Differentiation between pathogenic serotype 1 isolates of Marek's disease virus and the Rispens CVI988 vaccine in Australia using real-time PCR and high resolution melt curve analysis

被引:25
作者
Renz, K. G. [1 ]
Cheetham, B. F. [2 ]
Walkden-Brown, S. W. [1 ]
机构
[1] Univ New England, Sch Environm & Rural Sci, Armidale, NSW 2351, Australia
[2] Univ New England, Sch Sci & Technol, Armidale, NSW 2351, Australia
关键词
Rispens CVI988; Pathogenic MDV1; meq; Differentiation; qPCR; High resolution melt curve analysis (HRM); POLYMERASE-CHAIN-REACTION; SERIAL INVITRO PASSAGE; ABSOLUTE QUANTITATION; TISSUE CULTURE; VIRULENCE; REPEATS; GENOME; MDV; AMPLIFICATION; ASSOCIATION;
D O I
10.1016/j.jviromet.2012.09.018
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Two real-time PCR assays were developed which enable quantitation and differentiation between pathogenic Australian isolates of Marek's disease virus (MDV) serotype 1 and the serotype 1 vaccine strain Rispens CVI988. The assays are based on a DNA sequence variation in the meq gene between pathogenic and vaccinal MDV1 which has been confirmed by sequencing of 20 Australian field strains of MDV. Complete specificity has been demonstrated in samples containing pathogenic MDV (n = 20), Rispens (3 commercial vaccine strains), or both. The limit of detection of both the Rispens-specific and the pathogenic MDV1-specific assays was 10 viral copies/reaction. The tests successfully differentiated and quantified MDV in mixtures of pathogenic and vaccinal Rispens virus. A high resolution melt curve analysis targeting the same SNP used for the real-time PCR assays was also developed which successfully detected sequence variation between Md5, six Australian MDV1 isolates and the three Rispens vaccines. However it was ineffective at differentiating mixtures of pathogenic and vaccinal MDV1. The real-time PCR assays have both diagnostic and epidemiological applications as they enable differentiation and quantitation of Rispens CVI988 and pathogenic MDV1 in co-infected chickens in Australia. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:144 / 152
页数:9
相关论文
共 32 条
  • [1] [Anonymous], 2005, 8 ICTV
  • [2] Absolute quantitation of Marek's disease virus genome copy number in chicken feather and lymphocyte samples using real-time PCR
    Baigent, SJ
    Petherbridge, LJ
    Howes, K
    Smith, LP
    Currie, RJW
    Nair, VK
    [J]. JOURNAL OF VIROLOGICAL METHODS, 2005, 123 (01) : 53 - 64
  • [3] POLYMERASE CHAIN-REACTION FOR DIFFERENTIATION BETWEEN PATHOGENIC AND NONPATHOGENIC SEROTYPE-1 MAREKS-DISEASE VIRUSES (MDV) AND VACCINE VIRUSES OF MDV-SEROTYPE-2 AND MDV-SEROTYPE-3
    BECKER, Y
    ASHER, Y
    TABOR, E
    DAVIDSON, I
    MALKINSON, M
    WEISMAN, Y
    [J]. JOURNAL OF VIROLOGICAL METHODS, 1992, 40 (03) : 307 - 322
  • [4] Burgess G.W., 2003, AECL PUBLICATION, V03/05
  • [5] Cha R S, 1992, PCR Methods Appl, V2, P14
  • [6] AGENT OF MAREKS DISEASE IN TISSUE CULTURE
    CHURCHILL, AE
    BIGGS, PM
    [J]. NATURE, 1967, 215 (5100) : 528 - +
  • [7] Use of Marek's disease vaccines: could they be driving the virus to increasing virulence?
    Davison, F
    Nair, V
    [J]. EXPERT REVIEW OF VACCINES, 2005, 4 (01) : 77 - 88
  • [8] The development and evaluation of two tissue culture-grown Marek's disease challenge viruses
    De Laney, DB
    Morrow, CJ
    Read, KM
    Tannock, GA
    [J]. AVIAN PATHOLOGY, 1998, 27 (05) : 472 - 477
  • [9] Imperfect vaccines and the evolution of pathogen virulence
    Gandon, S
    Mackinnon, MJ
    Nee, S
    Read, AF
    [J]. NATURE, 2001, 414 (6865) : 751 - 756
  • [10] Absolute quantitation of Marek's disease virus and Herpesvirus of turkeys in chicken lymphocyte, feather tip and dust samples using real-time PCR
    Islam, A
    Cheetham, BF
    Mahony, TJ
    Young, PL
    Walkden-Brown, SW
    [J]. JOURNAL OF VIROLOGICAL METHODS, 2006, 132 (1-2) : 127 - 134