RNA interference-mediated functional analysis of vitellogenin and vitellogenin receptor in the predatory mite Neoseiulus californicus

IF 1.3 3区 农林科学 Q2 ENTOMOLOGY Systematic and Applied Acarology Pub Date : 2024-03-25 DOI:10.11158/saa.29.3.3
Rui Zhu, Tianci Yi, Run-dong Liu, Dao-chao Jin
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Abstract

Neoseiulus californicus is a key natural predator of spider mites and small arthropod pests. Although vitellogenin (Vg) and vitellogenin receptor (VgR) genes are important regulators of oocyte maturation, egg formation, and embryonic development in spider mites and ticks, their role in phytoseiid mites is less understood. Investigating the reproductive mechanism of predatory mites is crucial for understanding their reproduction and evolution. In this study, three Vg genes and one VgR gene were identified, cloned, and characterized in N. californicus. Vg1, Vg2, Vg3, and VgR mRNAs were 6066, 5728, 4515, and 5331 bp long, encoding proteins comprising 1851, 1849, 1471, and 1722 amino acids, respectively. Temporal expression analysis revealed elevated Vg1, Vg2, and VgR levels in fertilized female adult mites, whereas Vg3 exhibited peak expression during the developmental stage. RNA interference–mediated suppression of Vg1 and Vg2 resulted in 14.66% and 11.59% decreases in fecundity, respectively. Vg1 silencing notably reduced egg hatching rate and female offspring ratio. In contrast, Vg3 and VgR silencing had no significant impact on fecundity and egg hatching rate. These findings provide insights into the regulatory roles of Vg and VgR in predatory mite reproduction, offering a theoretical foundation for understanding their evolution and reproductive strategies.
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RNA 干扰介导的捕食螨 Neoseiulus californicus 体内卵黄素和卵黄素受体的功能分析
加利福尼亚新薮蛛是蜘蛛螨和小型节肢动物害虫的主要天敌。虽然卵黄原素(Vg)和卵黄原素受体(VgR)基因是蜘蛛螨和蜱卵母细胞成熟、卵形成和胚胎发育的重要调节因子,但它们在植食螨中的作用却鲜为人知。研究捕食螨的繁殖机制对于了解它们的繁殖和进化至关重要。在这项研究中,发现、克隆并鉴定了加利福尼亚螨(N. californicus)的三个 Vg 基因和一个 VgR 基因。Vg1、Vg2、Vg3和VgR mRNA长分别为6066、5728、4515和5331 bp,编码的蛋白质分别包含1851、1849、1471和1722个氨基酸。时间表达分析表明,受精雌成螨的 Vg1、Vg2 和 VgR 水平升高,而 Vg3 则在发育阶段达到表达峰值。RNA 干扰介导的 Vg1 和 Vg2 抑制分别导致受精率下降 14.66% 和 11.59%。Vg1 的沉默显著降低了卵孵化率和雌性后代比例。相比之下,Vg3 和 VgR 的沉默对繁殖力和卵孵化率没有显著影响。这些发现深入揭示了Vg和VgR在捕食螨繁殖过程中的调控作用,为理解捕食螨的进化和繁殖策略提供了理论基础。
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来源期刊
CiteScore
2.20
自引率
33.30%
发文量
152
期刊介绍: Systematic and Applied Acarology (SAA) is an international journal of the Systematic and Applied Acarology Society (SAAS). The journal is intended as a publication outlet for all acarologists in the world. There is no page charge for publishing in SAA. If the authors have funds to publish, they can pay US$20 per page to enable their papers published for open access. SAA publishes papers reporting results of original research on any aspects of mites and ticks. Due to the recent increase in submissions, SAA editors will be more selective in manuscript evaluation: (1) encouraging more high quality non-taxonomic papers to address the balance between taxonomic and non-taxonomic papers, and (2) discouraging single species description (see new special issues for single new species description) while giving priority to high quality systematic papers on comparative treatments and revisions of multiple taxa. In addition to review papers and research articles (over 4 printed pages), we welcome short correspondence (up to 4 printed pages) for condensed version of short papers, comments on other papers, data papers (with one table or figure) and short reviews or opinion pieces. The correspondence format will save space by omitting the abstract, key words, and major headings such as Introduction.
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