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The familyHerpesviridae: an update

  • Virology Division News
  • Published: September 1992
  • Volume 123, pages 425–449, (1992)
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The familyHerpesviridae: an update
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  • B. Roizmann1,
  • R. C. Desrosiers2,
  • B. Fleckenstein3,
  • C. Lopez4,
  • A. C. Minson5 &
  • …
  • M. J. Studdert6 

  • 1601 Accesses

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References

  1. Ablashi DV, Chopra HC, Armstrong GR (1972) A cytomegalovirus isolated from an owl monkey. Lab Anim Sci 22: 190–195

    Google Scholar 

  2. Allen GP, Bryans JT (1986) Molecular epizootiology, pathogenesis ans prophylaxis of equine herpesvirus 1 infections. Prog Vet Microbiol Immunol 2: 78–144

    Google Scholar 

  3. Armstrong JA, Pereira HG, Andrewes CH (1961) Observation of the virus of infectious bovine rhinotracheitis and its affinity with the herpesvirus group. Virology 14: 276–285

    Google Scholar 

  4. Asher Y, Heller M, Becker Y (1969) Incorporation of lipids into herpes simplex virus particles. J Gen Virol 4: 65–76

    Google Scholar 

  5. Asher DM, Gibbs CJ, Long DJ (1969) Rhesus monkey cytomegalovirus: persistent asymptomatic viruria. Bacteriol Proc Abstrct V269

  6. Baer R, Bankier AT, Biggin MD, Deininger PL, Farrell PJ, Gibson TG, Hatfull G, Hudson GS, Satchwell SC, Seguin C, Tuffnell PS, Barrell BG (1984) DNA sequence and expression of the B95-8 Epstein-Barr virus genome. Nature 310: 207–211

    Google Scholar 

  7. Barahona HH, Daniel MD, Katz SL, Ingalis JK, Melendez LV, King NW (1975) Isolation and in vitro characterization of a herpesvirus from ground squirrels (Citellus sp). Lab Anim Sci 25: 725–739

    Google Scholar 

  8. Barahona HH, Trum BF, Melendenz LV, Garcia FG, King NW, Daniel MD, Jackman DA (1973) A new herpes virus isolated from kinkajou (Botos flavus). Lab Anim Sci 23: 830–836

    Google Scholar 

  9. Bartha A, Juhasz M, Liebermann H (1966) Isolation of a bovine herpesvirus from calves with respiratory disease and keratoconjunctivitis. Acta Vet Acad Sci 16: 357–358

    Google Scholar 

  10. Basson PA, McCully RM, DeVoss B, Young E, Schulze P (1971) Some parasitic and other natural diseases of the African elephant in the Kruger National Park. Onderstepoort J Vet Res 38: 239–254

    Google Scholar 

  11. Baudet AETF (1928) Mortality in ducks in the Nederlands caused by a filterable virus: fowl plague. Tijdschr Diergeneeskd 50: 455–459

    Google Scholar 

  12. Ben-Porat T, Kaplan AS (1971) Phospholipid metabolism of herpesvirus-infected and uninfected rabbit kidney cells. Virology 45: 252–264

    Google Scholar 

  13. Ben-Porat T, Kaplan AS (1985) Molecular biology of pseudorabies virus. In: Roizman B (ed) The herpesviruses, vol 3. Plenum, New York, pp 105–173

    Google Scholar 

  14. Berezesky IK, Grimley PM, Tyrell SA (1971) Ultrastructure of a rat cytomegalovirus. Exp Mol Pathol 14: 337–349

    Google Scholar 

  15. Bhatt PN, Percy DH, Craft JL, Jonas AM (1971) Isolation and characterization of a herpes-like (Hsiung-Kaplow) virus from guinea pigs. J Infect Dis 123: 178–179

    Google Scholar 

  16. Bia FJ, Summers WC, Fong CKY, Hsiung GD (1980) New endogenous herpesvirus of guinea pigs: biological and molecular characterization. J Virol 36: 245–253

    Google Scholar 

  17. Black PH, Hartley J, Rowe WP (1963) Isolation of cytomegalovirus from African green monkey. Proc Soc Exp Biol Med 112: 601–605

    Google Scholar 

  18. Blakely GA, Lourie B, Morton WG, Evans HH, Kaufman AF (1973) A varicella-like disease in macaque monkeys. J Infect Dis 127: 617–625

    Google Scholar 

  19. Blaskovic D, Stancekova M, Svobodova J, Kresakova J (1980) Isolation of five strains of herpesvirus from two species of free living small rodents. Acta Virol 24: 468

    Google Scholar 

  20. Blaskovic D, Sekayova Z, Turna J, Kudelova M, Slavik J, Mucha V (1988) Purification of murine alpha-herpesvirus and some properties of its DNA. Acta Virol 32: 329–333

    Google Scholar 

  21. Bocker JF, Tiedemann K-H, Bornkamm GW, Zur Hausen M (1980) Characterization of an EBV-like virus from African green monkey lymphoblasts. Virology 101: 291–295

    Google Scholar 

  22. Bornkamm GW, Delius H, Fleckenstein B, Werner FJ, Mulder C (1976) Structure of herpes saimiri genomes: arrangement of heavy and light sequences in the M genome. J Virol 19: 154–161

    Google Scholar 

  23. Borst GHA, Walvoort HC, Reijnders PJH, Van der Kamp JS, Osterhaus ADME (1986) An outbreak of a herpesvirus infection in harbor seals (Phoca vitulina). J Wildl Dis 22: 1–6

    Google Scholar 

  24. Brake F, Studdert MJ (1985) Molecular epidemiology and pathogenesis of ruminant herpesviruses including bovine, buffalo, and caprine herpesvirus 1 and bovine encephalitis herpesvirus. Aust Vet J 62: 331–334

    Google Scholar 

  25. Breese SS Jr, Dardiri AH (1968) Electron microscopic characterization of duck plague virus. Virology 34: 160–169

    Google Scholar 

  26. Bridgen A (1991) The derivation of a restriction endonuclease map for alcelaphine herpesvirus 1 DNA. Arch Virol 117: 183–192

    Google Scholar 

  27. Brigden A, Herring AJ, Inglis NF, Reid HW (1989) Preliminary characterization of the alcelaphine herpesvirus 1 genome. J Gen Virol 70: 1141–1150

    Google Scholar 

  28. Bridgen A, Reid HW (1991) Deviation of a DNA clone corresponding to the viral agent of sheep-associated malignant catarrhal fever. Res Vet Sci 50: 38–44

    Google Scholar 

  29. Browning GF, Ficorilli N, Studdert MJ (1988) Asinine herpesvirus genomes: comparison with those of the equine herpesviruses. Arch Virol 101: 183–190

