Eiger pleiotropically regulates the immunity of Ostrinia furnacalis larvae

生物 玉米螟 黄色微球菌 免疫系统 先天免疫系统 MAPK/ERK通路 肿瘤坏死因子α 微生物学 信号转导 基因表达 细胞生物学 分子生物学 基因 幼虫 免疫学 大肠杆菌 生物化学 植物
作者
Honglun Bi,Wenlong Guo,Shiqi Lu,He Zhang,Yulin Liu,Qin Lu,Mengyao Dong,Shuzhong Li,Congjing Feng
出处
期刊:Insect Science [Wiley]
标识
DOI:10.1111/1744-7917.70108
摘要

Abstract The tumor necrosis factor (TNF) receptor superfamily is a set of essential inflammatory cytokines. In Drosophila , as a homolog of TNF, Eiger was first identified, which is involved in innate immunity signaling pathways. However, in Lepidoptera, the functions of Eiger and its molecular regulatory mechanisms on immune responses are unknown. In this study, Eiger was cloned from Ostrinia furnacalis . OfEiger has a conserved structural domain of the TNF family. The expression of OfEiger increased with the age of O. furnacalis larvae, and was the highest in the hemocytes. After O. furnacalis larvae were injected with Pseudomonas aeruginosa or Micrococcus luteus , the expression of OfEiger was significantly upregulated. The expression levels of several genes in the immune pathways of O. furnacalis larvae were downregulated at 60 h post‐injection of double‐stranded Eiger (ds Eiger ), including IMD, Toll, nitric oxide (NO), and mitogen‐activated protein kinase (MAPK) signaling pathways. Moreover, the expression levels of the 4 antimicrobial peptides (AMPs), OfLebocin , OfAttacin , OfGloverin , and OfMoricin , were downregulated. In addition, the phagocytosis of Escherichia coli by hemocytes was reduced in O. furnacalis larvae after ds Eiger injection. Injections of P. aeruginosa or M. luteus into O. furnacalis larvae following OfEiger RNA interference reduced the larvae's survival rate and increased the expression levels of OfMyD88 and OfJNK . Still, they suppressed the expression of OfNOS 1 and AMP genes and inhibited phenoloxidase (PO) activity in O. furnacalis larvae. In conclusion, OfEiger is a vital insect immune regulator, which synergistically regulates IMD, Toll, NO, and MAPK signaling pathways and adjusts PO activity, cellular immunity, AMPs, and other effectors.
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