北方农业学报 ›› 2026, Vol. 54 ›› Issue (3): 23-36.doi: 10.12190/j.issn.2096-1197.2026.03.03

• 作物遗传育种·分子生物学 • 上一篇    下一篇

斜纹夜蛾SlGNBP2基因的克隆及诱导表达分析

徐英杰1, 许小霞2, 金丰良2   

  1. 1.宁城县设施农业技术服务中心,内蒙古 宁城 024200;
    2.华南农业大学 植物保护学院/绿色农药全国重点实验室,广东 广州 510642
  • 收稿日期:2025-12-08 出版日期:2026-06-20 发布日期:2026-08-11
  • 通讯作者: 金丰良(1973—),男,教授,博士,主要从事害虫与植物/微生物互作及协同进化(昆虫免疫与病原物的互作机制)方面的研究工作。
  • 作者简介:徐英杰(1986—),女,经济师,硕士,主要从事设施蔬菜病虫害防治方面的研究工作。
  • 基金资助:
    国家自然科学基金项目(31972345); 有害生物控制与资源利用国家重点实验室基金项目(SKLBC16KF05)

Cloning and induced expression analysis of the SlGNBP2 gene in Spodoptera litura

XU Yingjie1, XU Xiaoxia2, JIN Fengliang2   

  1. 1. Facility Agriculture Technology Service Center of Ningcheng County,Ningcheng 024200,China;
    2. College of Plant Protection/State Key Laboratory of Green Pesticide,South China Agricultural University,Guangzhou 510642,China
  • Received:2025-12-08 Online:2026-06-20 Published:2026-08-11

摘要: 【目的】揭示斜纹夜蛾SlGNBP2基因在免疫应答病原微生物中的作用模式。【方法】通过同源克隆和cDNA末端快速扩增(RACE)技术获得SlGNBP2全长cDNA序列,利用生物信息学软件对其结构和进化特性进行分析,采用实时荧光定量PCR(qRT-PCR)对斜纹夜蛾不同发育历期、组织及病原微生物诱导后SlGNBP2的mRNA相对表达水平进行检测。【结果】克隆获得的SlGNBP2基因全长1 731 bp,开放阅读框(ORF)1 431 bp,编码476个氨基酸。生物信息学分析结果显示,预测蛋白具有GNBPs家族保守的糖苷水解酶活性结构域(Glyco_hydro_16)。同源性分析结果表明,斜纹夜蛾SlGNBP2与其他鳞翅目昆虫GNBP2的保守结构域高度相似,可能具有相同的功能,与粉纹夜蛾(Trichoplusia niTnGNBP2序列相似度最高,相似度为56%;系统进化树显示,SlGNBP2与粉纹夜蛾、烟草天蛾(Manduca sexta)、小菜蛾(Plutella xylostella)等鳞翅目昆虫高度同源,处于同一进化分支,其中与粉纹夜蛾TnGNBP2亲缘关系最近,二者聚为一支。qRT-PCR结果显示,斜纹夜蛾不同发育历期均检测到SlGNBP2基因表达,相对表达水平最高的是4龄幼虫,与卵的相对表达水平相比,其表达上调64.67倍;SlGNBP2基因在4龄幼虫的血细胞、脂肪体、中肠、表皮、头部和马氏管中均有表达,其中主要表达部位是中肠和脂肪体,与头部的相对表达水平相比,分别表达上调12.74倍和11.89倍。病原微生物诱导结果显示,SlGNBP2可被革兰氏阳性菌、革兰氏阴性菌和真菌诱导表达上调,其中,与对照相比,革兰氏阳性菌苏云金芽孢杆菌诱导24 h后SlGNBP2在脂肪体中表达上调14.47倍。【结论】SlGNBP2对革兰氏阳性菌苏云金芽孢杆菌的诱导最敏感,在斜纹夜蛾免疫防御病原微生物过程中发挥了重要的模式识别作用。

关键词: 斜纹夜蛾, SlGNBP2基因, 革兰氏阴性菌结合蛋白, 病原微生物诱导, 组织表达

Abstract: 【Objective】To reveal the action pattern of the SlGNBP2 gene in the immune response of Spodoptera litura against pathogenic microorganisms.【Methods】The full-length cDNA sequence of SlGNBP2 was obtained by homologous cloning and rapid amplification of cDNA ends (RACE). The structure and evolutionary characteristics of SlGNBP2 were analyzed using bioinformatics software. The relative mRNA expression levels of SlGNBP2 at different developmental stages,in various tissues,and after induction by pathogenic microorganisms in S. litura were detected by quantitative real-time PCR (qRT-PCR).【Results】The cloned SlGNBP2 gene was 1 731 bp in full-length,with an open reading frame (ORF) of 1 431 bp,encoding 476 amino acids. The results of bioinformatics analysis showed that the predicted protein had a conserved glycoside hydrolase domain (Glyco_hydro_16) of the GNBPs family. The results of homology analysis showed that the conserved domain of SlGNBP2 showed high similarity to those of GNBP2 from other Lepidoptera insects,and was likely to possess similar functions. The sequence similarity between SlGNBP2 and TnGNBP2 of Trichoplusia ni was the highest,with a similarity of 56%. The phylogenetic tree indicated that SlGNBP2 was highly homologous to Lepidoptera insects such as T. ni,Manduca sexta and Plutella xylostella,and was in the same evolutionary branch. Among them,SlGNBP2 showed the closest relationship with TnGNBP2 of T. ni,and the two were clustered into one branch. The results of qRT-PCR showed that the expression of the SlGNBP2 gene was detected at different developmental stages of S. litura,and the highest relative expression level was the 4th instar larvae,which was 64.67 times higher than the relative expression level of eggs. The SlGNBP2 gene was expressed in the hemocytes,fat body,midgut,epidermis,head and malpighian tubules of the 4th instar larvae,with predominant expression in the midgut and fat body,which were up-regulated by 12.74-fold and 11.89-fold compared with the relative expression level of the head. The results of pathogenic microorganism induction showed that SlGNBP2 could be up-regulated by Gram-positive bacteria,Gram-negative bacteria and fungi. Among them,compared with the control,the expression of SlGNBP2 in fat body was up-regulated by 14.47-fold after induction by Gram-positive bacteria Bacillus thuringiensis for 24 h.【Conclusion】SlGNBP2 is most sensitive to the induction of Gram-positive bacteria B. thuringiensis,and plays an important role in pattern recognition in the process of immune defense against pathogenic microorganisms in S. litura.

Key words: Spodoptera litura, SlGNBP2 gene, Gram-negative bacteria binding protein, Induction of pathogenic microorganisms, Tissue expression

中图分类号: 

  • S433.4