    Google Scholar 

  30. Browning GF, Studdert MJ (1987) Genomic heterogeneity of equine betaherpesviruses. J Gen Virol 68: 1441–1447

    Google Scholar 

  31. Browning GF, Studdert MJ (1989) Physical mapping of a genome of equine herpesvirus 2 (equine cytomegalovirus). Arch Virol 104: 77–86

    Google Scholar 

  32. Browning GF, Studdert MJ (1989) Physical mapping of the genomic heterogeneity of isolates of equine herpesvirus 2 (equine cytomegalovirus). Arch Virol 104: 87–94

    Google Scholar 

  33. Bublot M, Van Bressen M, Thiry E, Dubuisson J, Pastoret P (1990) Bovine herpesvirus 4 genomes: cloning, mapping, and strain variation analysis. J Gen Virol 71: 133–142

    Google Scholar 

  34. Bublot M, Dubuisson M-F, Van Bressem SD, Pastoret P-P, Thiry E (1991) Antigenic and genomic identity between simian herpesvirus aotus type 2 and bovine herpesvirus type 4. J Gen Virol 72: 715–719

    Google Scholar 

  35. Buchanan JS, Richards RH, Sommerville C, Madeley CR (1978) A herpestype virus from turbot (Scophthalamus maximus L). Vet Rec 102: 527–528

    Google Scholar 

  36. Buchman TG, Roizman B (1978) Anatomy of bovine mammillitis virus DNA. I. Restriction endonuclease maps of four populations of molecules that differ in the relative orientation of their long and short components. J Virol 25: 395–407

    Google Scholar 

  37. Buchman TG, Roizman B (1978) Anatomy of bovine mammillitis DNA. II. Size and arrangements of the deoxynucleotide sequences. J Virol 27: 239–254

    Google Scholar 

  38. Buckmaster AE, Scott SD, Sanderson MJS, Boursnell MEG, Ross NLJ, Binns MM (1988) Gene sequence and mapping data from Marek's disease virus and herpesvirus of turkeys: Implications for herpesvirus classification. J Gen Virol 69: 2033–2042

    Google Scholar 

  39. Bülow VV, Biggs PM (1975) Differentiation between strains of Marek's disease virus and turkey herpesvirus by immuno-fluorescence assays. Avian Pathol 4: 133–145

    Google Scholar 

  40. Bürki F, Burtscher H, Sibalin M (1973) Herpesvirus strigis: a new avian herpesvirus. I. Biological properties. Arch Ges Virusforsch 43: 14–24

    Google Scholar 

  41. Burtscher H, Grunberg W (1979) Herpesvirus-Hepatitis bei Kranichen (Aves-Gruidae). I. Pathomorphologische Befunde. Zentralbl Veterinaermed [B] 26: 561–569

    Google Scholar 

  42. Cameron KR, Stamminger T, Craxton M, Bodemer W, Honess RW, Fleckenstein B (1987) The 160,000 Mr virion protein encoded at the right end of the herpesvirus saimiri genome is homologous to the 140,000 Mr membrane antigen encoded at the left end of the Epstein-Barr virus genome. J Virol 61: 2063–2070

    Google Scholar 

  43. Cebrian J, Bucchini D, Sheldrick P (1983) Endless viral DNA in cells infected with channel catfish virus. J Virol 46: 405–412

    Google Scholar 

  44. Cebrian J, Kaschka-Dierich C, Berthelot N, and Sheldrick P (1982) Inverted repeat nucleotide sequences in the genomes of Marek's disease virus and the herpesvirus of the turkey. Proc Natl Acad Sci USA 79: 555–558

    Google Scholar 

  45. Chee MS, Bankier AT, Beck S, Bohni R, Brown CM, Cerny R, Horsnell T, Hutchinson III CA, Kouzarides T, Martignetti JA, Preddie E, Satchwell SC, Tomlinson P, Weston KM, Barrell BG (1990) Analysis of the protein-coding content of the sequence of human cytomegalovirus strain AD169. Curr Top Microbiol Immunol 154: 125–169

    Google Scholar 

  46. Chousterman S, Lacasa M, Sheldrick P (1979) Physical map of the channel catfish virus genome: location of sites for restriction endonucleasesEcoRI,HindIII, HpaI, andXbaI. J Virol 37: 73–85

    Google Scholar 

  47. Churchill AE, Biggs PM (1967) Agent of Marek's disease in tissue culture. Nature 215: 528–530

    Google Scholar 

  48. Clark HF, Karzon DT (1972) Iguana virus, a herpes-like virus isolated from cultured cells of a lizard,Iguana iguana. Infect Immun 5: 559–569

    Google Scholar 

  49. Clarkson MJ, Thorpe E, McCarthy K (1967) A virus disease of captive vervet monkeys (Cercopithecus aethiops) caused by a new herpesvirus. Arch Ges Virusforsch 22: 219–234

    Google Scholar 

  50. Cornwell HJC, Wright NG, McCusker HB (1970) Herpesvirus infection of pigeons. II. Experimental infection of pigeons and chicks. J Comp Pathol 80: 229–232

    Google Scholar 

  51. Cox WR, Rapley WA, Barker IK (1980) Herpesvirus-like infection in the painted turtle (Chrysemys picta). J Wildl Dis 16: 445–449

    Google Scholar 

  52. Cruickshank JO, Berry DM, Hay B (1963) The fine structure of infectious laryngotracheitis virus. J Virol 20: 376–378

    Google Scholar 

  53. Cullinane AA, Rixon FJ, Davison AJ (1988) Characterization of the genome of equine herpesvirus 1 subtype 2. J Gen Virol 69: 1575–1590

    Google Scholar 

  54. Daniel MD, Melendez LV, King NW, Fraser CEO, Barahona HH, Hunt RD, Garcia FG (1971) Herpes virus aotus: a latent herpesvirus from owl monkeys (Aotus trivirgatus). Isolation and characteristics. Proc Soc Exp Biol Med 138: 835–845

    Google Scholar 

  55. Darai G, Matz B, Schroder CH, Flugel RH, Berger U, Munk K, Gelderblom H (1979) Characterization of a tree shrew herpesvirus isolated from a lymphosarcoma. J Gen Virol 43: 541–551

    Google Scholar 

  56. Davison AJ, McGeoch DJ (1986) Evolutionary comparisons of the S segments in the genomes of herpes simplex virus type 1 and varicella-zoster virus. J Gen Virol 67: 597–611

    Google Scholar 

  57. Davison AJ, Scott JE (1986) The complete DNA sequence of varicella-zoster virus. J Gen Virol 67: 1759–1816

    Google Scholar 

  58. Davison AJ, Taylor P (1986) Genetic relations between varicella-zoster virus and Epstein-Barr virus. J Gen Virol 68: 1067–1079

