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Pathogenesis

  • Chapter
Bunyaviridae

Part of the book series: Current Topics in Microbiology and Immunology ((CT MICROBIOLOGY,volume 169))

Abstract

The family Bunyaviridae consists of over 250 individual virus species grouped into five genera. Most of these viruses rarely infect humans or domestic animals. This chapter focuses on the few viruses that are important pathogens

Table 1 Selected bunyaviruses that cause disease in humans or domestic animals

and which have been studied in experimental vertebrate hosts. Particular emphasis is given to the California serogroup since this group of agents has received the most detailed analysis. Several other viruses, such as Rift Valley fever virus, Hantaan virus, and Crimean-Congo hemorrhagic fever virus are important causes of disease but are difficult to study because they require special containment facilities and because of a paucity of animal models which mimic the human disease

Table 2 Animal models for selected pathogenic bunyaviruses

. A summary is presented of the information available on these agents.

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References

  • Al-Tikriti SK, Al-Ani F, Jurji FJ (1981 a) Congo-Crimean hemorrhagic fever in Iraq. Bull WHO 59: 85–90

    PubMed  CAS  Google Scholar 

  • Al-Tikriti SK, Hassan FK, Moslih IM, Jurji F, Mahmud MI, Tantawi HH (1981b) Congo-Crimean hemorrhagic fever in Iraq: a seroepidemiological survey. J Trop Med Hyg 84: 117–120

    Google Scholar 

  • Anderson AA, Campbell CH (1978) Experimental placental transfer of Akabane virus in the hamster. Am J Vet Res 39: 301–304

    Google Scholar 

  • Anderson GW, Peters CJ (1988) Viral determinants of virulence for Rift Valley fever (RVF) in rats. Microb Path 5: 241–250

    Google Scholar 

  • Anderson CR, Spence L, Downs WG, Aitken TH (1961) Oropouche virus: a new human disease agent from Trinidad. Am J Trop Med Hyg 10: 574–578

    PubMed  CAS  Google Scholar 

  • Anderson GW, Slone TW, Peters CJ (1987) Pathogenesis of Rift Valley fever virus (RVFV) in inbred rats. Microb Path 2: 283–293

    Google Scholar 

  • Anderson GW, Slone SW, Peters CJ (1988) The gerbil, Meriones unguiculatus, a model for Rift Valley fever virus encephalitis. Arch Virol 102: 187–196

    PubMed  Google Scholar 

  • Artsob H (1983) Distribution of California serogroup viruses and virus infection in Canada. In: Calisher CH, Thompson WH (eds) California serogroup viruses. Liss, New York, pp 277–292

    Google Scholar 

  • Asada H, Tamura M, Kondo K, Okuno Y, Takahashi Y, Dohi Y (1987) Role of T lymphocytes subsets in protection and recovery from Hantaan virus infection in mice. J Gen Virol 68: 1961–1969

    PubMed  Google Scholar 

  • Asada H, Tamura M, Kondo K, Dohi Y, Yamanishi K (1988) Cell-mediated immunity to virus causing haemorrhagic fever with renal syndrome: generation of cytotoxic T lymphocytes. J Gen Virol 69: 2179–2188

    PubMed  CAS  Google Scholar 

  • Asada H, Balachandra K, Tamura M, Kondo K, Yamanishi K (1989) Cross-reactive immunity among different serotypes of virus causing haemorrhagic fever with renal syndrome. J Gen Virol 70: 819–825

    PubMed  Google Scholar 

  • Balducci M, Fausto AM, Verani P (1985) Phlebotomus-transmitted viruses in Europe. In: Proceedings of the international congress for infectious diseases. Edizione Luigi Pozzi, Rome, pp 101–104

    Google Scholar 

  • Balfour HH, Edelman CK, Cook FE (1976) California arbovirus (La Crosse) infections. III. Epidemiology of California encephalitis in Minnesota. J Infect Dis 133: 293–301

    PubMed  Google Scholar 

  • Barnett IC, Suyemoto W (1961) Field studies on sandfly fever and kala-azar in Pakistan, in Iran, and in Baltistan (Little Tibet) Kashmir. Trans NY Acad Sci 23: 609–617

    Google Scholar 

  • Beaty BJ, Bishop DH (1988) Bunyavirus-vector interaction. Virus Res 10: 289–301

    PubMed  CAS  Google Scholar 

  • Beaty BJ, Thompson WH (1976) Delineation of La Crosse virus in developmental stages of transovarially infected Aedes triseriatus. Am J Trop Med Hyg 25: 685–691

    Google Scholar 

  • Beaty BJ, Rohzon EJ, Gensemer P, Bishop DH (1981) Formation of reassortant bunyaviruses in dually infected mosquitoes. Virology 111: 662–665

    PubMed  CAS  Google Scholar 

  • Beaty BJ, Miller BR, Shope RE, Rohzon EJ, Bishop DH (1982) Molecular basis of bunyavirus per os infection of mosquitoes: role of the middle-sized RNA segment. Proc Nat Acad Sci USA 79: 1295–1297

    PubMed  CAS  Google Scholar 

  • Beaty BJ, Sundin DR, Chandler LJ, Bishop DH (1985) Evolution of bunyaviruses by genome reassortment in dually infected mosquitoes (Aedes triseriatus). Science 230: 548–550

    PubMed  CAS  Google Scholar 

  • Berry RL, Parsons MA, Restifo RA (1975) Studies of the epidemiology of California encephalitis in an endemic area in Ohio in 1971. Am J Trop Med Hyg 24: 992–998

    PubMed  CAS  Google Scholar 

  • Bishop DH (1985a) Ambisense RNA genomes of arenaviruses and phleboviruses. Adv Virus Res 31: 1–51

    Google Scholar 

  • Bishop DH (1985b) The genetic basis for describing viruses as species. Intervirology 24: 79–93

    PubMed  CAS  Google Scholar 

  • Bishop DH, Shope RE (1979) Bunyaviridae. Comprehensive Virology. Virology 14: 1–156

    CAS  Google Scholar 

  • Bishop DH, Calisher CH, Casals J (1980) Bunyaviridae. Intervirology 14: 125–143

    PubMed  CAS  Google Scholar 

  • Bishop DH, Fuller F, Akashi H (1984a) The use of reassortant bunyaviruses to deduce their coding and pathogenic potentials. In: Kohn A, Fuchs P (eds) Mechanisms of virus pathogenesis. Nijhoff, Boston, pp 49–60

    Google Scholar 

  • Bishop DH, Rud E, Belloncik S (1984b) Coding analyses of bunyavirus RNA species. In: Compans RW, Bishop DH (eds) Segmented negative strand viruses. Academic, Orlando, pp 3–11

    Google Scholar 

  • Brown JL, Dominik JW, Morrissey RL (1981) Respiratory infectivity of a recently isolated Egyptian strain of Rift Valley fever virus. Infect Immun 33: 848–853

    PubMed  CAS  Google Scholar 

  • Brummer-Korvenkontio M, Vaheri A, Hovi T (1980) Nephropathia epidemica: detection of antigen in bank voles and serological diagnosis of human infection. J Infect Dis 141: 131–134

    PubMed  CAS  Google Scholar 

  • Brummer-Korvenkontio M, Hentonnen H, Vaheri A, (1982) Hemorrhagic fever with renal syndrome in Finland: ecology and virology of nephropathia epidemica. Scand J Infect Dis 36: 88–91

