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Genetic markers for discrimination and detection of a virus causing red sea bream iridovirus disease which is an infectious aquatic organism disease, and method of discriminating and detecting the virus using the same

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  • Publication Date:
    June 22, 2021
  • معلومة اضافية
    • Patent Number:
      11041,189
    • Appl. No:
      16/658113
    • Application Filed:
      October 20, 2019
    • نبذة مختصرة :
      Genetic markers are described for discriminating or detecting viruses causing infectious aquatic organism diseases, and a method of discriminating and detecting the viruses using the same is disclosed, in which the method includes selecting and amplifying a DNA nucleotide sequence encoding a gene specific for viral hemorrhagic septicemia virus (VHSV), red sea bream iridovirus (RSIV) or infectious spleen and kidney necrosis virus (ISKNV), which is a virus causing red sea bream iridovirus disease, or Koi herpesvirus (KHV); hybridizing a peptide nucleic acid (PNA) that specifically recognizes the amplification product; controlling the temperature of the hybridization product to obtain a temperature-dependent melting curve; and discriminating the viral type or detecting whether or not fish are infected with the viral type by analyzing the obtained melting curve to determine a melting temperature.
    • Inventors:
      National Institute of Fisheries Science (Busan, KR)
    • Assignees:
      NATIONAL INSTITUTE OF FISHERIES SCIENCE (Busan, KR)
    • Claim:
      1. A PNA probe consisting of SEQ ID NO: 2, for discrimination or detection of a virus causing red sea bream iridovirus disease which is a virus causing infectious aquatic organism disease, wherein the virus causing red sea bream iridovirus disease is red sea bream iridovirus (RSIV) or infectious spleen and kidney necrosis virus (ISKNV).
    • Claim:
      2. A PNA probe consisting of SEQ ID NO: 2 with one or more of a reporter and a quencher attached thereto, wherein the probe is for discrimination or detection of a virus causing red sea bream iridovirus disease which is a virus causing infectious aquatic organism disease.
    • Claim:
      3. A composition for discrimination or detection of a virus causing red sea bream iridovirus disease, the composition comprising: a primer consisting of SEQ ID NO: 7 and a PNA probe consisting of SEQ ID NO: 2.
    • Claim:
      4. A kit for discrimination or detection of a virus causing red sea bream iridovirus disease, the kit comprising: a primer consisting of SEQ ID NO: 7; and a PNA probe consisting of SEQ ID NO: 2.
    • Claim:
      5. A method for detecting a virus causing red sea bream iridovirus disease, the method comprising the steps of: (a) extracting a target nucleic acid from a fish sample; (b) amplifying a genetic marker nucleotide sequence for the virus causing red sea bream iridovirus disease contained in the target nucleic acid by use of a primer pair capable of amplifying a fragment consisting of SEQ ID NO: 17 or SEQ ID NO: 18; (c) producing a single-strand genetic marker sequence fragment using the amplified genetic marker nucleotide sequence as a template and a primer consisting of SEQ ID NO: 7; (d) hybridizing a PNA probe consisting of a reporter and quencher labeled SEQ ID NO: 2 to the produced single-strand genetic marker sequence fragment; (e) obtaining a temperature-dependent melting curve while increasing the temperature of a PNA probe-hybridized product resulting from step (d); and (f) detecting whether or not the fish sample is infected with the virus causing red sea bream iridovirus disease by analyzing the melting curve obtained in step (e) to determine a melting temperature, wherein the virus causing red sea bream iridovirus disease is red sea bream iridovirus (RSIV) or infectious spleen and kidney necrosis virus (ISKNV).
    • Claim:
      6. The method of claim 5 , the single-strand genetic marker sequence fragment in step (c) is produced by adding a single strand generation buffer (SSG buffer).
    • Claim:
      7. The method of claim 6 , wherein the single strand generation buffer comprises DNA polymerase, dNTPs (deoxynucleotides) and a stabilizer.
    • Claim:
      8. The method of claim 5 , wherein step (b) of amplifying the genetic marker nucleotide sequence by use of the primer pair further comprises adding a TaqMan probe to obtain an amplification curve.
    • Patent References Cited:
      2004/0121371 June 2004 Andersen et al.
      2018/0195114 July 2018 Cho et al.
      10-2008-0066301 July 2008
      10-2014-0091944 July 2014
      10-2015-0028063 March 2015
      10-1642784 July 2016
      101642783 July 2016
      101644776 August 2016













    • Other References:
      Machine Translation for KR 10-1644776; obtained from K-PION http://kposd.kipo.go.kr:8088/kiponet/up/kpion/patent/publication/selectPatentPublication.do?decorator=popupp on Dec. 9, 2020. 12 pages (Year: 2016). cited by examiner
      Machine Translation for KR 10-1642783; obtained from K-PION http://kposd.kipo.go.kr:8088/kiponet/up/kpion/patent/publication/selectPatentPublication.do?decorator=popup on Dec. 9, 2020. 12 pages. (Year: 2016). cited by examiner
      Mohr et al. (Dis Aquat Org., vol. 116: 103-110, 2015) (Year: 2015). cited by examiner
      Petersen et al. Molecular and Cellular Probes. 2004, vol. 18, pp. 117-122. (Year: 2004). cited by examiner
      Matejusova et al. (Dis Aquat Org., vol. 80: 137-144, 2008) (Year: 2008). cited by examiner
      Clustal multiple sequence alignment of Mohr sequences. Obtained from https://www.ebi.ac.uk/Tools/services/rest/clustalo/result/clustalo-I20201210-194045-0208-36631904-p1m/aln-clustal_num on Dec. 10, 2020. 3 pages. (Year: 2020). cited by examiner
      Bercovier, H., et al., “Cloning of the Koi Herpesvirus (KHV) Gene Encoding Thymidine Kinase and its use for a Highly Sensitive PCR Based Diagnosis”, “BMC Microbiology”, Mar. 17, 2005, p. 1-9, vol. 5, No. 13. cited by applicant
      Genbank, “Cyprinid Herpesvirus 3 (KHV, CyHV-3) DNA, Enlarged Sphl-5 PCR Region, Genotype/Variant: A1, A2”, “GenBank AB375381”, Jun. 2009. cited by applicant
      Genbank, “Cyprinid Herpesvirus 3 Isolate KHV-GZ11 Thymidine Kinase Gene, Compete cds”, “GenBank JQ247183”, Jan. 2013. cited by applicant
      Kim, I.-W., et al., “Diagnosis Case of Viral Hemorrhagic Septicemia (VHS) in Adult Olive F lounder Paralichthys olivaceus”, “Korean Journal of Fisheries and Aquatic Sciences”, Dec. 2012, pp. 666-674 (English Abstract), vol. 45, No. 6. cited by applicant
      Kurita, J., et al., “Molecular Epidemiology of Koi Herpesvirus”, “Fish Pathology”, 2009, pp. 59-66, vol. 44, No. 2. cited by applicant
      OIE Aquatic Animals Commission, “Red Sea Bream Iridoviral Disease”, “Manual of Diagnostic Tests for Aquatic Animals”, 2009, pp. 251-261. cited by applicant
      Petersen, K., et al., “Short PNA Molecular Beacons for Real-Time PCR Allelic Discrimination of Single Nucleotide Polymorphisms”, “Molecular and Cellular Probes”, 2004, pp. 117-122, vol. 18. cited by applicant
      Pokorova, D., et al., “Tests for the Presence of KOI Herbesvirus (KHV) in Common Carp (Cyprinus Carpio Carpio) and Koi Carp (Cyprinus Carpio koi) in the Czech Republic”, “Veterinami Medicina”, 2007, pp. 562-568, vol. 52. cited by applicant
    • Primary Examiner:
      Switzer, Juliet C
    • Attorney, Agent or Firm:
      Hultquist, PLLC
      Hultquist, Steven J.
    • الرقم المعرف:
      edspgr.11041189