| 注册
首页|期刊导航|昆虫学报|基于微滴式数字PCR技术多重精准检测鉴定三种常见检疫性粉蚧

基于微滴式数字PCR技术多重精准检测鉴定三种常见检疫性粉蚧

李鑫 李辉 李立梅 杨力凤 孟凡泽 褚栋 付海滨

昆虫学报2026,Vol.69Issue(2):255-265,11.
昆虫学报2026,Vol.69Issue(2):255-265,11.DOI:10.16380/j.kcxb.2026.02.010

基于微滴式数字PCR技术多重精准检测鉴定三种常见检疫性粉蚧

Droplet digital PCR for the multiplex and precise identification of three common quarantine mealybug species(Hemiptera:Pseudococcidae)

李鑫 1李辉 2李立梅 3杨力凤 4孟凡泽 5褚栋 4付海滨6

作者信息

  • 1. 大连海关技术中心,大连 116000
  • 2. 东港海关综合技术服务中心,丹东 118300
  • 3. 吉林省林业科学研究院,长春 130000
  • 4. 青岛农业大学植物医学学院,青岛 266109
  • 5. University of Minnesoda,Twin Cities,Twin 55455,Unites States of America
  • 6. 沈阳海关技术中心,沈阳 110000
  • 折叠

摘要

Abstract

[Aim]To apply the droplet digital PCR(ddPCR)technology to establish a multiplex and precise detection method for three quarantine mealybug species,Planococcus minor,Pl.lilacinus and Paracoccus marginatus intercepted at high frequency.[Methods]Using common mealybug species Pl.minor,Pl.lilacinu,Pa.marginatus,Dysmicoccus neobrevipes,Pseudococcus jackbeardsleyi,Maconellicoccus hirsutus,Ps.comstocki and Pl.citri intercepted at ports and collected domestically as test insects,the CO I gene sequence was used as the target.Homology alignment and design of specific primers and probes were performed using the GenBank database,MEGA11 and Beacon Designer 8.Based on the single ddPCR detection system of the three mealybug species Pl.minor,Pl.lilacinus and Pa.marginatus,the reaction system was optimized by screening the optimal concentrations of primers and probes,thereby establishing a multiplex ddPCR method for the rapid and absolute quantitative detection of the genomic copy numbers of Pl.minor,Pl.lilacinus and Pa.marginatus in the same reaction system,and compared with TaqMan qPCR method to determine the sensitivity,quantification limit and accuracy of this method.[Results]All sets of primers and probes could amplify the genomes of target mealybugs in the multiplex ddPCR detection system without cross-reactivity,and the lowest DNA concentration detected was consistent with that of TaqMan qPCR.The lower limit of absolute quantification of this nultiplex ddPCR detection system for the genomic detection of Pl.minor was 0.44 copies/μL,that for the genomic detection of Pl.lilacinus was 0.43 copies/μL,and that for the genomic detection of Pa.marginatus was 0.44 copies/μL.The linear coefficients of determination R2 for the quantitative assay of this nultiplex ddPCR detection system were all greater than 0.99 within the range of quantification,and the reproducibility and linear correlation were good.[Conclusion]The multiplex ddPCR detection method established in this study can realize the rapid and precise identification of three quarantine mealybug species Pl.minor,Pl.lilacinus and Pa.marginatus intercepted at high frequency,and provide technical service and support for the prevention and control of foreign pests at ports and the protection of China's ecological security.

关键词

大洋臀纹粉蚧/南洋臀纹粉蚧/木瓜秀粉蚧/分子鉴定/分子标记/微滴式数字PCR

Key words

Planococcus minor/Planococcus lilacinus/Paracoccus marginatus/molecular identification/molecular marker/droplet digital PCR

分类

生物科学

引用本文复制引用

李鑫,李辉,李立梅,杨力凤,孟凡泽,褚栋,付海滨..基于微滴式数字PCR技术多重精准检测鉴定三种常见检疫性粉蚧[J].昆虫学报,2026,69(2):255-265,11.

基金项目

国家"十四五"重点研发计划项目(2021YFD1400100) (2021YFD1400100)

海关总署科研项目(2024HK175,2023HK083) (2024HK175,2023HK083)

昆虫学报

0454-6296

访问量0
|
下载量0
段落导航相关论文