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Functional transcriptome analyses of Drosophila suzukii midgut reveal mating-dependent reproductive plasticity in females

BACKGROUND: Insect females undergo a huge transition in energy homeostasis after mating to compensate for nutrient investment during reproduction. To manage with this shift in metabolism, mated females experience extensive morphological, behavioral and physiological changes, including increased food...

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Autores principales: Xing, Shisi, Deng, Dan, wen, Wen, Peng, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9598023/
https://www.ncbi.nlm.nih.gov/pubmed/36284272
http://dx.doi.org/10.1186/s12864-022-08962-2
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author Xing, Shisi
Deng, Dan
wen, Wen
Peng, Wei
author_facet Xing, Shisi
Deng, Dan
wen, Wen
Peng, Wei
author_sort Xing, Shisi
collection PubMed
description BACKGROUND: Insect females undergo a huge transition in energy homeostasis after mating to compensate for nutrient investment during reproduction. To manage with this shift in metabolism, mated females experience extensive morphological, behavioral and physiological changes, including increased food intake and altered digestive processes. However, the mechanisms by which the digestive system responds to mating in females remain barely characterized. Here we performed transcriptomic analysis of the main digestive organ, the midgut, to investigate how gene expression varies with female mating status in Drosophila suzukii, a destructive and invasive soft fruit pest. RESULTS: We sequenced 15,275 unique genes with an average length of 1,467 bp. In total, 652 differentially expressed genes (DEGs) were detected between virgin and mated D. suzukii female midgut libraries. The DEGs were functionally annotated utilizing the GO and KEGG pathway annotation methods. Our results showed that the major GO terms associated with the DEGs from the virgin versus mated female midgut were largely appointed to the metabolic process, response to stimulus and immune system process. We obtained a mass of protein and lipid metabolism genes which were up-regulated and carbohydrate metabolism and immune-related genes which were down-regulated at different time points after mating in female midgut by qRT-PCR. These changes in metabolism and immunity may help supply the female with the nutrients and energy required to sustain egg production. CONCLUSION: Our study characterizes the transcriptional mechanisms driven by mating in the D. suzukii female midgut. Identification and characterization of the DEGs between virgin and mated females midgut will not only be crucial to better understand molecular research related to intestine plasticity during reproduction, but may also provide abundant target genes for the development of effective and ecofriendly pest control strategies against this economically important species. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-022-08962-2.
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spelling pubmed-95980232022-10-27 Functional transcriptome analyses of Drosophila suzukii midgut reveal mating-dependent reproductive plasticity in females Xing, Shisi Deng, Dan wen, Wen Peng, Wei BMC Genomics Research BACKGROUND: Insect females undergo a huge transition in energy homeostasis after mating to compensate for nutrient investment during reproduction. To manage with this shift in metabolism, mated females experience extensive morphological, behavioral and physiological changes, including increased food intake and altered digestive processes. However, the mechanisms by which the digestive system responds to mating in females remain barely characterized. Here we performed transcriptomic analysis of the main digestive organ, the midgut, to investigate how gene expression varies with female mating status in Drosophila suzukii, a destructive and invasive soft fruit pest. RESULTS: We sequenced 15,275 unique genes with an average length of 1,467 bp. In total, 652 differentially expressed genes (DEGs) were detected between virgin and mated D. suzukii female midgut libraries. The DEGs were functionally annotated utilizing the GO and KEGG pathway annotation methods. Our results showed that the major GO terms associated with the DEGs from the virgin versus mated female midgut were largely appointed to the metabolic process, response to stimulus and immune system process. We obtained a mass of protein and lipid metabolism genes which were up-regulated and carbohydrate metabolism and immune-related genes which were down-regulated at different time points after mating in female midgut by qRT-PCR. These changes in metabolism and immunity may help supply the female with the nutrients and energy required to sustain egg production. CONCLUSION: Our study characterizes the transcriptional mechanisms driven by mating in the D. suzukii female midgut. Identification and characterization of the DEGs between virgin and mated females midgut will not only be crucial to better understand molecular research related to intestine plasticity during reproduction, but may also provide abundant target genes for the development of effective and ecofriendly pest control strategies against this economically important species. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-022-08962-2. BioMed Central 2022-10-25 /pmc/articles/PMC9598023/ /pubmed/36284272 http://dx.doi.org/10.1186/s12864-022-08962-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Xing, Shisi
Deng, Dan
wen, Wen
Peng, Wei
Functional transcriptome analyses of Drosophila suzukii midgut reveal mating-dependent reproductive plasticity in females
title Functional transcriptome analyses of Drosophila suzukii midgut reveal mating-dependent reproductive plasticity in females
title_full Functional transcriptome analyses of Drosophila suzukii midgut reveal mating-dependent reproductive plasticity in females
title_fullStr Functional transcriptome analyses of Drosophila suzukii midgut reveal mating-dependent reproductive plasticity in females
title_full_unstemmed Functional transcriptome analyses of Drosophila suzukii midgut reveal mating-dependent reproductive plasticity in females
title_short Functional transcriptome analyses of Drosophila suzukii midgut reveal mating-dependent reproductive plasticity in females
title_sort functional transcriptome analyses of drosophila suzukii midgut reveal mating-dependent reproductive plasticity in females
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9598023/
https://www.ncbi.nlm.nih.gov/pubmed/36284272
http://dx.doi.org/10.1186/s12864-022-08962-2
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