Analyze Diet
Vaccine2009; 27(12); 1797-1810; doi: 10.1016/j.vaccine.2008.12.063

Immunoprophylaxis against important virus disease of horses, farm animals and birds.

Abstract: Since the refinement of tissue culture techniques for virus isolation and propagation from the mid 1960s onwards, veterinary virology has received much academic and industrial interest, and has now become a major global industry largely centred on vaccine development against economically important virus diseases of food animals. Bio-tech approaches have been widely used for improved vaccines development. While many viral diseases are controlled through vaccination, many still lack safe and efficacious vaccines. Additional challenges faced by academia, industry and governments are likely to come from viruses jumping species and also from the emergence of virulent variants of established viruses due to natural mutations. Also viral ecology is changing as the respective vectors adapt to new habitats as has been shown in the recent incursion by bluetongue virus into Europe. In this paper the current vaccines for livestock, horses and birds are described in a species by species order. The new promising bio-tech approaches using reverse genetics, non-replicating viral vectors, alpha virus vectors and genetic vaccines in conjunction with better adjuvants and better ways of vaccine delivery are discussed as well
Publication Date: 2009-04-30 PubMed ID: 19402200PubMed Central: PMC7130586DOI: 10.1016/j.vaccine.2008.12.063Google Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
  • Journal Article
  • Review

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

The research article discusses the progress in the development of vaccines for viral diseases affecting horses, farm animals, and birds. The paper examines the current state of vaccines for each species, and also considers promising new biotechnological strategies for improved vaccine development.

Exploring the Field of Veterinary Virology

  • This paper contextualizes the field of veterinary virology, which has advanced significantly since the mid-1960s following the refinement of virus isolation and propagation techniques through tissue culture. It emphasizes that this area of study has seen increasing academic and industrial interest over the years.
  • Currently, veterinary virology plays a significant role in the global industry, primarily focusing on developing vaccines against virus diseases prevalent in animals raised for food. This has important economic implications as it safeguards the food supply chain from disruptions due to these diseases.

Challenges and Evolving Viral Trends

  • Despite the industry’s expansion and progress in controlling many viral diseases through vaccination, some diseases continue to lack safe and effective solutions. This reveals significant gaps in the current state of veterinary vaccine development.
  • Other challenges discussed include the viral diseases jumping between species and the emergence of more virulent virus variants due to natural mutations. These issues complicate the attempts to control and eradicate these diseases.
  • Significant changes in viral ecology are resulting from various vectors adapting to new habitats. The example cited is the bluetongue virus’s incursion into Europe, underscoring the importance of monitoring and understanding these diseases’ shifting geographical profiles.

Future of Vaccine Development

  • The paper provides a review of the current vaccines available for livestock, horses, and birds, describing the state of each on a species-by-species basis.
  • Potential methods for improved vaccine development are discussed in light of emerging biotechnological tools. These include the use of reverse genetics, non-replicating viral vectors, alpha virus vectors, and genetic vaccines.
  • More efficient vaccine delivery methods and the use of better adjuvants—substances that enhance the body’s immune response to an antigen—are also considered. These cutting-edge approaches may shape the future direction of veterinary vaccine development and help address the current challenges in the field.

Cite This Article

APA
Patel JR, Heldens JG. (2009). Immunoprophylaxis against important virus disease of horses, farm animals and birds. Vaccine, 27(12), 1797-1810. https://doi.org/10.1016/j.vaccine.2008.12.063

Publication

ISSN: 0264-410X
NlmUniqueID: 8406899
Country: Netherlands
Language: English
Volume: 27
Issue: 12
Pages: 1797-1810

Researcher Affiliations

Patel, J R
  • JAS Biologicals Limited, The Centre for Veterinary Science, Madingley Road, Cambridge, CB3 0ES, UK. jasltd@aol.com
Heldens, J G M