    Google Scholar 

  59. Deinhardt F, Falk LA, Wolfe LG (1973) Simian herpesviruses. Cancer Res 33: 1424–1426

    Google Scholar 

  60. Deiss LP, Chou J, Frenkel N (1986) Functional domains with the a sequence involved in the cleavage-packaging of herpes simplex virus DNA. J Virol 59: 605–618

    Google Scholar 

  61. De Villiers EM, Els HJ, Verwoerd DW (1975) Characteristics of an ovine herpesvirus associated with pulmonary adenomatosis (jaagsiekte) in sheep. S Afr J Med Sci 40: 165–170

    Google Scholar 

  62. De Villiers EM (1979) Purification of the JS-3 isolate of herpesvirus ovis (bovid herpesvirus 4) and some properties of its DNA. J Virol 32: 705–709

    Google Scholar 

  63. Diosi P, Babusceac L, David C (1967) Recovery of cytomegalovirus from the submaxillary glands of ground squirrels. Arch Ges Virusforsch 20: 383–386

    Google Scholar 

  64. Diosi P, Plavosin L, Arcan P, David C (1975) Recovery of a new herpesvirus form the ground squirrel. Pathol Microbiol 42: 42–48

    Google Scholar 

  65. Ditchfield J, Grinyer I (1965) Feline rhinotracheitis virus: a feline herpesvirus. Virology 26: 504–506

    Google Scholar 

  66. Docherty DE, Romaine RI, Knight RL (1983) Isolation of a herpesvirus from a bald eagle nesting. Avian Dis 27: 1162–1165

    Google Scholar 

  67. Dubuisson J, Danyi S, Bublot M, Pastoret P-P, Thiry E (1991) Comparison of proteins of simian aotus type 2 and bovine herpesvirus 4. J Gen Virol 72: 1145–1150

    Google Scholar 

  68. Dumas AM, Geelen JLMC, Maris W, Van der Noordaa J (1980) Infectivity and molecular weight of varicella-zoster virus DNA. J Gen Virol 47: 233–235

    Google Scholar 

  69. Ebeling A, Keil G, Nowak B, Fleckenstein B, Berthelot N, Sheldrick P (1983) Genome structure and virion polypeptides of the primate herpesviruses,Herpesvirus aotus types 1 and 3; comparison with human cytomegalovirus. J Virol 45: 715–726

    Google Scholar 

  70. Ebeling A, Keil GM, Knust E, Koszinowski UH (1983) Molecular cloning and physical mapping of murine cytomegalovirus DNA. J Virol 47: 421–433

    Google Scholar 

  71. Efstathiou S, Ho YM, Minson AC (1990) Cloning and molecular characterization of the murine herpesvirus 68 genome. J Gen Virol 71: 1355–1364

    Google Scholar 

  72. Ek-Kommonen C, Pelkonen S, Nettleton PF (1986) Isolation of herpesvirus serologically related to bovine herpesvirus 1 from a reindeer (Rangifer tarandus). Acta Vet Scand 27: 299–301

    Google Scholar 

  73. Engles M, Giuliani C, Wild P, Beck TM, Loepfe E, Wyler R (1986) The genome of bovine herpesvirus 1 (BHV-1) strains exhibiting a neuropathogenic potential compared to known BHV-1 strains by restriction site mapping and cross hybridization. Virus Res 6: 57–73

    Google Scholar 

  74. Engles M, Loepfe E, Wild P, Schraner E, Wyler R (1987) The genome of caprine herpesvirus 1: genome structure and relatedness to bovine herpesvirus 1. J Gen Virol 68: 2019–2023

    Google Scholar 

  75. Epstein MA (1962) Observations on the fine structure of mature herpes simplex virus and on the composition of its nucleoid. J Exp Med 115: 1–12

    Google Scholar 

  76. Epstein MA, Henle W, Achong BG, Barr YM (1965) Morphological and biological studies on virus in cultured lymphoblasts from Burkitt's lymphoma. J Exp Med 121: 761–770

    Google Scholar 

  77. Falk L, Deinhardt F, Nonoyama M, Wolfe LG, Bergholz C, Lapin B, Yakovleva L, Agrba V, Henle G, Henle W (1976) Properties of a baboon lymphotropic herpesvirus related to Epstein-Barr virus. Int J Cancer 18: 798–807

    Google Scholar 

  78. Falke D, Siegert R, Vogell W (1959) Elektronenmikroskopische Befunde zur Frage der Doppelmembranbildung des Herpes-simplex-Virus. Arch Ges Virusforsch 9: 484–496

    Google Scholar 

  79. Fleckenstein B, Bornkamm GW, Mulder C, Werner F-J, Daniel MD, Falk LA, Delius H (1978) Herpesvirus ateles DNA and its homology with herpesvirus saimiri nucleic acid. J Virol 25: 361–373

    Google Scholar 

  80. Fleckenstein B, Desrosiers RC (1982) Herpesvirus saimiri and herpesvirus ateles. In: Roizman B (ed) The herpesviruses, vol 1. Plenum, New York, pp 253–332

    Google Scholar 

  81. Fong CKY, Tenser RB, Hsiung GD, Gross PA (1973) Ultrastructural studies of the envelopment and release of guinea pig herpeslike virus in cultured cells. Virology 52: 468–477

    Google Scholar 

  82. Frye FL, Oshiro LO, Dutra FR, Carney JD (1977) Herpesvirus-like infection in two Pacific pond turtles. J Am Vet Med Assoc 171: 882–884

    Google Scholar 

  83. Fukuchi K, Sudo M, Lee Y-S, Tanaka A, Nonoyama M (1984) Structure of Marek's disease DNA: detailed restriction enzyme map. J Virol 102–109

  84. Furlong D, Swift H, Roizman B (1972) Arrangement of herpesvirus deoxyribonucleic acid in the core. J Virol 10: 1071–1074

    Google Scholar 

  85. Frank AL, Bissell JA, Rowe DS, Dunnick NR, Mayner RE, Hopps HE, Parkman PD, Meyer HM Jr (1973) Rhesus leucocyte-associated herpesvirus. I. Isolation and characterization of a new herpesvirus recovered from rhesus monkey leukocytes. J Infect Dis 128: 618–629

    Google Scholar 

  86. French EL (1961) Relationship between infectious bovine rhinotracheitis (IBR) virus and a virus isolated from calves with encephalitis. Aust Vet J 38: 555–556

    Google Scholar 

  87. French EL, Purchase HG, Nazerian K (1973) A new herpesvirus isolated from a nestling cormorant (Phalacrocorax melanoleucos). Avian Pathol 2: 3–15