    CAS  Google Scholar 

  • Burney MI, Ghafoor A, Saleen M, Webb PA, Casals J (1980) Nosocomial outbreak of viral hemorrhagic fever caused by Crimean hemorrhagic lever-Congo virus in Pakistan, Jan 1976. Am J Trop Med Hyg 29: 941–947

    PubMed  CAS  Google Scholar 

  • Calisher CH (1983) Taxonomy, classification, and geographic distribution of California serogroup bunyaviruses. In: Calisher CH, Thompson WH (eds) California serogroup viruses. Liss, New York, pp1–18

    Google Scholar 

  • Calisher CH and Thompson WH (1983) California serogroup viruses. Liss, New York

    Google Scholar 

  • Calisher CH, Kokernot RH, de Moore JF, Boyd KR, Hayes J, Chappell WA (1969) Arbovirus studies in the Ohio-Mississippi basin, 1964–1967. VI. Mermet: a Simbu group arbovirus. Am J Trop Med Hyg 18: 779–792

    PubMed  CAS  Google Scholar 

  • Calisher CH, Lazuick JS, Liev S, Monath TP, Castro KG (1988) Human infections with Tensaw virus in South Florida: evidence that Tensaw virus subtypes stimulate the production of antibodies reactive with closely related Bunyamwera serogroup viruses. Am J Trop Med Hyg 39:117–122

    PubMed  CAS  Google Scholar 

  • Caplen H, Peters CJ, Bishop DHL (1985) Mutagen-directed attenuation of Rift Valley fevr virus as a method for vaccine development. J Gen Virol 66: 2271–2277

    PubMed  Google Scholar 

  • Casals J (1969) Antigenic similarity between the virus causing Crimean hemorrhagic fever and Congo virus. Proc Soc Exp Biol Med 131: 233–236

    PubMed  CAS  Google Scholar 

  • Casals J, Henderson B, Hoogstraal H, Johnson KM, Shelokov A (1970) A review of Soviet viral hemorrhagic fevers, 1969. J Infect Dis 122: 437–453

    PubMed  CAS  Google Scholar 

  • Causey OR, Kemp GE, Causey CE, Lee VH (1972) Isolations of Simbu-group viruses in Ibadan, Nigeria 1964–1969, including the new types Sango, Shamonda, Sabo, and Shuni. Am J Trop Med Hyg 66: 357–363

    CAS  Google Scholar 

  • Chambers PG, Swanepoel R (1980) Rift Valley fever in abattoir workers. Cent Afr J Med 26:122–126

    PubMed  CAS  Google Scholar 

  • Childs JE, Korch GW, Glass GE, LeDuc JW, Shah KV (1987) Epizootology of hantavirus infections in Baltimore, isolation of a virus from Norway rats, and characteristics of infected rat populations. Am J Epidemiol 126: 55–68

    PubMed  CAS  Google Scholar 

  • Chumakov MP (1963) Study of viral haemorrhagic fevers. J Hyg Epidemiol 7: 125–140

    Google Scholar 

  • Chumakov MP, Butenko AM, Shalunova NV (1968) New data on the virus causing Crimean haemorrhagic fever (in Russian). Vopr Virusol 13: 377–390

    PubMed  CAS  Google Scholar 

  • Chumakov MP, Smirnova SE, Tkachenko EA (1970) Relationship between strains of Crimean hemorrhagic fever and Congo viruses. Acta Virol 14: 82–85

    PubMed  CAS  Google Scholar 

  • Chun RW (1983) Clinical aspects of La Crosse encephalitis: neurological and psychological sequelae. In: Calisher CH, Thompson WH (eds) California serogroup viruses. Liss, New York, pp 193–201

    Google Scholar 

  • Chun RW, Thompson WH, Grawbow JD (1968) California arbovirus encephalitis in children. Neurology 18: 369–375

    PubMed  CAS  Google Scholar 

  • Coates DM, Sweet C (1990) Studies on the pathogenicity of a nairovirus, Dugbe virus, in normal and immunosuppressed mice. J Gen. Virol 71: 325–332

    PubMed  Google Scholar 

  • Cosgriff TM, Morrill JC, Jennings GB, Hodgson LA, Slayter MV, Gibbs PH, Peters CJ (1989) Hemostatic derangement produced by Rift Valley fever virus in rhesus monkeys. Rev Infect Dis (S4): 807–814

    Google Scholar 

  • Danielova V (1975) Growth of Tahyna virus at low temperatures. Acta Virol 19: 327–332

    PubMed  CAS  Google Scholar 

  • Daubney R, Hudson JR (1931) Enzootic hepatitis or Rift Valley fever: an undescribed virus disease of sheep, cattle and man from East Africa. J Pathol Bacteriol 34: 545–557

    Google Scholar 

  • David-West TS (1972) World distribution and antigenic variation of Simbu arboviruses. Microbios 5: 213–217

    PubMed  CAS  Google Scholar 

  • Davies FG (1975) Observations on the epidemiology of Rift Valley fever in Kenya. J Hyg (Cambr) 75: 219–230

    CAS  Google Scholar 

  • Davies FG, Jessett DM (1985) A study of the host range and distribution of antibody to Akabane virus (genus Bunyavirus, family Bunyaviridae) in Kenya. J Hyg (Cambr) 95: 191–196

    CAS  Google Scholar 

  • Davies FG, Linthicum KJ, James AD (1985) Rainfall and epizootic Rift Valley fever. Bull WHO 63: 941–943

    PubMed  CAS  Google Scholar 

  • DeFoliart GR (1983) Aedes triseriatus: vector biology in relationship to the persistence of La Crosse virus in endemic foci. In: Calisher CH, Thompson WH (eds) California serogroup viruses. Liss, New York, pp 89–105

    Google Scholar 

  • Desmyter J, Johnson KM, Deckers C, LeDuc JW, Brasseru F, van Ypersele de Strihou C (1983) Laboratory rat associated outbreak of haemorrhagic fever with renal syndrome due to Hantaan-like virus in Belgium. Lancet i: 1445–1448

    Google Scholar 

  • Diebel R, Srihongse S, Grayson MA (1983) Jamestown Canyon virus: the etiologic agent of an emerging human disease? In: Calisher CH, Thompson WH (eds) California serogroup viruses. Liss, New York, pp 313–328

    Google Scholar 

  • Dixon KE, Travassos da Rosa AP, Travassos da Rosa JF, Llewellyn CH (1981) Oropouche virus II. Epidemiological observations during an epidemic in Santaram, Para, Brazil in 1975. Am J Trop Med Hyg 30: 161–171

    PubMed  CAS  Google Scholar 

  • Doherty RL, Carley JG, Standfast A, Dyce AL, Snowdon WA (1972) Virus strains isolated from arthropods during an epizootic of bovine ephemeral fever in queensland. Aust Vet J 48: 81–86

    PubMed  CAS  Google Scholar 

  • Earle DP (1954) Symposium on epidemic hemorrhagic fever. Am J Med 16: 619–709

    Google Scholar 

  • Easterday BC (1965) Rift Valley fever Adv Vet Sci 10: 65–127

    CAS  Google Scholar 

  • Eddy GA, Peters CJ (1980) The extended horizons of Rift Valley fever: current and projected immunogens. New developments with human and veterinary vaccines. Liss, New York, pp 179–191

    Google Scholar 

  • Edwards JF, Livingston CW, Chung SI, Collisson EC (1989) Ovine arthrogryposis and central nervous system malformations associated with in utero Cache Valley virus infection: spontaneous disease. Vet Pathol 26: 33–39

