Department of Bioresource Sciences, Andong National University, Andong 760-749, Republic of Korea.
J Invertebr Pathol. 2011 Feb;106(2):217-22. doi: 10.1016/j.jip.2010.09.023. Epub 2010 Oct 16.
Apolipophorin III (ApoLpIII) has been known to play critical roles in lipid transport and immune activation in insects. This study reports a partial ApoLpIII gene cloned from the diamondback moth, Plutella xylostella. It showed that the gene was expressed in all developmental stages of P. xylostella. In larval stage, it was expressed in all tested tissues of hemocyte, fat body, gut, and epidermis. In response to bacterial challenge, the larvae showed an enhanced level of ApoLpIII expression by a quantitative real-time RT-PCR. RNA interference of ApoLpIII by its specific double stranded RNA (dsRNA) caused significant knockdown of its expression level and resulted in significant suppression in hemocyte nodule formation in response to bacterial challenge. However, larvae treated with the dsRNA exhibited a significant recovery in the cellular immune response by addition of a recombinant ApoLpIII. Parasitization by an endoparasitoid wasp, Cotesia plutellae, suppressed expression of ApoLpIII and resulted in a significant suppression in the hemocyte nodule formation. The addition of the recombinant ApoLpIII to the parasitized larvae significantly restored the hemocyte activity. Infection of an entomopathogenic bacterium, Xenorhabdus nematophila, caused potent pathogenicity of P. xylostella. However, the addition of the recombinant ApoLpIII to the infected larvae significantly prevented the lethal pathogenicity. This study suggests that ApoLpIII limits pathogenicity induced by parasitization or bacterial infection in P. xylostella.
载脂蛋白 LpIII(ApoLpIII)在昆虫的脂质运输和免疫激活中起着关键作用。本研究从小菜蛾中克隆了一个载脂蛋白 LpIII 的部分基因。结果表明,该基因在小菜蛾的所有发育阶段都有表达。在幼虫期,它在血细胞、脂肪体、肠道和表皮的所有测试组织中都有表达。在受到细菌挑战时,幼虫通过定量实时 RT-PCR 显示出 ApoLpIII 表达水平的增强。用其特异性双链 RNA(dsRNA)对 ApoLpIII 进行 RNA 干扰会导致其表达水平的显著下调,并导致对细菌挑战时血细胞结节形成的显著抑制。然而,用 dsRNA 处理的幼虫通过添加重组 ApoLpIII 显著恢复了细胞免疫反应。内寄生蜂 Cotesia plutellae 的寄生会抑制 ApoLpIII 的表达,导致血细胞结节形成的显著抑制。向被寄生的幼虫中添加重组 ApoLpIII 可显著恢复血细胞的活性。昆虫病原细菌 Xenorhabdus nematophila 的感染会导致小菜蛾产生强烈的致病性。然而,向受感染的幼虫中添加重组 ApoLpIII 可显著防止致命的致病性。本研究表明,ApoLpIII 限制了小菜蛾寄生或细菌感染引起的致病性。