    MeSH Terms

    • Animal Diseases / immunology
    • Animal Diseases / prevention & control
    • Animals
    • Animals, Domestic / immunology
    • Bird Diseases / immunology
    • Bird Diseases / prevention & control
    • Horse Diseases / immunology
    • Horse Diseases / prevention & control
    • Horses
    • Sheep
    • Sheep Diseases / immunology
    • Sheep Diseases / prevention & control
    • Swine
    • Swine Diseases / immunology
    • Swine Diseases / prevention & control
    • Virus Diseases / immunology
    • Virus Diseases / prevention & control

    References

    This article includes 144 references
    1. Reidel S. Edward Jenner and the history of smallpox and vaccination.. Baylor University Medical Centre Proceedings 2005;18:21–5.
    2. Heldens JG, Patel JR, Chanter N, Ten Thij GJ, Gravendijck M, Schijns VE, Langen A, Schetters TP. Veterinary vaccine development from an industrial perspective.. Vet J 2008 Oct;178(1):7-20.
      pmc: PMC7110856pubmed: 18313956doi: 10.1016/j.tvjl.2007.11.009google scholar: lookup
    3. Anonymous Office international des epizooties. Animal Health Code. 1997:1997.
    4. Westergaard J.M. Control strategies of major viral infectious diseases of live stock in Europe, ten years of experience.. Proceedings of the 5th international congress of the European society for veterinary virology 2000. pp. 3–12.
    5. Kitching P, Hammond J, Jeggo M, Charleston B, Paton D, Rodriguez L, Heckert R. Global FMD control--is it an option?. Vaccine 2007 Jul 26;25(30):5660-4.
      pubmed: 17126959doi: 10.1016/j.vaccine.2006.10.052google scholar: lookup
    6. Patel JR, Heldens J. Equine herpesviruses 1 (EHV-1) and 4 (EHV-4)--epidemiology, disease and immunoprophylaxis: a brief review.. Vet J 2005 Jul;170(1):14-23.
      pubmed: 15993786doi: 10.1016/j.tvjl.2004.04.018google scholar: lookup
    7. Heldens JG, Hannant D, Cullinane AA, Prendergast MJ, Mumford JA, Nelly M, Kydd JH, Weststrate MW, van den Hoven R. Clinical and virological evaluation of the efficacy of an inactivated EHV1 and EHV4 whole virus vaccine (Duvaxyn EHV1,4). Vaccination/challenge experiments in foals and pregnant mares.. Vaccine 2001 Jul 20;19(30):4307-17.
      pubmed: 11457558doi: 10.1016/s0264-410x(01)00131-1google scholar: lookup
    8. Patel JR, Bateman H, Williams J, Didlick S. Derivation and characterisation of a live equid herpes virus-1 (EHV-1) vaccine to protect against abortion and respiratory disease due to EHV-1.. Vet Microbiol 2003 Jan 2;91(1):23-39.
      pubmed: 12441229doi: 10.1016/s0378-1135(02)00259-6google scholar: lookup
    9. Patel JR, Földi J, Bateman H, Williams J, Didlick S, Stark R. Equid herpesvirus (EHV-1) live vaccine strain C147: efficacy against respiratory diseases following EHV types 1 and 4 challenges.. Vet Microbiol 2003 Mar 20;92(1-2):1-17.
      pubmed: 12488066doi: 10.1016/s0378-1135(02)00358-9google scholar: lookup
    10. Patel JR, Didlick S, Bateman H. Efficacy of a live equine herpesvirus-1 (EHV-1) strain C147 vaccine in foals with maternally-derived antibody: protection against EHV-1 infection.. Equine Vet J 2004 Jul;36(5):447-51.
      pubmed: 15253088doi: 10.2746/0425164044868332google scholar: lookup
