Development of a real-time enzymatic recombinase amplification assay for rapid detection of infectious hypodermal and hematopoietic necrosis virus (IHHNV) in shrimp Penaeus vannamei

被引:5
|
作者
Zhang, Lu [1 ,2 ]
Liu, Kexin [1 ,2 ]
Liu, Mengran [1 ,2 ,3 ,4 ]
Hu, Jingjie [1 ,2 ,3 ]
Bao, Zhenmin [1 ,2 ,3 ]
Wang, Mengqiang [1 ,2 ,3 ,4 ]
机构
[1] Ocean Univ China, MOE Key Lab Marine Genet & Breeding, Qingdao 266003, Peoples R China
[2] Ocean Univ China, Sanya Oceanog Inst, Key Lab Trop Aquat Germplasm Hainan Prov, Sanya 572024, Peoples R China
[3] Hainan Yazhou Bay Seed Lab, Sanya 572024, Peoples R China
[4] MOE Key Lab Marine Genet & Breeding, Qingdao 266003, Peoples R China
关键词
Enzymatic recombinase amplification; Infectious hypodermal and hematopoietic; necrosis virus; Penaeus vannamei; Endogenous viral elements; STYLIROSTRIS; PATHOGENS; SEQUENCE; MONODON;
D O I
10.1016/j.jip.2023.108024
中图分类号
Q95 [动物学];
学科分类号
071002 ;
摘要
Infectious hypodermal and hematopoietic necrosis virus (IHHNV) is classified as a reportable crustacean disease by the World Organisation for Animal Health (WOAH), which causes poor growth in Penaeus vannamei. Ac-cording to genome sequence alignment analysis, enzymatic recombinase amplification (ERA) primers and probe were designed based on the ORF1 region of IHHNV, and a real-time ERA assay for IHHNV detection (IHHNV-ERA) was established. The experimental results show that IHHNV-F2/IHHNV-R2 and IHHNV-Probe can effec-tively amplify the target gene, and the sensitivity is 1.4 x 101 copies/mu L within 14.97 +/- 0.19 min, while the qPCR using primers 309F/309R could reach the detection limit of 1.4 x 101 copies/mu L within 21.76 +/- 0.63 min, and the sensitivity results of one-step PCR could be as low as 1.4 copies/mu L with expense of time and false positives. The IHHNV-ERA system can effectively amplify the target gene at 42 celcius within 20 min, and has no cross-reaction with white spot syndrome virus (WSSV), Ecytonucleospora hepatopenaei (EHP), Vibrio para-haemolyticus causing acute hepatopancreatic necrosis disease (VpAHPND), and healthy shrimp genomic DNA. Test results of practical samples showed that the detection rate of IHHNV-ERA (18/20) was better than the industrial standard qPCR assay (17/20). Compared with the existing technology, the useful results of this detection assay are: (1) get rid of the dependence on the thermal cycle instrument in the PCR process; (2) the experimental procedure is simple, time-consuming and fast; (3) the detection sensitivity is high. This study provides an ERA based detection assay for IHHNV, which can be used not only for the rapid detection of IHHNV infection, but also for the field screening of pathogens. This assay can also be applied to clinical inspection, customs detection, enterprise quality inspection and other fields, and has obvious practical application value.
