Integration of transcriptomic and proteomic data uncovers the nutritional requirement of the immature development of an endoparasitoid wasp

Endoparasitic wasps produce several factors, such as polydnavirus, venom and a specialized group of wasp embryonic cells named teratocytes, to condition their hosts and support the development of parasitoid offspring. However, the role of the developing parasitoid larvae in host adaption and regulation remains largely unknown. By analyzing RNA-seq data of Cotesia vestalis, an endolarval parasitoid of the diamondback moth Plutella xylostella, we discovered that most of the larval stage highly expressed genes are associated with nutrient metabolism, including carbohydrate, protein, and lipid metabolism. We also identified hundreds of C. vestalis larvae-secreted proteins. A large proportion of the secreted proteins (126/404) are encoded by larval highly expressed genes. Besides several immune-related proteins, most of the secreted proteins are closely related to carbohydrate, protein, and amino acid metabolism. We further demonstrated that eleven genes linked to amino acid metabolism that encode secretory proteins were upregulated in 2nd instar larvae. These results suggest a relatively positive correlation between gene expression and secreted proteins. In summary, our study presents the secretory proteome of an endolarval parasitoid, highlighting its potential function in nutritional and immune regulation within the host, which would benefit the growth and development of parasitoid progeny.

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Publication Details

Journal
Scientific Reports
Published
2025-05-22
DOI
https://doi.org/10.1038/s41598-025-02290-7
Citations
2
Primary Topic
Insect and Arachnid Ecology and Behavior
Type
article
Field-Weighted Citation Impact
3.63

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article

Integration of transcriptomic and proteomic data uncovers the nutritional requirement of the immature development of an endoparasitoid wasp

Xue‐Xin Chen, Peng-Zhan Wang, Zhizhi Wang, Xiqian Ye et al.
2 citations
Scientific Reports
Insect and Arachnid Ecology and Behavior
3.63
article

Integration of transcriptomic and proteomic data uncovers the nutritional requirement of the immature development of an endoparasitoid wasp

Xue‐Xin Chen, Peng-Zhan Wang, Zhizhi Wang, Xiqian Ye, Jianhua Huang, Zihan Wang, Lizhi Wang, Shuang Xie
article en
2 citations

Abstract

Endoparasitic wasps produce several factors, such as polydnavirus, venom and a specialized group of wasp embryonic cells named teratocytes, to condition their hosts and support the development of parasitoid offspring. However, the role of the developing parasitoid larvae in host adaption and regulation remains largely unknown. By analyzing RNA-seq data of Cotesia vestalis, an endolarval parasitoid of the diamondback moth Plutella xylostella, we discovered that most of the larval stage highly expressed genes are associated with nutrient metabolism, including carbohydrate, protein, and lipid metabolism. We also identified hundreds of C. vestalis larvae-secreted proteins. A large proportion of the secreted proteins (126/404) are encoded by larval highly expressed genes. Besides several immune-related proteins, most of the secreted proteins are closely related to carbohydrate, protein, and amino acid metabolism. We further demonstrated that eleven genes linked to amino acid metabolism that encode secretory proteins were upregulated in 2nd instar larvae. These results suggest a relatively positive correlation between gene expression and secreted proteins. In summary, our study presents the secretory proteome of an endolarval parasitoid, highlighting its potential function in nutritional and immune regulation within the host, which would benefit the growth and development of parasitoid progeny.

Scientific ReportsVol. 15(1)
Ministry of Agriculture and Rural Affairs (CN), China National Rice Research Institute (CN), State Key Laboratory of Rice Biology, Zhejiang University (CN)
National Natural Science Foundation of China, Fundamental Research Funds for the Central Universities
Zero hunger
Openalex Percentile: Top 8%
Insect and Arachnid Ecology and Behavior
3.63
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