DIFFERENTIATION OF VACCINE STRAINS AND GEORGIA FIELD ISOLATES OF INFECTIOUS LARYNGOTRACHEITIS VIRUS BY THEIR RESTRICTION ENDONUCLEASE FRAGMENT PATTERNS

被引:46
|
作者
ANDREASEN, JR
GLISSON, JR
VILLEGAS, P
机构
[1] Department of Avian Medicine, College of Veterinary Medicine, University of Georgia, Athens
关键词
D O I
10.2307/1591259
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Seven restriction endonucleases (REs) were used to cleave the DNA from seven vaccine strains of infectious laryngotracheitis (ILT) virus and from six Georgia field isolates of ILT virus. After electrophoresis of the resulting RE fragments, the patterns were compared in order to differentiate strains of ILT virus. The six chicken-embryo-origin (CEO) vaccines were identical with each RE, but the tissue-culture-origin (TCO) vaccine strain differed from the CEO vaccines using five of the REs. Four of the six field isolates were identical by each RE, but two field isolates differed from each other and from the four identical field isolates on the basis of patterns produced by some but not all of the REs. The four identical field isolates could not be differentiated from the CEO vaccine strains by any RE, but the other two field isolates were not identical to either strain of vaccine virus. This work demonstrates that differentiable strains of ILT virus exist in the United States and that viruses other than vaccine viruses are involved in field outbreaks of ILT.
引用
收藏
页码:646 / 656
页数:11
相关论文
共 50 条
  • [1] Rapid differentiation of vaccine strains and field isolates of infectious laryngotracheitis virus by restriction fragment length polymorphism of PCR products
    Chang, PC
    Lee, YL
    Shien, JH
    Shieh, HK
    JOURNAL OF VIROLOGICAL METHODS, 1997, 66 (02) : 179 - 186
  • [2] DIFFERENCES AMONG RESTRICTION ENDONUCLEASE DNA FINGERPRINTS OF PENNSYLVANIA FIELD ISOLATES, VACCINE STRAINS, AND CHALLENGE STRAINS OF INFECTIOUS LARYNGOTRACHEITIS VIRUS
    KELLER, LH
    BENSON, CE
    DAVISON, S
    ECKROADE, RJ
    AVIAN DISEASES, 1992, 36 (03) : 575 - 581
  • [3] Differentiation of field isolates and vaccine strains of infectious laryngotracheitis virus by DNA sequencing
    Sadeghi, Majid
    Bozorgemehrifard, Mohammad Hasan
    Keyvanfar, Hadi
    Momtaz, Hassan
    Shooshtari, Abdolhamid
    Charkhkar, Saied
    AFRICAN JOURNAL OF MICROBIOLOGY RESEARCH, 2011, 5 (24): : 4112 - 4117
  • [4] Differentiation of field isolates and vaccine strains of infectious laryngotracheitis virus by DNA sequencing
    Chacon, Jorge Luis
    Piantino Ferreira, Antonio J.
    VACCINE, 2009, 27 (48) : 6731 - 6738
  • [5] RESTRICTION-ENDONUCLEASE ANALYSIS OF DELMARVA FIELD ISOLATES OF INFECTIOUS LARYNGOTRACHEITIS VIRUS
    KEELER, CL
    HAZEL, JW
    HASTINGS, JE
    ROSENBERGER, JK
    AVIAN DISEASES, 1993, 37 (02) : 418 - 426
  • [6] RESTRICTION ENDONUCLEASE PATTERNS OF SOME EUROPEAN AND AMERICAN ISOLATES OF AVIAN INFECTIOUS LARYNGOTRACHEITIS VIRUS
    LEIB, DA
    BRADBURY, JM
    GASKELL, RM
    HUGHES, CS
    JONES, RC
    AVIAN DISEASES, 1986, 30 (04) : 835 - 837
  • [7] Characterization of Western European Field Isolates and Vaccine Strains of Avian Infectious Laryngotracheitis Virus by Restriction Fragment Length Polymorphism and Sequence Analysis
    Neff, C.
    Sudler, C.
    Hoop, R. K.
    AVIAN DISEASES, 2008, 52 (02) : 278 - 283
  • [8] Characterization by restriction fragment length polymorphism and sequence analysis of field and vaccine strains of infectious laryngotracheitis virus involved in severe outbreaks
    Chacon, Jorge Luis
    Mizuma, Matheus Y.
    Piantino Ferreira, Antonio J.
    AVIAN PATHOLOGY, 2010, 39 (06) : 425 - 433
  • [9] DIFFERENTIATION OF INFECTIOUS LARYNGOTRACHEITIS VIRUS-STRAINS USING RESTRICTION ENDONUCLEASES
    KOTIW, M
    WILKS, CR
    MAY, JT
    AVIAN DISEASES, 1982, 26 (04) : 718 - 731
  • [10] Characterization of field strains of infectious laryngotracheitis virus in China by restriction fragment length polymorphism and sequence analysis
    Yan, Zhuanqiang
    Li, Shengpeng
    Xie, Qingmei
    Chen, Feng
    Bi, Yingzuo
    JOURNAL OF VETERINARY DIAGNOSTIC INVESTIGATION, 2016, 28 (01) : 46 - 49