    PubMed  CAS  Google Scholar 

  • Elliott RM (1989) Nucleotide sequence analysis of the large (L) genomic RNA segment of Bunyamwera virus, the prototype of the family Bunyaviridae. Virology 173: 426–436

    PubMed  CAS  Google Scholar 

  • Elliott RM (1990) Molecular biology of the Bunyaviridae. J Gen Virol 71: 501–522

    PubMed  CAS  Google Scholar 

  • Elliott RM, Lees JF, Watret GE (1984) Genetic diversity of bunyaviruses and the mechanism of genetic variation, In: Kohn A, Fuchs P (eds) Mechanisms of virus pathogenesis Nijhoff, Boston, pp 61–75

    Google Scholar 

  • Endres MJ, Jacoby DR, Janssen RS, Gonzalez-Scarano F, Nathanson N (1989) The large viral RNA segment of bunyaviruses encodes the large viral protein. J Gen Virol 70: 223–228

    PubMed  CAS  Google Scholar 

  • Endres MJ, Valsamakis, A, Gonzalez-Scarano F, Nathanson N (1990) A neuroattenuated clone of California bunyavirus: derivation, characterization, and revertants. J Virol 64: 1927–1933

    PubMed  CAS  Google Scholar 

  • Endris RG, Tesh RB, Young DG (1983) Transovarial transmission of Rio Grande virus (Bunyaviridae: Phlebovirus) by the sand fly, Luztomyia anthophora. Am J Trop Med Hyg 32: 862–864

    PubMed  CAS  Google Scholar 

  • Faran ME, Turell MJ, Romoser WS, Routier RG, Gibbs PH, Cannon TL, Bailey CL (1987) Reduced survival of adult Culex pipiens infected with Rift Valley fever virus. Am J Trop Med Hyg 37: 403–409

    PubMed  CAS  Google Scholar 

  • Faran ME, Romoser WS, Routier RG, Bailey CL (1988) The distribution of Rift Valley fever virus in the mosquito Culex pipiens as revealed by viral titration of dissected organs and tissues. Am J Trop Med Hyg 39: 206–213

    PubMed  CAS  Google Scholar 

  • French GR, Fulke RS, Brand OA, Eddy GA, Lee HW, Lee PW (1981) Korean hemorrhagic fever: propagation of the etiologic agent in a cell line of human origin. Science 211: 1046–1048

    PubMed  CAS  Google Scholar 

  • Gavrilovskaya IN, Apenkina NS, Myasnikov YA (1983) Features of circulation of hemorrhagic fever with renal syndrome (HFRS) virus among small mammals in the European U.S.S.R. Arch Virol 75: 313–316

    PubMed  CAS  Google Scholar 

  • Gentsch J, Bishop DH (1976) Recombination and complementation between temperature-sensitive mutants of a bunyavirus, snowshoe hare virus. J Virol 20: 351–354

    PubMed  CAS  Google Scholar 

  • Gentsch J, Bishop DH (1978) Small viral RNA segment of bunyaviruses codes for viral nucleocapsid protein. J Virol 28: 417–419

    PubMed  CAS  Google Scholar 

  • Gentsch J, Robeson G, Bishop DH (1979) Recombination between snowshoe hare and La Crosse bunyaviruses. J Virol 31: 707–717

    PubMed  CAS  Google Scholar 

  • Gonzalez-Scarano F, Shope RE, Calisher CH (1983) Monoclonal antibodies against the G1 and nucleocapsid proteins of La Crosse and Tahyna viruses. In: Calisher CH, Thompson WH (eds) California serogroup viruses. Liss, New York, pp. 145–156

    Google Scholar 

  • Gonzalez-Scarano F, Janssen RS, Najjar JA, Pobjecky N, Nathanson N (1985) An avirulent G1 glycoprotein variant of La Crosse bunyavirus with a defective fusion function. J Virol 54: 757–763

    PubMed  CAS  Google Scholar 

  • Gonzalez-Scarano F, Beaty BJ, Sundin DR, Janssen R, Endres MJ, Nathanson N (1988) Genetic determinants of the virulence and infectivity of La Crosse virus. Microb Path 4: 1–7

    CAS  Google Scholar 

  • Gonzalez-Scarano F, Nathanson N (1989) California serogroup viruses. In: Gilden DH, Lipton HL (eds) Clinical and molecular aspects of neurotropic virus infection. Kluwer, New York, pp 43–68

    Google Scholar 

  • Gonzalez-Scarano F, Nathanson N (1990) Bunyaviruses. In: Fields BN, Knipe DM (eds) Virology. Raven, New York, pp 1195–1228

    Google Scholar 

  • Gonzalez-Scarano F, Nathanson N (1989) California serogroup viruses. In: Gilden DH, Lipton HL (eds) Clinical and molecular aspects of neurotropic virus infection. Kluwer, Boston, pp 43–68

    Google Scholar 

  • Grimstad PR, Barrett RL, Humphrey RL (1984a) Serologic evidence for widespread infection with La Crosse and St. Louis encephalitis viruses in the Indiana human population. Am J Epidemiol 119: 913–930

    PubMed  CAS  Google Scholar 

  • Grimstad PR, Calisher CH, Haroff RN (1984b) Jamestown Canyon virus (California serogroup) is the etiologic agent of widespread infection in Michigan humans. Am J Trop Med Hyg 35: 376–386

    Google Scholar 

  • Gundersen CB, Brown KL (1983) Clinical aspects of La Crosse encephalitis: preliminary report. In: Calisher CH, Thompson WH (eds) California serogroup viruses. Liss, New York, pp 169–177

    Google Scholar 

  • Hammon WM, Reeves WC (1952) California encephalitis virus—a newly described agent. I. Evidence of natural infection in man and other animals. Calif Med 77: 303–309

    PubMed  CAS  Google Scholar 

  • Hardy JL, Scrivani RP, Lyness RP, Nelson RL, Roberts DR (1970) Ecologie studies on Buttonwillow virus in Kern County, California, 1961–1968. Am J Trop Med Hyg 19: 552–561

    PubMed  CAS  Google Scholar 

  • Hartley WJ, Wanner RA, Della-Porta AJ, Snowdon WA (1975) Serological evidence for the association of Akabane virus with epizootic bovine congenital arthrogryposis and hydranencephaly syndromes in New South Wales. Aust Vet J 51: 103–104

    PubMed  CAS  Google Scholar 

  • Haughey KG, Hartley WJ, Della-Porta AJ, Murray MD (1988) Akabane disease in sheep. Aust Vet J 65: 136–140

    PubMed  CAS  Google Scholar 

  • Henderson BE, Coleman PH (1971) The growing importance of California arboviruses in the etiology of human disease. Prog Med Virol 13: 404–461

    PubMed  CAS  Google Scholar 

  • Hoogstraal H (1979) The epidemiology of tick-borne Crimean-Congo hemorrhagic fever in Asia, Europe, and Africa. J Med Entomol 15: 307–417

    PubMed  CAS  Google Scholar 

  • Hoogstraal H, Meegan JM, Khalil GM, Adham FK (1979) The Rift Valley fever epizootic in Egypt 1977–1978. 2. Ecological and entomological studies. Trans R Soc Trop Med Hyg 73: 624–629

    PubMed  CAS  Google Scholar 

  • Inaba Y, Kurogi H, Omori T (1975) Akabane disease: epizootic abortion, premature birth, stillbirth, and congenital arthrogryposis-hydranencephaly in cattle, sheep, and goats caused by Akabane virus. Aust Vet J 51: 584–585

