Viral zoonoses in Europe

FEMS Microbiology Reviews

Volumn 29, Issue 5, 2005, Pages 1051-1077

  Kallio Kokko, Hannimari ^a,b   Uzcategui, Nathalie ^a   Vapalahti, Olli ^a,b,c   Vaheri, Antti ^a,b  

^a UNIVERSITY OF HELSINKI   (Finland)

^b HELSINKI UNIVERSITY CENTRAL HOSPITAL   (Finland)

^c UNIVERSITY OF HELSINKI   (Finland)

Author keywords

Arbovirus; Emerging infections; Europe; Vector borne viruses; Vertebrate borne viruses; Viral zoonoses

Indexed keywords

ALPHA INTERFERON; ANTISERUM; ORTHOPOXVIRUS VACCINE; RABIES VACCINE; RIBAVIRIN; VIRUS VACCINE;

ALPHA VIRUS; ARENAVIRUS; BUNYAVIRUS; COWPOX; EUROPE; FLAVIVIRUS; HANTAVIRUS; HUMAN; NAIRO VIRUS; NONHUMAN; ORTHOPOXVIRUS; PATHOGENESIS; PUUMALA VIRUS; RABIES; RABIES VIRUS; REVIEW; SINDBIS VIRUS; TICK BORNE ENCEPHALITIS; TICK BORNE ENCEPHALITIS FLAVIVIRUS; VIROLOGY; VIRUS HEMORRHAGIC FEVER; VIRUS INFECTION; VIRUS MENINGITIS; ZOONOSIS;

ANIMALS; ARTHROPOD VECTORS; BIRD DISEASES; CARNIVORA; EUROPE; HUMANS; RODENT DISEASES; VERTEBRATES; VIRUS DISEASES; ZOONOSES;

ACARI; ALPHAVIRUS; ANIMALIA; ARBOVIRUS; ARENAVIRUS; FLAVIVIRUS; HANTAVIRUS; NAIROVIRUS; ORTHOBUNYAVIRUS; ORTHOPOXVIRUS; PUUMALA VIRUS; RABIES VIRUS; SINDBIS VIRUS; TICK-BORNE ENCEPHALITIS VIRUS; VERTEBRATA;

EID: 26444537521     PISSN: 01686445     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.femsre.2005.04.012     Document Type: Review

References (237)

