Multiplex qPCR development for the simultaneous and rapid detection of largemouth bass virus and infectious spleen and kidney necrosis virus in aquaculture

被引:0
|
作者
Cao, Weiwei [1 ]
Huang, Baiqi [1 ]
Xu, Qian [1 ]
Xie, Hui [2 ]
Gao, Jinyan [3 ]
Mai, Xiaodong [4 ]
Lin, Xuejin [3 ]
Tian, Chi [5 ]
Huang, Xianpei [6 ]
Zhang, Huang [3 ]
机构
[1] Guangdong Polytech Sci & Trade, Coll Food Sci & Bioengn, Guangzhou 510640, Peoples R China
[2] Guangdong Xuanda Testing Technol Serv Co Ltd, Guangzhou 510320, Peoples R China
[3] Guangzhou Double Helix Gene Technol Co Ltd, Guangzhou 510320, Peoples R China
[4] Xinjiang Agr Univ, Urumqi 830046, Xinjiang, Peoples R China
[5] Lianyungang Xuanda Testing Technol Serv Co Ltd, Nanjing 222000, Jiangsu, Peoples R China
[6] Shanwei Marine Ind Inst, Shanwei 516600, Peoples R China
关键词
Largemouth bass virus; Infectious spleen and kidney necrosis virus; Multiplex qPCR; REAL-TIME PCR; FISH;
D O I
10.1016/j.jviromet.2024.115012
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Largemouth bass virus (LMBV) and infectious spleen and kidney necrosis virus (ISKNV) are both belong to Iridoviridae that cause considerable economic losses in the fish industry. There is no reported literature that can detect these two viruses simultaneously. In this study, we established a multiplex quantitative polymerase chain reaction (qPCR) assay that can specifically and simultaneously detect both LMBV and ISKNV in fish samples. The specificity experiment showed that the method only amplified LMBV and ISKNV but not the other 10 common fish viruses. The slope (m), efficiency (E) and linearity (R2) determined from the generated standard curve were all within the optimal range of qPCR values. The detection limit of the multiplex qPCR assay was as low as 4 copies/mu L for LMBV DNA and 7 copies/mu L for ISKNV DNA, respectively. The established method exhibited adequate repeatability and reproducibility, and the intra- and inter-assay coefficients of variation were both less than 3 %. The accuracy of the multiplex qPCR method was validated using 229 fish samples and was more precise than that of the conventional PCR assay. In summary, the established multiplex qPCR assay can simultaneously detect LMBV and ISKNV to monitor the risk of infection LMBV and ISKNV and control the disease early.
引用
收藏
页数:9
相关论文
共 50 条
  • [1] Rapid simultaneous detection and quantitation of infectious pancreatic necrosis virus (IPNV)
    Espinoza, JC
    Kuznar, J
    JOURNAL OF VIROLOGICAL METHODS, 2002, 105 (01) : 81 - 85
  • [2] Development and application of a sensitive droplet digital PCR (ddPCR) for the detection of infectious spleen and kidney necrosis virus
    Lin, Qiang
    Fu, Xiaozhe
    Liu, Lihui
    Liang, Hongru
    Niu, Yinjie
    Wen, Yuanya
    Huang, Zhibin
    Li, Ningqiu
    AQUACULTURE, 2020, 529
  • [3] Rapid and sensitive detection of infectious spleen and kidney necrosis virus by recombinase polymerase amplification combined with lateral flow dipsticks
    Li, Haoxuan
    Yuan, Gailing
    Luo, Yangzhi
    Yu, Yunzhen
    Ai, Taoshan
    Su, Jianguo
    AQUACULTURE, 2020, 519
  • [4] Identification of infectious spleen and kidney necrosis virus (ISKNV)-encoded microRNAs
    Jian-hui He
    Qiong Xia
    Shaoping Weng
    Jianguo He
    Xiaopeng Xu
    Virus Genes, 2020, 56 : 724 - 733
  • [5] Identification of infectious spleen and kidney necrosis virus (ISKNV)-encoded microRNAs
    He, Jian-hui
    Xia, Qiong
    Weng, Shaoping
    He, Jianguo
    Xu, Xiaopeng
    VIRUS GENES, 2020, 56 (06) : 724 - 733
  • [6] Global Landscape of Structural Proteins of Infectious Spleen and Kidney Necrosis Virus
    Dong, Chuan-Fu
    Xiong, Xiao-Peng
    Shuang, Fan
    Weng, Shao-Ping
    Zhang, Jing
    Zhang, Ye
    Luo, Yong-Wen
    He, Jian-Guo
    JOURNAL OF VIROLOGY, 2011, 85 (06) : 2869 - 2877
  • [7] Autophagy promoted infectious kidney and spleen necrosis virus replication and decreased infectious virus yields in CPB cell line
    Li, Chen
    Fu, Xiaozhe
    Lin, Qiang
    Liu, Lihui
    Liang, Hongru
    Huang, Zhibin
    Li, Ningqiu
    FISH & SHELLFISH IMMUNOLOGY, 2017, 60 : 25 - 32
  • [8] Rapid and sensitive detection of infectious spleen and kidney necrosis virus by loop-mediated isothermal amplification combined with a lateral flow dipstick
    W. C. Ding
    Jiong Chen
    Y. H. Shi
    X. J. Lu
    M. Y. Li
    Archives of Virology, 2010, 155 : 385 - 389
  • [9] Rapid and sensitive detection of infectious spleen and kidney necrosis virus by loop-mediated isothermal amplification combined with a lateral flow dipstick
    Ding, W. C.
    Chen, Jiong
    Shi, Y. H.
    Lu, X. J.
    Li, M. Y.
    ARCHIVES OF VIROLOGY, 2010, 155 (03) : 385 - 389
  • [10] Stability of Infectious spleen and kidney necrosis virus and susceptibility to physical and chemical disinfectants
    Fusianto, Cahya
    Hick, Paul M.
    Becker, Joy A.
    AQUACULTURE, 2019, 506 : 104 - 111