David B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7644658/
https://www.ncbi.nlm.nih.gov/pubmed/33154410
http://dx.doi.org/10.1038/s41598-020-75064-y
_version_ 1783606498905030656
author Chou, Hsuan
Jima, Dereje D.
Funk, David H.
Jackson, John K.
Sweeney, Bernard W.
Buchwalter, David B.
author_facet Chou, Hsuan
Jima, Dereje D.
Funk, David H.
Jackson, John K.
Sweeney, Bernard W.
Buchwalter, David B.
author_sort Chou, Hsuan
collection PubMed
description To better understand the effects of transient thermal stress in an aquatic insect, we first identified static temperatures associated with fitness deficits, and then reared larvae from egg hatch to adulthood under diurnally variable regimens including daily forays into deleterious temperatures. We sampled mature larvae at the coolest and warmest portions of their respective regimens for RNA-seq analysis. Few transcripts (28) were differentially expressed when larvae oscillated between favorable temperatures, while 614 transcripts were differentially expressed when experiencing daily transient thermal stress. Transcripts associated with N-glycan processing were downregulated while those associated with lipid catabolism and chitin turnover were significantly upregulated in heat stressed larvae. An across-regimen comparison of differentially expressed transcripts among organisms sampled at comparable temperatures demonstrated that the effects of daily thermal stress persisted even when larvae were sampled at a more optimal temperature (806 differentially expressed transcripts). The chronically stressed population had reduced expression of transcripts related to ATP synthesis, mitochondrial electron chain functions, gluconeogenesis and glycolytic processes while transcripts associated with cell adhesion, synaptic vesicle transport, regulation of membrane potential and lipid biosynthesis increased. Comparisons of constant vs. variable temperatures revealed that the negative consequences of time spent at stressful temperatures were not offset by more time spent at optimal temperatures.
format Online
Article
Text
id pubmed-7644658
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-76446582020-11-06 Transcriptomic and life history responses of the mayfly Neocloeon triangulifer to chronic diel thermal challenge Chou, Hsuan Jima, Dereje D. Funk, David H. Jackson, John K. Sweeney, Bernard W. Buchwalter, David B. Sci Rep Article To better understand the effects of transient thermal stress in an aquatic insect, we first identified static temperatures associated with fitness deficits, and then reared larvae from egg hatch to adulthood under diurnally variable regimens including daily forays into deleterious temperatures. We sampled mature larvae at the coolest and warmest portions of their respective regimens for RNA-seq analysis. Few transcripts (28) were differentially expressed when larvae oscillated between favorable temperatures, while 614 transcripts were differentially expressed when experiencing daily transient thermal stress. Transcripts associated with N-glycan processing were downregulated while those associated with lipid catabolism and chitin turnover were significantly upregulated in heat stressed larvae. An across-regimen comparison of differentially expressed transcripts among organisms sampled at comparable temperatures demonstrated that the effects of daily thermal stress persisted even when larvae were sampled at a more optimal temperature (806 differentially expressed transcripts). The chronically stressed population had reduced expression of transcripts related to ATP synthesis, mitochondrial electron chain functions, gluconeogenesis and glycolytic processes while transcripts associated with cell adhesion, synaptic vesicle transport, regulation of membrane potential and lipid biosynthesis increased. Comparisons of constant vs. variable temperatures revealed that the negative consequences of time spent at stressful temperatures were not offset by more time spent at optimal temperatures. Nature Publishing Group UK 2020-11-05 /pmc/articles/PMC7644658/ /pubmed/33154410 http://dx.doi.org/10.1038/s41598-020-75064-y Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Chou, Hsuan
Jima, Dereje D.
Funk, David H.
Jackson, John K.
Sweeney, Bernard W.
Buchwalter, David B.
Transcriptomic and life history responses of the mayfly Neocloeon triangulifer to chronic diel thermal challenge
title Transcriptomic and life history responses of the mayfly Neocloeon triangulifer to chronic diel thermal challenge
title_full Transcriptomic and life history responses of the mayfly Neocloeon triangulifer to chronic diel thermal challenge
title_fullStr Transcriptomic and life history responses of the mayfly Neocloeon triangulifer to chronic diel thermal challenge
title_full_unstemmed Transcriptomic and life history responses of the mayfly Neocloeon triangulifer to chronic diel thermal challenge
title_short Transcriptomic and life history responses of the mayfly Neocloeon triangulifer to chronic diel thermal challenge
title_sort transcriptomic and life history responses of the mayfly neocloeon triangulifer to chronic diel thermal challenge
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7644658/
https://www.ncbi.nlm.nih.gov/pubmed/33154410
http://dx.doi.org/10.1038/s41598-020-75064-y
work_keys_str_mv AT chouhsuan transcriptomicandlifehistoryresponsesofthemayflyneocloeontriangulifertochronicdielthermalchallenge
AT jimaderejed transcriptomicandlifehistoryresponsesofthemayflyneocloeontriangulifertochronicdielthermalchallenge
AT funkdavidh transcriptomicandlifehistoryresponsesofthemayflyneocloeontriangulifertochronicdielthermalchallenge
AT jacksonjohnk transcriptomicandlifehistoryresponsesofthemayflyneocloeontriangulifertochronicdielthermalchallenge
AT sweeneybernardw transcriptomicandlifehistoryresponsesofthemayflyneocloeontriangulifertochronicdielthermalchallenge
AT buchwalterdavidb transcriptomicandlifehistoryresponsesofthemayflyneocloeontriangulifertochronicdielthermalchallenge