    Google Scholar 

  88. Frenkel N, Schirmer EC, Wyatt LS, Katsafanas G, Roffman E, Danovich RM, June CH (1990) Isolation of a new herpesvirus from human CD4+ T cells. Proc Natl Acad Sci USA 87: 748–752

    Google Scholar 

  89. Gelb LD (1990) Varicella-zoster virus. In: Fields BN, Knipe DM (eds) Fields' virology, vol 2, 2nd edn. Raven Press, New York, pp 2011–2054

    Google Scholar 

  90. Gibbs EPJ, Rweyemamu MM (1977) Bovine herpesviruses. Vet Bull 47: 317–425

    Google Scholar 

  91. Gilles NG, Ogstron CW (1991) Structure and expression of the woodchuck herpesvirus genome. Virology 180: 434–438

    Google Scholar 

  92. Gompels UA, Craxton MA, Honess RW (1988) Conservation of gene organization in the lymphotropic herpesviruses herpesvirus saimiri and Epstein-Barr virus. J Virol 62: 757–767

    Google Scholar 

  93. Gompels UA, Craxton MA, Honess RW (1988) Conservation of glycoprotein H (gH) in herpesviruses: nucleotide sequence of the gH gene from herpesvirus saimiri. J Gen Virol 69: 2819–2829

    Google Scholar 

  94. Goodheart C, Plummer G (1974) The densities of herpes viral DNAs. Prog Med Virol 19: 324

    Google Scholar 

  95. Gravell M (1971) Viruses and renal carcinoma ofRana pipiens. X. Comparison of herpes type viruses associated with Lucké tumour-bearing frogs. Virology 43: 730–733

    Google Scholar 

  96. Gruter W (1924) Das Herpesvirus, seine aetiologische und klinische Bedeutung. Muench Med Wochenschr 71: 1058–1060

    Google Scholar 

  97. Gustafson DP (1986) Pseudorabies. In: Leman AD (ed) Diseases of swine, 6th edn. Iowa State University Press, Ames, pp 274–289

    Google Scholar 

  98. Haines H, Kleese WC (1977) Effect of water temperatures on a herpesvirus infection of sea turtles. Infect Immun 15: 756–759

    Google Scholar 

  99. Hamparian VV, Hilleman MR, Ketler A (1963) Contributions to characterization and classification of animal viruses. Proc Soc Exp Biol Med 112: 1040–1052

    Google Scholar 

  100. Hartley HW, Rowe WP, Huebner RJ (1971) Serial propagation of the guinea pig salivary gland virus in tissue culture. Proc Soc Exp Biol Med 96: 281–285

    Google Scholar 

  101. Hauser B, Mettler F, Rubel A (1983) Herpes-like infection in two young boas. J Comp Pathol 93: 515–519

    Google Scholar 

  102. Heller M, Gerber P, Kieff E (1982) DNA of herpesvirus PAN, a third member of the Epstein-Barr virusherpesvirus papio group. J Virol 41: 931–939

    Google Scholar 

  103. Heller M, Kieff ED (1981) Colinearity between the DNAs of Epstein-Barr virus and herpes virus papio. J Virol 37: 698–709

    Google Scholar 

  104. Hinze HC (1971) New member of the herpesvirus group isolated from wild cottontail rabbits. Infect Immun 3: 350–354

    Google Scholar 

  105. Holmes AW, Caldwell RG, Dedmon RE, Deinhardt F (1964) Isolation and characterization of a new herpes virus. J Immunol 92: 602–610

    Google Scholar 

  106. Honess RW, Gompels UA, Barrell BG, Craxton M, Cameron KR, Staden R, Chang Y-N, Hayward GS (1989) Deviations from expected frequencies of CpG dinucleotides in herpesvirus DNAs may be diagnostic of differences in the states of their latent genomes. J Gen Virol 70: 837–855

    Google Scholar 

  107. Hsiung GD, Kaplow LS (1969) Herpes like virus isolated from spontaneously degenerated tissue culture derived from leukemia-susceptible guinea pigs. J Virol 3: 355–357

    Google Scholar 

  108. Hull RN, Dwyer AC, Holmes AW, Nowakowski E, Deinhardt F, Lennette EH, Emmons RW (1972) Recovery and characterization of a new simian herpesvirus from a fatally infected spider monkey. J Natl Cancer Inst 49: 225–230

    Google Scholar 

  109. Inglis DM, Bowie JM, Allan MJ, Nettleton PF (1983) Ocular disease in red deer calves associated with a herpesvirus infection. Vet Rec 113: 182–183

    Google Scholar 

  110. Jackman DA, King NW, Daniel MD, Sehgal DK, Fraser CEO (1977) M. cyclopis: a new herpesvirus isolated fromMacaca cyclopis. In: Abstracts of the Annual Meeting of the American Society for Microbiology, V348

  111. Jacob RJ, Cohen D, Bouchey D, Davis T, Borchelt J (1988) Molecular pathogenesis of equine coital exanthema a new equine herpesvirus isolated from lesions reminiscent of coital exanthema in a donkey. In: Powell DG (ed) Equine infectious diseases V. The University of Kentucky Press, Lexington, pp 140–146

    Google Scholar 

  112. Jacobson ER, Clubb S, Gaskin JM, Gardner C (1985) Herpesvirus like infection in Argentine tortoises. J Am Vet Med Assoc 187: 1227–1229

    Google Scholar 

  113. Jacobson ER, Gaskin JM, Wahlquist H (1982) Herpes-like infection in map turtles. Am J Vet Res 181: 1322–1324

    Google Scholar 

  114. Johnson MA, Whalley JM (1987) Restriction enzyme maps of the macropodid herpesvirus 2 genome. Arch Virol 96: 153–168

    Google Scholar 

  115. Johnson MA, Whalley JM, Littlejohns IR, Dickson J, Smith VW, Wilks CR, Reisner AH (1985) Macropodid herpesviruses 1 and 2: two herpesviruses from Australian marsupials differentiated by restriction endonucleases, DNA composition and hybridization. Arch Virol 85: 313–319

    Google Scholar 

  116. Kaleta EF, Marschall HJ, Glunder G, Stiburek B (1980) Isolation and serological differentation of a herpesvirus from bobwhite quail (Colinus virginianus, L. 1758). Arch Virol 66: 359–364

    Google Scholar 

  117. Kaleta EF, Mikami T, Marschall HJ, Heffels U, Heidenreich M, Stiburek B (1980) A new herpesvirus isolated from black storks (Ciconia nigra). Avian Pathol 9: 301–310

    Google Scholar 

  118. Kawamura H, King DJ, Anderson DP (1969) A herpesvirus isolated from kidney cell culture of normal turkeys. Avian Dis 13: 853–863

    Google Scholar 

  119. Kelly RK, Nielsen O, Yamamoto T (1980) A new herpes-like virus (HLV) of fish (Stizostedion vitreum-vitreum). In Vitro 16: 225