    PubMed  CAS  Google Scholar 

  • Iroegbu CU, Pringle CR (1981a) Genetics of the Bunyamwera complex. In: Bishop DH, Compans R (eds) The replication of negative strand RNA viruses. Elsevier, New York, pp 159–165

    Google Scholar 

  • Iroegbu CU and Pringle CR (1981 b) Genetic interactions among viruses of the Bunyavirus complex. J Virol 37: 383–394

    PubMed  CAS  Google Scholar 

  • Janssen R, Gonzalez-Scarano F, Nathanson N (1984) Mechanisms of bunyavirus virulence. Comparative pathogenesis of a virulent strain of La Crosse virus and an avirulent strain of Tahyna virus. Lab Invest 50: 447–455

    PubMed  CAS  Google Scholar 

  • Janssen RS, Nathanson N, Endres MJ, Gonzalez-Scarano F (1986) Virulence of La Crosse virus is under polygenic control. J Virol 59: 1–7

    PubMed  CAS  Google Scholar 

  • Jennings M, Boorman J (1983) Laboratory infection of the sandfly Phlebotomus papatasii Scopoli (Diptera, Psychodidae) with three phleboviruses. Trans R Soc Trop Med Hyg 77: 62–64

    PubMed  CAS  Google Scholar 

  • Jennings M, Mellor PS (1987) Culicoides: biological vectors of Akabane virus. Vet Microbiol 21: 125–131

    Google Scholar 

  • Johnson KP, Johnson RT (1968) California encephalitis. II. Studies of experimental infection in the mouse. J Neuropathol Exp Neurol 27: 390–400

    Google Scholar 

  • Johnson RT (1983) Pathogenesis of La Crosse virus in mice. In: Calisher CH, Thompson WH (eds) California serogroup viruses. Liss, New York, pp 139–144

    Google Scholar 

  • Johnston RE, Smith JF (1988) Selection for accelerated penetration in cell culture coselects for attenuated mutants of Venezuelan equine encephalitis virus. Virology 162: 437–443

    PubMed  CAS  Google Scholar 

  • Joubert JD, Ferguson AL, Gear J (1951) Rift Valley fever in South Africa 2. The occurrence of human cases in the Orange Free State, the North-Western Cape Province, the Western and Southern Transvaal. A. epidemiological and clinical findings. S Afr Med J 25: 890–891

    PubMed  CAS  Google Scholar 

  • Kalfayan B (1983) Pathology of La Crosse virus infections in humans. Calisher CH, Thompson WH, editors. California serogroup viruses. Liss, New York, pp 179–186

    Google Scholar 

  • Kappus KD, Monath TP, Kaminski RM (1983) Reported encephalitis associated with California serogroup virus infections in the United States, 1963–1981. In: Calisher CH, Thompson WH (eds) California serogroup viruses. Liss, New York, pp 31–41

    Google Scholar 

  • Kim GR, McKee KT (1985) Pathogenesis of Hantaan virus infection in suckling mice: clinical, virologie, and serologic observations. Am J Trop Med Hyg 34: 388–395

    PubMed  CAS  Google Scholar 

  • Kinney RM, Calisher CH (1981) Antigenic relationships among Simbu serogroup (Bunyaviridae) viruses. Am J Trop Med Hyg 30: 1307–1318

    PubMed  CAS  Google Scholar 

  • Klimas RA, Thompson WH, Calisher CH (1984) Genotypic varieties of La Crosse virus isolated from different geographic regions of the continental United States and evidence for a naturally occurring intertypic recombinant La Crosse virus. Am J Epidemiol 114: 112–131

    Google Scholar 

  • Konno S, Moriwaki M, Nakagawa M, Uchimura M, Kamimirata M, Tojinbara K (1975) Congenital abnormality of calves with arthrogryposis and hydranencephaly in Japan in 1972–1973. Nat Inst Anim Health Q 15: 52–53

    CAS  Google Scholar 

  • Konno S, Koeda T, Madarame H (1988) Myopathy and encephalopathy in chick embryos experimentally infected with Akabane virus. Vet Pathol 25: 1–8

    PubMed  CAS  Google Scholar 

  • Ksiazek TG, Yuill TM (1977) Viremia and antibody response to La Crosse virus in sentinel gray squirrels (Sciuris carolinensis) and chipmunks (Tamiasstriatus). Am J Trop Med Hyg 26: 815–821

    PubMed  CAS  Google Scholar 

  • Ksiazek TG, Jouan A, Meegan JM (1989) Rift Valley fever among domestic animals in the recent West African outbreak. Res Virol 140: 67–77

    PubMed  CAS  Google Scholar 

  • Kurata T, Tsai TF, Bauer SP, McCormick JB (1983) Immunofluorescence studies of disseminated Hantaan virus infection of suckling mice. Infect Immun 41: 391–398

    PubMed  CAS  Google Scholar 

  • Kurogi H, Inaba Y, Goto Y (1975) Serologic evidence for etiologic role of Akabane virus in epizootic abortion-arthrogryposis-hydranencephaly in cattle in Japan, 1972–1974. Arch Virol 47: 71–83

    PubMed  CAS  Google Scholar 

  • Kurogi H, Inaba Y, Takahashi E (1976) Epizootic congenital arthrogryposis-hydranencephaly syndrome in cattle: isolation of Akabane virus from affected fetuses. Arch Virol 51: 67–74

    PubMed  CAS  Google Scholar 

  • Kurogi H, Inaba Y, Tkahashi E (1977) Congenital abnormalities in newborn cattle after inoculation of pregnant cows with Akabane virus. Infect Immun 17: 338–343

    PubMed  CAS  Google Scholar 

  • Lahdevirta J (1982) Clinical features of HFRS in Scandinavia as compared with East Asia. Scand J Infect Dis 36: 93–95

    CAS  Google Scholar 

  • Laughlin LW, Meegan JM, Strausbuagh LH, Morens DM, Watten RH (1979) Epidemic Rift Valley fever in Egypt: Observations of the spectrum of human illness. Trans R Soc Trop Med Hyg 73: 630–633

    PubMed  CAS  Google Scholar 

  • LeDuc JW (1987) Epidemiology of Hantaan and related viruses. Lab Anim Sci 37: 413–418

    PubMed  CAS  Google Scholar 

  • LeDuc JW, Smith GA, Johnson KM (1984) Hantaan-like viruses from domestic rats captured in the United States. Am J Trop Med Hyg 33: 992–998

    PubMed  CAS  Google Scholar 

  • LeDuc JW, Smith GA, Childs JE (1986) Global survey of antibody to Hantaan-related viruses among peridomestic rodents. Bull WHO 64: 139–144

    PubMed  CAS  Google Scholar 

  • Lee HW (1982) Korean hemorrhagic fever. Prog Med Virol 28: 96–113

    PubMed  CAS  Google Scholar 

  • Lee HW (1989) Hemorrhagic fever with renal syndrome. Prog Med Virol 36: 62–102

    PubMed  CAS  Google Scholar 

  • Lee HW, Johnson KM (1982) Laboratory-acquired infections with Hantaan virus, the etiologic agent of Korean hemorrhagic fever. J Infect Dis 146: 645–651

    PubMed  CAS  Google Scholar 

  • Lee HW, Lee PW, Johnson KM (1978) Isolation of the etiologic agent of Korean hemorrhagic fever. J Infect Dis 137: 298–308

