Yang Yao, Xu Li-ming, Zhao Jing-zhuang, Ren Guang-ming, Lu Tong-yan, Yin Hai-fu. Establishment of RT-LAMP Assay for Infectious Pancreatic Necrosis Virus[J]. Journal of Northeast Agricultural University(English Edition), 2020, 27(2): 90-98.
Citation: Yang Yao, Xu Li-ming, Zhao Jing-zhuang, Ren Guang-ming, Lu Tong-yan, Yin Hai-fu. Establishment of RT-LAMP Assay for Infectious Pancreatic Necrosis Virus[J]. Journal of Northeast Agricultural University(English Edition), 2020, 27(2): 90-98.

Establishment of RT-LAMP Assay for Infectious Pancreatic Necrosis Virus

Funds: 

Supported by the National Natural Science Foundation of China(31802345)

China Postdoctoral Science Foundation(2018M630893)

Heilongjiang Province Postdoctoral Science Foundation(LBH-Z18275)

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  • The purpose of this study was to establish a method for the rapid detection of infectious pancreatic necrosis virus (IPNV,Jasper serotype) using reverse transcription loop-mediated isothermal amplification (RT-LAMP).Four groups of specific primers were designed,according to the genome sequence of a Chinese IPNV isolate ChRtm213.The results showed that primer set B2 had the best amplification effect.When the final concentration of Mg2+ was 6 mmol·L-1,dNTPs were 1 mmol·L-1 and betaine was 0.4 mol·L-1,the reaction could be completed in a 63℃ water bath within 60 min.This RT-LAMP assay for the detection of IPNV had no cross-reactivity with infectious hematopoietic necrosis virus,viral hemorrhagic septicemia virus,grass carp reovirus and spring viremia of carp virus.The detection limit was 3.2×10-12 ng·μL-1.The sensitivity of this method was 10-fold higher than that of a previously published RT-LAMP assay for detecting the Spajarup (Sp) serotype of IPNV.This method,aimed at detecting IPNV isolates that were currently prevalent in China,possessed the characteristics of strong specificity,high sensitivity and direct interpretation by the naked eyes.The IPNV RT-LAMP was successfully applied to determine the clinical samples,which indicated the IPNV RT-LAMP assay was suitable for the rapid and large-scale detections of IPNV in China.
  • [1]
    Bain N,Gregory A,Raynard R S.2010.Genetic analysis of infectious pancreatic necrosis virus from Scotland.Journal of Fish Diseases,31(1):37-47.
    [2]
    Blake S,Ma J Y,Caporale D A,et al.2001.Phylogenetic relationships of aquatic birnaviruses based on deduced amino acid sequences of genome segment A cDNA.Diseases of Aquatic Organisms,45(2):89-102.
    [3]
    Biering E,Villoing S,Sommerset I,et al.2005.Update on viral vaccines for fish.Developments in Biologicals,121:97-113.
    [4]
    Caipang C M A,Haraguchi I,Ohira T,et al.2004.Rapid detection of a fish iridovirus using loop-mediated isothermal amplification (LAMP).Journal of Virological Methods,121(2):155-161.
    [5]
    Chang N,Macdonald R D,Yamamoto T.1978.Purification of infectious pancreatic necrosis (IPN) virus and comparison of polypeptide composition of different isolates.Canadian Journal of Microbiology,24(1):19-27.
    [6]
    Dobos P,Hill B J,Hallett R,et al.1979.Biophysical and biochemical characterization of 5 animal viruses with bisegmented double-stranded RNA genomes.Journal of Virology,32(2):593-605.
    [7]
    Dobos P.1995.The molecular biology of infectious pancreatic necrosis virus (IPNV).Annual Review of Fish Diseases,5:25-54.
    [8]
    Hill B J,Way K.1955.Serological classification of infectious pan-creatic necrosis (IPN) virus and other aquatic birnaviruses.Annual Review of Fish Diseases,5(95):55-77.
    [9]
    Hoferer M,Braun A,Skrypski J,et al.2017.One-step cross-genogroup multiplex RT-qPCR with an internal control system for the detec-tion of infectious pancreatic necrosis virus (IPNV).Journal of Virological Methods,247:68-76.
    [10]
    Hong T C,Mai Q L,Cuong D V,et al.2004.Development and evaluation of a novel loop-mediated isothermal amplification method for rapid detection of severe acute respiratory syndrome coronavirus.Journal of Clinical Microbiology,42(5):1956-1961.
    [11]
    Hsu Y L,Leong J C.1985.A comparison of detection methods for infectious haematopoietic necrosis virus.Journal of Fish Diseases,8(1):1-12.
    [12]
    Ji F,Zhao J Z,Liu M,et al.2017.Complete genomic sequence of an infectious pancreatic necrosis virus isolated from rainbow trout (Oncorhynchus mykiss) in China.Virus Genes,53(2):1-11.
    [13]
    Jiang Y L,Xu B L,Li Z Q,et al.1989.Isolation and identification of infectious pancreatic necrosis virus (IPNV) from imported rainbow trout (Salmon gairdneri) in P.R.China.Acta Hydrobiologica Sinica,13(4):353-358,394.
    [14]