    11. Baker DJ. Rationale for the use of influenza vaccines in horses and the importance of antigenic drift.. Equine Vet J 1986 Mar;18(2):93-6.
    12. Wilson WD. Equine influenza.. Vet Clin North Am Equine Pract 1993 Aug;9(2):257-82.
      pubmed: 8358645doi: 10.1016/s0749-0739(17)30395-4google scholar: lookup
    13. Paillot R, Hannant D, Kydd JH, Daly JM. Vaccination against equine influenza: quid novi?. Vaccine 2006 May 8;24(19):4047-61.
      pubmed: 16545507doi: 10.1016/j.vaccine.2006.02.030google scholar: lookup
    14. Mumford JA, Jessett DM, Rollinson EA, Hannant D, Draper ME. Duration of protective efficacy of equine influenza immunostimulating complex/tetanus vaccines.. Vet Rec 1994 Feb 12;134(7):158-62.
      pubmed: 8160328doi: 10.1136/vr.134.7.158google scholar: lookup
    15. Heldens JG, Kersten AJ, Weststrate MW, van den Hoven R. Duration of immunity induced by an adjuvanted and inactivated equine influenza, tetanus and equine herpesvirus 1 and 4 combination vaccine.. Vet Q 2001 Nov;23(4):210-7.
      pubmed: 11765243doi: 10.1080/01652176.2001.9695116google scholar: lookup
    16. Heldens JG, Pouwels HG, van Loon AA. Efficacy and duration of immunity of a combined equine influenza and equine herpesvirus vaccine against challenge with an American-like equine influenza virus (A/equi-2/Kentucky/95).. Vet J 2004 Mar;167(2):150-7.
      pubmed: 14975389doi: 10.1016/s1090-0233(03)00028-5google scholar: lookup
    17. Cullinane A, Weld J, Osborne M, Nelly M, Mcbride C, Walsh C. Field studies on equine influenza vaccination regimes in thoroughbred foals and yearlings.. Vet J 2001 Mar;161(2):174-85.
      pubmed: 11243687doi: 10.1053/tvjl.2000.0546google scholar: lookup
    18. Youngner JS, Whitaker-Dowling P, Chambers TM, Rushlow KE, Sebring R. Derivation and characterization of a live attenuated equine influenza vaccine virus.. Am J Vet Res 2001 Aug;62(8):1290-4.
      pubmed: 11497453doi: 10.2460/ajvr.2001.62.1290google scholar: lookup
    19. Drane D, Pearse M.J. The ISCOM matrix adjuvant.. Immune potentiators in modern vaccines 2006. pp. 191–216.
    20. Wood JL, Mumford JA, Mair TS, Slater J. Boosting in equine influenza vaccination schedules: timing and time for a re-evaluation of requirements of national and international authorities.. Vet J 2007 Nov;174(3):449-50.
      pubmed: 17702620doi: 10.1016/j.tvjl.2007.06.012google scholar: lookup
    21. Monath TP. Prospects for development of a vaccine against the West Nile virus.. Ann N Y Acad Sci 2001 Dec;951:1-12.
    22. Wetzel H, Nevill EM, Erasmus BJ. Studies on the transmission of African horsesickness.. Onderstepoort J Vet Res 1970 Sep;37(3):165-8.
      pubmed: 5526278
    23. Rodriguez M, Hooghuis H, Castaño M. African horse sickness in Spain.. Vet Microbiol 1992 Nov;33(1-4):129-42.
      pubmed: 1481352doi: 10.1016/0378-1135(92)90041-qgoogle scholar: lookup
    24. Ranz AI, Miguet JG, Anaya C, Venteo A, Cortés E, Vela C, Sanz A. Diagnostic methods for African horsesickness virus using monoclonal antibodies to structural and non-structural proteins.. Vet Microbiol 1992 Nov;33(1-4):143-53.
      pubmed: 1481354doi: 10.1016/0378-1135(92)90042-rgoogle scholar: lookup
    25. Craigo JK, Li F, Steckbeck JD, Durkin S, Howe L, Cook SJ, Issel C, Montelaro RC. Discerning an effective balance between equine infectious anemia virus attenuation and vaccine efficacy.. J Virol 2005 Mar;79(5):2666-77.
