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中国生物防治学报 ›› 2026, Vol. 42 ›› Issue (1): 208-217.DOI: 10.16409/j.cnki.2095-039x.2025.09.014

• 研究论文 • 上一篇    

一株侵染斜纹夜蛾的核型多角体病毒的分离鉴定及毒力分析

杨光源1,3, 张轲1, 王广1, 蔡浩升1, 李政宾1, 谢永辉2, 茶陈文3, 顾小飞2, 陈斌1   

  1. 1. 云南农业大学植物保护学院/云南生物资源保护与利用国家重点实验室, 昆明 650201;
    2. 云南省烟草公司昆明市公司, 昆明 650051;
    3. 云南省烟草公司永平县分公司, 永平 672699
  • 收稿日期:2025-01-03 发布日期:2026-02-11
  • 通讯作者: 陈斌, 顾小飞
  • 基金资助:
    云南省昆明市烟草公司科技计划项目(KMYC202402);云南省科技计划项目重点专项(202401AS070089);云南省教育厅科技创新团队项目(2022-69)

Isolation, Identification and Virulence Analysis of a Nucleopolyhedrovirus Infecting Spodoptera litura

YANG Guangyuan1,3, ZHANG Ke1, WANG Guang1, CAI Haosheng1, LI Zhengbin1, XIE Yonghui2, CHA Chenwen3, GU Xiaofei2, CHEN Bin1   

  1. 1. State Key Laboratory for Conservation and Utilization of Bio-Resources in Yunnan/College of Plant Protection, Yunnan Agricultural University, Kunming 650201, China;
    2. Yunnan Tobacco Co., Ltd of Kunming Branch, Kunming 650051, China;
    3. Dali Tobacco Co., Ltd. Yongping Branch, Yongping 672699, China
  • Received:2025-01-03 Published:2026-02-11

摘要: 从云南省大理州湾桥镇烟田采集的自然罹病死亡的疑似被病毒感染的斜纹夜蛾幼虫,对体内病原物进行富集分离,通过形态学观察、分子鉴定及系统发育分析对该病原种类进行了鉴定,并采用含有病毒的人工饲料饲喂法生物测定了该病原物在斜纹夜蛾体内的复制特征和对3龄斜纹夜蛾幼虫的毒力。结果表明,罹病斜纹夜蛾幼虫体的病原为斜纹夜蛾核型多角体病毒(Spodoptera litura Nucleopolyhedrovirus),编号为SpltMNPV-DL01。该病毒毒株可在斜纹夜蛾幼虫体内迅速复制,当1.0×106 PIB/mL病毒饲喂斜纹夜蛾3龄幼虫5 d后,体内SpltMNPV-DL01基因组拷贝数多达8.85×106拷贝数/μL。用1.0×104、1.0×105、1.0×106、1.0×107和1.0×108 PIB/mL核型多角体病毒悬浮液饲喂斜纹夜蛾3龄幼虫,LT50分别为7.3 d、7.0 d、6.3 d、5.2 d和4.8 d,毒力回归方程分别为Y= -3.452+0.474XY= -3.551+0.508XY= -3.314+0.524XY= -3.043+0.560XY= -2.722+0.573X,处理后第5、6和7 d的LC50分别是107.806、106.285和104.700 PIB/mL,第8 d时,斜纹夜蛾3龄幼虫的累计死亡率分别为72.22%、75.60%、84.72%、91.67%和98.61%。该研究将丰富斜纹夜蛾核型多角体病毒毒株资源,毒株SpltMNPV-DL01能够有效侵染斜纹夜蛾幼虫并将其致死,可作为优良菌株用于防治斜纹夜蛾生物农药的进一步研发。

关键词: 斜纹夜蛾, 核型多角体病毒, 毒力测定, 生物防治

Abstract: This study enriched and isolated the pathogens from the dead Spodoptera litura larvae collected from the tobacco fields in Wanqiao Town, Dali Prefecture, Yunnan Province. Through morphological observation, molecular identification, and phylogenetic analysis, the pathogen species was identified. The droplet-feeding method was used to determine the replication characteristics of the pathogen in S. litura and its virulence to the 3rd instar S. litura larvae. The results showed that the pathogen of the diseased S. litura larvae was S. litura nucleopolyhedrovirus, named SpltMNPV-DL01. This virus strain can replicate rapidly in the larvae of S. litura. When the 3rd instar S. litura larvae were infected with 1.0×106 PIB/mL virus for 5 days, the genomic copy number of SpltMNPV-DL01 in the body was as many as 8.85× 106 copies/μL. When the 3rd instar S. litura larvae were inoculated with 1.0× 104, 1.0 ×105, 1.0×106, 1.0×107, and 1.0× 108 PIB/mL nucleopolyhedrovirus, the LT50 values were 7.3 d, 7.0 d, 6.3 d, 5.2 d, and 4.8 d, respectively. The corresponding virulence regression equations were Y=-3.452+0.474X, Y= -3.551+0.508X, Y= -3.314+0.524X, Y= -3.043+0.560X, and Y= -2.722+0.573X, respectively. The LC50 on the 5th, 6th, and 7th days of treatment were 107.806, 106.285, and 104.700 PIB/mL, respectively. On the 8th day, the cumulative mortality rates of the 3rd instar S. litura larvae were 72.22%, 75.60%, 84.72%, 91.67%, and 98.61%, respectively. The results provide prospective for the application and development of S. litura nucleopolyhedrovirus.

Key words: Spodoptera litura, nuclear polyhedrosis virus, virulence determination, biological control

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