    Google Scholar 

  120. Kieff E, Liebowitz D (1990) Epstein-Barr virus and its replication. In: Fields BN, Knipe DM et al (eds) Fields' virology, vol 2, 2nd edn. Raven Press, New York, pp 1889–1920

    Google Scholar 

  121. Kimura T, Ioshimizu M, Tanaka M (1980) Salmonid viruses: effect ofOncorhynchus mason virus (OMV) in fry of chum salmon (Oncorhynchus keta). Fish Health News 9: 2–3

    Google Scholar 

  122. Kincaid AL, Bunton TE, Cranfield M (1988) Herpes-like infection in black-footed penguins (Spheniscus dermersus). J Wildl Dis 24: 173–175

    Google Scholar 

  123. Knipe DM, Ruyechan WT, Roizman B, Halliburton IW (1978) Molecular genetics of herpes simplex virus: demonstration of regions of obligatory and nonobligatory identity within diploid regions of the genome by sequence replacement and insertion. Proc Natl Acad Sci USA 75: 3896–3900

    Google Scholar 

  124. Koch H-G, Delius H, Matz B, Flugel RM, Clarke J, Darai G (1985) Molecular cloning and physical mapping of the tupaia herpesvirus genome. J Virol 55: 86–95

    Google Scholar 

  125. Kouzarides T, Bankier AT, Satchwell SC, Weston K, Tomlinson P, Barrell BG (1987) Large scale rearrangements of homologous regions in the genomes of HCMV and EBV. Virology 157: 397–413

    Google Scholar 

  126. Koch H-G, Rosen A, Ernst F, Becker Y, Darai G (1987) Determination of the nucleotide sequence flanking the deletion (0.762 and 0.789 map units) in the genome of and intraperitoneally avirulent HSV-1 strain HFEM. Virus Res 7: 105–115

    Google Scholar 

  127. Landon JE, Ellis LB, Zeve VH, Fabrizio DP (1968) Herpes-type virus in cultured leukocytes from chimpanzees. J Natl Cancer Inst 40: 181–192

    Google Scholar 

  128. L'Ecuyer C, Corner AH (1966) Propagation of porcine cytomegalic inclusion disease virus in cell cultures: preliminary report. Can J Comp Med Vet Sci 30: 321–326

    Google Scholar 

  129. Lee LF, Armstrong RL, Nazerian K (1972) Comparative studies of six avian herpesviruses. Avian Dis 16: 799–805

    Google Scholar 

  130. Leib DA, Bradbury JM, Hart CA, McCarthy K (1987) Genome isomerism in two alphaherpesviruses: Herpesvirus saimiri-1 (herpesvirus tamarinus) and avian infectious laryngotracheitis virus. Arch Virol 93: 287–294

    Google Scholar 

  131. Lewis MA, Frye LD, Gibbs CJ Jr, Chou SM, Cutchins EC, Gajdusek DC, Ward G (1976) Isolation and characterization of two new herpes-like viruses from Capuchin monkeys. Infect Immun 14: 759–766

    Google Scholar 

  132. Lindquester GJ, Pellett PE (1991) Properties of the human herpesvirus 6 strain Z29 genome: G + C content, length, and the presence of variable-length repeated terminal sequence elements. Virology 182: 102–110

    Google Scholar 

  133. Lopez C, Honess RW (1990) Human herpesvirus-6. In: Fields BN, Knipe DM et al (eds) Fields' virology, vol 2, 2nd edn. Raven Press, New York, pp 2055–2075

    Google Scholar 

  134. Lopez C, Pellett P, Stewart J, Goldsmith C, Sanderlin K, Black J, Warfield D, Feorino P (1988) Characteristics of human herpesvirus-6. J Infect Dis 157: 1271–1273

    Google Scholar 

  135. Lucke B (1938) Carcinoma of the leopard frog: its probable causation by a virus. J Exp Med 68: 457–466

    Google Scholar 

  136. Ludwig H, Biswal N, Bryans JT, McCombs RM (1971) Some properties of the DNA from a new equine herpesvirus. Virology 45: 534–537

    Google Scholar 

  137. Lunger PD, Clark HF (1978) Reptilia-related viruses. Adv Virus Res 23: 159–204

    Google Scholar 

  138. MacKay JMK (1969) Tissue culture studies of sheep pulmonary adenomatosis (Jaagsiekte). I. Direct culture of affected lungs. J Comp Pathol 79: 141–146

    Google Scholar 

  139. Madin SH, York CJ, McKercher DG (1956) Isolation of the infectious bovine rhinotracheitis virus. Science 124: 721–722

    Google Scholar 

  140. Malherbe M, Harwin R, Ulrich M (1963) The cytopathic effects of vervet monkey viruses. S Afr Med J 37: 407–411

    Google Scholar 

  141. Mare CJ, Graham DL (1973) Falcon herpesvirus, the etiologic agent of inclusion body disease of falcons. Infect Immun 8: 118–126

    Google Scholar 

  142. Martin MED, Thomson BJ, Honess RW, Craxton MA, Gompels UA, Liu M-Y, Littler E, Arrand JR, Teo I, Jones MD (1991) The genome of human herpesvirus 6: maps of unit-length and concatemeric genomes for nine restriction endonucleases. J Gen Virol 72: 157–168

    Google Scholar 

  143. Martin WB, Hay D, Crawford LV, Lebouvier GL, Crawford EM (1966) Characteristics of bovine mammillitis virus. J Gen Microbiol 45: 325–332

    Google Scholar 

  144. May HG, Tittsler RP (1925) Tracheo-laryngitis in poultry. J Am Vet Med Assoc 67: 229–231

    Google Scholar 

  145. Mayfield JE, Good PJ, van Oort HJ, Campbell AR, Reed DE (1983) Cloning and cleavage site mapping of DNA from bovine herpesvirus 1 (Cooper strain). J Virol 47: 259–264

    Google Scholar 

  146. McCarthy K, Thorpe E, Laursen AC, Heymann CS, Beale JA (1968) Exanthematous disease in patas monkeys caused by a herpes virus. Lancet 2: 856–857

    Google Scholar 

  147. McCombs R, Brunschwig JP, Mirkovic R, Benyesh-Melnick M (1971) Electron microscopic characterization of a herpes-like virus isolated from tree shrews. Virology 45: 816–820

    Google Scholar 

  148. McGeoch DJ, Dalrymple MA, Davison AJ, Dolan A, Frame MC, McNab D, Perry LJ, Scott JE, Taylor P (1988) The complete DNA sequence of the long unique region in the genome of herpes simplex virus type 1. J Gen Virol 69: 1531–1574