    26. Patel JR. Evaluation of a quadrivalent inactivated vaccine for the protection of cattle against diseases due to common viral infections.. J S Afr Vet Assoc 2004 Sep;75(3):137-46.
      pubmed: 15628806doi: 10.4102/jsava.v75i3.469google scholar: lookup
    27. Peters AR, Thevasagayam SJ, Wiseman A, Salt JS. Duration of immunity of a quadrivalent vaccine against respiratory diseases caused by BHV-1, PI3V, BVDV, and BRSV in experimentally infected calves.. Prev Vet Med 2004 Dec 15;66(1-4):63-77.
    28. Salt JS, Thevasagayam SJ, Wiseman A, Peters AR. Efficacy of a quadrivalent vaccine against respiratory diseases caused by BHV-1, PI3V, BVDV and BRSV in experimentally infected calves.. Vet J 2007 Nov;174(3):616-26.
      pubmed: 17276108doi: 10.1016/j.tvjl.2006.10.007google scholar: lookup
    29. Bowland SL, Shewen PE. Bovine respiratory disease: commercial vaccines currently available in Canada.. Can Vet J 2000 Jan;41(1):33-48.
      pmc: PMC1476343pubmed: 10642871
    30. Straub O.C. Advantages and disadvantages of common vaccination programmes.. Recent developments and perspectives in bovine medicine: keynote lectures of the XXII World Buiatrics Congress 2002. pp. 86–96.
    31. Patel JR. Characteristics of live bovine herpesvirus-1 vaccines.. Vet J 2005 May;169(3):404-16.
      pubmed: 15848783doi: 10.1016/j.tvjl.2004.03.005google scholar: lookup
    32. Alvarez M, Bielsa JM, Santos L, Makoschey B. Compatibility of a live infectious bovine rhinotraheitis (IBR) marker vaccine and an inactivated bovine viral diarrhoea virus (BVDV) vaccine.. Vaccine 2007 Sep 4;25(36):6613-7.
      pubmed: 17669560doi: 10.1016/j.vaccine.2007.06.050google scholar: lookup
    33. Brownlie J. Bovine virus diarrhoea: pathogenesis and control.. Recent developments and perspectives in bovine medicine: keynote lectures of the XXII World Buiatrics Congress 2002. pp. 24–32.
    34. Brownlie J, Clarke MC, Hooper LB, Bell GD. Protection of the bovine fetus from bovine viral diarrhoea virus by means of a new inactivated vaccine.. Vet Rec 1995 Jul 15;137(3):58-62.
      pubmed: 8533232doi: 10.1136/vr.137.3.58google scholar: lookup
    35. Patel JR, Shilleto RW, Williams J, Alexander DC. Prevention of transplacental infection of bovine foetus by bovine viral diarrhoea virus through vaccination.. Arch Virol 2002 Dec;147(12):2453-63.
      pubmed: 12491111doi: 10.1007/s00705-002-0878-3google scholar: lookup
    36. Salt J.S, Anthonis A.F.G, Peters A.R, Brune A, Jahnecke S, Traeder W. Breite kreuzneutralisation von europäische BVDV Typ-1 und Typ-2 Stämmen und signifikante Verbesserung der Fertilität nach Testinfektionen.. Tierärzlicher Praxis 2004;32:191–195.
    37. Patel JR, Didlick SA. Evaluation of efficacy of an inactivated vaccine against bovine respiratory syncytial virus in calves with maternal antibodies.. Am J Vet Res 2004 Apr;65(4):417-21.
      pubmed: 15077682doi: 10.2460/ajvr.2004.65.417google scholar: lookup
    38. Warzecha H, Mason HS. Benefits and risks of antibody and vaccine production in transgenic plants.. J Plant Physiol 2003 Jul;160(7):755-64.
      pubmed: 12940544doi: 10.1078/0176-1617-01125google scholar: lookup