1. A. Plyusnin, O. Vapalahti, and A. Vaheri Hantaviruses: genome structure, expression and evolution J. Gen. Virol. 77 1996 2677 2687
2. Jonsson, C.B. and Schmaljohn, C.S. (2001) Replication of hantaviruses. Volume "Hantaviruses" (Schmaljohn, C.S., Nichol, S.T., Eds.). Curr. Top. Microbiol. Immunol. 256, 15-32.
3. Plyusnin, A. and Morzunov, S.P. (2001) Virus evolution and genetic diversity of hantaviruses and their rodent hosts. Volume " Hantaviruses" (Schmaljohn, C.S., Nichol, S.T., Eds.). Curr. Top. Microbiol. Immunol. 256, 47-75.
4. A. Plyusnin, O. Vapalahti, H. Lehväslaiho, N. Apekina, T. Mikhailova, I. Gavrilovskaya, J. Laakkonen, J. Niemimaa, H. Henttonen, M. Brummer-Korvenkontio, and A. Vaheri Genetic variation of wild Puumala viruses within the serotype, local rodent populations and individual animal Virus Res. 38 1995 25 41
5. A. Plyusnin, Y. Cheng, H. Lehväslaiho, and A. Vaheri Quasispecies in wild-type Tula hantavirus populations J. Virol. 70 1996 9060 9063
6. C. Sibold, H. Meisel, D.H. Krüger, M. Labuda, J. Lysy, O. Kozuch, M. Pejcoch, A. Vaheri, and A. Plyusnin Recombination in Tula hantavirus evolution: analysis of genetic lineages from Slovakia J. Virol. 73 1999 667 675
7. A. Plyusnin, S.K.J. Kukkonen, A. Plyusnina, O. Vapalahti, and A. Vaheri Transfection-mediated generation of functionally competent Tula hantavirus with recombinant S RNA segment EMBO J. 21 2002 1497 1503
8. O. Vapalahti, J. Mustonen, Å. Lundkvist, H. Henttonen, A. Plyusnin, and A. Vaheri Hantavirus infections in Europe Lancet Infect. Dis. 3 2003 653 661
9. A. Plyusnin, O. Vapalahti, H. Lankinen, H. Lehväslaiho, N. Apekina, Y. Myasnikov, H. Kallio-Kokko, H. Henttonen, Å. Lundkvist, M. Brummer-Korvenkontio, I. Gavrilovskaya, and A. Vaheri Tula virus: a newly detected hantavirus carried by European common voles J. Virol. 68 1994 7833 7839
10. O. Vapalahti, Å. Lundkvist, S.K.J. Kukkonen, Y. Cheng, M. Gilljam, M. Kanerva, T. Manni, M. Pejcoch, J. Niemimaa, A. Kaikusalo, H. Henttonen, A. Vaheri, and A. Plyusnin Isolation and characterization of Tula hantavirus, a distinct serotype in the genus Hantavirus, family Bunyaviridae J. Gen. Virol. 77 1996 3063 3067
11. O. Vapalahti, Å. Lundkvist, V. Fedorov, C.J. Conroy, S. Hirvonen, A. Plyusnina, K. Nemirov, K. Fredga, J.A. Cook, J. Niemimaa, A. Kaikusalo, H. Henttonen, A. Vaheri, and A. Plyusnin Isolation and characterization of a hantavirus from Lemmus sibiricus : evidence for host-switch during hantavirus evolution J. Virol. 73 1999 5586 5592
12. J. Desmyter, J.W. LeDuc, K.M. Johnson, F. Brasseur, C. Deckers, and C. van Ypersele de Strihou Laboratory rat associated outbreak of haemorrhagic fever with renal syndrome due to Hantaan-like virus in Belgium Lancet 2 1983 1445 1448
13. G. Lloyd, E.T. Bowen, N. Jones, and A. Pendry HFRS outbreak associated with laboratory rats in UK Lancet 1 1984 1175 1176
14. P. Heyman, A. Plyusnina, P. Berny, C. Cochez, M. Artois, M. Zizi, J.P. Pirnay, and A. Plyusnin Seoul hantavirus in Europe: first demonstration of the virus genome in wild Rattus norvegicus captured in France Eur. J. Clin. Microbiol. Infect. Dis. 23 2004 711 717
15. M. Brummer-Korvenkontio, O. Vapalahti, H. Henttonen, P. Koskela, P. Kuusisto, and A. Vaheri Epidemiological study of nephropathia epidemica in Finland 1989-1996 Scand. J. Infect. Dis. 31 1999 427 435
16. K. Vapalahti, M. Paunio, A. Vaheri, and O. Vapalahti Puumala virus infections in Finland: increased occupational risk for farmers Am. J. Epidemiol. 149 1999 1142 1151
17. M. Kanerva, J. Mustonen, and A. Vaheri Pathogenesis of Puumala and other hantavirus infections Rev. Med. Virol. 8 1998 67 86
18. J. Mustonen, J. Partanen, M. Kanerva, K. Pietilä, O. Vapalahti, A. Pasternack, and A. Vaheri Genetic susceptibility to severe course of nephropathia epidemica caused by Puumala hantavirus Kidney Int. 49 1996 217 221
19. S. Mäkelä, I. Ala-Houhala, J. Mustonen, A.-M. Koivisto, T. Kouri, V. Turjanmaa, O. Vapalahti, A. Vaheri, and A. Pasternack Renal function and blood pressure five years after Puumala virus-induced nephropathy Kidney Int. 58 2000 1711 1718
20. T. Hautala, T. Sironen, O. Vapalahti, E. Pääkkö, T. Särkioja, P.I. Salmela, A. Vaheri, A. Plyusnin, and H. Kauma Hypophyseal hemorrhage and panhypopituitarism during Puumala virus infection: magnetic resonance imaging and detection of viral antigen in the hypophysis Clin. Infect. Dis. 35 2002 96 101
21. M. Terajima, O. Vapalahti, H. Van Epps, A. Vaheri, and F.A. Ennis Immune responses to Puumala virus infection and the pathogenesis of nephropathia epidemica Microbes Infect. 6 2004 238 245
22. Mackow, E.R. and Gavrilovskaya, I.N. (2001) Cellular pathogenesis and hantavirus pathogenesis. Volume "Hantaviruses" (Schmaljohn, C.S., Nichol, S.T., Eds.). Curr. Top. Microbiol. Immunol. 256, 91-115.
23. J.I. Kang, S.H. Park, P.W. Lee, and B.Y. Ahn Apoptosis is induced by hantaviruses in cultured cells Virology 264 1999 99 105
24. N.K. Akhmatova, R.S. Yusupova, S.F. Khaiboullina, and S.V. Sibiryak Lymphocyte apoptosis during Hemorrhagic Fever with Renal Syndrome Russ. J. Immunol. 8 2003 37 46
25. A. Markotic, L. Hensley, T. Geisbert, K. Spik, and C. Schmaljohn Hantaviruses induce cytopathic effects and apoptosis in continuous human embryonic kidney cells J. Gen. Virol. 84 2003 2197 2202
26. X.D. Li, S. Kukkonen, O. Vapalahti, A. Plyusnin, H. Lankinen, and A. Vaheri Tula hantavirus infection of Vero E6 cells induces apoptosis involving caspase 8 activation J. Gen. Virol. 85 2004 3261 3268
27. M. Linderholm, C. Ahlm, B. Settergren, A. Waage, and A. Tarnvik Elevated plasma levels of tumor necrosis factor (TNF)-alpha, soluble TNF receptors, interleukin (IL)-6, and IL-10 in patients with hemorrhagic fever with renal syndrome J. Infect. Dis. 173 1996 38 43
28. M. Temonen, J. Mustonen, H. Helin, A. Pasternack, A. Vaheri, and H. Holthöfer Cytokines, adhesion molecules, and cellular infiltration in nephropathia epidemica kidneys: an immunohistochemical study Clin Immunol Immunopathol. 78 1996 47 55
29. S. Mäkelä, J. Mustonen, I. Ala-Houhala, M. Hurme, A.-M. Koivisto, A. Vaheri, and A. Pasternack Urinary excretion of interleukin-6 correlates with proteinuria in acute Puumala hantavirus-induced nephritis Am. J. Kidney Dis. 43 2004 809 816
30. J. Klingström, A. Plyusnin, A. Vaheri, and Å. Lundkvist Wild-type Puumala hantavirus infection induces cytokines, C-reactive protein, creatinine and nitric oxide in Cynomolgus macaques J. Virol. 76 2002 444 449
31. Vapalahti, O., Lundkvist, Å. and Vaheri, A. (2001). Human immune response, host genetics and severity of disease. Volume "Hantaviruses" (Schmaljohn, C.S., Nichol, S.T., Eds.). Curr. Top. Microbiol. Immunol. 256, 153-169.
32. H.L. Van Epps, M. Terajima, J. Mustonen, T.P. Arstila, E.A. Corey, A. Vaheri, and F.A. Ennis Long-lived memory T lymphocytes after hantavirus infection J. Exp. Med. 196 2002 579 588
