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基于vp19基因检测克氏原螯虾WSSV高灵敏度一步式PCR方法的建立

陈楠 罗小红 廖明聪 胡瑞雪 李丹 顾泽茂

中国水产科学2025,Vol.32Issue(5):689-699,11.
中国水产科学2025,Vol.32Issue(5):689-699,11.DOI:10.12264/JFSC2024-0306

基于vp19基因检测克氏原螯虾WSSV高灵敏度一步式PCR方法的建立

Establishment of a highly sensitive one-step PCR assay for detecting white spot syndrome virus(WSSV)in Procambarus clarkii based on the vp19 gene

陈楠 1罗小红 2廖明聪 2胡瑞雪 2李丹 1顾泽茂2

作者信息

  • 1. 华中农业大学水产学院/双水双绿研究院,湖北武汉 430070||农业农村部水生动物疫病专业实验室(华中农业大学),湖北武汉 430070||湖北省水生动物病害防控工程技术研究中心,湖北武汉 430070||长江经济带大宗水生生物产业绿色发展教育部工程研究中心,湖北武汉 430070
  • 2. 华中农业大学水产学院/双水双绿研究院,湖北武汉 430070||湖北洪山实验室,湖北武汉 430070||农业农村部水生动物疫病专业实验室(华中农业大学),湖北武汉 430070||湖北省水生动物病害防控工程技术研究中心,湖北武汉 430070||长江经济带大宗水生生物产业绿色发展教育部工程研究中心,湖北武汉 430070
  • 折叠

摘要

Abstract

White spot syndrome virus(WSSV)poses a significant threat to red swamp crayfish(Procambarus clarkii)aquaculture,a major crustacean industry in China.This virus' ability to remain latent in hosts and its complex transmission pathways make prevention and early detection crucial.However,current diagnostic methods,including the WOAH-recommended nested PCR,have limitations in speed,sensitivity,and convenience.This study aimed to develop a rapid,sensitive,and specific one-step conventional PCR assay for WSSV detection in P.clarkii,addressing the need for improved surveillance and early intervention strategies.In our study,specific primers(V1)were designed to target a 196 bp region within the WSSV vp19 gene.The assay's analytical specificity was rigorously evaluated using DNA/cDNA from 10 different pathogens in crayfish(5 viruses and 5 bacteria).To determine analytical sensitivity,serial dilutions of a recombinant plasmid(pMD19T-Vl)containing the vp19 target sequence were employed.WOAH recommended TaqMan qPCR was used as the reference method in performance parameters evaluation.The assay's performances parameters including analytical specificity(ASp),analytical sensitivity(ASe),diagnostic specificity(DSp),diagnostic sensitivity(DSe),and positive rate between the one-step PCR and nested PCR were compared.Results showed that developed one-step PCR assay demonstrated high ASp for WSSV detection,no cross-reactivity was detected against other 9 common pathogen samples.ASe tests revealed impressive detection limits:using the WSSV standard plasmid as a template,the theoretical minimum detection limit was 1.83 copies/μL,while with mixed DNA from field samples,the limit reached 0.82 fg/μL.Notably,in both scenarios,this method outperformed the WOAH-recommended nested PCR in terms of sensitivity.Comparison of diagnostic performance on 317 field samples showed that the one-step PCR achieved a DSp of 97.01%and a DSe of 95.08%,both superior to the WOAH-recommended nested PCR.In conclusion,this study introduces an innovative one-step PCR method for WSSV detection in P.clarkii,based on the vp19 gene,achieving a remarkable detection limit of 1.83 copies/μL while maintaining simplicity and cost-effectiveness.Outperforming the WOAH-recommended nested PCR,this highly sensitive approach excels in identifying latent infections and facilitating epidemiological investigations.Its ability to detect low-level infections enhances its versatility for both routine screening and research,providing a powerful tool for year-round dynamic monitoring and early warning of WSSV.While acknowledging current limitations,this groundbreaking method lays a solid foundation for future advancements in aquatic pathogen detection.By combining accuracy,sensitivity,and practicality,this research represents a significant step forward in WSSV detection technology,with far-reaching implications for the sustainable development of crayfish aquaculture in both scientific and economic contexts.

关键词

克氏原螯虾/白斑综合征病毒/囊膜蛋白VP19/一步式PCR/特异性/灵敏性

Key words

Procambarus clarkii/white spot syndrome virus/VP19/one-step PCR/specificity/sensitivity

分类

农业科技

引用本文复制引用

陈楠,罗小红,廖明聪,胡瑞雪,李丹,顾泽茂..基于vp19基因检测克氏原螯虾WSSV高灵敏度一步式PCR方法的建立[J].中国水产科学,2025,32(5):689-699,11.

基金项目

国家重点研发计划项目(2022YFD2400700) (2022YFD2400700)

湖北省重点研发计划项目(2023BBB169) (2023BBB169)

湖北洪山实验室重大项目(2021HSZD002) (2021HSZD002)

湖北省农业科技创新中心项目(2024-620-000-001-33) (2024-620-000-001-33)

中央高校基本科研业务费专项基金项目(2662023SCPY003,20062023SCYJ004) (2662023SCPY003,20062023SCYJ004)

湖北省支持种业高质量资金项目(HBZY2023B009). (HBZY2023B009)

中国水产科学

OA北大核心

1005-8737

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