    39. Rosas CT, König P, Beer M, Dubovi EJ, Tischer BK, Osterrieder N. Evaluation of the vaccine potential of an equine herpesvirus type 1 vector expressing bovine viral diarrhea virus structural proteins.. J Gen Virol 2007 Mar;88(Pt 3):748-757.
      pubmed: 17325347doi: 10.1099/vir.0.82528-0google scholar: lookup
    40. Schmitt J, Becher P, Thiel HJ, Keil GM. Expression of bovine viral diarrhoea virus glycoprotein E2 by bovine herpesvirus-1 from a synthetic ORF and incorporation of E2 into recombinant virions.. J Gen Virol 1999 Nov;80 ( Pt 11):2839-2848.
      pubmed: 10580045doi: 10.1099/0022-1317-80-11-2839google scholar: lookup
    41. Saif L.J, Jackwood D.J. Enteric virus vaccines.. Viral diarrhoeas of man and animals 1990. pp. 313–329.
    42. Grubman MJ, Mason PW. Prospects, including time-frames, for improved foot and mouth disease vaccines.. Rev Sci Tech 2002 Dec;21(3):589-600.
      pubmed: 12523699doi: 10.20506/rst.21.3.1360google scholar: lookup
    43. Grubman MJ, Baxt B. Foot-and-mouth disease.. Clin Microbiol Rev 2004 Apr;17(2):465-93.
    44. Wu Q, Moraes MP, Grubman MJ. Recombinant adenovirus co-expressing capsid proteins of two serotypes of foot-and-mouth disease virus (FMDV): in vitro characterization and induction of neutralizing antibodies against FMDV in swine.. Virus Res 2003 Jun;93(2):211-9.
      pubmed: 12782369doi: 10.1016/s0168-1702(03)00116-3google scholar: lookup
    45. Mayr GA, O'Donnell V, Chinsangaram J, Mason PW, Grubman MJ. Immune responses and protection against foot-and-mouth disease virus (FMDV) challenge in swine vaccinated with adenovirus-FMDV constructs.. Vaccine 2001 Feb 28;19(15-16):2152-62.
      pubmed: 11228388doi: 10.1016/s0264-410x(00)00384-4google scholar: lookup
    46. Plowright W. The duration of immunity in cattle following inoculation of rinderpest cell culture vaccine.. J Hyg (Lond) 1984 Jun;92(3):285-96.
      pmc: PMC2129311pubmed: 6736639doi: 10.1017/s0022172400064524google scholar: lookup
    47. Kitching RP, Hammond JM, Taylor WP. A single vaccine for the control of capripox infection in sheep and goats.. Res Vet Sci 1987 Jan;42(1):53-60.
      pubmed: 3029848
    48. Berhe G, Minet C, Le Goff C, Barrett T, Ngangnou A, Grillet C, Libeau G, Fleming M, Black DN, Diallo A. Development of a dual recombinant vaccine to protect small ruminants against peste-des-petits-ruminants virus and capripoxvirus infections.. J Virol 2003 Jan;77(2):1571-7.
    49. Aspden K, Passmore JA, Tiedt F, Williamson AL. Evaluation of lumpy skin disease virus, a capripoxvirus, as a replication-deficient vaccine vector.. J Gen Virol 2003 Aug;84(Pt 8):1985-1996.
      pubmed: 12867628doi: 10.1099/vir.0.19116-0google scholar: lookup
    50. Kihm U, Flamand A, Pastoret PP, Peterhans E. Round table on epidemiology and control of fox rabies.. Vet Microbiol 1992 Nov;33(1-4):297-301.
      pubmed: 1481362doi: 10.1016/0378-1135(92)90057-zgoogle scholar: lookup
    51. Pastoret PP, Brochier B. The development and use of a vaccinia-rabies recombinant oral vaccine for the control of wildlife rabies; a link between Jenner and Pasteur.. Epidemiol Infect 1996 Jun;116(3):235-40.
      pmc: PMC2271442pubmed: 8666066doi: 10.1017/s0950268800052535google scholar: lookup