    PubMed  CAS  Google Scholar 

  • Lee HW, French GR, Lee PW, Baek LJ, Tsuchiya K, Foulke RS (1981a) Observations on natural and laboratory infection of rodents with the etiologic agent of Korean hemorrhagic fever. Am J Trop Med Hyg 30: 477–482

    PubMed  CAS  Google Scholar 

  • Lee HW, Lee PW, Baek LJ, Song CK, Seong IW (1981b) Intraspecific transmission of Hantaan virus, the etiologic agent of Korean hemorrhagic fever, in the rodent Apodemus agragrius. Am J Trop Med Hyg 30: 1106–1112

    PubMed  CAS  Google Scholar 

  • Lee HW, Baek LJ, Johnson KM (1982) Isolation of Hantaan virus, the etiologic agent of Korean hemorrhagic fever, from wild urban rats. J Infect Dis 146: 638–644

    PubMed  CAS  Google Scholar 

  • Lee M, Kim BK, Park S, Han JS, Kim ST, Lee JS (1989) Coagulopathy in hemorrhagic fever with renal syndrome (Korean hemorrhagic fever). Rev Inf Dis 11 (SA): 877–883

    Google Scholar 

  • Lee PW, Amyx HL, Gibbs CJ, Gajdusek DC, Lee HW (1981) Propagation of Korean hemorrhagic fever virus in laboratory rats. Infect Immun 31: 334–338

    PubMed  CAS  Google Scholar 

  • Lee PW, Amyx HL, Yanagihara R, Gajdusek DC, Goldgaber D, Gibbs CJ (1985) Partial characterization of Prospect Hill virus isolated from meadow voles in the United States. J Infect Dis 152: 826–829

    PubMed  CAS  Google Scholar 

  • Lewis RM, Cosgriff TM, Peters CJ, Morrill JC (1987) Differentiation of a human monocytic cell line associated with increased production of Rift Valley fever virus by infected cells. J Med Virol 23: 207–215

    PubMed  CAS  Google Scholar 

  • Linthicum KJ, Davies FG, Kairo A, Bailey CL (1985) Rift Valley fever virus (family Bunyaviriae, genus Phlevobirus). Isolations from Diptera collected during an inter-epizootic period in Kenya. J Hyg (Cambr) 95: 197–209

    CAS  Google Scholar 

  • Ludwig GV, Christensen BM, Yuill TM, Schultz KT (1989) Enzyme processing of La Crosse virus glycoprotein G1: a bunyavirus-vector infection model. Virology 17: 108–113

    Google Scholar 

  • Lyons MJ, Heyduk J (1973) Aspects of the developmental morphology of California encephalitis virus in cultured vertebrate and arthropod cells and in mouse brain. Virology 54: 37–52

    PubMed  CAS  Google Scholar 

  • Mackenzie RD, Finlay GM, Stern RO (1936) Studies on neurotropic Rift Valley fever virus: the susceptibility of rodents. Br J Exp Pathol 17: 352–361

    Google Scholar 

  • McGavran MH, Easterday BC (1963) Rift Valley fever virus hepatitis. Am J Pathol 42: 587–607

    PubMed  CAS  Google Scholar 

  • McKee KT, Lim GR, Green DE, Peters CJ (1985) Hantaan virus infection in suckling mice: virologie and pathologic correlates. J Med Virol 17: 107–117

    PubMed  Google Scholar 

  • McLean DM (1983) Yukon isolates of snowshoe hare virus, 1972–1982. In: Calisher CH, Thompson WH (eds) California serogroup viruses. Liss, New York, pp 247–256

    Google Scholar 

  • McLean DM, Gubash SM, Grass PN, Miller MA, Petric M, Walters TE (1975) California encephalitis development in mosquitoes as revealed by transmission studies, immunoperoxidase staining, and electron microscopy. Can J Microbiol 21: 453–462

    PubMed  CAS  Google Scholar 

  • McLean DM, Grass PN, Judd BD, Stolz KJ (1979) Bunyavirus development in arctic and Aedes aegypti mosquitoes as revealed by glucose oxidase staining and immunofluorescence. Arch Virol 62: 313–322

    PubMed  CAS  Google Scholar 

  • McPhee DA, Parsonson IM, Della-Porta AJ, Jarre« RG (1984) Teratogenicity of Australian Simbu serogroup and some other Bunyaviridae viruses: the embryonated chicken egg as a model. Infect Immun 43: 413–420

    PubMed  CAS  Google Scholar 

  • Meegan JM (1979) The Rift Valley fever epizootic in Egypt, 1977–1978.1. Description of the epizootic and virological studies. Trans R Soc Trop Med Hyg 73: 618–623

    PubMed  CAS  Google Scholar 

  • Meegan JM, Shope RE (1981) Emerging concepts on Rift Valley fever. Perspect Virol 11: 267–287

    Google Scholar 

  • Miller BR (1983) A variant of La Crosse virus attenuated for Aedes triseriatus mosquitoes. Am J Trop Med Hyg 32: 1422–1428

    PubMed  CAS  Google Scholar 

  • Mims CA (1956a) Rift Valley fever virus in mice I. General features of the infection. Br J Exp Pathol 37: 99–109

    PubMed  CAS  Google Scholar 

  • Mims CA (1956b) Rift Valley fever virus in mice. II. Adsorption an multiplication of the virus. Br J Exp Pathol 37: 110–119

    PubMed  CAS  Google Scholar 

  • Mims CA (1956c) Rift Valley fever virus in mice. III. Further quantitative features of the infective process. Br J Exp Pathol 37: 120–128

    PubMed  CAS  Google Scholar 

  • Mims CA (1956d) Rift Valley fever virus in mice. IV. Incomplete virus, its production and properties. Br J Exp Pathol 37: 129–143

    PubMed  CAS  Google Scholar 

  • Mitten JQ, Remmele NS, Walker JS, Carter RC, Stephen EL, Klein F (1970) The clinical aspects of Rift Valley fever virus in household pets. III. Pathologic changes in the dog and cat. J Infect Dis 121: 25–31

    PubMed  CAS  Google Scholar 

  • Miura Y, Hayashi S, Ishihara T, Inaba Y, Omori T, Matumoto M (1974) Neutralizing antibody against Akabane virus in precolostral sera from calves with congenital arthrogryposis-hydranencephaly syndrome. Arch Gesamte Virusforsch 46: 377–380

    PubMed  CAS  Google Scholar 

  • Monath TP, Nuckolls JG, Berall J, Bauer H, Chappell WA, Coleman PH (1970) Studies of California encephalitis in Minnesota. Am J Epiemiol 92: 40–50

    CAS  Google Scholar 

  • Montgomery E (1917) On a tick-borne gastro-enteritis of sheep and goats occurring in British East Africa. J Comp Pathol Ther 30: 28–57

    Google Scholar 

  • Morrill JC, Jennings GB, Caplen H, Turell MJ, Johnson AJ, Peters CJ (1987) Pathogenicity and immunogenicity of a mutagen-attenuated Rift Valley fever virus immunogen in pregnant ewes. Am J Vet Res 48: 1042–1047

    PubMed  CAS  Google Scholar 

  • Morrill JC, Jennings GB, Cosgriff TM, Gibbs PH, Peters CJ (1989) Prevention of Rift Valley fever in rhesus monkeys with interferon-alpha. Rev Infect Dis 11(54): 815–825

    Google Scholar 

  • Morrill JC, Jennings GB, Johnson AJ, Cosgriff TM, Gibbs PH, Peters CJ (1990) Pathogenesis of Rift Valley fever in rhesus monkeys: role of interferon response. Arch Virol 110: 195–212

