Differential detection of Newcastle disease virus strains by degenerate primers based RT-PCR

被引:16
|
作者
Tiwari, AK [1 ]
Kataria, RS
Nanthakumar, T
Dash, BB
Desai, G
机构
[1] Indian Vet Res Inst, Natl Biotechnol Ctr, Izatnagar 243122, Uttar Pradesh, India
[2] Indian Vet Res Inst, Div Avian Dis, Izatnagar 243122, Uttar Pradesh, India
[3] High Secur Anim Dis Lab, Bhopal 462021, India
关键词
Newcastle disease virus; differentiation; F gene; degenerate primers; RT-PCR;
D O I
10.1016/j.cimid.2003.09.002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Degenerate primers based RT-PCR (previously described by [Avian Dis 26 (1997) 837]) has been used for the detection and differentiation of Newcastle disease (ND) viruses. Two sets of primers (A + B and A + C), with common forward primer and distinct reverse degenerate primers, designed from fusion protein gene encoding for cleavage site, could differentiate virulent and avirulent Newcastle disease viruses (NDV). Both sets of primers amplified 'F' gene sequence of virulent (velogenic and mesogenic) viruses, whereas in avirulent strains, amplification was only with primer set A + C. Total 10 NDV isolates and two clinical samples including both known and unknown pathotypes, were checked. Based on amplification results 5 viruses were found to be virulent type and 6 as avirulent with one of the two clinical samples, earlier positive by RT-PCR using non-degenerate V gene specific primers was found negative in this study. The technique has been found to be a simple and quick for the detection and differentiation of virulent and avirulent NDV, which is important for control of the disease in the events of the outbreaks. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:163 / 169
页数:7
相关论文
共 50 条
  • [41] Differential detection of transmissible gastroenteritis virus and porcine epidemic diarrhea virus by duplex RT-PCR
    Kim, SY
    Song, DS
    Park, BK
    JOURNAL OF VETERINARY DIAGNOSTIC INVESTIGATION, 2001, 13 (06) : 516 - 520
  • [42] Multiplex RT-PCR for Virulence Detection and Differentiation Between Newcastle Disease Virus and Goose-Origin APVM-1
    Kong, Ling-Chen
    Ren, Tao
    Ao, Yan-Hua
    Xi, Rui-Zhen
    Liao, Ming
    AVIAN DISEASES, 2007, 51 (03) : 668 - 673
  • [43] RAPID ASSESSMENT OF PROTEIN-TYROSINE-PHOSPHATASE EXPRESSION LEVELS BY RT-PCR WITH DEGENERATE PRIMERS
    HENDRIKS, W
    BRUGMAN, C
    SCHEPENS, J
    WIERINGA, B
    MOLECULAR BIOLOGY REPORTS, 1994, 19 (02) : 105 - 108
  • [44] Pathotyping of Newcastle Disease Viruses by RT-PCR and Restriction Enzyme Analysis
    T. Nanthakumar
    R.S. Kataria
    A.K. Tiwari
    G. Butchaiah
    J.M. Kataria
    Veterinary Research Communications, 2000, 24 : 275 - 286
  • [45] Sensitive, semi-nested RT-PCR amplification of fusion gene sequences for the rapid detection and differentiation of Newcastle disease virus
    Zhang, Lei
    Pan, Zhiming
    Geng, Shizhong
    Chen, Xiang
    Hu, Shunlin
    Liu, Huimo
    Wu, Yantao
    Jiao, Xinan
    Liu, Xiufan
    RESEARCH IN VETERINARY SCIENCE, 2010, 89 (02) : 282 - 289
  • [46] Pathotyping of Newcastle disease viruses by RT-PCR and restriction enzyme analysis
    Nanthakumar, T
    Kataria, RS
    Tiwari, AK
    Butchaiah, G
    Kataria, JM
    VETERINARY RESEARCH COMMUNICATIONS, 2000, 24 (04) : 275 - 286
  • [47] RT-PCR for detecting five distinct Tospovirus species using degenerate primers and dsRNA template
    Okuda, M
    Hanada, K
    JOURNAL OF VIROLOGICAL METHODS, 2001, 96 (02) : 149 - 156
  • [48] Detection of Beet yellows virus by RT-PCR and immunocapture RT-PCR in Tetragonia expansa and Beta vulgaris
    Kundu, K
    Rysánek, P
    ACTA VIROLOGICA, 2004, 48 (03) : 177 - 182
  • [49] RT-PCR based diagnosis of infectious bursal disease virus in Pakistan
    Zahoor, M. A.
    Hussain, I.
    Mansoor, M. K.
    Masood, S.
    Khan, Q. M.
    JOURNAL OF DAIRY SCIENCE, 2004, 87 : 109 - 110