    Google Scholar 

  149. Medveczky MM, Geck P, Clarke C, Byrnes J, Sullivan JL, Medveczky PG (1989) Arrangement of repetitive sequences in the genome of herpesvirus sylvilagus. J Virol 63: 1010–1014

    Google Scholar 

  150. Meijer H, Dreesen JCFM, Van Boven CPA (1986) Molecular cloning and restriction endonuclease mapping of the rat cytomegalovirus genome. J Gen Virol 67: 1327–1342

    Google Scholar 

  151. Melendez LV, Daniel MD, Hunt RD, Garcis FG (1968) An apparently new herpesvirus from primary kidney cultures of the squirrel monkey (Saimiri sciureus). Lab Anim Care 18: 374–381

    Google Scholar 

  152. Melendez LV, Daniel MD, King NW, Calvo FC, Thorington RW, Jackman DA, Cadwallader J (1973) Isolation and in vitro characterization of a herpesvirus from field mouse (Microtus pennsylvanicus). Lab Anim Sci 23: 385–390

    Google Scholar 

  153. Melendez LV, Hunt RD, Daniel MD, Trum BF (1970) New World monkeys, herpesviruses, and cancer. In: H Balner, WIB Beveridge (eds) Infectious and immunosuppression in subhuman primates. Munksgaard, Copenhagen, pp 111–117

    Google Scholar 

  154. Melendez LV, Hunt RD, King NW, Barahona HH, Daniel MD, Fraser CEO, Garcia FG (1972) Herpesvirus ateles, a new lymphoma virus of monkeys. Nature (New Biol) 235: 182–184

    Google Scholar 

  155. Melendez LV, Hunt RD, King NW, Garcia FG, Like AA, Miki E (1967) A herpesvirus from sand rats (Psammomys obesus). Lab Animal Care 17: 302–309

    Google Scholar 

  156. Middelkamp JN, Patrizi G, Reed CA (1967) Light and electron microscopic studies of the guinea pig cytomegalovirus. J Ultrastruct Res 18: 85–101

    Google Scholar 

  157. Mirkovic R, Voss WR, Benyesh-Melnick M (1970) Characterization of a new herpes type virus indigenous for tree shrews. In: Proceedings of the 10th International Congress of Microbiology, Mexico City, pp 181–189

  158. Monroe JH, Shibley GP, Schidlovsky G, Nakai T, Howalson AF, Wivel NW, O'Connor TE (1968) Action of snake venom on Rauscher virus. J Natl Cancer Inst 40: 135–145

    Google Scholar 

  159. Morgan C, Rose HM, Holden M, Jones EP (1959) Electron microscopic observations on the development of herpes simplex virus. J Exp Med 110: 643–656

    Google Scholar 

  160. Morgan C, Rose HM, Mednis B (1968) Electron microscopy of herpes simplex virus. I. Entry. J Virol 2: 507–516

    Google Scholar 

  161. Mosmann TR, Hudson JB (1973) Some properties of the genome of murine cytomegalovirus (MCV). Virology 54: 135–149

    Google Scholar 

  162. Nayak DP (1971) Isolation and characterization of a herpesvirus from leukemic guinea pigs. J Virol 8: 579–588

    Google Scholar 

  163. Nazerian K (1974) DNA configuration in the core of Marek's disease virus. J Virol 13: 1148–1150

    Google Scholar 

  164. Nesburn AB (1969) Isolation and characterization of a herpes-like virus from New Zealand albino rabbit kidney cultures: a probable reisolation of virus III of Rivers. J Virol 3: 59–69

    Google Scholar 

  165. Nettleton PF, Sinclair JA, Herring JA, Inglis DM, Fletcher TJ, Ross HM, Bonniwell MA (1986) Prevalence of herpesvirus infectio in British red deer and investigations of further disease outbreaks. Vet Rec 118: 267–270

    Google Scholar 

  166. Neubauer RH, Rabin H, Strnad BC, Nonoyama M, Nelson-Rees WA (1979) Establishment of a lymphoblastoid cell line and isolation of a Epstein-Barr-related virus of gorilla origin. J Virol 31: 845–848

    Google Scholar 

  167. Nicholas J, Gompels UA, Craxton MA, Honess RW (1988) Conservation of sequence and function between the product of the 52-kilodalton immediate-early gene of herpesvirus saimiri and the BMLF1-encoded transcriptional effector (EB2) of Epstein-Barr virus. J Virol 62: 3250–3257

    Google Scholar 

  168. Nigida SM, Falk LA, Wolfe G, Deinhardt F (1979) Isolation of a cytomegalovirus from salivary glands of white-lipped marmosets (Saguinus fuscicollis). Lab Anim Sci 29: 53–60

    Google Scholar 

  169. Osterhaus ADME, Yang H, Spijkers HEM, Groen J, Teppema JS, Van Steenis G (1985) The isolation and partial characterization of a highly pathogenic herpesvirus from the harbor seal (Phoca vitulina). Arch Virol 86: 239–251.26

    Google Scholar 

  170. Parker JC, Vernon ML, Cross SS (1973) Classification of mouse thymic virus as a herpesvirus. Infect Immun 7: 305–308

    Google Scholar 

  171. Pellett PE, Biggin MD, Barrell B, Roizman B (1985) The Epstein-Barr virus may encode a protein showing significant amino acid and predicted secondary structure homology with the glycoprotein B of herpes simplex virus 1. J Virol 56: 807–813

    Google Scholar 

  172. Pensaert MB, Kluge JP (1989) Pseudorabies virus (Aujeszkys disease). In: Pensaert MB (ed) Virus infections of porcines. Elsevier, New York, pp 39–64

    Google Scholar 

  173. Plowright W, Ferris RD, Scott GR (1960) Blue wildebeest and the aetiological agent of bovine malignant catarrhal fever. Nature 188: 1167–1169

    Google Scholar 

  174. Plowright W, Macadam RF, Armstrong JA (1965) Growth and characterization of the virus of bovine malignant catarrhal fever in East Africa. J Gen Microbiol 39: 253–266

    Google Scholar 

  175. Plummer G, Goodheart CR, Henson D, Bowling CP (1969) A comparative study of the DNA density and behavior in tissue cultures of fourteen different herpesviruses. Virology 39: 134–137

    Google Scholar 

  176. Plummer G, Goodheart CR, Studdert MJ (1973) Equine herpesviruses: Antigenic relationships and DNA densities. Infect Immun 8: 621–627

    Google Scholar 

  177. Poffenberger KL, Roizman B (1985) Studies on non-inverting genome of a viable herpes simplex virus 1. Presence of head-to-tail linkages in packaged genomes and requirements for circularization after infection. J Virol 53: 589–595

    Google Scholar 

  178. Rafferty KA Jr (1965) The cultivation of inclusion-associated virus from Lucké tumour frogs. Ann NY Acad Sci 126: 3–21

