Development of a loop-mediated isothermal amplification assay for the detection and quantification of epizootic epitheliotropic disease virus (salmonid herpesvirus-3)

被引:3
作者
Zhang, Qingli [1 ,2 ]
Shavalier, Megan [3 ]
Standish, Isaac [2 ]
Glenney, Gavin W. [4 ]
Loch, Thomas P. [2 ]
Faisal, Mohamed [2 ,3 ,5 ,6 ]
机构
[1] Chinese Acad Fishery Sci, Funct Lab Marine Fisheries Sci & Food Prod Proc, Qingdao Natl Lab Marine Sci & Technol, Yellow Sea Fisheries Res Inst, Qingdao 266071, Peoples R China
[2] Michigan State Univ, Coll Vet Med, Dept Pathobiol & Diagnost Invest, E Lansing, MI 48824 USA
[3] Michigan State Univ, Coll Vet Med, Comparat Med & Integrat Biol, E Lansing, MI 48824 USA
[4] US Fish & Wildlife Serv, Lamar Fish Hlth Ctr, Lamar, PA 16848 USA
[5] Michigan State Univ, Coll Agr & Nat Resources, Dept Fisheries & Wildlife, E Lansing, MI 48824 USA
[6] 1129 Farm Lane,Room 342, E Lansing, MI 48824 USA
关键词
Epizootic epitheliotropic disease virus; Salmonid Herpesvirus-3 (SaHV-3); Loop-mediated isothermal amplification; Calcein; TROUT SALVELINUS-NAMAYCUSH; POLYMERASE-CHAIN-REACTION; RAPID DETECTION; MOLECULAR CHARACTERIZATION; VISUAL DETECTION; LAMP;
D O I
10.1016/j.jviromet.2018.11.006
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Epizootic Epitheliotropic Disease Virus (EEDV; Salmonid Herpesvirus-3) causes a serious disease hatchery-reared lake trout (Salvelinus namaycush), threatening restoration efforts of this species in North America. The current inability to replicate EEDV in vitro necessitates the search for a reproducible, sensitive, and specific assay that allows for its detection and quantitation in a time- and cost-effective manner. Herein, we describe a loop-mediated isothermal amplification (LAMP) assay that was developed for the quantitative detection of EEDV in infected fish tissues. The newly developed LAMP reaction was optimized in the presence of calcein, and the best results were produced using 2 mM MgCl2, 1.8 mM dNTPs and at an incubation temperature of 67.1 degrees C. This method was highly specific to EEDV, as it showed no cross-reactivity with several fish viruses, including Salmonid Herpesvirus(-1), -2, -4, and -5, Infectious Pancreatic Necrosis Virus, Spring Viremia of Carp Virus, Infectious Hematopoietic Necrosis Virus, Golden Shiner Reovirus, Fathead Minnow Nidovirus, and Viral Hemorrhagic Septicemia Virus. The analytical sensitivity of the EEDV-LAMP method was estimated to be as low as 16 copies of plasmid per reaction. When infected fish tissue was used, a positive reaction could be obtained when an infected gill tissue sample that contained 430 viral copies/mu g was diluted up to five orders of magnitude. The sensitivity and specificity of the newly developed LAMP assay compared to the SYBR Green qPCR assay were 84.3% and 93.3%, respectively. The quantitative LAMP for EEDV had a correlation coefficient (R-2 = 0.980), and did not differ significantly from the SYBR Green quantitative PCR assay (p > 0.05). Given its cost- and time-effectiveness, this quantitative LAMP assay is suitable for screening lake trout populations and for the initial diagnosis of clinical cases.
引用
收藏
页码:44 / 50
页数:7
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