    PubMed  CAS  Google Scholar 

  • Moussa MI, Wood OL, Abdel-Wahab KS (1982) Reduced pathogenicity associated with a small plaque variant of the Egyptian strain of Rift Valley fever virus (ZH501). Trans R Soc Trop Med Hyg 76: 482–486

    PubMed  CAS  Google Scholar 

  • Murphy FA, Harrison AK, Tzianabos T (1968a) Electron microscopic observations of mouse brain infected with Bunyamwera serologic supergroup viruses and several other arthropod-borne viruses. J Virol 2: 1315–1325

    PubMed  CAS  Google Scholar 

  • Murphy FA, Whitfield SG, Coleman PH, Calisher CH (1968b) California group arboviruses: electron microscopic studies. Exp Mol Pathol 9: 44–56

    PubMed  CAS  Google Scholar 

  • Murphy FA, Harrison AK, Whitfield SG (1973) Bunyaviridae: morphologic and morphogenetic similarities of Bunyamwera serologic supergroup viruses and several other arthropod-borne viruses. Intervirology 1: 297–316

    PubMed  CAS  Google Scholar 

  • Murphy FA, Whitfield SG, Sudia WD (1975) Interactions of vector with vertebrate pathogenic viruses. Mamamorosch K, Shope RE, editors. Invertebrate immunity. Academic, Oralando, pp 25–37

    Google Scholar 

  • Murray MD (1987) An outbreak of Akabane disease in calves in New South Wales. Aust Vet J 64: 305–308

    PubMed  CAS  Google Scholar 

  • Myrhman G (1951) Nephropathia epidemica: a new infectious disease in Northern Scandinavia. Acta Med Scand 140: 52–56

    Google Scholar 

  • Nakamura T, Yanagihara R, Gibbs CJ, Amyx HL, Gajddusek DC (1985a) Differential susceptibility and resistance of immunocompetent and immunodeficient mice to fatal Hantaan virus infection. Arch Virol 86: 109–120

    PubMed  CAS  Google Scholar 

  • Nakamura T, Yanagihara R, Gibbs CJ, Gajdusek DC (1985b) Immune spleen cell-mediated protection against fatal Hantaan virus infection in infant mice. J Infect Dis 151: 691–697

    PubMed  CAS  Google Scholar 

  • Nicoletti L, Verani P (1985) Growth of the phlebovirus Toscana in a mosquito (Aedes pseudo-scutellaris) cell line (AP-61): establishment of a persistent infection. Arch Virol 85: 35–45

    PubMed  CAS  Google Scholar 

  • Niklasson B, LeDuc JW (1987) Epidemiology of nephropathia epidemica in Sweden. J Infect Dis 155: 269–276

    PubMed  CAS  Google Scholar 

  • Oker-Blom N, von Bonsdorff C-H, Korvenkontio M (1979) Nephropathia epidemica in Finland. In: Kurstak E (ed) Arctic and tropical arboviruses. Academic, Orlando, pp 197–209

    Google Scholar 

  • Oliver J, McDowell M (1957) The renal lesion in epidemic hemorrhagic fever. J Clin Invest 36: 99–22

    PubMed  Google Scholar 

  • Oya A, Okino T, Ogata T, Kobayashi I, Matsuyama T (1961) Akabane, a new arbor virus isolated in Japan. Jpn J Med Sci Biol 14: 101–108

    PubMed  CAS  Google Scholar 

  • Paci P, Balucci M, Verani P (1983) Toscana virus, a new Phlebotomus-transmitted virus isolated from Italy. In: Proceedings of the international congress of infectious diseases. Luigi Pozzi, Rome, pp 35–39

    Google Scholar 

  • Pantuwatana S, Thompson WH, Watts DM (1972) Experimental infection of chipmunks an squirrels with La Crosse and trivittatus viruses an biological transmission of La Crosse virus by Aedes triseriatus. Am J Trop Med Hyg 21: 476–481

    PubMed  CAS  Google Scholar 

  • Parkin WE, Hammon WM, Sather GE (1972) Review of current epidemiologic literature on viruses of the California arbovirus group. Am J Trop Med Hyg 14: 964–978

    Google Scholar 

  • Parsonson IM, Della-Porta AJ, Snowdon WA (1975) Congenital abnormalities in fetal lambs after inoculation of pregnant ewes with Akabane virus. Aust Vet J 51: 585–586

    PubMed  CAS  Google Scholar 

  • Parsonson IM, Della-Porta AJ, Snowon WA (1977) Congenital abnormalities in fetal lambs after infection of pregnant sheep with Akabane virus. Infect Immun 15: 254–262

    PubMed  CAS  Google Scholar 

  • Parsonson IM, McPhee DA (1985) Bunyavirus pathogenesis. Adv Virus Res 30: 279–316

    PubMed  CAS  Google Scholar 

  • Patrican LA, DeForliart GR, Yuill TM (1985) La Crosse viremia in juvenile, subadult and adult chipmunks (Tamias striatus) following feeding by transovarially-infected Aedes triseriatus. Am J Trop Med Hyg 34: 596–602

    PubMed  CAS  Google Scholar 

  • Paulson SL, Grimstad PR (1989) Replication and dissemination of La Crosse virus in the competent vector Aedes triseriatus and the incompetent vector Aedes hendersoni and evidence for transovarial transmission by Aedes hendersoni (Diptera: Culicidae). J Med Entomol 26: 602–609

    PubMed  CAS  Google Scholar 

  • Penttinen K, Lahdevirta J, Kekomaki R (1981) Circulating immune complexes, immunoconglutinins, and rheumatoid factors in nephrophathia epidemica. J Infect Dis 143: 15–21

    PubMed  CAS  Google Scholar 

  • Peters CJ, Anderson GW (1981) Pathogenesis of Rift Valley fever. Contrib Epidemiol Biostat 3: 21–41

    Google Scholar 

  • Peters CJ, Jones D, Trotter R (1988) Experimental Rift Valley fever in rhesus macaques. Arch Virol 99: 31–44

    PubMed  CAS  Google Scholar 

  • Peters CJ, Lui CT, Anderson GW, Morrill JC, Jahrling PB (1989) Pathogenesis of viral hemorrhagic fevers: Rift Valley fever and Lassa fever contrasted. Rev Infect Dis 11(54): 743–749

    Google Scholar 

  • Pifat D, Smith JF (1987) Punta Toro virus infection of C57BL/6J mice: a model for phlebovirus-induced disease. Microb Path 3: 409–422

    CAS  Google Scholar 

  • Pinheiro FP, Travassos da Rosa AP, Travassos da Rosa JF (1981a) Oropouche virus. I. A review of clinical, epidemiological, and ecological findings. Am J Trop Med Hyg 30: 149–160

    PubMed  CAS  Google Scholar 

  • Pinheiro FP, Hoch AL, Gomes MD, Roberts DR (1981 b) Oropouche virus. IV. Laboratory transmission by Culicoides paraensis. Am J Trop Med Hyg 30: 172–176

    PubMed  CAS  Google Scholar 

  • Pinheiro FP, Travassos da Rosa AP, Gomes ML, Leduc JW, Hoch HL (1982) Transmission of Oropouche virus from man to hamster by the midge Culicoides paraensis. Science 215:1251–1252

    PubMed  CAS  Google Scholar 

  • Pringle CR and Iroegbu CU (1982) Mutant identifying a third recombination group in a bunyavirus. J Virol 42: 873–879

