College of Life Sciences, Anhui Agricultural University, Hefei 230036, China.
Protein Pept Lett. 2020;27(10):953-961. doi: 10.2174/0929866527666200505210113.
Antibacterial peptides play important roles in the innate immune system of insects and are divided into four categories according to their structures. Although many antibacterial peptides have been reported in lepidopteran insects, the roles of an attacin-like gene in immune response of Antheraea pernyi remain unclear.
In this study, the cloning and immunological functions of an attacin-like gene from Antheraea pernyi were investigated.
The open reading frame of Ap-attacin-like gene was cloned by PCR using the specific primers and then was ligated to the pET-32a vector to construct the recombinant plasmids Ap-attacin- like-pET-32a. The recombinant Ap-attacin-like protein was expressed in E. coli (BL21 DE3) cells and purified by Ni-NTA affinity chromatography. The expression patterns of Ap-attacin-like in different tissues or under microorganism challenges were investigated by real-time PCR and western blotting. Finally, agar well diffusion assay was performed to determine the antimicrobial activity of the recombinant Ap-attacin-like proteins based on the inhibition rate.
The expression level of Ap-attacin-like was highest in the fat body compared with the other examined tissues. The expression of Ap-attacin-like in the fat body was significantly elevated after E. coli, Beauveria bassiana, Micrococcus luteus or Nuclear Polyhedrosis Virus challenges. In addition, the recombinant Ap-attacin-like proteins had obvious antibacterial activity against E. coli.
Ap-attacin-like was highly expressed in immune-related tissues and its expression level was significantly induced by different microorganism challenges, suggesting that Ap-attacin-like participated in the innate immunity of A. pernyi.
抗菌肽在昆虫的先天免疫系统中发挥着重要作用,根据其结构可分为四类。尽管鳞翅目昆虫中已报道了许多抗菌肽,但在野蚕(Antheraea pernyi)中,抗菌肽基因在免疫反应中的作用仍不清楚。
本研究旨在克隆野蚕抗菌肽基因,并探讨其免疫功能。
采用特异性引物通过 PCR 克隆 Ap-attacin-like 基因的开放阅读框,然后将其连接到 pET-32a 载体上,构建重组质粒 Ap-attacin-like-pET-32a。将重组 Ap-attacin-like 蛋白在大肠杆菌(BL21 DE3)细胞中表达,并通过 Ni-NTA 亲和层析进行纯化。通过实时 PCR 和 Western blot 检测 Ap-attacin-like 在不同组织或在微生物挑战下的表达模式。最后,根据抑菌率测定重组 Ap-attacin-like 蛋白的抗菌活性。
与其他检测组织相比,Ap-attacin-like 在脂肪体中的表达水平最高。在大肠杆菌、金龟子绿僵菌、微球菌或核型多角体病毒挑战后,脂肪体中的 Ap-attacin-like 表达显著上调。此外,重组 Ap-attacin-like 蛋白对大肠杆菌具有明显的抗菌活性。
Ap-attacin-like 在免疫相关组织中高度表达,其表达水平在受到不同微生物挑战后显著诱导,表明 Ap-attacin-like 参与了野蚕的先天免疫反应。