引用
收藏
页数:8
相关论文
共 50 条
  • [21] Prevalence and genomic analysis of infectious hypodermal and hematopoietic necrosis virus (IHHNV) in Litopenaeus vannamei shrimp farmed in Shanghai, China
    Chao Chai
    Yuchen Liu
    Xiaoming Xia
    Hongming Wang
    Yingjie Pan
    Shuling Yan
    Yongjie Wang
    Archives of Virology, 2016, 161 : 3189 - 3201
  • [22] An enzymatic recombinase amplification assay combined with CRISPR-Cas12a for the rapid detection of acute hepatopancreatic necrosis disease in shrimp Penaeus vannamei
    Liu, Kexin
    Zhang, Lu
    Yang, Jing
    Zeng, Qifan
    Hu, Jingjie
    Bao, Zhenmin
    Wang, Mengqiang
    AQUACULTURE INTERNATIONAL, 2024, 32 (06) : 7695 - 7718
  • [23] Real-time triplex loop-mediated isothermal amplification (LAMP) using a turbidimeter for detection of shrimp infectious hypodermal and hematopoietic necrosis virus <bold>(</bold>IHHNV<bold>)</bold>
    Arunrut, Narong
    Jitrakorn, Sarocha
    Tondee, Benyatip
    Saksmerprome, Vanvimon
    Kiatpathomchai, Wansika
    JOURNAL OF AQUATIC ANIMAL HEALTH, 2024, 36 (03) : 205 - 219
  • [24] ISOLATION, PURIFICATION AND CHARACTERIZATION OF INFECTIOUS HYPODERMAL AND HEMATOPOIETIC NECROSIS VIRUS (IHHNV) FROM PENAEID SHRIMP
    LU, Y
    LOH, PC
    BROCK, JA
    JOURNAL OF VIROLOGICAL METHODS, 1989, 26 (03) : 339 - 343
  • [25] PCR assay for discriminating between infectious hypodermal and hematopoietic necrosis virus (IHHNV) and virus-related sequences in the genome of Penaeus monodon
    Tang, Kathy F. J.
    Navarro, Solangel A.
    Lightner, Donald V.
    DISEASES OF AQUATIC ORGANISMS, 2007, 74 (02) : 165 - 170
  • [26] Development of a real-time enzymatic recombinase amplification assay (RT-ERA) and an ERA combined with lateral flow dipsticks (LFD) assay (ERA-LFD) for rapid detection of acute hepatopancreatic necrosis disease (AHPND) in shrimp Penaeus vannamei
    Zhou, Qingqian
    Wang, Yan
    Hu, Jingjie
    Bao, Zhenmin
    Wang, Mengqiang
    AQUACULTURE, 2023, 566
  • [27] Studies on infectious myonecrosis virus (IMNV) and infectious hypodermal and hematopoietic necrosis virus (IHHNV) in cultured penaeid shrimp in Egypt
    Aly, Salah M.
    Mansour, Shimaa M.
    Thabet, Randa Y.
    Mabrok, Mahmoud
    DISEASES OF AQUATIC ORGANISMS, 2021, 143 : 57 - 67
  • [28] Low impact of infectious hypodermal and hematopoietic necrosis virus (IHHNV) on growth and reproductive performance of Penaeus monodon
    Withyachumnarnkul, Boonsirm
    Chayaburakul, Kanokporn
    Supak, Lao-Aroon
    Plodpai, Pornthep
    Sritunyalucksana, Kallaya
    Nash, Gary
    DISEASES OF AQUATIC ORGANISMS, 2006, 69 (2-3) : 129 - 136
  • [29] Reduced replication of infectious hypodermal and hematopoietic necrosis virus (IHHNV) in Litopenaeus vannamei held in warm water
    Montgomery-Brock, Dee
    Tacon, Albert G. J.
    Poulos, Bonnie
    Lightner, Donald
    AQUACULTURE, 2007, 265 (1-4) : 41 - 48
  • [30] Detection of infectious hypodermal and hematopoietic necrosis virus and white spot syndrome virus in whiteleg shrimp (Penaeus vannamei) imported from Vietnam to South Korea
    Park, Seul Chan
    Choi, Seong-Kyoon
    Han, Se-Hyeon
    Park, Song
    Jeon, Hye Jin
    Lee, Seung Chan
    Kim, Kyeong Yeon
    Lee, Young Seo
    Kim, Ji Hyung
    Han, Jee Eun
    JOURNAL OF VETERINARY SCIENCE, 2020, 21 (02)