33. A. Plyusnin, J. Hörling, M. Kanerva, J. Mustonen, Y. Cheng, J. Partanen, O. Vapalahti, S.K.J. Kukkonen, J. Niemimaa, H. Henttonen, B. Niklasson, Å. Lundkvist, and A. Vaheri Puumala hantavirus genome in patients with nephropathia epidemica: correlation of PCR positivity with HLA haplotype and link to viral sequences in local rodents J. Clin. Microbiol. 35 1997 1090 1096
34. A. Plyusnin, J. Mustonen, K. Asikainen, A. Plyusnina, J. Niemimaa, H. Henttonen, and A. Vaheri Analysis of Puumala hantavirus genome in patients with nephropathia epidemica and rodent carriers from the sites of infection J. Med. Virol. 59 1999 397 405
35. K. Hedman, A. Vaheri, and M. Brummer-Korvenkontio Rapid diagnosis of hantavirus disease with an IgG-avidity assay Lancet 338 1991 1353 1356
36. H. Kallio-Kokko, O. Vapalahti, K. Hedman, M. Brummer-Korvenkontio, and A. Vaheri Puumala virus antibody and immunoglobulin G avidity assays based on recombinant nucleocapsid antigen J. Clin. Microbiol. 31 1993 677 680
37. K. Brus Sjölander, F. Elgh, H. Kallio-Kokko, O. Vapalahti, M. Hägglund, V. Palmcrantz, P. Juto, A. Vaheri, B. Niklasson, and Å. Lundkvist Evaluation of serological methods for diagnosis of Puumala hantavirus infection (nephropathia epidemica) J. Clin. Microbiol. 35 1997 3264 3268
38. H. Hujakka, V. Koistinen, P. Eerikäinen, I. Kuronen, I. Mononen, M. Parviainen, Å. Lundkvist, A. Vaheri, A. Närvänen, and O. Vapalahti New immunochromatographic rapid test for diagnosis of acute Puumala virus infection J. Clin. Microbiol. 39 2001 2146 2150
39. H. Hujakka, V. Koistinen, I. Kuronen, P. Eerikäinen, M. Parviainen, Å. Lundkvist, A. Vaheri, O. Vapalahti, and A. Närvänen Diagnostic rapid tests for acute hantavirus infections: specific tests for Hantaan, Dobrava and Puumala viruses versus a hantavirus combination test J. Virol. Methods 108 2003 117 122
40. Hooper, J.W. and Li, D. (2001) Vaccines against hantaviruses. Volume "Hantaviruses" (Schmaljohn, C.S., Nichol, S.T., Eds.). Curr. Top. Microbiol. Immunol. 256, 171-191.
41. J.W. Huggins, C.M. Hsiang, T.M. Cosgriff, M.Y. Guang, J.I. Smith, Z.O. Wu, J.W. Le Duc, Z.M. Zheng, J.M. Meegan, and Q.N. Wang Prospective, double-blind, concurrent, placebo-controlled clinical trial of intravenous ribavirin therapy of hemorrhagic fever with renal syndrome J. Infect. Dis. 164 1991 1119 1127
42. J. Bai, K. Zhu, and G. Zhou The therapeutic effect of purified human leucocytic interferon-alpha on hemorrhagic fever with renal syndrome Zhonghua Nei Ke Za Zhi 36 1997 90 93
43. C. Bahloul, Y. Jacob, N. Tordo, and P. Perrin DNA-based immunisation for exploring the enlargement of immunological cross-reactivity against the lyssaviruses Vaccine 16 1998 417 425
44. C. Jallet, Y. Jacob, C. Bahloul, A. Drings, E. Desmeziè res, N. Tordo, and P. Perrin Chimeric lyssavirus glycoproteins with increased immunological potential J. Virol. 73 1999 225 233
45. A.D. Botvinkin, E.M. Poleschuk, I.V. Kuzmin, T.I- Borisova, S.V. Gazaryan, P. Yager, and C.E. Rupprecht Novel lyssaviruses isolated from bats in Russia Emerg. Infect. Dis. 9 2003 1623 1625
46. H. Bourhy, B. Kissi, L. Audry, M. Smreczak, M. Sadkowska-Todys, K. Kulonen, N. Tordo, J.F. Zmudzinski, and E.C. Holmes Ecology and evolution of rabies virus in Europe J. Gen. Virol. 180 1999 2545 2557
47. H. Badrane, and N. Tordo Host-switching in lyssavirus history from chiroptera to carnivora orders J. Virol. 75 2001 8096 8104
48. M.J. Warrrell, and D.A. Warrell Rabies and other lyssavirus disesases Lancet 363 2004 959 969
49. J.E. Echevarria, A. Avellon, J. Juste, M. Vera, and C. Ibanez Screening of active lyssavirus infection in wild bat populations by viral RNA detection on oropharyngeal swabs J. Clin. Microbiol. 39 2001 3678 3683
50. B. Amengual, J.E. Whitby, A. King, J.S. Cobo, and H. Bourhy Evolution of European bat lyssaviruses J. Gen. Virol. 78 1997 2319 2328
51. J.E. Whitby, P.R. Heaton, E.M. Black, M. Wooldridge, L.M. McElhinney, and P. Johnstone First isolation of a rabies-related virus from a Daubenton's bat in the United Kingdom Vet. Rec. 147 2000 385 388
52. D. Nathwani, P.G. McIntyre, K. White, A.J. Shearer, N. Reynolds, D. Walker, G.V. Orange, and A. Fooks Fatal human rabies caused by European bat Lyssavirus type 2a infection in Scotland Clin. Infect. Dis. 37 2003 598 601
53. P.C. Grauballe, H.J. Baagøe, M. Fekadu, J.M. Westergaard, and H. Zoffmann Bat rabies in Denmark Lancet 1 1987 379 380
54. J. Serra-Cobo, B. Amengual, C. Abellan, and H. Bourhy European bat lyssavirus infection in Spanish bat populations Emerg. Infect. Dis. 8 2002 413 420
55. D. Nathwani, P.G. McIntyre, K. White, A.J. Shearer, N. Reynolds, D. Walker, G.V. Orange, and A.R. Fooks Fatal human rabies caused by European bat Lyssavirus type 2a infection in Scotland Clin Infect Dis. 37 2003 598 601
56. S. Plotkin Rabies Clin. Infect. Dis. 30 2000 4 12
57. T. Hemachudha, J. Laothamatas, and C.E. Rupprecht Human rabies: a disease of complex neuropathogenetic mechanisms and diagnostic challenges Lancet Neurol. 1 2002 101 109
58. H. Raux, A. Flamand, and D. Blondel Interaction of the rabies virus P protein with the LC8 dynein light chain J. Virol. 74 2000 10212 10216
59. Y. Jacob, H. Badrane, P.E. Ceccaldi, and N. Tordo Cytoplasmic dynein LC8 interacts with lyssavirus phosphoprotein J. Virol. 74 2000 10217 10222
60. M. Lafon, H. Bourhy, and P. Sureau Immunity against the European bat rabies (Duvenhage) virus induced by rabies vaccines: an experimental study in mice Vaccine 6 1988 362 368
61. H. Badrane, C. Bahloul, P. Perrin, and N. Tordo Evidence of two Lyssavirus phylogroups with distinct pathogenicity and immunogenicity J. Virol. 75 2001 3268 3276
62. T. Mebatsion Extensive attenuation of rabies virus by simultaneously modifying the dynein light chain binding site in the P protein and replacing Arg333 in the G protein J. Virol. 75 2001 11496 11502
63. A.C. Jackson, M.J. Warrell, C.E. Rupprecht, H.C. Ertl, B. Dietzschold, M. O'Reilly, R.P. Leach, Z.F. Fu, W.H. Wunner, T.P. Bleck, and H. Wilde Management of rabies in humans Clin. Infect. Dis. 36 2003 60 63
64. M. Perez, R.C. Craven, and J.C. de la Torre The small RING finger protein Z drives arenavirus budding: implications for antiviral strategies Proc. Natl. Acad. Sci. USA 100 2003 12978 12983
65. J. Salazar-Bravo, L.A. Ruedas, and T.L. Yates M.B.A. Oldstone Arenaviruses I 2002 Springer-Verlag Berlin, Heidelberg, New York 25 64
66. M.D. Bowen, C.J. Peters, and S.T. Nichol Phylogenetic analysis of the Arenaviridae: patterns of virus evolution and evidence for cospeciation between arenaviruses and their rodent hosts Mol. Phylogenet. Evol. 8 1997 301 316
67. J.S.C. Clegg M.B.A. Oldstone Arenaviruses I 2002 Springer-Verlag Berlin, Heidelberg, New York 1 24
68. R.N. Charrel, H. Feldmann, C.F. Fulhorst, R. Khelifa, R. de Chesse, and X. de Lamballerie Phylogeny of New World arenaviruses based on the complete coding sequences of the small genomic segment identified an evolutionary lineage produced by intrasegmental recombination Biochem. Biophys. Res. Commun. 296 2002 1118 1124
69. M.C. Rousseau, M.F. Saron, P. Broqui, and A. Bourgeade Lymphocytic choriomeningitis virus in southern France: four case reports and a review of the literature Eur. J. Epidemiol. 13 1997 817 823
70. L. Lledo, M.I. Gegundez, J.V. Saz, N. Bahamontes, and M. Beltran Lymphocytic choriomeningitis virus infection in a province of Spain: analysis of sera from the general population and wild rodents J. Med. Virol. 70 2003 273 275
71. J.C. Peters M.B.A. Oldstone Arenaviruses I 2002 Springer-Verlag Berlin, Heidelberg, New York 65 74
72. J.B. McGormick, and S.P. Fisher-Hoch M.B.A. Oldstone Arenaviruses I 2002 Springer-Verlag Berlin, Heidelberg, New York 75 110
73. S. Gunther, P. Emmerich, T. Laue, O. Kuhle, M. Asper, A. Jung, T. Grewing, J. ter Meulen, and H. Schmitz Imported lassa fever in Germany: molecular characterization of a new lassa virus strain Emerg. Infect. Dis. 6 2000 466 476
74. H. Schmitz, B. Kohler, T. Laue, C. Drosten, P.J. Veldkamp, S. Gunther, P. Emmerich, H.P. Geisen, K. Fleischer, M.F. Beersma, and A. Hoerauf Monitoring of clinical and laboratory data in two cases of imported Lassa fever Microbes Infect. 4 2002 43 50
75. W.H. Haas, T. Breuer, G. Pfaff, H. Schmitz, P. Kohler, M. Asper, P. Emmerich, C. Drosten, U. Golnitz, K. Fleischer, and S. Gunther Imported Lassa fever in Germany: surveillance and management of contact persons Clin. Infect. Dis. 36 2003 1254 1258
76. M.B. Mets Childhood blindness and visual loss: an assessment at two institutions including a "new" cause Trans. Am. Ophthalmol. Soc. 97 1999 653 696
77. R. Wright, D. Johnson, M. Neumann, T.G. Ksiazek, P. Rollin, R.V. Keech, D.J. Bonthius, P. Hitchon, C.F. Grose, W.E. Bell, and J.F. Bale Jr. Congenital lymphocytic choriomeningitis virus syndrome: a disease that mimics congenital toxoplasmosis or Cytomegalovirus infection Pediatrics 100 1997 E9
78. L.L. Barton, M.B. Mets, and C.L. Beauchamp Lymphocytic choriomeningitis virus: emerging fetal teratogen Am. J. Obstet. Gynecol. 187 2002 1715 1716
79. R.N. Charrel, and X. de Lamballerie Arenaviruses other than Lassa virus Antiviral Res. 57 2003 89 100
80. J.Y. Park, C.J. Peters, P.E. Rollin, T.G. Ksiazek, B. Gray, K.B. Waites, and C.B. Stephensen Development of a reverse transcription-polymerase chain reaction assay for diagnosis of lymphocytic choriomeningitis virus infection and its use in a prospective surveillance study J. Med. Virol. 51 1997 107 114
81. C. Drosten, S. Gottig, S. Schilling, M. Asper, M. Panning, H. Schmitz, and S. Gunther Rapid detection and quantification of RNA of Ebola and Marburg viruses, Lassa virus, Crimean-Congo hemorrhagic fever virus, Rift Valley fever virus, dengue virus, and yellow fever virus by real-time reverse transcription-PCR J. Clin. Microbiol. 40 2002 2323 2330
82. C. Drosten, S. Gottig, S. Schilling, M. Asper, M. Panning, H. Schmitz, and S. Gunther Rapid detection and quantification of RNA of Ebola and Marburg viruses, Lassa virus, Crimean-Congo hemorrhagic fever virus, Rift Valley fever virus, dengue virus, and yellow fever virus by real-time reverse transcription-PCR J. Clin. Microbiol. 40 2002 2323 2330
83. C. Drosten, B.M. Kummerer, H. Schmitz, and Gunther Molecular diagnostics of viral hemorrhagic fevers Antiviral Res 57 2003 61 87
84. S. Gunther, M. Asper, C. Roser, L.K. Luna, C. Drosten, B. Becker-Ziaja, P. Borowski, H.M. Chen, and R. Hosmane Application of real-time PCR for testing antiviral compounds against Lassa virus, SARS coronavirus and Ebola virus in vitro Antiviral Res. 63 2004 209 215
85. J.B. McCormick, I.J. King, P.A. Webb, C.L. Scribner, R.B. Craven, K.M. Johnson, L.H. Elliott, and R. Belmont-Williams Lassa fever. Effective therapy with ribavirin N. Engl. J. Med. 314 1986 20 26
86. S.P. Fisher-Hoch, and J.B. McCormick Towards a human Lassa fever vaccine Rev. Med. Virol. 11 2001 331 341
87. K.T. McKee Jr., J.G. Oro, A.I. Kuehne, J.A. Spisso, and B.G. Mahlandt Safety and immunogenicity of a live-attenuated Junin (Argentine hemorrhagic fever) vaccine in rhesus macaques Am. J. Trop. Med. Hyg. 48 1993 403 411
88. M. del Carmen Saavedra, J.M. Sottosanti, L. Riera, and A.M. Ambrosio IgG subclasses in human immune response to wild and attenuated (vaccine) Junin virus infection J. Med. Virol. 69 3 2003 447 450
89. J.J. Esposito, and F. Fenner Poxviruses D.M. Knipe P.M. Howley Fields Virology 4th ed. 2001 Lippincott Williams & Wilkins Philadelphia 2885 2921
90. G.L Smith, A. Vanderplasschenã, and M. ja Law The formation and function of extracellular enveloped vaccinia virus J. Gen. Virol. 83 2002 2915 2931
91. T. Sandvik, M. Tryland, H. Hansen, M. Mehl, M. Moens, Ø. Olsvik, and T. ja Traavik Naturally occurring orthopoxviruses: potential for recombination with vaccine vectors J. Clin. Microbiol. 36 1998 2542 2547
92. E. Jenner An Inquiry into the Causes and Effects of the Variolae Vaccinae, a Disease Discovered in some of the Western Counties of England, Particularly Gloucestershire, and known by the Name of the Cow Pox 1798 Sampson Low London
93. C.R.A. Damaso, J.J. Esposito, R.C. Condit, and N. Moussatché An emergent poxvirus from humans and cattle in Rio de Janeiro state: Cantagalo virus may derive from Brazilian smallpox vaccine Virology 277 2000 439 449
94. J. Chantrey, H. Meyer, D. Baxby, M. Begon, K.J. Bown, S.M. Hazel, T. Jones, W.I. Montgomery, and M. Bennett Cowpox: reservoir hosts and geographic range Epidemiol. Infect. 122 1999 455 460
95. H. Meyer, C. Schay, H. Mahnel, and M. Pfeffer Characterization of orthopoxviruses isolated from man and animals in Germany Arch. Virol. 144 1999 491 501
96. D. Baxby, M. Bennett, and B. Getty Human cowpox 1969-93: a review based on 54 cases Br. J. Dermatol. 131 1994 598 607
97. R. Wienecke, H. Wolff, M. Schaller, H. Meyer, and G. Plewig Cowpox virus infection in an 11-year-old girl J. Am. Acad. Dermatol. 42 2000 892 894
98. P.M. Pelkonen, K. Tarvainen, A. Hynninen, E.R.K. Kallio, H. Henttonen, A. Palva, A. Vaheri, and O. ja Vapalahti Cowpox with severe generalized eruption, Finland Emerg. Infect. Dis. 9 2003 1458 1461
99. P. Schupp, M. Pfeffer, H. Meyer, G. Burck, K. Kölmel, and C. Neumann Cowpox virus in a 12-year-old boy: rapid identification by an orthopoxvirus-specific polymerase chain reaction Br. J. Dermatol. 145 2001 146 150
100. M. Tryland, H. Myrmel, L. Holtet, G. Haukenes, and T. Traavik Clinical cowpox cases in Norway Scan J. Infect. Dis. 30 1998 301 303
101. C.P. Czerny, A.M. Eis-Hübinger, A. Mayr, K.E. Schneweis, and B. Pfeiff Animal poxviruses transmitted from cat to man: current event with lethal end J. Vet. Med. B38 1991 421 431
102. D.F. Smee, K.W. Bailey, M. Wong, and R.W. Sidwell Intranasal treatment of cowpox virus respiratory infection in mice with cidofovir Antiviral Res. 47 2000 171 177
103. S.L. Ropp, Q. Jin, J.C. Knight, R.F. Massung, and J.J. ja Esposito PCR Strategy for Identification and Differentiation of Smallpox and Other Orthopoxviruses J. Clin. Microbiol. 33 1995 2069 2076
104. M.J. Espy, F.R. Cockerill III, R.F. Meyer, M.D. Bowen, G.A. Poland, T.L. Hadfield, and T.F. ja Smith Detection of Smallpox Virus DNA by LightCycler PCR. J. Clin. Microbiol. 40 2002 1985 1988
105. M. Niedrig, H. Schmitz, S. Becker, S. Gunther, J. ter Meulen, H. Meyer, H. Ellerbrok, A. Nitsche, H.R. Gelderblom, and C. ja Drosten First international quality assurance study on the rapid detection of viral agents of bioterrorism J. Clin. Microbiol. 42 2004 1753 1755
106. F Fenner, D.A. Henderson, I. Arita, Z. Ježek, and I.D. ja Ladnyi Smallpox and its Eradication 1988 Office of publications, WHO Geneve, Switzerland
107. D.B. Di Giulio, and P.B. Eckbur Human monkeypox: an emerging zoonosis Lancet Infect. Dis. 4 2004 15 25
108. S.J. Baigent, and J.W. McCauley Influenza type A in humans,mammals and birds: determinants of virus virulence, host-range and interspecies transmission BioEssays 25 2003 657 671
109. F.A. Murphy, E.P.J. Gibbs, M.C. Horzinek, and M.J. Studdert Veterinary Virology 3rd ed. 1999 Academic Press
110. M.L. Perdue, and D.L. Suarez Structural features of avian influenza virus hemagglutinin that influence virulence Vet. Microbiol. 74 2000 77 86
111. D.J. Alexander A review of avian influenza in different bird species Vet. Microbiol. 74 2000 3 13
112. K. Iwatsuki-Horimoto, R. Kanazawa, S. Sugii, Y. Kawaoka, and T. Horimoto The index influenza A virus subtype H5N1 isolated from a human in 1997 differs in its receptor-binding properties from a virulent avian influenza virus J. Gen. Virol. 85 2004 1001 1005
113. R.G. Webster, J. Geraci, and G. Petursson Conjunctivitis in human beings caused by influenza A virus of seals N. Engl. J. Med. 304 1981 911
114. J. Kurtz, R.J. Manvell, and J. Banks Avian influenza virus isolated from a woman with conjunctivitis Lancet 348 1996 901 902
115. P.K.S. Chan Outbreak of Avian Influenza A(H5N1) Virus infection in Hong Kong in 1997 Clin. Infect. Dis. 34 2002 S58 S64
116. I. Capua, F. Mutinelli, S. Marangon, and D.J. Alexander H7N1 avian influenza in Italy (1999 to 2000) in intensively reared chickens and turkeys Avian Pathol. 29 2000 537 543
117. M. Koopmans, B. Wilbrink, M. Conyn, G. Natrop, H. van der Nat, H. Vennema, A. Meijer, J. van Steenbergen, R. Fouchier, A. Osterhaus, and A. Bosman Transmission of H7N7 avian influenza A virus to human beings during a large outbreak in commercial poultry farms in the Netherlands Lancet 363 2004 587 593
118. R.A. Fouchier, P.M. Schneeberger, F.W. Rozendaal, J.M. Broekman, S.A. Kemink, V. Munster, T. Kuiken, G.F. Rimmelzwaan, M. Schutten, G.J. Van Doornum, G. Koch, A. Bosman, M. Koopmans, and A.D. Osterhaus Avian influenza A virus (H7N7) associated with human conjunctivitis and a fatal case of acute respiratory distress syndrome Proc. Natl. Acad. Sci. USA. 101 2004 1356 1361
119. R.A. Fouchier, T.M. Bestebroer, S. Herfst, L. Van Der Kemp, G.F. Rimmelzwaan, and A.D. Osterhaus Detection of influenza A viruses from different species by PCR amplification of conserved sequences in the matrix gene J. Clin. Microbiol. 38 2000 4096 4101
120. V.S. Hinshaw, J.M. Wood, R. Webster, R. Deibel, and B. Turner Bull World Health Organ. 63 1985 711 719
121. D.E. Stallknecht, S.M. Shane, M.T. Kearney, and P.J. Zwank Persistence of Avian Influenza Viruses in Water Avian Dis. 34 1990 406 411
122. K.F. Shortridge, N.N. Zhou, Y. Guan, P. Gao, T. Ito, Y. Kawaoka, S. Kodihalli, S. Krauss, D. Markwell, K.G. Murti, M. Norwood, D. Senne, L. Sims, A. Takada, and R.G. Webster Characterization of avian H5N1 influenza viruses from poultry in Hong Kong Virology 252 1998 331 342
123. M. Brummer-Korvenkontio, O. Vapalahti, P. Kuusisto, P. Saikku, T. Manni, P. Koskela, T. Nygren, H. Brummer-Korvenkontio, and A. Vaheri Epidemiology of Sindbis virus infections in Finland 1981-96: possible factors explaining a peculiar disease pattern Epidemiol. Infect. 129 2002 335 345
124. J.O. Lundstrom Mosquito-borne viruses in western Europe: a review J Vector Ecol. 24 1999 1 39
125. B. Niklasson, A. Espmark, J.W. LeDuc, T.P. Gargan, W.A. Ennis, R.B. Tesh, and A.J. Main Jr. Association of a Sindbis-like virus with Ockelbo disease in Sweden Am. J. Trop. Med. Hyg. 33 1984 1212 1217
126. D.K. Lvov, T.M. Skvortsova, L.K. Berezina, V.L. Gromashevsky, B.I. Yakovlev, B.V. Gushchin, V.A. Aristova, G.A. Sidorova, E.L. Gushchina, and S.M. Klimenko Isolation of Karelian fever agent from Aedes communis mosquitoes Lancet 2 1984 399 400
127. J.O. Lundström, K.M. Lindström, B. Olsen, R. Dufva, and D.S. Krakower Prevalence of Sindbis virus neutralizing antibodies among Swedish passerines indicates that thrushes are the main amplifying hosts J. Med. Entomol. 38 2001 289 297
128. H. Norder, J.O. Lundström, O. Kozuch, and L.O. Magnius Genetic relatedness of Sindbis virus strains from Europe, Middle East, and Africa Virology 222 1996 440 445
129. J.O. Lundström, M.J. Turell, and B. Niklasson Viremia in three orders of birds (Anseriformes, Galliformes and Passeriformes) inoculated with Ockelbo virus J. Wildl. Dis. 29 1993 189 195
130. S. Kurkela, T. Manni, A. Vaheri, and O. Vapalahti Causative agent of Pogosta disease isolated from blood and skin lesions Emerg. Infect. Dis. 10 2004 889 894
131. B. Niklasson, and A. Espmark Ockelbo disease: arthralgia 3-4 years after infection with a Sindbis virus related agent Lancet 1 1986 1039 1040
132. B. Niklasson, A. Espmark, and J. Lundström Occurrence of arthralgia and specific IgM antibodies three to four years after Ockelbo disease J. Infect. Dis. 157 1988 832 835
133. M. Skogh, and A. Espmark Ockelbo disease: epidemic arthritis-exanthema syndrome in Sweden caused by Sindbis-virus like agent Lancet 1 1982 795 796
134. M. Turunen, P. Kuusisto, P.E. Uggeldahl, and A. Toivanen Pogosta disease: clinical observations during an outbreak in the province of North Karelia, Finland Br. J. Rheumatol. 37 1998 1177 1180
135. S. Kurkela, T. Manni, J. Myllynen, A. Vaheri, and O. Vapalahti Clinical and laboratory manifestations of Sindbis virus infection: Prospective study, Finland 2002-2003 J. Infect. Dis. 191 2005 1820 1829
136. S. Vene, C. Franzen, and B. Niklasson Development of specific antibody patterns and clinical symptoms following Ockelbo virus infection Arch. Virol. 134 1994 61 71
137. J. Hörling, S. Vene, C. Franzen, and B. Niklasson Detection of Ockelbo virus RNA in skin biopsies by polymerase chain reaction J. Clin. Microbiol. 31 1993 2004 2009
138. C. Chastel, A.J. Main, C. Guiguen, G. le Lay, M.C. Quillien, J.Y. Monnat, and J.C. Beaucournu The isolation of Meaban virus, a new Flavivirus from the seabird tick Ornithodoros (Alectorobius) maritimus in France Arch. Virol. 83 1985 129 140
139. E.A. Henchal, and J.R. Putnak The dengue viruses Clin. Microbiol. Rev. 3 1990 376 396
140. Lindenbach, B. and Rice, C. (2001) Flaviviridae: The viruses and their replication. In: Knipe, D., Howley, P. (Eds.), Virology, Fourth edition, vols. 1 and 2. Lippincott Williams & Wilkins, Philadelphia, pp. 991-1041 [Chapter 32].
141. F.X. Heinz, M.S. Collett, R.H. Purcell, E.A. Gould, C.R. Howard, M. Houghton, R.J.M. Moorman, C.M. Rice, and H.J. Thiel Family Flaviviridae M.H.V. Regenmortel C.M. Fauquet D.H.L. Bishop E. Carstens M.K. Estes S. Lemon J. Maniloff M.A. Mayo D. McGeogch C.R. Pringle R.B. Wickner Virus Taxonomy. 7th International committee for the Taxonomy of Viruses 2000 Academic Press San Diego 859 878
142. Burke, M. (2001) Flaviviruses. In: Knipe, D., Howley, P. (Eds.), Virology, Fourth edition ed., vols. 1 and 2. Lippincott Williams & Wilkins, Philadelphia, pp. 1043-1125 [Chapter 33].
143. M. Theiler, and W.G. Downs The Arthropod-borne Viruses of Vertebrates. An Account of the Rockefeller Foundation Virus Program (1951-1970) 1973 Yale University Press London
144. M.W. Gaunt, A.A. Sall, X. Lamballerie, A.K. Falconar, T.I. Dzhivanian, and E.A. Gould Phylogenetic relationships of flaviviruses correlate with their epidemiology, disease association and biogeography J. Gen. Virol. 82 2001 1867 1876
145. E.A. Gould, X. de Lamballerie, P.M. Zanotto, and E.C. Holmes Evolution, epidemiology, and dispersal of flaviviruses revealed by molecular phylogenies Adv. Virus Res. 57 2001 71 103
146. WHO. (2002) Dengue and dengue haemorrhagic fever. Fact sheet No. 117.
147. I. Takashima, K. Morita, M. Chiba, D. Hayasaka, T. Sato, C. Takezawa, A. Igarashi, H. Kariwa, K. Yoshimatsu, J. Arikawa, and N. Hashimoto A case of tick-borne encephalitis in Japan and isolation of the virus J. Clin. Microbiol. 35 1997 1943 1947
148. I. Kohl, O. Kozuch, E. Eleckova, M. Labuda, and J. Zaludko Family outbreak of alimentary tick-borne encephalitis in Slovakia associated with a natural focus of infection Eur J Epidemiol. 12 4 1996 373 375
149. T.S. Gritsun, V.A. Lashkevich, and E.A. Gould Tick-borne encephalitis Antiviral Res. 57 2003 129 146
150. T.S. Gritsun, P.A. Nuttall, and E.A. Gould Tick-borne flaviviruses Adv. Virus Res. 61 2003 17 71
151. M. Gresikova, and C.H. Calisher Tick-borne Encephalitis T.P. Monath The Arboviviruses: Ecology and Epidemiology Vol. IV 1988 CRC Press Boca Raton, FL 177 203
152. X. Han, M. Aho, S. Vene, M. Brummer-Korvenkontio, A. Juceviciene, P. Leinikki, A. Vaheri, and O. Vapalahti Studies on TBE epidemiology in Finland (and Lithuania) Int. J. Med. Microbiol. 291 2002 48 49
153. M. Ecker, S.L. Allison, T. Meixner, and F.X. Heinz Sequence analysis and genetic classification of tick-borne encephalitis viruses from Europe and Asia J. Gen. Virol. 80 1999 179 185
154. V. Maytchoutko, S. Vene, M. Haglund, M. Forsgren, A. Duks, V. Kalnina, J. Horling, and A. Lundkvist Characterization of tick-borne encephalitis virus from Latvia J. Med. Virol. 60 2000 216 222
155. Å Lundkvist, S. Vene, I. Golovljova, V. Mavtchoutko, M. Forsgren, V. Kalnina, and A. Plyusnin Characterization of tick-borne encephalitis virus from Latvia: evidence for co-circulation of three distinct subtypes J. Med. Virol. 65 2001 730 735
156. C. Kunz Tick borne encephalitis in Europe Acta Leidensia 60-62 1992 1 14
157. M. Haglund, M. Forsgren, G. Lindh, and L. Lindquist A 10-year Follow-up study of TBE in the Stockholm Area and a review of the litterature: Need for a vaccination strategy Scand J. Infect. Dis. 28 1996 217 224
158. G. Gunther, M. Haglund, L. Lindquist, M. Forsgren, and B. Skoldenberg Tick-bone encephalitis in Sweden in relation to aseptic meningo-encephalitis of other etiology: a prospective study of clinical course and outcome J. Neurol. 244 1997 230 238
159. R. Kaiser The clinical and epidemiological profile of tick-borne encephalitis in southern Germany 1994-98: a prospective study of 656 patients Brain 122 1999 2067 2078
160. L. Gilbert, L.D. Jones, P.J. Hudson, E.A. Gould, and H.W. Reid Role of small mammals in the persistence of Louping-ill virus: field survey and tick co-feeding studies Med. Vet. Entomol. 14 2000 277 282
161. C.E.G. Smith, and M.G.R. Varma Louping ill C.W. Beran CRC Handbook Series in Zoonoses, Section B: Viral Zoonoses vol I 1981 CRC Press Boca Raton, FL 191 200
162. H.E. Webb, J.H. Connolly, F.F. Kane, K.J. O'Reilly, and D.I. Simpson Laboratory infections with Louping ill with associated encephalitis Lancet 3 1968 255 258
163. Gilbert, L., Jones, L.D., Laurenson, M.K., Gould, E.A., Reid, H.W. and Hudson, P.J. (2004) Ticks need not bite their red grouse hosts to infect them with louping ill virus. Proc R Soc Lond B Biol Sci. May 7;271 (Suppl. 4):S202-5.
164. M.M. Davidson, H. Williams, and J.A. MacLeod Louping ill in man: A forgotten disease J. Infect. 23 1991 241 249
165. H. Reid Controlling tick-borne diseases of sheep in Britain Practice 9 1987 189 191
166. K. McGuire, E.C Holmes, G.F. Gao, H.W. Reid, and E.A. Gould Tracing the origins of Louping ill virus by molecular phylogenetic analysis J. Gen. Virol. 79 1998 981 988
167. K.C. Smithburn, T.P. Hughes, A.W. Burke, and J.H. Paul A neurotropic virus isolated from the blood of a native of Uganda Am. J. Trop. Med. Hyg. 20 1940 471
168. B. Murgue, H. Zeller, and V. Deubel The ecology and epidemiology of West Nile virus in Africa, Europe and Asia Curr. Top. Microbiol. Immunol. 267 2002 195 221
169. Z. Hubalek, and J. Halouzka West Nile Fever-a Reemerging Mosquito-Borne Viral Disease in Europe Emerg. Infect. Dis. 5 1999 643 650
170. T.F. Tsai, F. Popovici, C. Cernescu, G.L. Campbell, and NI. Nedelcu West Nile encephalitis epidemic in southeastern Romania Lancet 352 1998 767 771
171. J.T. Roehrig, M. Layton, P. Smith, G.L. Campbell, R. Nasci, and R.S. Lanciotti The emergence of West Nile virus in North America: ecology, epidemiology, and surveillance Curr. Top. Microbiol. Immunol. 267 2002 223 240
172. F.J. Burt, A.A. Grobbelaar, P.A. Leman, F.S. Anthony, G.V. Gibson, and R. Swanepoel Phylogenetic relationships of southern African West Nile virus isolates Emerg. Infect. Dis. 8 2002 820 826
173. R.S. Lanziotti, J.T. Roehrig, V. Deubel, J. Smith, M. Parker, K. Steele, B. Crise, K.E. Volpe, M.B. Crabtree, J.H. Scherret, R.A. Hall, J.S. MacKenzie, C.B. Cropp, B. Panigrahy, E. Ostlund, B. Schmitt, M. Malkinson, C. Banet, J. Weissman, N. Komar, H.M. Savage, W. Stone, T. McNamara, and D.J. Gubler Origin of the West Nile virus responsible for an outbreak of encephalitis in the northeastern United States Science 286 1999 2333 2337
174. H. Weissenbock, J. Kolodziejek, A. Url, H. Lussy, B. Rebel-Bauder, and N. Nowotny Emergence of Usutu virus, an African mosquito-borne flavivirus of the Japanese encephalitis virus group, central Europe Emerg. Infect. Dis. 8 2002 652 656
175. J.P. Woodhall The viruses isolated from arthropods at the East African Virus Research Institute in the 26 years ending December 1963 Proc. E African Acad. 2 1964 141 146
176. H. Weissenbock, J. Kolodziejek, K. Fragner, R. Kuhn, M. Pfeffer, and N. Nowotny Usutu virus activity in Austria, 2001-2002 Microbes. Infect. 5 2003 1132 1136
177. D.K. Lvov, A.M. Butenko, V.L. Gromashevsky, V.P. Larichev, S.Y. Gaidamovich, O.I. Vyshemirsky, A.N. Zhukov, V.V. Lazorenko, V.N. Salko, A.I. Kovtunov, K.M. Galimzyanov, A.E. Platonov, T.N. Morozova, N.V. Khutoretskaya, E.O. Shishkina, and T.M. Skvortsova Isolation of two strains of West Nile virus during an outbreak in southern Russia, 1999 Emerg. Infect. Dis. 6 2000 373 376
178. F. Berthet, H.G. Zeller, M. Drouetm, J. Rauzier, J. Digoutte, and V. Deubel Extensive nucleotide changes and deletions within the envelope gene of Euro-African West Nile viruses J. Gen. Virol. 78 1997 2293 2297
179. H.M. Savage, C. Ceianu, G. Nicolescu, N. Karabatsos, R.S. Lanciotti, A. Vladimirescu, L. Laiv, A. Ungureanu, C. Romanca, and T.F. Tsai Entomologic and avian investigations of an epidemic of West Nile fever in Romania, 1996, with serologic and molecular characterization of a virus from mosquitoes Am. J. Trop. Med. Hyg. 61 1999 600 611
180. R.S. Lanciotti, J.T. Roehrig, V. Deubel, J. Smith, M. Parker, K. Steele, B. Crise, K.E. Volpe, M.B. Crabtree, J.H. Scherret, R.A. Hall, J.S. MacKenzie, C.B. Cropp, B. Panigrahy, E. Ostlund, B. Schmitt, M. Malkinson, C. Banet, J. Weissman, N. Komar, H.M. Savage, W. Stone, T. McNamara, and D.J. Gubler Origin of the West Nile virus responsible for an outbreak of encephalitis in the northeastern US Science 286 1999 2333 2337
181. R.N. Charrel, A.C. Brault, P. Gallian, J.J. Lemasson, B. Murgue, S. Murri, B. Pastorino, H. Zeller, R. de Chesse, P. de Micco, and X. de Lamballerie Evolutionary relationship between Old World West Nile virus strains evidence for viral gene flow between Africa, the Middle East and Europe Virology 315 2003 381 388
182. T. Bakonyi, Z. Huba'lek, I. Rudolf, and N. Nowotny Novel Flavivirus or new lineage of West Nile virus, Central Europe Emerg. Infect. Dis. 11 2004 225 231
183. A.E. Platonov, G.A. Shipulin, O.Y. Shipulina, E.N. Tyutyunnik, T.I. Frolochkina, R.S. Lanciotti, S. Yazyshina, O.V. Platonova, I.L. Obukhov, A.N. Zhukov, Y.Y. Vengerov, and V.I. Pokrovskii Outbreak of West Nile virus infection, Volgograd Region, Russia, 1999 Emerg Infect Dis. Jan-Feb 7 1 2001 128 132
184. R. George, and S.K. Lam Dengue virus infection-the Malaysian experience Ann. Acad. Med. Singapore 26 1997 815 819
185. R. Rico-Hesse Molecular evolution and distribution of dengue viruses type 1 and 2 in nature Virology 174 1990 479 493
186. T. Jelinek, N. Muhlberger, G. Harms, M. Corachan, M.P. Grobusch, J. Knobloch, U. Bronner, H. Laferl, A. Kapaun, Z. Bisoffi, J. Clerinx, S. Puente, G. Fry, M. Schulze, U. Hellgren, I. Gjorup, P. Chalupa, C. Hatz, A. Matteelli, M. Schmid, L.N. Nielsen, S. da Cunha, J. Atouguia, B. Myrvang, and K. Fleischer European Network on Imported Infectious Disease Surveillance. 2002. Epidemiology and clinical features of imported dengue fever in Europe: sentinel surveillance data from TropNetEurop Clin. Infect. Dis. 35 2002 1047 1052
187. E.A. Gould, X. de Lamballerie, P.M. Zanotto, and E.C. Holmes Origins, evolution, and vector/host coadaptations within the genus Flavivirus Adv Virus Res. 59 2003 277 314
188. H. Holzmann Diagnosis of tick-borne encephalitis Vaccine 21 2003 S1/36 S1/40
189. L.H. Gould, and E. Fikrig West Nile virus: a growing concern? J. Clin. Invest. 113 2004 1102 1107
190. S.T. Nichol Bunyaviruses D.M. Knipe P.M. Howley Fields Virology vol. 2 2001 Lippincott Williams & Wilkins Philadelphia 1603 1634
191. E. Kinsella, S.G. Martin, A. Grolla, M. Czub, H. Feldmann, and R. Flick Sequence determination of the Crimean-Congo hemorrhagic fever virus L segment Virology 321 2004 23 28
192. J.E. Honig, J.C. Osborne, and S.T. Nichol Crimean-Congo hemorrhagic fever virus genome L RNA segment and encoded protein Virology 321 2004 29 35
193. A.J. Sanchez, M.J. Vincent, and S.T. Nichol Characterization of the glycoproteins of Crimean-Congo hemorrhagic fever virus J. Virol. 76 2002 7263 7275
194. I. Andersson, L. Bladh, M. Mousavi-Jazi, K.-E. Magnusson, Å. Lundkvist, O. Haller, and A. Mirazimi Human MxA protein inhibits the replication of Crimean-Congo hemorrhagic fever virus J. Virol. 78 2004 4323 4329
195. J.E. Honig, J.C. Osborne, and S.T. Nichol Crimean-Congo hemorrhagic fever virus genome L RNA segment and encoded protein Virology 321 2004 29 35
196. R. Hewson, A. Gmyl, L. Gmyl, S.E. Smirnova, G. Karganova, B. Jamil, R. Hasan, J. Chamberlain, and C. Clegg Evidence of segment reassortment in Crimean-Congo hemorrhagic fever virus J. Gen. Virol. 85 2004 3059 3070
197. R. Flick, K. Flick, H. Feldmann, and F. Elgh Reverse genetics for Crimean-Congo hemorrhagic fever virus J. Virol. 77 2003 5997 6000
198. R. Swanepoel S.R. Palmer L. Soulsby D.I.H. Simpson Crimean-Congo Hemorrhagic Fever 1998 Oxford University Press Oxford, New York, Tokyo 311 317
199. M. Isaäcson Viral hemorrhagic fever hazards for travelers in Africa Clin. Infect. Dis. 33 2001 1707 1712
200. M. Saijo, Q. Tang, B. Shimay, L. Han, Y. Zhang, M. Asiguma, D. Tianshu, A. Maeda, I. Kurane, and S. Morikawa Possible horizontal transmission of Crimean-Congo hemorrhagic fever virus from mother to her child Jpn. J. Infect. Dis. 57 2004 55 57
201. R. Hewson, J. Chamberlain, V. Mioulet, G. Lloyd, B. Jamil, R. Hasan, A. Gmyl, L. Gmyl, S.E. Smirnova, A. Lukashev, G. Karganova, and C. Clegg Crimean-Congo hemorrhagic fever virus: sequence analysis of the small RNA segments from a collection of viruses world wide Virus Res. 102 2004 185 189
202. A. Papa, B. Bozov, V. Pavlidou, E. Papadimitriou, M. Pelemis, and A. Antoniadis Genetic detection and isolation of Crimean-Congo hemorrhagic fever virus, Kosovo, Yugoslavia Emerg. Infect. Dis. 8 2002 852 854
203. A. Papa, S. Bino, A. Llagami, B. Brahimaj, E. Papadimitriou, V. Pavlidou, E. Velo, G. Cahani, M. Hajdini, A. Pilaca, A. Harxhi, and A. Antoniadis Crimean-Congo hemorrhagic fever in Albania, 2001 Eur. J. Microbiol. Infect. Dis. 21 2002 603 606
204. M. Saijo, T. Qing, M. Niikura, A. Maeda, T. Ikegami, K. Sakai, C. Prehaud, I. Kurane, and S. Morikawa Immunofluorescence technique using HeLa cells expressing recombinant nucleoprotein for detection of immunoglobulin G antibodies to Crimean-Congo hemorrhagic fever virus J. Clin. Microbiol. 40 2002 372 375
205. M. Saijo, T. Qing, M. Niikura, A. Maeda, T. Ikegami, C. Prehaud, I. Kurane, and S. Morikawa Recombinant nucleoprotein-based enzyme-linked immunosorbent assay for detection of immunoglobulin G antibodies to Crimean-Congo hemorrhagic fever virus J. Clin. Microbiol. 40 2002 1587 1591
206. T. Qing, M. Saijo, H. Lei, M. Niikura, A. Maeda, T. Ikegami, W. Xinjung, I. Kurane, and S. Morikawa Detection of immunoglobulin G to Crimean-Congo hemorrhagic fever virus in sheep sera by recombinant nucleoprotein-based enzyme-linked immunosorbent and immuno-fluorescence assays J. Virol. Methods 108 2003 111 116
207. Q. Tang, M. Saijo, V. Zhang, M. Asiguma, D. Tianshu, L. Han, B. Shimay, A. Maeda, I. Kurane, and S. Morikawa A patient with Crimean-Congo hemorrhagic fever serologically diagnosed by recombinant nucleoprotein-based antibody detection systems Clin. Diagn. Lab. Immunol. 10 2003 489 491
208. C. Drosten, S. Göttig, S. Schilling, M. Asper, M. Panning, H. Schmitz, and S. Günther Rapid detection and quantification of RNA of Ebola and Marburg viruses, Lassa virus, Crimean-Congo hemorrhagic fever virus, dengue virus, and yellow fever virus by real-time reverse transcription-PCR. J. Clin. Microbiol. 40 2002 2323 2330
209. S.P. Fisher-Hoch, J.A. Khan, S. Rehman, S. Mirza, M. Khurshid, and J.B. McCormick Crimean-Congo hemorrhagic fever treated with oral Ribavirin Lancet 346 1995 472 475
210. O. Ergonui, A. Celikbas, B. Dokuzoguz, S. Eren, N. Baykam, and H. Esener Characteristics of patients with Crimean-Congo hemorrhagic fever in a recent outbreak in Turkey and impact of oral Ribavirin therapy Clin. Infect. Dis. 39 2004 284 287
211. J. Lundström Vector competence of Western European mosquitoes for arboviruses: A review of field and experimental studies Bull. Soc. Vector Ecol. 19 1994 23 36
212. T. Jaenson Vector roles of Fennoscandian mosquitoes attracted to mammals, birds, and dogs Med. Vet. Entomol. 4 1990 221 226
213. M. Brummer-Korvenkontio, P. Saikku, P. Korhonen, I. Ulmanen, T. Rennala, and J. Karvonen Arboviruses in Finland Am. J. Trop. Med. Hyg. 22 1973 404 413
214. Z. Hubalek, P. Zeman, J. Halouzka, Z. Juricova, E. Stovickova, H. Balkova, S. Sikutova, and Rudolf Mosquitoborne viruses, Czech Republic, 2002 Emerg. Infect. Dis. 11 2005 116 118
215. Stuart, T. (2001). Bunyaviruses. In: Knipe, D., Howley, P. (Eds.), Virology, Fourth edition ed., vol. 2. Lippincott Williams & Wilkins, Philadelphia, pp. 1603-1633 [Chapter 49].
216. R.M. Elliott, M. Bouloy, C.H. Calisher, R. Goldbach, J.T. Moyer, S.T. Nichol, R. Petersson, A. Plyusnin, and C.S. Schmaljohn Family Bunyaviridae M.H.V. Regenmortel C.M. Fauquet D.H.L. Bishop E. Carstens M.K. Estes S. Lemon J. Maniloff M.A. Mayo D. McGeogch C.R. Pringle R.B Wickner Virus Taxonomy. 7th International committee for the Taxonomy of Viruses 2000 Academic Press San Diego 859 878
217. R. Swanepoel, and J.A.W. Coetzer Rift Valley fever J.A.W. Coetzer G.R. Thomson R.C. Tustin Infectious Diseases of Livestocks with Special Reference to Southern Africa 1994 Oxford University Press Cape Town, South Africa 668 717
218. R. Daubney, J.R. Hudson, and P.C. Garnham Enzootic hepatitis or Rift Valley fever: an undescribed virus disease of sheep, cattle and man from East Africa J. Pathol. Bacteriol. 34 1931 545 579
219. G.A. Eddy, and C.J. Peters The extended horizons of Rift Valley fever: current and projected immunogens Prog. Clin. Biol. Res. 47 1980 179 191
220. T.M. Cosgriff, J.C. Morrill, G.B. Jennings, L.A. Hodgson, M.V. Slayter, P.H. Gibbs, and C.J. Peters Hemostatic derangement produced by Rift Valley fever virus in rhesus monkeys Rev. Infect. Dis. 11 1989 S807 S814
221. R. Swanepoel, J.K. Struthers, M.J. Erasmus, S.P. Shepherd, G.M. McGillivray, A.J. Shepherd, D.E. Hummitzsch, B.J. Erasmus, and B.J. Barnard Comparative pathogenicity and antigenic cross-reactivity of Rift Valley fever and other African phleboviruses in sheep J. Hyg. 97 1986 331 346
222. M.K. Goverdhan, V. Dhanda, and G.B. Modi Isolation of phlebotomus (sandfly) fever virus from sandflies and humans during the same season in Aurangabad district, maharashtra State, India Indian J. Med. Res. 64 1976 57 63
223. J.R. Schmidt, M.L. Schmidt, and M.I. Said Phlebotomus fever in Egypt: Isolation of phlebotomus fever viruses from Phlebotomus papatasi Am. J. Trop. Med Hyg. 20 1971 483 490
224. R.B. Tesh The genus Phlebovirus and its vectors Ann. Rev. Entomol. 33 1988 169 181
225. P.J. Bartelloni, and R.B. Tesh Clinical and serologic responses of volunteers infected with phlebotomus fever virus (Sicilian type) Am. J. Trop. Med. Hyg. 25 1976 456 462
226. A. Braito, M.G. Ciufolini, L. Pippi, R. Corbisiero, C. Fiorentini, A. Gistri, and L. Toscano Phlebotomus-transmitted toscana virus infections of the central nervous system: a seven-year experience in Tuscany Scand. J. Infect. Dis. 30 1998 505 508
227. A. Braito, R. Corbisiero, S. Corradini, C. Fiorentini, and M.G. Ciufolini Toscana virus infections of the central nervous system in children: a report of 14 cases J. Pediatr. 132 1998 144 148
228. A. Braito, R. Corbisiero, S. Corradini, B. Marchi, N. Sancasciani, C. Fiorentini, and M.G. Ciufolini Evidence of Toscana virus infections without central nervous system involvement: a serological study Eur. J. Epidemiol. 13 1997 761 764
229. R. Eitrem, M. Stylianou, and B. Niklasson High prevalence rates of antibody to three sandfly fever viruses (Sicilian, Naples, and Toscana) among Cypriots Epidemiol. Infect. 107 1991 685 691
230. J. Mendoza-Montero, M.I. Gamez-Rueda, J.M. Navarro-Mari, M. de la Rosa-Fraile, and S. Oyonarte-Gomez Infections due to sandfly fever virus serotype Toscana in Spain Clin. Infect. Dis. 27 1998 434 436
231. L. Nicoletti, P. Verani, S. Caciolli, M.G. Ciufolini, A. Renzi, D. Bartolozzi, P. Paci, F. Leoncini, P. Padovani, and E. Traini Central nervous system involvement during infection by Phlebovirus toscana of residents in natural foci in central Italy (1977-1988) Am. J. Trop. Med. Hyg. 45 1991 429 434
232. M.L. Martin, H. Lindsey-Regnery, D.R. Sasso, J.B. McCormick, and E. Palmer Distinction between Bunyaviridae genera by surface structure and comparison with Hantaan virus using negative stain electron microscopy Arch. Virol. 86 1985 17 28
233. D.Y. Liu, R.B. Tesh, A.P. Travassos Da Rosa, C.J. Peters, Z. Yang, H. Guzman, and S.Y. Xiao Phylogenetic relationships among members of the genus Phlebovirus (Bunyaviridae) based on partial M segment sequence analyses J. Gen. Virol. 84 2003 465 473
234. K.J. Linthicum, A. Anyamba, C.J. Tucker, P.W. Kelley, M.F. Myers, and C.J. Peters Climate and satellite indicators to forecast Rift Valley fever epidemics in Kenya Science 285 1999 397 400
235. G.F. Meadors 3rd, P.H. Gibbs, and C.J. Peters Evaluation of a new Rift Valley fever vaccine: safety and immunogenicity trials Vaccine 4 1986 179 184
236. R. Randall, L.N. Binn, and V.R. Harrison Immunization against Rift Valley Fever Virus. Studies of the immunogenicity of lyophilized formalin-inactivated vaccine J. Immunol. 93 1964 293 299
237. T. Shuchin, K. Naoto, T. Kazuaki, and M. Shunji Zoonotic transmission of hepatitis E virus from deer to human beings Lancet 362 2003 371 373