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
  • [21] Proteomic analysis of zebrafish (Danio rerio) infected with infectious spleen and kidney necrosis virus
    Xiong, Xiao-Peng
    Dong, Chuan-Fu
    Xu, Xiaopeng
    Weng, Shao-Ping
    Liu, Zhao-Yu
    He, Jian-Guo
    DEVELOPMENTAL AND COMPARATIVE IMMUNOLOGY, 2011, 35 (04): : 431 - 440
  • [22] A zebrafish (Danio rerio) model of infectious spleen and kidney necrosis virus (ISKNV) infection
    Xu, Xiaopeng
    Zhang, Lichun
    Weng, Shaoping
    Huang, Zhijian
    Lu, Jing
    Lan, Dongming
    Zhong, Xuejun
    Yu, Xiaoqiang
    Xu, Anlong
    He, Jianguo
    VIROLOGY, 2008, 376 (01) : 1 - 12
  • [23] Antigenic identification of virion structural proteins from infectious spleen and kidney necrosis virus
    Xiong, Xiao-Peng
    Dong, Chuan-Fu
    Weng, Shao-Ping
    Zhang, Jing
    Zhang, Ye
    He, Jian-Guo
    FISH & SHELLFISH IMMUNOLOGY, 2011, 31 (06) : 919 - 924
  • [24] The impact of pooling samples on surveillance sensitivity for the megalocytivirus Infectious spleen and kidney necrosis virus
    Johnson, Sophia J.
    Hick, Paul M.
    Robinson, Andrew P.
    Rimmer, Anneke E.
    Tweedie, Alison
    Becker, Joy A.
    TRANSBOUNDARY AND EMERGING DISEASES, 2019, 66 (06) : 2318 - 2328
  • [25] Tetraodon nigroviridis as a nonlethal model of infectious spleen and kidney necrosis virus (ISKNV) infection
    Xu, Xiaopeng
    Huang, Lichao
    Weng, Shaoping
    Wang, Jing
    Lin, Ting
    Tang, Junliang
    Li, Zhongsheng
    Lu, Qingxia
    Xia, Qiong
    Yu, Xiaoqiang
    He, Jianguo
    VIROLOGY, 2010, 406 (02) : 167 - 175
  • [26] Asparagine Availability Is a Critical Limiting Factor for Infectious Spleen and Kidney Necrosis Virus Replication
    Ma, Baofu
    Li, Fangying
    Fu, Xiaozhe
    Luo, Xia
    Lin, Qiang
    Liang, Hongru
    Niu, Yinjie
    Li, Ningqiu
    VIRUSES-BASEL, 2024, 16 (10):
  • [27] A Multiplex PCR Method for Simultaneous Detection of Infectious Laryngotracheitis Virus and Ornithobacterium rhinotracheale
    Nguyen, Van-Giap
    Cao, Thi-Bich-Phuong
    Le, Van-Truong
    Truong, Ha-Thai
    Chu, Thi-Thanh-Huong
    Dang, Huu-Anh
    Nguyen, Thi-Hoa
    Le, Thi-Luyen
    Huynh, Thi-My-Le
    VETERINARY SCIENCES, 2023, 10 (04)
  • [28] Development of a multiplex loop-mediated isothermal amplification (mLAMP) method for the simultaneous detection of white spot syndrome virus and infectious hypodermal and hematopoietic necrosis virus in penaeid shrimp
    He, Lin
    Xu, Hai-sheng
    AQUACULTURE, 2011, 311 (1-4) : 94 - 99
  • [29] Development of polymer chain reaction and nucleic acid probe diagnostic methods for the detection of infectious spleen and kidney necrosis virus from mandarin fish
    Deng, M
    He, JG
    Weng, SP
    Lu, L
    Wang, YQ
    Long, QX
    Chan, SM
    PROCEEDINGS OF THE THIRD WORLD FISHERIES CONGRESS: FEEDING THE WORLD WITH FISH IN THE NEXT MILLENIUM-THE BALANCE BETWEEN PRODUCTION AND ENVIRONMENT, 2003, 38 : 181 - 188
  • [30] Partial validation of a TaqMan quantitative polymerase chain reaction for the detection of the three genotypes of Infectious spleen and kidney necrosis virus
    Koda, Samantha A. A.
    Subramaniam, Kuttichantran
    Hick, Paul M. M.
    Hall, Evelyn
    Waltzek, Thomas B. B.
    Becker, Joy A. A.
    PLOS ONE, 2023, 18 (02):