    52. Wittmann G, Rziha H.J. Aujeszky's disease (pseudo rabies) in pigs.. Herpesvirus disease of cattle, horses and pigs 1989. pp. 230–325.
    53. Mettenleiter TC. Molecular biology of pseudorabies (Aujeszky's disease) virus.. Comp Immunol Microbiol Infect Dis 1991;14(2):151-63.
      pubmed: 1657509doi: 10.1016/0147-9571(91)90128-zgoogle scholar: lookup
    54. Kimman TG, Pol JM, de Wind N, Oei-Lie N, Berns AJ, Gielkens AL. Role of different genes in the virulence and pathogenesis of Aujeszky's disease virus.. Vet Microbiol 1992 Nov;33(1-4):45-52.
      pubmed: 1336250doi: 10.1016/0378-1135(92)90034-qgoogle scholar: lookup
    55. Kit S, Sheppard M, Ichimura H, Kit M. Second-generation pseudorabies virus vaccine with deletions in thymidine kinase and glycoprotein genes.. Am J Vet Res 1987 May;48(5):780-93.
      pubmed: 3035972
    56. Marchioli CC, Yancey RJ Jr, Wardley RC, Thomsen DR, Post LE. A vaccine strain of pseudorabies virus with deletions in the thymidine kinase and glycoprotein X genes.. Am J Vet Res 1987 Nov;48(11):1577-83.
      pubmed: 2829665
    57. Quint W, Gielkens A, Van Oirschot J, Berns A, Cuypers HT. Construction and characterization of deletion mutants of pseudorabies virus: a new generation of 'live' vaccines.. J Gen Virol 1987 Feb;68 ( Pt 2):523-34.
      pubmed: 3029289doi: 10.1099/0022-1317-68-2-523google scholar: lookup
    58. Pensaert M, Gielkens AL, Lomniczi B, Kimman TG, Vannier P, Eloit M. Round table on control of Aujeszky's disease and vaccine development based on molecular biology.. Vet Microbiol 1992 Nov;33(1-4):53-67.
      pubmed: 1336251doi: 10.1016/0378-1135(92)90035-rgoogle scholar: lookup
    59. Van Oirschot J.T. Present and future of veterinary viral vaccinology.. Proceedings of the 5th international congress of the European society for veterinary virology 2000. pp. 18–27.
    60. Kuiper A.F.C, Dazelle C.J, Zantinga J.W. Oil adjuvanted modified live vaccine against Aujeszky's disease, based on the Bartha strain.. Proceedings of 8th international pig veterinary society congress 1984. p. 33.
    61. Pensaert MB, De Smet K, De Waele K. Extent and duration of virulent virus excretion upon challenge of pigs vaccinated with different glycoprotein-deleted Aujeszky's disease vaccines.. Vet Microbiol 1990 Apr;22(2-3):107-17.
      pubmed: 2162094doi: 10.1016/0378-1135(90)90098-ggoogle scholar: lookup
    62. Chenut G, Saintilan AF, Burger C, Rosenthal F, Crucière C, Picard M, Bruyère V, Albina E. Oral immunisation of swine with a classical swine fever vaccine (Chinese strain) and transmission studies in rabbits and sheep.. Vet Microbiol 1999 Feb 12;64(4):265-76.
      pubmed: 10063532doi: 10.1016/s0378-1135(98)00256-9google scholar: lookup
    63. Kaden V, Lange E. Vaccination as strategy of CSF control in wild boar.. Proceedings of the 5th international congress of the European society for veterinary virology 2000. pp. 110–114.
    64. Lin TC, Lee RCT. An overall report on the development of a highly safe and potent lapinized hog cholera virus strain for hog cholera control in Taiwan.. NSC special publication no. 5 1981.
