Cargando…

Identification and functional analysis of serine protease inhibitor gene family of Eocanthecona furcellata (Wolff)

The predatory natural enemy Eocanthecona furcellata plays a crucial role in agricultural ecosystems due to its effective pest control measures and defensive venom. Predator venom contains serine protease inhibitors (SPIs), which are the primary regulators of serine protease activity and play key rol...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Man, Dai, Zhenlin, Chen, Xiao, Qin, Deqiang, Zhu, Guoyuan, Zhu, Tao, Chen, Gang, Ding, Yishu, Wu, Guoxing, Gao, Xi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10545863/
https://www.ncbi.nlm.nih.gov/pubmed/37795265
http://dx.doi.org/10.3389/fphys.2023.1248354
_version_ 1785114753459290112
author Zhang, Man
Dai, Zhenlin
Chen, Xiao
Qin, Deqiang
Zhu, Guoyuan
Zhu, Tao
Chen, Gang
Ding, Yishu
Wu, Guoxing
Gao, Xi
author_facet Zhang, Man
Dai, Zhenlin
Chen, Xiao
Qin, Deqiang
Zhu, Guoyuan
Zhu, Tao
Chen, Gang
Ding, Yishu
Wu, Guoxing
Gao, Xi
author_sort Zhang, Man
collection PubMed
description The predatory natural enemy Eocanthecona furcellata plays a crucial role in agricultural ecosystems due to its effective pest control measures and defensive venom. Predator venom contains serine protease inhibitors (SPIs), which are the primary regulators of serine protease activity and play key roles in digestion, development, innate immunity, and other physiological regulatory processes. However, the regulation mechanism of SPIs in the salivary glands of predatory natural enemies is still unknown. In this study, we sequenced the transcriptome of E. furcellata salivary gland and identified 38 SPIs genes named EfSPI1∼EfSPI38. Through gene structure, multiple sequence alignment and phylogenetic tree analysis, real-time quantitative PCR (RT-PCR) expression profiles of different developmental stages and different tissues were analyzed. RNAi technology was used to explore the gene function of EFSPI20. The results showed that these 38 EfSPIs genes contained 8 SPI domains, which were serpin, TIL, Kunitz, Kazal, Antistasin, Pacifastin, WAP and A2M. The expression profile results showed that the expression of different types of EfSPIs genes was different at different developmental stages and different tissues. Most of the EfSPIs genes were highly expressed in the egg stage. The EfSPI20, EfSPI21, EfSPI22, and EfSPI24 genes of the Pacifastin subfamily and the EfSPI35 gene of the A2M subfamily were highly expressed in the nymphal and adult stages, which was consistent with the RT-qPCR verification results. These five genes are positively correlated with each other and have a synergistic effect on E. furcellata, and they were highly expressed in salivary glands. After interfering with the expression of the EfSPI20 gene, the survival rate and predatory amount of male and female adults were significantly decreased. Taken together, we speculated some EfSPIs may inhibit trypsin, chymotrypsin, and elastase, and some EfSPIs may be involved in autoimmune responses. EfSPI20 was essential for the predation and digestion of E. furcellata, and the functions of other EfSPIs were discussed. Our findings provide valuable insights into the diversity of EfSPIs in E. furcellata and the potential functions of regulating their predation, digestion and innate immunity, which may be of great significance for developing new pest control strategies.
