Genome sequences of three koi herpesvirus isolates representing the expanding distribution of an emerging disease threatening koi and common carp worldwide

被引:218
作者
Aoki, Takashi
Hirono, Ikuo
Kurokawa, Ken
Fukuda, Hideo
Nahary, Ronen
Eldar, Avi
Davison, Andrew J.
Waltzek, Thomas B.
Bercovier, Herve
Hedrick, Ronald P.
机构
[1] MRC, Virol Unit, Inst Virol, Glasgow G11 5JR, Lanark, Scotland
[2] Tokyo Univ Marine Sci & Technol, Lab Genome Sci, Tokyo, Japan
[3] Nara Inst Sci & Technol, Lab Comparat Genom, Keihanna Science City, Nara 6300192, Japan
[4] Hebrew Univ Jerusalem, Hadassah Med Sch, Inst Microbiol, Dept Clin Microbiol, IL-91010 Jerusalem, Israel
[5] Kimron Vet Inst, IL-50250 Bet Dagan, Israel
[6] Univ Calif Davis, Sch Vet Med, Dept Med & Epidemiol, Davis, CA 95616 USA
基金
英国医学研究理事会;
关键词
D O I
10.1128/JVI.00146-07
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Since the mid-1990s, lethal infections of koi herpesvirus (KHV) have been spreading, threatening the worldwide production of common carp and koi (both Cyprinus carpio). The complete genome sequences of three KHV strains from Japan, the United States, and Israel revealed a 295-kbp genome containing a 22-kbp terminal direct repeat. The finding that 15 KHV genes have clear homologs in the distantly related channel catfish virus (ictalurid herpesvirus 1) confirms the proposed place of KHV in the family Herpesviridae, specifically in the branch with fish and amphibian hosts. KHV thus has the largest genome reported to date for this family. The three strains were interpreted as having arisen from a wild-type parent encoding 156 unique protein-coding genes, 8 of which are duplicated in the terminal repeat. In each strain, four to seven genes from among a set of nine are fragmented by frameshifts likely to render the encoded proteins nonfunctional. Six of the affected genes encode predicted membrane glycoproteins. Frameshifts or other mutations close to the 3' ends of coding sequences were identified in a further six genes. The conclusion that at least some of these mutations occurred in vivo prompts the hypothesis that loss of gene functions might be associated with emergence of the disease and provides a basis for further investigations into the molecular epidemiology of the virus.
引用
收藏
页码:5058 / 5065
页数:8
相关论文
共 50 条
  • [1] An enzyme linked immunosorbent assay (ELISA) for detection of antibodies to the koi herpesvirus (KHV) in the serum of koi Cyprinus carpio
    Adkison, MA
    Gilad, O
    Hedrick, RP
    [J]. FISH PATHOLOGY, 2005, 40 (02): : 53 - 62
  • [2] BASIC LOCAL ALIGNMENT SEARCH TOOL
    ALTSCHUL, SF
    GISH, W
    MILLER, W
    MYERS, EW
    LIPMAN, DJ
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 1990, 215 (03) : 403 - 410
  • [3] ORIGIN AND DOMESTICATION OF THE WILD CARP, CYPRINUS-CARPIO - FROM ROMAN GOURMETS TO THE SWIMMING FLOWERS
    BALON, EK
    [J]. AQUACULTURE, 1995, 129 (1-4) : 3 - 48
  • [4] Cloning of the koi herpesvirus (KHV) gene encoding thymidine kinase and its use for a highly sensitive PCR based diagnosis
    Bercovier, H
    Fishman, Y
    Nahary, R
    Sinai, S
    Zlotkin, A
    Eyngor, M
    Gilad, O
    Eldar, A
    Hedrick, RP
    [J]. BMC MICROBIOLOGY, 2005, 5 (1)
  • [5] Bretzinger A, 1999, BULL EUR ASSN FISH P, V19, P182
  • [6] Human cytomegalovirus-encoded interleukin-10 homolog inhibits maturation of dendritic cells and alters their functionality
    Chang, WLW
    Baumgarth, N
    Yu, D
    Barry, PA
    [J]. JOURNAL OF VIROLOGY, 2004, 78 (16) : 8720 - 8731
  • [7] CHANNEL CATFISH VIRUS - A NEW TYPE OF HERPESVIRUS
    DAVISON, AJ
    [J]. VIROLOGY, 1992, 186 (01) : 9 - 14
  • [8] A novel class of herpesvirus with bivalve hosts
    Davison, AJ
    Trus, BL
    Cheng, NQ
    Steven, AC
    Watson, MS
    Cunningham, C
    Le Deuff, RM
    Renault, T
    [J]. JOURNAL OF GENERAL VIROLOGY, 2005, 86 : 41 - 53
  • [9] Evolution of the herpesviruses
    Davison, AJ
    [J]. VETERINARY MICROBIOLOGY, 2002, 86 (1-2) : 69 - 88
  • [10] IDENTIFICATION OF STRUCTURAL PROTEINS OF CHANNEL CATFISH VIRUS BY MASS-SPECTROMETRY
    DAVISON, AJ
    DAVISON, MD
    [J]. VIROLOGY, 1995, 206 (02) : 1035 - 1043