    65. De Smit A.J, Van De Wetering G, Colijn E.C, Hulst M, Kramps J.A, Van Den Blink A. The detection of antibodies against the ERNS envelope protein of classical swine fever virus.. Proceedings of the 5th international congress of the European society for veterinary virology 2000. pp. 414–415.
    66. Ahrens U, Kaden V, Drexler C, Visser N. Efficacy of the classical swine fever (CSF) marker vaccine Porcilis Pesti in pregnant sows.. Vet Microbiol 2000 Nov 15;77(1-2):83-97.
      pubmed: 11042402doi: 10.1016/s0378-1135(00)00265-0google scholar: lookup
    67. Bouma A, de Smit AJ, de Kluijver EP, Terpstra C, Moormann RJ. Efficacy and stability of a subunit vaccine based on glycoprotein E2 of classical swine fever virus.. Vet Microbiol 1999 Apr 1;66(2):101-14.
      pubmed: 10227472doi: 10.1016/s0378-1135(99)00003-6google scholar: lookup
    68. van Gennip HG, van Rijn PA, Widjojoatmodjo MN, de Smit AJ, Moormann RJ. Chimeric classical swine fever viruses containing envelope protein E(RNS) or E2 of bovine viral diarrhoea virus protect pigs against challenge with CSFV and induce a distinguishable antibody response.. Vaccine 2000 Oct 15;19(4-5):447-59.
      pubmed: 11027808doi: 10.1016/s0264-410x(00)00198-5google scholar: lookup
    69. van Zijl M, Wensvoort G, de Kluyver E, Hulst M, van der Gulden H, Gielkens A, Berns A, Moormann R. Live attenuated pseudorabies virus expressing envelope glycoprotein E1 of hog cholera virus protects swine against both pseudorabies and hog cholera.. J Virol 1991 May;65(5):2761-5.
    70. Hill H. Overview and history of mystery swine disease (swine infertility respiratory syndrome).. Proceedings of the mystery swine disease committee meeting Denver Colorado, 6 October, 1990; 1990.
    71. Terpstra C, Wensvoort G, Pol JM. Experimental reproduction of porcine epidemic abortion and respiratory syndrome (mystery swine disease) by infection with Lelystad virus: Koch's postulates fulfilled.. Vet Q 1991 Jul;13(3):131-6.
      pubmed: 1949539doi: 10.1080/01652176.1991.9694297google scholar: lookup
    72. Zuckermann FA, Garcia EA, Luque ID, Christopher-Hennings J, Doster A, Brito M, Osorio F. Assessment of the efficacy of commercial porcine reproductive and respiratory syndrome virus (PRRSV) vaccines based on measurement of serologic response, frequency of gamma-IFN-producing cells and virological parameters of protection upon challenge.. Vet Microbiol 2007 Jul 20;123(1-3):69-85.
      pubmed: 17376612doi: 10.1016/j.vetmic.2007.02.009google scholar: lookup
    73. Coggins L. African swine fever virus. Pathogenesis.. Prog Med Virol 1974;18(0):48-63.
      pubmed: 4418259
    74. Mettraux C, Ackermann M, Tratschin JD, Kihm U. Approaches to the identification of non-essential genes of African swine fever virus.. Vet Microbiol 1992 Nov;33(1-4):101-15.
      pubmed: 1481351doi: 10.1016/0378-1135(92)90039-vgoogle scholar: lookup
    75. Kihm U, Ackerman M, Műller H.K, Pool R. Approaches to vaccination.. Developments in veterinary virology, African swine fever 1987. pp. 127–144.
    76. Van Reeth K, Van Gucht S, Pensaert M. Investigations of the efficacy of European H1N1- and H3N2-based swine influenza vaccines against the novel H1N2 subtype.. Vet Rec 2003 Jul 5;153(1):9-13.
      pubmed: 12877210doi: 10.1136/vr.153.1.9google scholar: lookup