    Jiang Y L,Yu P L,Li Zh Q.1990.Rapid detection of infectious pancreatic necrosis virus (IPNV) with the enzyme-linked immuno-sorbent assay (ELISA).Acta Hydrobiologica Sinica,14(3):276-279.
    [15]
    Liu M,Xu L M,Lu T Y,et al.2014.Development and application of reverse transcription loop-mediated isothermal amplification for detection of IHNV.Journal of Fishery Sciences of China,21(5):1065-1071.
    [16]
    Liu M,Xu L M,Zhao,J Z,et al.2017.Isolation,identification and cluster analysis of an infectious pancreatic necrosis virus.Journal of Dalian Fisheries University,32(1):56-61.
    [17]
    Liu Y H,Ren T,Tan Y M,et al.2018.Development of a RT-LAMP detection method for salmonid alphavirus.China Animal Health Inspection,35(10):99-103.
    [18]
    Nagamine K,Watanabe K,Ohtsuka K,et al.2001.Loop-mediated isothermal amplification reaction using a nondenatured template.Clinical Chemistry,47(9):1742-1743.
    [19]
    Nakamura N,Ito K,Takahashi M,et al.2007.Detection of six single-nucleotide polymorphisms associated with Rheumatoid arthritis by a loop-mediated isothermal amplification method and an electrochemical DNA Chip.Analytical Chemistry,79(24):9484-9493.
    [20]
    Niu L Q,Zhao Z Z.The epidemiological IHN and IPN of rainbow trout in northeast China.Journal of fisheries of China,12(4):327-332.
    [21]
    Notomi T,Okayama H,Masubuchi H,et al.2000.Loop-mediated isothermal amplification of DNA.Nucleic Acids Research,28(12):E63.
    [22]
    Pedersen T,Skjesol A,Jørgensen J B.2007.VP3,a structural pro-tein of infectious pancreatic necrosis virus,interacts with RNA-dependent RNA polymerase VP1 and with double-stranded RNA.Journal of Virology,81(12):6652-6663.
    [23]
    Roberts R J,Pearson M D.2010.Infectious pancreatic necrosis in Atlantic salmon,Salmo salar L.Journal of Fish Diseases,28(7):383-390.
    [24]
    Santi N,Vakharia V N,Evensen Ø.2004.Identification of putative motifs involved in the virulence of infectious pancreatic necrosis virus.Virology,322:31-40.
    [25]
    Soliman H,Elmatbouli M.2006.Reverse transcription loop-mediated isothermal amplification (RT-LAMP) for rapid detection of viral hemorrhagic septicaemia virus (VHS).Veterinary Microbiology,114(3):205-213.
    [26]
    Soliman H,Midtlyng P J,El-Matbouli M.2009.Sensitive and rapid detection of infectious pancreatic necrosis virus by reverse transcription loop mediated isothermal amplification.Journal of Virological Methods,158(1/2):77-83.
    [27]
    Tong S L,Hetrick F M.1989.A study infectious pancreatic necrosis disease of rainbow trout Salmon gairdneri.Journal of Ocean University of QINGDAO,20(2):119-122.
    [28]
    Wang J N.2012.Establishment of indirect immunocolour assay (IFA) with Epitope of VP2 of infectious pancreatic necrosis virus.Northeast Agricultural University,Harbin.
    [29]
    Wolf K,Snieszko S F,Dunbar C E,et al.1960.Virus nature of infectious pancreatic necrosis in trout.Proc Soc Exp Biol Med,104(1):105-108.
    [30]
    Wood E M,Snieszko S F,Yasutake W T.1955.Infectious pancreatic necrosis in brook trout.A M A Archives of Pathology,60(1):26-28.
    [31]
    Xu H D,Feng J,Guo Z X,et al.2010.Detection of red-spotted grouper nervous necrosis virus by loop-mediated isothermal amplification.Journal of Virological Methods,163(1):123-128.
    [32]
    Xu L M,Liu H B,Lu T Y.2014.Genotype of IHNV-Sn1203 iso-late and the bioinformatics analysis of its glycoprotein.Journal of Fishery Sciences of China,21(1):180-188.
    [33]
    Xu Y,Duan H A,Zhou Y,et al.2011.Establishment of real-time RT-PCR assay for detection of IPNV.Journal of Anhui Agricultural Sciences,39(31):19224-19226.
    [34]
    Xiong J.2011.Sequening and analysis of partial genme of Scylla serrata reovirus and RT-LAMP detection methods development.Huazhong Agricultural University,Wuhan.
    [35]
    Yao K,Vakharia V N.1998.Generation of infectious pancreatic necrosis virus from cloned cDNA.Journal of Virology,72(11):8913-8920.
    [36]
    Zhang C X,Mei Q.2002.Protein microarray–a new tool for detection of torch infection.Adv Nanomat Nanodev,7:397-407.
    [37]
    Zhang H,Zeng L,Fan Y,et al.2014.A loop-mediated isothermal amplification assay for rapid detection of cyprinid herpesvirus 2 in gibel carp (Carassius auratus gibelio).The Scientific World Journal,doi: 10.1155/2014/716413.
    [38]
    Zhang J F,Zeng L B,Zhang H,et al.2013.Development of a reverse transcription-loop mediated isothermal amplification (RT-LAMP) assay for detection of grass carp reovirus.Journal of Fishery Sciences of China,20(1):129-136.
    [39]
    Zhu L,Wang X L,Huang X L,et al.2017.Outbreak of infectious pancreatic necrosis virus (IPNV) in farmed rainbow trout in China.Acta Tropica,170:63-69.

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