format Online
Article
Text
id pubmed-10545863
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-105458632023-10-04 Identification and functional analysis of serine protease inhibitor gene family of Eocanthecona furcellata (Wolff) Zhang, Man Dai, Zhenlin Chen, Xiao Qin, Deqiang Zhu, Guoyuan Zhu, Tao Chen, Gang Ding, Yishu Wu, Guoxing Gao, Xi Front Physiol Physiology The predatory natural enemy Eocanthecona furcellata plays a crucial role in agricultural ecosystems due to its effective pest control measures and defensive venom. Predator venom contains serine protease inhibitors (SPIs), which are the primary regulators of serine protease activity and play key roles in digestion, development, innate immunity, and other physiological regulatory processes. However, the regulation mechanism of SPIs in the salivary glands of predatory natural enemies is still unknown. In this study, we sequenced the transcriptome of E. furcellata salivary gland and identified 38 SPIs genes named EfSPI1∼EfSPI38. Through gene structure, multiple sequence alignment and phylogenetic tree analysis, real-time quantitative PCR (RT-PCR) expression profiles of different developmental stages and different tissues were analyzed. RNAi technology was used to explore the gene function of EFSPI20. The results showed that these 38 EfSPIs genes contained 8 SPI domains, which were serpin, TIL, Kunitz, Kazal, Antistasin, Pacifastin, WAP and A2M. The expression profile results showed that the expression of different types of EfSPIs genes was different at different developmental stages and different tissues. Most of the EfSPIs genes were highly expressed in the egg stage. The EfSPI20, EfSPI21, EfSPI22, and EfSPI24 genes of the Pacifastin subfamily and the EfSPI35 gene of the A2M subfamily were highly expressed in the nymphal and adult stages, which was consistent with the RT-qPCR verification results. These five genes are positively correlated with each other and have a synergistic effect on E. furcellata, and they were highly expressed in salivary glands. After interfering with the expression of the EfSPI20 gene, the survival rate and predatory amount of male and female adults were significantly decreased. Taken together, we speculated some EfSPIs may inhibit trypsin, chymotrypsin, and elastase, and some EfSPIs may be involved in autoimmune responses. EfSPI20 was essential for the predation and digestion of E. furcellata, and the functions of other EfSPIs were discussed. Our findings provide valuable insights into the diversity of EfSPIs in E. furcellata and the potential functions of regulating their predation, digestion and innate immunity, which may be of great significance for developing new pest control strategies. Frontiers Media S.A. 2023-09-18 /pmc/articles/PMC10545863/ /pubmed/37795265 http://dx.doi.org/10.3389/fphys.2023.1248354 Text en Copyright © 2023 Zhang, Dai, Chen, Qin, Zhu, Zhu, Chen, Ding, Wu and Gao. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Zhang, Man
Dai, Zhenlin
Chen, Xiao
Qin, Deqiang
Zhu, Guoyuan
Zhu, Tao
Chen, Gang
Ding, Yishu
Wu, Guoxing
Gao, Xi
Identification and functional analysis of serine protease inhibitor gene family of Eocanthecona furcellata (Wolff)
title Identification and functional analysis of serine protease inhibitor gene family of Eocanthecona furcellata (Wolff)
title_full Identification and functional analysis of serine protease inhibitor gene family of Eocanthecona furcellata (Wolff)
title_fullStr Identification and functional analysis of serine protease inhibitor gene family of Eocanthecona furcellata (Wolff)
title_full_unstemmed Identification and functional analysis of serine protease inhibitor gene family of Eocanthecona furcellata (Wolff)
title_short Identification and functional analysis of serine protease inhibitor gene family of Eocanthecona furcellata (Wolff)
title_sort identification and functional analysis of serine protease inhibitor gene family of eocanthecona furcellata (wolff)
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10545863/
https://www.ncbi.nlm.nih.gov/pubmed/37795265
http://dx.doi.org/10.3389/fphys.2023.1248354
work_keys_str_mv AT zhangman identificationandfunctionalanalysisofserineproteaseinhibitorgenefamilyofeocantheconafurcellatawolff
AT daizhenlin identificationandfunctionalanalysisofserineproteaseinhibitorgenefamilyofeocantheconafurcellatawolff
AT chenxiao identificationandfunctionalanalysisofserineproteaseinhibitorgenefamilyofeocantheconafurcellatawolff
AT qindeqiang identificationandfunctionalanalysisofserineproteaseinhibitorgenefamilyofeocantheconafurcellatawolff
AT zhuguoyuan identificationandfunctionalanalysisofserineproteaseinhibitorgenefamilyofeocantheconafurcellatawolff
AT zhutao identificationandfunctionalanalysisofserineproteaseinhibitorgenefamilyofeocantheconafurcellatawolff
AT chengang identificationandfunctionalanalysisofserineproteaseinhibitorgenefamilyofeocantheconafurcellatawolff
AT dingyishu identificationandfunctionalanalysisofserineproteaseinhibitorgenefamilyofeocantheconafurcellatawolff
AT wuguoxing identificationandfunctionalanalysisofserineproteaseinhibitorgenefamilyofeocantheconafurcellatawolff
AT gaoxi identificationandfunctionalanalysisofserineproteaseinhibitorgenefamilyofeocantheconafurcellatawolff