高级检索

    舞毒蛾V-ATPaseA基因dsRNA原核表达及其对生长发育的影响

    Prokaryotic-expressed V-ATPaseA dsRNA and its effects on growth and development in Lymantria dispar

    • 摘要:
      目的 探究舞毒蛾液泡型H+-ATP酶V-ATPaseA基因对蜕皮、生殖和生长发育等生理活动的影响,评估其作为舞毒蛾RNA干扰(RNAi)绿色防控靶标的潜力,为鳞翅目害虫新型生物农药开发提供参考。
      方法 首先,克隆舞毒蛾V-ATPaseA基因开放阅读框(ORF)序列,利用qRT-PCR分析舞毒蛾不同发育时期及组织中V-ATPaseA基因的表达特征。随后,构建LdV-ATPaseA基因原核表达载体,并转化至HT115(DE3)菌株,经IPTG诱导后制备表达dsRNA的菌液,连续饲喂舞毒蛾2龄和3龄幼虫。试验统计取食量、体重、体重累计增长率、死亡率、化蛹率、蛹质量、产卵量和发育历期等指标。
      结果 结果显示,LdV-ATPaseA基因在舞毒蛾整个生命周期中持续表达,且表达水平呈组织特异性,其中精巢表达量最高(为对照脂肪体的30.80倍),其次为卵巢(12.82倍)和表皮(9.66倍)。对舞毒蛾2龄和3龄幼虫连续饲喂添加表达dsLdV-ATPaseA菌液的人工饲料均可显著沉默靶标基因,导致3龄 ~ 5龄幼虫取食量、体重、体重累计增长率显著降低,幼虫累计死亡率显著增加,雌蛹质量显著降低;此外,对舞毒蛾2龄幼虫连续饲喂添加表达dsLdV-ATPaseA菌液的人工饲料可导致2龄 ~ 6龄幼虫及蛹期发育历期显著延长,化蛹率显著降低,蛹期畸形率显著升高,雌成虫产卵量显著降低。
      结论 V-ATPaseA基因显著干扰舞毒蛾蜕皮、生殖及生长发育,表现为取食减少、生长受阻、死亡率升高、发育延迟、蛹畸形增加及繁殖力下降。因此,LdV-ATPaseA基因可作为RNAi介导绿色防控的理想靶点,本研究为鳞翅目害虫生物农药的研发提供了新的理论依据。

       

      Abstract:
      Objective The objective of this study was to thoroughly investigate how the LdV-ATPaseA gene affects various physiological activities of Lymantria dispar, including molting, reproduction, growth, and development. Furthermore, we evaluated its potential as a green control target for Lymantria dispar RNA interference (RNAi) and provide reference for the development of new biopesticides for L. dispar.
      Method The ORF sequence of V-ATPase was successfully cloned, and quantitative reverse transcription PCR (qRT-PCR) was used to measure gene expression levels across various developmental stages and tissues in L. dispar. Additionally, an in vitro prokaryotic expression system was developed to produce dsRNA targeting the LdV-ATPaseA gene, continuous feeding of 2nd and 3rd instar larvae of L. dispar. Subsequently, we conducted experimental statistics on indicators such as food intake, body mass, cumulative mass gain rate, mortality rate, pupation rate, pupal mass, egg production, and developmental duration.
      Result The LdV-ATPaseA gene showed consistent expression levels across all developmental phases of L. dispar, with distinct tissue specific expression levels. The highest expression level was detected in the tests, with 30.80-fold of that in the control fat body. This was followed by ovary and epidermis, with 12.82-fold and 9.66-fold of that in the fat body, respectively. The recombinant expression of LdV-ATPaseA vector was successfully constructed to generate dsRNA which specifically induces V-ATPaseA gene silencing. Moreover, the dsRNA ingested by 2nd and 3rd instar L. dispar resulted in decreased food intake, reduced larval mass, decreased larval growth rate, decreased pupal mass of females and increased mortality. Additionally, the dsRNA ingested by 2nd instar L. dispar resulted larval and pupal life span was significantly longer, increased the pupal malformation rate, and reduced the pupation and egg production in female adults.
      Conclusion The LdV-ATPaseA plays a crucial role in the molting, reproduction, growth, and development of L. dispar. These findings highlight its potential as an RNAi-based green control target and offer valuable insights for developing biopesticides against Lepidoptera pests.

       

    /

    返回文章
    返回