    77. Loeffen WL, Kamp EM, Stockhofe-Zurwieden N, van Nieuwstadt AP, Bongers JH, Hunneman WA, Elbers AR, Baars J, Nell T, van Zijderveld FG. Survey of infectious agents involved in acute respiratory disease in finishing pigs.. Vet Rec 1999 Jul 31;145(5):123-9.
      pubmed: 10466829doi: 10.1136/vr.145.5.123google scholar: lookup
    78. Wesley RD, Tang M, Lager KM. Protection of weaned pigs by vaccination with human adenovirus 5 recombinant viruses expressing the hemagglutinin and the nucleoprotein of H3N2 swine influenza virus.. Vaccine 2004 Sep 3;22(25-26):3427-34.
      pubmed: 15308368doi: 10.1016/j.vaccine.2004.02.040google scholar: lookup
    79. Allan GM, Ellis JA. Porcine circoviruses: a review.. J Vet Diagn Invest 2000 Jan;12(1):3-14.
      pubmed: 10690769doi: 10.1177/104063870001200102google scholar: lookup
    80. Krakowka S, Ellis JA, McNeilly F, Gilpin D, Meehan B, McCullough K, Allan G. Immunologic features of porcine circovirus type 2 infection.. Viral Immunol 2002;15(4):567-82.
      pubmed: 12513928doi: 10.1089/088282402320914511google scholar: lookup
    81. Fenaux M, Opriessnig T, Halbur PG, Elvinger F, Meng XJ. A chimeric porcine circovirus (PCV) with the immunogenic capsid gene of the pathogenic PCV type 2 (PCV2) cloned into the genomic backbone of the nonpathogenic PCV1 induces protective immunity against PCV2 infection in pigs.. J Virol 2004 Jun;78(12):6297-303.
    82. Fan H, Ju C, Tong T, Huang H, Lv J, Chen H. Immunogenicity of empty capsids of porcine circovius type 2 produced in insect cells.. Vet Res Commun 2007 May;31(4):487-96.
      pubmed: 17225085doi: 10.1007/s11259-007-3469-7google scholar: lookup
    83. Ju C, Fan H, Tan Y, Liu Z, Xi X, Cao S, Wu B, Chen H. Immunogenicity of a recombinant pseudorabies virus expressing ORF1-ORF2 fusion protein of porcine circovirus type 2.. Vet Microbiol 2005 Aug 30;109(3-4):179-90.
      pubmed: 16006077doi: 10.1016/j.vetmic.2005.06.001google scholar: lookup
    84. Wang X, Jiang W, Jiang P, Li Y, Feng Z, Xu J. Construction and immunogenicity of recombinant adenovirus expressing the capsid protein of porcine circovirus 2 (PCV2) in mice.. Vaccine 2006 Apr 12;24(16):3374-80.
      pubmed: 16524646doi: 10.1016/j.vaccine.2005.12.068google scholar: lookup
    85. Wang X, Jiang P, Li Y, Jiang W, Dong X. Protection of pigs against post-weaning multisystemic wasting syndrome by a recombinant adenovirus expressing the capsid protein of porcine circovirus type 2.. Vet Microbiol 2007 Apr 15;121(3-4):215-24.
      pubmed: 17215092doi: 10.1016/j.vetmic.2006.11.027google scholar: lookup
    86. Opriessnig T, McKeown NE, Harmon KL, Meng XJ, Halbur PG. Porcine circovirus type 2 infection decreases the efficacy of a modified live porcine reproductive and respiratory syndrome virus vaccine.. Clin Vaccine Immunol 2006 Aug;13(8):923-9.
      pmc: PMC1539115pubmed: 16893993doi: 10.1128/cvi.00074-06google scholar: lookup
    87. Opriessnig T, Ramamoorthy S, Madson DM, Patterson AR, Pal N, Carman S, Meng XJ, Halbur PG. Differences in virulence among porcine circovirus type 2 isolates are unrelated to cluster type 2a or 2b and prior infection provides heterologous protection.. J Gen Virol 2008 Oct;89(Pt 10):2482-2491.
      pubmed: 18796717doi: 10.1099/vir.0.2008/001081-0google scholar: lookup
    88. Gardner IA, Carpenter TE, Leontides L, