Development of Two Quantitative Real-Time PCR Diagnostic Kits for HPV Isolates from Korea

被引:4
|
作者
Jeeva, Subbiah [1 ]
Kim, Nam-Il [2 ]
Jang, In-Kwon [3 ]
Choi, Tae-Jin [1 ]
机构
[1] Pukyong Natl Univ, Dept Microbiol, Pusan 608737, South Korea
[2] Bioneer Corp, Mol Sci Div, Taejon 306220, South Korea
[3] Natl Fisheries Res & Dev Inst, Inchon 400420, South Korea
关键词
Real-time PCR kit; Green Star; Dual Star; hepatopancreatic parvovirus; HEPATOPANCREATIC PARVOVIRUS HPV; COMPLETE NUCLEOTIDE-SEQUENCE; POLYMERASE-CHAIN-REACTION; PENAEUS-MONODON; SHRIMP; VIRUS; AMPLIFICATION; INFECTION; DISEASE; ASSAY;
D O I
10.4014/jmb.1205.05028
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Viral pathogens, alongside other pathogens, have major effects on crustacean aquaculture. Hepatopancreatic parvovirus (HPV) is an emerging virus in the shrimp industry and has been detected in shrimp farms worldwide. The HPV genome has greater diversity than other shrimp viruses owing to its wide host range and geographical distribution. Therefore, developing diagnostic tools is essential to detect even small copy numbers from the target region of native HPV isolates. We have developed two easy to use quantitative real-time PCR kits, called Green Star and Dual Star, which contain all of the necessary components for real-time PCR, including HPV primers, using the primers obtained from the sequences of HPV isolates from Korea, and analyzed their specificity, efficiency, and reproducibility. These two kits could detect from 1 to 1 x 109 copies of cloned HPV DNA. The minimum detection limits obtained from HPV-infected shrimp were 7.74 x 10(1) and 9.06 x 10(1) copies in the Green Star and Dual Star assay kits, respectively. These kits can be used for rapid, sensitive, and efficient screening for HPV isolates from Korea before the introduction of postlarval stages into culture ponds, thereby decreasing the incidence of early development of the disease.
引用
收藏
页码:1350 / 1358
页数:9
相关论文
共 50 条
  • [41] Real-time quantitative PCR of telomere length
    Gil, ME
    Coetzer, TL
    MOLECULAR BIOTECHNOLOGY, 2004, 27 (02) : 169 - 172
  • [42] Real-time quantitative PCR for toxoplasmosis diagnosis
    Ordinaire, I
    Simon, A
    Fréalle, E
    Soula, F
    Valat, AS
    Rouland, V
    Subtil, D
    Dei-Cas, E
    Camus, D
    Delhaes, L
    ANNALES DE BIOLOGIE CLINIQUE, 2005, 63 (01) : 67 - 73
  • [43] Basic principles of real-time quantitative PCR
    Arya, M
    Shergill, IS
    Williamson, M
    Gommersall, L
    Arya, N
    Patel, HRH
    EXPERT REVIEW OF MOLECULAR DIAGNOSTICS, 2005, 5 (02) : 209 - 219
  • [44] Real-time quantitative PCR of telomere length
    Marcel E. Gil
    Thérèsa L. Coetzer
    Molecular Biotechnology, 2004, 27 : 169 - 172
  • [45] Accuracy of quantitative real-time PCR analysis
    D. G. Sochivko
    A. A. Fedorov
    D. A. Varlamov
    V. E. Kurochkin
    R. V. Petrov
    Doklady Biochemistry and Biophysics, 2013, 449 : 105 - 108
  • [46] Applications and advances in Real-Time quantitative PCR
    Roque-Biewer, M
    Shannon, M
    Hunkapiller, K
    Fuller, A
    Bluestone, J
    Seyfert-Margolis, V
    Ruff, D
    HUMAN IMMUNOLOGY, 2004, 65 : S118 - S118
  • [47] Quantitative real-time PCR in cancer research
    Mocellin, S
    Rossi, CR
    Marincola, FM
    ARCHIVUM IMMUNOLOGIAE ET THERAPIAE EXPERIMENTALIS, 2003, 51 (05) : 301 - 313
  • [48] Accuracy of quantitative real-time PCR analysis
    Sochivko, D. G.
    Fedorov, A. A.
    Varlamov, D. A.
    Kurochkin, V. E.
    Petrov, R. V.
    DOKLADY BIOCHEMISTRY AND BIOPHYSICS, 2013, 449 (01) : 105 - 108
  • [49] Evaluation of three commercial real-time PCR kits for dengue diagnosis
    Najioullah, F.
    Angla-Gre, M.
    Viron, F.
    Cesaire, R.
    INTERNATIONAL JOURNAL OF INFECTIOUS DISEASES, 2014, 21 : 373 - 373
  • [50] Quantitative analysis of two genetically modified maize lines by real-time PCR
    Lee, SH
    Kang, SH
    Park, YH
    Min, DM
    Kim, YM
    JOURNAL OF MICROBIOLOGY AND BIOTECHNOLOGY, 2006, 16 (02) : 205 - 211