    Google Scholar 

  179. Rajcani J, Blaskovic D, Svobodova J, Ciampor F, Huckova D, Stanekova D (1985) Pathogenesis of acute and persistent murine herpesvirus infection in mice. Acta Virol 29: 51–60

    Google Scholar 

  180. Randall CC, Ryden FW, Doll ER, Shell FS (1953) Cultivation of equine abortion virus in fetal horse tissue in vitro. Am J Pathol 29: 139–153

    Google Scholar 

  181. Rangan SRS, Martin LN, Bozelka BE, Wang N, Gormus BJ (1986) Epstein-Barr virus-related herpesvirus from a rhesus monkey (Macaca mulatta) with a malignant lymphoma. Int J Cancer 38: 425–432

    Google Scholar 

  182. Rasheed S, Rongey RW, Bruszewski J, Nelson-Rees WA, Rabin H, Neubaner RH, Esra G, Gardner MB (1977) Establishment of a cell line with associated Epstein-Barr like virus from a leukemic orangutan. Science 198: 407–409

    Google Scholar 

  183. Raynaud A, Adrian M (1970) Lésions cutanées à structure papillomateuse associés à des virus chez le lézard vert (Lacerta virelis laur.). CR Acad Sci Ser D 283: 845–847

    Google Scholar 

  184. Rebell G, Rywlin A, Haines H (1975) A herpesvirus-type agent associated with skin lesions of green sea turtle in aquaculture. Am J Vet Res 36: 1221–1224

    Google Scholar 

  185. Reid HW, Rowe LW (1973) The attenuation of a herpesvirus (malignant catarrhal fever virus) isolated from hartebeest (Alcelaphus buselaphus cokei Gunther). Res Vet Sci 15: 144–146

    Google Scholar 

  186. Roizman B (1990) An introduction to herpesviruses. In: Fields BN, Knipe DM et al (eds) Fields' virology, vol 2, 2nd edn. Raven Press, New York, pp 1787–1793

    Google Scholar 

  187. Roizman B, Carmichael LE, Deinhardt F, de The G, Nahmias AJ, Plowright W, Rapp F, Sheldrick P, Takahashi M, Wolf K (1981) Herpesviridae. Definition, provisional nomenclature and taxonomy. Intervirology 16: 201–217

    Google Scholar 

  188. Roizman B, Furlong D (1974) The replication of herpesvirus. In: Fraenkel-Conrat H, Wagner RR (eds) Comprehensive virology, vol 3. Plenum, New York, pp 229–403

    Google Scholar 

  189. Roizman B, Sears AE (1990) Herpes simplex viruses and their replication. In: Fields BN, Knipe DM, et al (eds) Fields' virology, vol 2, 2nd edn. Raven Press, New York, pp 1795–1894

    Google Scholar 

  190. Rota PA, Maes RK, Ruyechan WT (1986) Physical characterization of the genome of feline herpesvirus 1. Virology 154: 168–179

    Google Scholar 

  191. Rowe WP, Capps WI (1961) A new mouse virus causing necrosis of the thymus in newborn mice. J Exp Med 113: 831–844

    Google Scholar 

  192. Sabin AB (1934) Studies of B virus. I: the immunological identity of a virus isolated from a human case of ascending myelitis associated with visceral necrosis. Br J Exp Pathol 15: 248–268

    Google Scholar 

  193. Sabin AB, Wright AM (1934) Acute ascending myelitis following a monkey bite with the isolation of a virus capable of producing the disease. J Exp Med 59: 115–136

    Google Scholar 

  194. Sabine M, Robertson GR, Whalley JM (1981) Differentiation of the subtypes of equine herpesvirus 1 by restriction endonuclease analysis. Equine Vet J 57: 148–149

    Google Scholar 

  195. Saito JK, Gribble DH, Berrios PE, Knight HD (1974) A new herpesvirus isolate from goats: preliminary report. Am J Vet Res 35: 847–848

    Google Scholar 

  196. Salahuddin SZ, Ablashi DV, Markham PD, Josephs SF, Sturzenegger S, Kaplan M, Halligan G, Biberfeld P, Wong-Staal F, Kramarsky B, Gallo RC (1986) Isolation of a new virus, HTLV, in patients with lymphoproliferative disorders. Science 234: 596–601

    Google Scholar 

  197. Schechter EM, Summers J, Ogston CW (1988) Characterization of herpesvirus isolated from woodchuck hepatocytes. J Gen Virol 69: 1591–1599

    Google Scholar 

  198. Schetter CH (1970) In vitro-Untersuchungen über die Eigenschaften des Virus der Hepatitis et Splenitis Infectiosa Strigum. In: Verhandlungsberichte des XII Internationalen Symposiums über Erkrankungen der Zootiere, Budapest, pp 205–209

  199. Schneweis KE (1962) Serologische Untersuchungen zur Typendifferenzierung des herpesvirus hominis. Z Immunitaetsforsch Exp Ther 124: 24–48

    Google Scholar 

  200. Schriemer EC, Wyatt LS, Yamanishi K, Rodriguez WJ, Frenkel N (1991) Differentiation between two distinct classes of viruses now classified as human herpesvirus 6. Proc Natl Acad Sci USA 88: 5922–5926

    Google Scholar 

  201. Schubert von G (1964) Elektronenmikroskopische Untersuchungen zur Pockenkrankheit des Karpfens. Z Naturforsch 19: 675–682

    Google Scholar 

  202. Shat KA, Calneck BW (1978) Characterization of an apparently nononcogenic Marek's disease virus. J Natl Cancer Inst 60: 1075–1082

    Google Scholar 

  203. Simpson CF, Hanley JE, Gaskin JM (1975) Psittacine herpesvirus infection resembling Pacheco's parrot disease. J Infect Dis 13: 390–396

    Google Scholar 

  204. Sixbey JW, Shirley P, Sloas M, Raab-Traub N, Israele V (1991) A transformation incompetent nuclear antigen 2-deleted Epstein-Barr virus associated with replicative infection. J Infect Dis 163: 1008–1015

    Google Scholar 

  205. Smith MG (1954) Propagation of salivary gland virus of the mouse in tissue cultures. Proc Soc Exp Biol Med 86: 435–440

    Google Scholar 

  206. Smith MG (1956) Propagation in tissue cultures of a cytopathogenic virus from human salivary gland virus (SGV) disease. Proc Soc Exp Biol Med 92: 424–430

    Google Scholar 

  207. Smith MG (1959) The salivary gland viruses of man and animals (cytomegalic inclusion disease). Prog Med Virol 2: 171–202

    Google Scholar 

  208. Spear PG, Roizman B (1972) Proteins specified by herpes simplex virus. V. Purification and structural proteins of the herpesvirion. J Virol 9: 431–439

