ONE-STEP TYPING OF EPSTEIN-BARR-VIRUS BY POLYMERASE CHAIN-REACTION - PREDOMINANCE OF TYPE-1 VIRUS IN JAPAN

被引:70
作者
KUNIMOTO, M
TAMURA, S
TABATA, T
YOSHIE, O
机构
[1] SHIONOGI INST MED SCI, 2-5-1 MISHIMA, SETTSU, OSAKA 566, JAPAN
[2] WAKAYAMA MED COLL, WAKAYAMA 640, JAPAN
关键词
D O I
10.1099/0022-1317-73-2-455
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
The prevalence of two types of Epstein-Barr virus (EBV) in Japan was studied by using the polymerase chain reaction (PCR). The U2 region encoding EBV nuclear antigen 2 (EBNA-2) was chosen as the target of amplification. Consensus primers were synthesized from sequences common to the two types but encompassing a large stretch of deletion in the sequence of type 1 EBV. The primers were capable of amplifying both types at the same time but allowed differentiation of each type by the size of the amplification products. Thus we could carry out detection and typing of EBV in a one-step PCR. EBV was detected in mouth washings of 21 (23%) of 91 seropositive healthy adults. Twenty samples (22%) contained type 1 and only one (1%) type 2. Seventy-nine patients suffering from various types of tonsillitis were also studied. EBV was detected in mouth washings of 37 patients (47%). Thirty-four (43%) contained type 1 and three (4%) type 2. Double infection was not seen in either healthy donors or patients. These results indicate that type 1 EBV is highly dominant and the type 2 variant is quite rare in Japan.
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页码:455 / 461
页数:7
相关论文
共 31 条
  • [1] A PUTATIVE TRANSFORMING GENE OF JIJOYE VIRUS DIFFERS FROM THAT OF EPSTEIN-BARR VIRUS PROTOTYPES
    ADLDINGER, HK
    DELIUS, H
    FREESE, UK
    CLARKE, J
    BORNKAMM, GW
    [J]. VIROLOGY, 1985, 141 (02) : 221 - 234
  • [2] BERGER J, 1969, TRANSPL P, V1, P939
  • [3] DETECTION OF EPSTEIN-BARR-VIRUS DNA-SEQUENCES IN NASOPHARYNGEAL CARCINOMA-CELLS BY ENZYMATIC DNA AMPLIFICATION
    CHANG, YS
    TYAN, YS
    LIU, ST
    TSAI, MS
    PAO, CC
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 1990, 28 (11) : 2398 - 2402
  • [4] DETECTION OF EPSTEIN-BARR-VIRUS GENOMES IN NORMAL HUMAN LACRIMAL GLANDS
    CROUSE, CA
    PFLUGFELDER, SC
    CLEARY, T
    DEMICK, SM
    ATHERTON, SS
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 1990, 28 (05) : 1026 - 1032
  • [5] U2 REGION OF EPSTEIN-BARR VIRUS-DNA MAY ENCODE EPSTEIN-BARR NUCLEAR ANTIGEN-2
    DAMBAUGH, T
    HENNESSY, K
    CHAMNANKIT, L
    KIEFF, E
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (23): : 7632 - 7636
  • [6] VIRUS PARTICLES IN CULTURED LYMPHOBLASTS FROM BURKITTS LYMPHOMA
    EPSTEIN, MA
    ACHONG, BG
    BARR, YM
    [J]. LANCET, 1964, 1 (733) : 702 - +
  • [7] FOX RI, 1986, J IMMUNOL, V137, P3162
  • [8] DETECTION BY PCR OF HHV-6 AND EBV DNA IN BLOOD AND OROPHARYNX OF HEALTHY-ADULTS AND HIV-SEROPOSITIVES
    GOPAL, MR
    THOMSON, BJ
    FOX, J
    TEDDER, RS
    HONESS, RW
    [J]. LANCET, 1990, 335 (8705) : 1598 - 1599
  • [9] EBNA SIZE POLYMORPHISM CAN BE USED TO TRACE EPSTEIN-BARR-VIRUS SPREAD WITHIN FAMILIES
    GRATAMA, JW
    OOSTERVEER, MAP
    KLEIN, G
    ERNBERG, I
    [J]. JOURNAL OF VIROLOGY, 1990, 64 (10) : 4703 - 4708
  • [10] REPLICATION OF EPSTEIN-BARR VIRUS WITHIN THE EPITHELIAL-CELLS OF ORAL HAIRY LEUKOPLANKIA, AN AIDS-ASSOCIATED LESION
    GREENSPAN, JS
    GREENSPAN, D
    LENNETTE, ET
    ABRAMS, DI
    CONANT, MA
    PETERSEN, V
    FREESE, UK
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1985, 313 (25) : 1564 - 1571