Department of Plant Medicals, Andong National University, Andong 36729, Korea.
Department of Plant Medicals, Andong National University, Andong 36729, Korea
J Exp Biol. 2020 Nov 4;223(Pt 21):jeb233221. doi: 10.1242/jeb.233221.
Several prostaglandins (PGs) and PG-synthesizing enzymes have been identified from insects. PGs mediate cellular and humoral immune responses. However, uncontrolled and prolonged immune responses might have adverse effects on survival. PG catabolism in insects has not been reported. Here, using a transcriptomic analysis, we predicted the presence of two PG-degrading enzymes, () and (), in , a lepidopteran insect. and expression levels were upregulated after immune challenge. However, their expression peaks occurred after those of PG biosynthesis genes, such as those encoding PGE synthase or PGD synthase. and expression levels were upregulated after injection with PGE or PGD In contrast, such upregulated expression was not detected after injection with leukotriene B, an eicosanoid inflammatory mediator. RNA interference (RNAi) using double-stranded RNAs specific to or suppressed their expression levels. The RNAi treatment resulted in an excessive and fatal melanization of larvae even after a non-pathogenic bacterial infection. Phenoloxidase (PO) activity mediating the melanization in larval plasma was induced by bacterial challenge or PGE injection. Although the induced PO activity decreased after 8 h in control larvae, those treated with dsRNAs specific to PG-degrading enzyme genes kept a high PO activity for a longer period. These results suggest that SePGDH and SePGR are responsible for PG degradation at a late phase of the immune response.
已经从昆虫中鉴定出几种前列腺素 (PG) 和 PG 合成酶。PG 介导细胞和体液免疫反应。然而,不受控制和延长的免疫反应可能对生存产生不利影响。昆虫中 PG 的分解代谢尚未报道。在这里,我们使用转录组分析预测了鳞翅目昆虫 中两种 PG 降解酶 () 和 () 的存在。在免疫挑战后, 和 表达水平上调。然而,它们的表达峰值出现在 PG 生物合成基因(如 PGE 合酶或 PGD 合酶)之后。用 PGE 或 PGD 注射后, 和 表达水平上调。相比之下,用花生四烯酸的炎症介质白三烯 B 注射后,没有检测到这种上调表达。针对 或 的双链 RNA (dsRNA) 的 RNAi 处理抑制了它们的表达水平。RNAi 处理导致幼虫过度和致命的黑化,即使在非致病性细菌感染后也是如此。幼虫血浆中介导黑化的酚氧化酶 (PO) 活性被细菌挑战或 PGE 注射诱导。尽管对照幼虫中的诱导 PO 活性在 8 小时后下降,但用针对 PG 降解酶基因的 dsRNA 处理的幼虫保持高 PO 活性的时间更长。这些结果表明,SePGDH 和 SePGR 负责免疫反应后期的 PG 降解。