    Google Scholar 

  209. Spring SB, Roizman B (1968) Herpes simplex virus products in productive and abortive infection. III. Differentiation of infectious virus derived from nucleus and cytoplasm with respect to stability and size. J Virol 2: 979–985

    Google Scholar 

  210. Stack MJ, Higgins RJ, Challones DJ, Gregory MW (1990) Herpesvirus in the liver of a hedgehog (Erinaceus europaeus). Vet Rec 620–621

  211. Stannard LM, Fuller AO, Spear PG (1987) Herpes simplex virus glycoproteins associated with different morphological entities projecting from the virion envelope. J Gen Virol 68: 715–725

    Google Scholar 

  212. (deleted)

  213. Stinski MF (1990) Cytomegalovirus and its replication. In: Fields BN, Knipe DM, et al (eds) Fields' virology, vol 2, 2nd edn. Raven Press, New York, pp 1959–1980

    Google Scholar 

  214. Storz H, Ludwig H, Rott R (1974) Immunologic and genetic relationship between herpes simplex virus and bovine herpes mammillitis virus. Intervirology 2: 1–13

    Google Scholar 

  215. Strandberg JD, Carmichael LE (1965) Electron microscopy of a canine herpesvirus. J Bacteriol 90: 1790–1791

    Google Scholar 

  216. Studdert MJ (1974) Comparative aspects of equine herpesviruses. Cornell Vet 64: 94–122

    Google Scholar 

  217. Studdert MJ, Simpson T, Roizman B (1981) Differentiation of respiratory and abortigenic isolates of equine herpesvirus 1 by restriction endonucleases. Science 214: 562–564

    Google Scholar 

  218. Sugaya K, Bradley G, Nonoyama M, Tanaka A (1990) Latent transcripts of Marek's disease virus are clustered in the short and long repeat regions. J Virol 64: 5773–5782

    Google Scholar 

  219. Sullivan DC, Atherton SS, Staczek J, O'Callaghan DJ (1984) Structure of the genome of equine herpesvirus type 3. Virology 132: 352–367

    Google Scholar 

  220. Thiry E, Bublot M, Dubuisson J, Pastoret PP (1989) Bovine herpesvirus-4 (BHV-4) infections of cattle. In: Witmann G (ed) Herpesvirus diseases of cattle, horses, and pigs. Kluwer, Norwell, pp 96–115

    Google Scholar 

  221. Thiry E, Dubuisson J, Bublot M, Van Bressem M-F, Pastoret P-P (1990) The biology of bovine herpesvirus-4 infection of cattle. DTW Dtsch Tierarzt Wochenschr 97: 72–77

    Google Scholar 

  222. Todd WJ, Storz J (1983) Morphogenesis of a cytomegalovirus from an American bison affected with malignant catarrhal fever. J Gen Virol 64: 1025–1030

    Google Scholar 

  223. Trimble JJ, Desrosiers RC (1991) Transformation by herpesvirus saimiri. Adv Cancer Res 56: 335–355

    Google Scholar 

  224. Valicek L, Smid B, Pleva V, Mensik J (1970) Porcine cytomegalic inclusion disease virus. Arch Ges Virusforsch 32: 19–30

    Google Scholar 

  225. Wagner EK, Roizman B, Savage T, Spear PG, Mizell M, Durr FE, Sypowicz D (1970) Characterization of the DNA of herpesviruses associated with Lucke adenocarcinoma of the frog and Burkitt lymphoma of man. Virology 42: 257–261

    Google Scholar 

  226. Weller TH (1953) Serial propagation in vitro of agents producing inclusion bodies derived from varicella and herpes zoster. Proc Soc Exp Biol Med 83: 3440–3446

    Google Scholar 

  227. Whalley JM, Robertson GR, Davison AJ (1981) Analysis of the genome of equine herpesvirus type 1: arrangement of cleavage sites for restriction endonucleasesEcoRI,BglII andBamHI. J Gen Virol 57: 307–323

    Google Scholar 

  228. Whalley JM, Webber CE (1979) Characteristics of Parma wallaby herpesvirus grown in marsupial cells. J Gen Virol 45: 423–430

    Google Scholar 

  229. Whalley JM, Robertson GR, Scott NA, Hudson GC, Bell CW, Woodworth LM (1986) Identification and nucleotide sequence of a gene in equine herpesvirus 1 analogous to the herpes simplex virus gene encoding the major envelope glycoprotein gB. J Gen Virol 70: 383–394

    Google Scholar 

  230. Whitley RJ (1990) Herpes simplex viruses. In: Fields BN, Knipe DM, et al (eds) Fields' virology, vol 2, 2nd edn. Raven Press, New York, pp 1843–1887

    Google Scholar 

  231. Wildy P, Watson DH (1963) Electron microscopic studies on the architecture of animal viruses. Cold Spring Harbor Symp Quant Biol 27: 25–47

    Google Scholar 

  232. Wolf K, Darlington RW (1971) Channel catfish virus: a new herpesvirus of ictalurid fish. J Virol 8: 525–533

    Google Scholar 

  233. Wolf K, Darlington RW, Taylor WG, Quimby MC, Nagabayashi T (1978) Herpesvirus salmonis: characteristics of a new pathogen of rainbow trout. J Virol 27: 659–666

    Google Scholar 

  234. Yamamoto T, Kelly RK, Nielson O (1983) Epidermal hyperplasias of Northern pike (Esox lucius) associated with herpesvirus and C-type particles. Arch Virol 79: 255–272

    Google Scholar 

  235. Zeigel RF, Clark HF (1972) Electron microscopic observation on a new herpes-type virus isolated fromIguana iguana and propagated in reptilian cells in vitro. Infect Immun 5: 570–582

    Google Scholar 

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Authors and Affiliations

  1. Majorie B. Kovler Viral Oncology Laboratories, The University of Chicago, 60637, Chicago, Illinois, USA

    B. Roizmann

  2. New England Regional Primate Center, Harvard Medical School, Boston, Massachusetts, USA

    R. C. Desrosiers

  3. Institut für Klinische und Molekulare Virologie der Universität Erlangen-Nürnberg, Erlangen, Federal Republic of Germany

    B. Fleckenstein

  4. Lilly Research Laboratories, Indianapolis, Indiana, USA

    C. Lopez

  5. Department of Pathology, Cambridge University, Cambridge, England

    A. C. Minson

  6. School of Veterinary Science, The University of Melbourne, Parkville, Victoria, Australia

    M. J. Studdert

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Roizmann, B., Desrosiers, R.C., Fleckenstein, B. et al. The familyHerpesviridae: an update. Archives of Virology 123, 425–449 (1992). https://doi.org/10.1007/BF01317276

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