    PubMed  CAS  Google Scholar 

  • Raju R, Kolakofsky D (1989) The translational requirement for complete La Crosse virus mRNA synthesis is cell-type dependent. J Virol 63: 5159–5165

    PubMed  CAS  Google Scholar 

  • Reeves WC, Hammon WM (1962) Epidemiology of the arthropod-borne viral encephalitides in Kern County, California, 1943–1952. Univ Calif Publ Public Health 4: 1–257

    CAS  Google Scholar 

  • Reeves WC, Emmons RW, Hardy JL (1983) Historical perspective on California encephalitis virus in California. In: Calisher CH, Thompson WH (eds) California serogroup viruses. Liss, New York, pp 19–30

    Google Scholar 

  • Roberts DR, Hoch AL, Dixon KE, Llewellyn CH (1981) Oropouche virus. III. Entomological observations from three epidemics in Para, Brazil, 1975. Am J Trop Med Hyg 30: 339–350

    Google Scholar 

  • Rossier C, Raju R, Kolakofsky D (1988) La Crosse virus gene expresion in mammalian and mosquito cells. Virology 165: 539–548

    PubMed  CAS  Google Scholar 

  • Rowley WA, Wong YW, Dorsey DC, Hunsler WJ, Carrier RW (1988) California serogroup viruses in Iowa. In: Calisher CH and Thompson WH (eds) California serogroup viruses. Liss, New York, pp 237–246

    Google Scholar 

  • Sabatino DA, Cramblett HG (1968) Behavioral sequelae of California encephalitis virus infection in children. Dev Med Child Neurol 10: 331–337

    PubMed  CAS  Google Scholar 

  • Sabin AB (1948) Phlebotomus fever. In: Rivers TM (ed) Viral and rickettsial diseases of man. Lippincott, Philadelphia, pp 454–460

    Google Scholar 

  • Sabin AB (1951) Experimental studies on Phlebotomus (pappataci, sandfly) fever during World War II. Arch Virusforsch 4: 367–410

    PubMed  CAS  Google Scholar 

  • Sabin AB, Blumberg RW (1947) Human infection with Rift Valley fever virus and immunity twelve years after a single attack. Proc Soc Exp Biol Med 64: 385–389

    PubMed  CAS  Google Scholar 

  • Settergren B, Juto P, Trollfors B, Wadell G, Norrby SR (1989) Clinical characteristics of nephropathia epidemica in Sweden. Rev Infect Dis 11: 921–927

    PubMed  CAS  Google Scholar 

  • Seymour C, Amundson TE, Yuill TM, Bishop DH (1983) Experimental infection of chipmunks and snowshoe hares with La Crosse and snowshoe hare viruses and four of their reassortants. Am J Trop Med Hyg 32: 1147–1153

    PubMed  CAS  Google Scholar 

  • Shepherd AJ, Swanepoel R, Leman PA, Blackburn NK, Haliett AF (1985) A nosocomial outbreak of Crimean-Congo hemorrhagic fever at Typerberg Hospital, part V. Virological and serological observations. S Afr Med J 68: 733–736

    PubMed  CAS  Google Scholar 

  • Shepherd AJ, Swanepoel R, Shepherd SP, McGillivray GM, Searle LA (1987) Antibody to Crimean-Congo hemorrhagic fever virus in wild mammals from southern Africa. Am J Trop Med Hyg 36: 133–142

    PubMed  CAS  Google Scholar 

  • Shimshony A, Barzilai R (1983) Rift Valley fever. Adv Vet Sci Comp Med 27: 347–425

    PubMed  CAS  Google Scholar 

  • Shope RE (1985) Bunyaviruses. In: Fields BN (ed) Virology, Raven, New York, pp 1055–1082

    Google Scholar 

  • Shope RE, Rozhon EJ, Bishop DH (1981) Role of the middle-sized bunyavirus segment in mouse virulence. Virology 114: 273–276

    PubMed  CAS  Google Scholar 

  • Shope RE, Peters CJ, Dives FG (1982) The spread of Rift Valley fever and approaches to its control. Bull WHO 60: 299–304

    PubMed  CAS  Google Scholar 

  • Siam AL, Meegan JM, Gharbawi KF (1980) Rift Valley fever ocular manifestations: observations during the 1977 epidemic in Egypt. Br J Ophthalmol 64: 366–374

    PubMed  CAS  Google Scholar 

  • Simpson DI, Knight EM, Courtois G, Williams MC, Weibren MP, Kibukamosoke JW (1967) Congo virus: a hitherto undescribed virus occurring in Africa. I. Human isolations-clinical notes. East Afr Med J 44: 87–92

    Google Scholar 

  • Smirnova SE (1979) A comparative study of the Crimean hemorrhagic fever Congo group of viruses. Arch Virol 62: 137–145

    PubMed  CAS  Google Scholar 

  • Smithburn KC (1949) Rift Valley fever: the neurotropic adaptation of the virus and the experimental use of this modified virus as a vaccine. Br J Exp Pathol 30: 1–16

    PubMed  CAS  Google Scholar 

  • Sommer A-I, Traavik TM, Traavik R., Berdal BP, Dalrymple JM (1985) Reservoir animals for nephropathia epidemica in Norway: indicaton of a major role for the bank vole (C. glareolus) in comparison with the woodmouse (A sylvaticus). J Hyg (Cambr) 94: 123–127

    CAS  Google Scholar 

  • Srihongse S, Grayson MA, Diebel R (1984) California serogroup viruses in New York State: the role of subtypes in human infections. Am J Trop Med Hyg 33: 1218–1227

    PubMed  CAS  Google Scholar 

  • Sugiyama K, Morikawa S, Matsura Y (1987) Four serotypes of hemorrhagic fever with renal syndrome viruses identified by polyclonal and monoclonal antibodies. J Gen Virol 68: 979–987

    PubMed  Google Scholar 

  • Suleiman MN, Muscat-Baron JM, Harries JR, Platt GS, Bowen ET, Simpson DI (1980) Congo/Crimean hemorrhagic fever in Dubai, an outbreak at the Rashid hospital. Lancet ii: 939–941

    Google Scholar 

  • Sundin DR, Beaty BR, Nathanson N, Gonzalez-Scarano F (1987) A G1 glycoprotein epitope of La Crosse virus: a determinant of infection of Aedes triseriatus. Science 235: 591–593

    PubMed  CAS  Google Scholar 

  • Swanepoel R, Struthers JK, Shepherd AJ, McGillivray GM, Nel MJ, Jupp PG (1983) Crimean-Congo hemorrhagic fever in South Africa. Am J Trop Med Hyg 32: 1407–1415

    PubMed  CAS  Google Scholar 

  • Swanepoel R, Shepherd AJ, Leman PA (1987) Epidemiologic and clinical features of Crimean-Congo hemorrhagic fever in Southern Africa. Am J Trop Med Hyg 36: 120–132

    PubMed  CAS  Google Scholar 

  • Swanepoel R, Gill DE, Shepherd AJ, Leman PA, Mynhardt JH, Harvey S (1989) The clinical pathology of Crimean-Congo hemorrhagic fever. Rev Infect Dis 11(54): 794–800

    Google Scholar 

  • Takahara K, Min MN, Battles JK, Sugiyama K, Emery VC, Dalrymple JM, Bishop DH (1989) Identification of mutations in the M RNA segment of a candidate vaccine strain of Rift Valley fever virus. Virology 169: 452–456

    Google Scholar 

  • Tamara M, Asada H, Kondo K, Tanishita O, Kurata T, Yamanishi K (1989) Pathogenesis of Hantaan virus in mice. J Gen Virol 70: 2897–2906

    Google Scholar 

  • Tanashita O, Tsakahashi Y, Okuno Y (1986) Persistent infection of rats with hemorrhagic fever with renal syndrome virus and their antibody responses. J Gen Virol 67: 2819–2824

    Google Scholar 

  • Tesh RB (1988) Phlevovirus and its vectors. Annu Rev Entomol 33: 169–181

    PubMed  CAS  Google Scholar 

  • Tesh RB, Beaty BR (1983) Localization of California serogroup viruses in mosquitoes. In: Calisher CH, Thompson WH (eds) California serogroup viruses. Liss, New York, pp 67–75

    Google Scholar 

  • Tesh RB, Modi GB (1984) Studies on the biology of Phleboviruses in sand flies (Diptera: Psychodidae). I. Experimental infection of the vector. Am J Trop Med Hyg 33: 1007–1016

    PubMed  CAS  Google Scholar 

  • Tesh RB, Modi GB (1987) Maintenance of Toscana virus in Phlebotomus perniciosus by vertical transmission. Am J Trop Med Hyg 36: 189–193

    PubMed  CAS  Google Scholar 

  • Tesh RB, Chaniotis BN, Peralta PH, Johnson KM (1974) Ecology of viruses isolated from Panamanian sandflies. Am J Trop Med Hyg 23: 258–266

    PubMed  CAS  Google Scholar 

  • Thompson WH, Beaty BJ (1978) Venereal transmission of La Crosse virus from male to female Aedes triseriatus. Am J Trop Med Hyg 27: 187–195

    PubMed  CAS  Google Scholar 

  • Thompson WH, Evans AS (1965) California encephalitis virus studies in Wisconsin. Am J Epidemiol 81: 230–244

    PubMed  CAS  Google Scholar 

  • Thompson WH, Gundersen CB (1983) La Crosse encephalitis: occurrence of disease and control in a suburban area. In: Calisher CH, Thompson WH (eds) California serogroup viruses. Liss, New York, pp 225–236

    Google Scholar 

  • Thompson WH, Kalfayan B, Anslow RO (1965) Isolation of California encephalitis virus from a fatal human illness. Am J Epidemiol 81: 245–253

    PubMed  CAS  Google Scholar 

  • Tignor GH, Smith AL, Casals J, Ezekoli CD, Okoli J (1980) Close relationship of Crimean hemorrhagic fever-Congo (CHF-C) virus strains by neutralizing antibody assays. Am J Trop Med Hyg 29: 676–685

    PubMed  CAS  Google Scholar 

  • Tignor GH, Burrage TG, Smith AL (1983) California serogroup gene structure-function relationships; virulence and tissue tropisms. In: Calisher CH, Thompson WH (eds) California serogroup viruses. Liss, New York, pp 129–138

    Google Scholar 

  • Tomori O (1980) Rift Valley fever infection in man in Nigeria. J Med Virol 5: 343–350

    PubMed  CAS  Google Scholar 

  • Tsai TF, Bauer S, McCormick JB, Kurata T (1982) Intracerebral inoculation of suckling mice with Hantaan virus. Lancet i: 503–504

    Google Scholar 

  • Turell MJ, Hardy JL (1980) Carbon dioxie sensitivity of mosquitoes infected with California encephalitis virus. Science 209: 1029–1030

    PubMed  CAS  Google Scholar 

  • Turell MJ, Gargan TP, Bailey CL (1984) Replication and dissemination of Rift Valley fever virus in Culex pipiers Am J Trop Med Hyg BB 176–181

    Google Scholar 

  • Turell MJ, Rossignol PA, Spielman A, Rossi CA, Bailey CL (1984) Enhanced arboviral transmission by mosquitoes that concurrently ingested microfilariae. Science 225: 1039–1041

    PubMed  CAS  Google Scholar 

  • van Eeden PJ, Joubert RR, van de Wal BW, King JB, de Kock A, Gorenwald JH (1985) A nosocomial outbreak of Crimean-Congo hemorrhagic fever at Tygerberg Hospital, part I. Clinical features. S Afr Med J 68:711–717

    PubMed  Google Scholar 

  • Verani P, Nicoletti L, Ciufolini MG (1984) Antigenic and biological characterization of Toscana virus, a new phleblotomus fever group virus isolated in Italy. Acta Virol 28: 39–47

    PubMed  CAS  Google Scholar 

  • Vezza AC, Repik DM, Cash P, Bishop DH (1979) In vivo transcription and protein synthesis capabilities of bunyaviruses: wild-type snowshoe hare virus and its temperature-sensitive group I, group II, and group l/ll mutants. J Virol 31: 426–436

    PubMed  CAS  Google Scholar 

  • Walsh J (1988) Rift Valley fever virus rears its head. Science 240: 1397–1399

    PubMed  CAS  Google Scholar 

  • Watts DM, Panuwatana S, DeFoliart GR, Yuill TM, Thompson WH (1973) Transovarial tramsmission of La Crosse virus (California encephalitis group) in the mosquito, Aedes triseriatus. Science 182: 1140–1143

    PubMed  CAS  Google Scholar 

  • Whitman L, Shope RE (1962) The California complex of arthropod-borne viruses and its relationship to the Bunyamwera serogroup through Guaroa virus. Am J Trop Med Hyg 11: 691–696

    PubMed  CAS  Google Scholar 

  • Whittem JH (1957) Congenital abnormalities in calves: arthrogryposis and hydranencephally. J Pathol Bacteriol 73: 375–387

    Google Scholar 

  • Yanagihara R, Svedmyr A, Amyx HL (1984) Isolation and propagation of nephropathia epidemica virus in bank voles. Scand J Infect Dis 16: 225–228

    PubMed  CAS  Google Scholar 

  • Yanagihara R, Golgaber D, Gajdusek DC (1985) Propagation of nephropathia epidemica virus in Mongolian gerbils. J Virol 53: 973–975

    PubMed  CAS  Google Scholar 

  • Yanagihara R, Daum CA, Lee PW (1987) Serological servey of Prospect Hill virus infection in indigenous wild rodents in the USA. Trans R Soc Trop Med Hyg 81: 42–45

    PubMed  CAS  Google Scholar 

  • Yanagihara R, Amyx HL, Lee PW, Asher DM, Gibbs CJ, Gajusek DC (1988) Experimental hantavirus infection in nonhuman primates. Arch Virol 10: 125–130

    Google Scholar 

  • Yu-Chen Y, Ling-Xiong K, Ling L (1985) Characteristics of Crimean-Congo hemorrhagic fever virus (Xinjiang strain) in China. Am J Trop Med Hyg 34: 1179–1182

    Google Scholar 

  • Zhang XK, Takashima I, Hashimoto N (1989a) Characteristics of passive immunity against hantavirus infections in rats. Arch Virol 105: 235–246

    PubMed  CAS  Google Scholar 

  • Zhang XK, Takashima I, Mori F, Hashimoto N (1989b) Comparison of virulence between two strains of Rattus serotype hemorrhagic fever with renal syndrome (HFRS) virus in newborn rats. Microbiol Immunol 33: 195–205

    PubMed  CAS  Google Scholar 

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Gonzalez-Scarano, F., Endres, M.J., Nathanson, N. (1991). Pathogenesis. In: Kolakofsky, D. (eds) Bunyaviridae. Current Topics in Microbiology and Immunology, vol 169. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-76018-1_8

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