Park Youngjin, Kim Yonggyun
School of Bioresource Sciences, College of Natural Sciences, Andong National University, Andong, Korea.
Arch Insect Biochem Physiol. 2003 Nov;54(3):134-42. doi: 10.1002/arch.10108.
Xenorhabdus nematophilus is a Gram-negative symbiotic bacterium of the entomopathogenic nematode, Steinernema carpocapsae. The bacteria delivered into the insect hemocoel by the nematodes cause immunodepression of the target insects to protect host nematodes and themselves from the cellular immune reaction. Previous reports suggest that the immunodepression is caused by inhibition of the eicosanoid pathway that is known to be critically important to mediate cellular immunity. This study focused on the inhibitory effect of X. nematophilus on PLA2 activity of Spodoptera exigua. The PLA2 activity was functionally associated with the activation cascade of prophenoloxidase (pPO). Dexamethasone (DEX), a specific PLA2 inhibitor, inhibited pPO activation completely at the higher doses of approximately 2.4 muM in vitro condition. The inhibitory effect of DEX was reversed by the addition of arachidonic acid, the catalytic product of PLA2. By means of this in vitro PLA2 inhibitor assay system, two different PLA2 inhibitors were used to compare their inhibitory effects on the hemolymph PLA2 of S. exigua. p-Bromophenacyl bromide (BPB), a specific inhibitor of secretory PLA2 (sPLA2), significantly inhibited pPO activation, but methylarachidonyl fluorophosphates (MAFP), a specific inhibitor of cytosolic PLA2 (cPLA2), did not show any inhibitory effect. BPB also inhibited pPO activation of the plasma, though much higher PO activation and its inhibition by BPB was found in the hemocytes. Growth medium of X. nematophilus at the stationary phase had a PLA2 inhibitory effect. Via the in vitro PLA2 inhibitor assay, it was shown that the ethyl ether extract of the medium contained significant PLA2 inhibitor activity. These results indicate that X. nematophilus produces and secretes PLA2 inhibitor, which acts on BPB-susceptible PLA2 of S. exigua.
嗜线虫致病杆菌是昆虫病原线虫小卷蛾斯氏线虫的革兰氏阴性共生菌。线虫将细菌传递到昆虫血腔中,导致靶标昆虫免疫抑制,以保护宿主线虫及其自身免受细胞免疫反应的影响。先前的报道表明,免疫抑制是由类花生酸途径的抑制引起的,已知该途径对介导细胞免疫至关重要。本研究聚焦于嗜线虫致病杆菌对甜菜夜蛾磷脂酶A2(PLA2)活性的抑制作用。PLA2活性与前酚氧化酶(pPO)的激活级联功能相关。地塞米松(DEX)是一种特异性PLA2抑制剂,在体外条件下,约2.4 μM的较高剂量可完全抑制pPO激活。添加PLA2的催化产物花生四烯酸可逆转DEX的抑制作用。通过这种体外PLA2抑制剂检测系统,使用两种不同的PLA2抑制剂比较它们对甜菜夜蛾血淋巴PLA2的抑制作用。分泌型PLA2(sPLA2)的特异性抑制剂对溴苯甲酰溴(BPB)显著抑制pPO激活,但胞质型PLA2(cPLA2)的特异性抑制剂氟磷酸甲酯(MAFP)未显示任何抑制作用。BPB也抑制血浆中的pPO激活,尽管在血细胞中发现了更高的PO激活及其被BPB的抑制作用。嗜线虫致病杆菌稳定期的生长培养基具有PLA2抑制作用。通过体外PLA2抑制剂检测表明,培养基的乙醚提取物具有显著的PLA2抑制剂活性。这些结果表明,嗜线虫致病杆菌产生并分泌PLA2抑制剂,其作用于甜菜夜蛾对BPB敏感的PLA2。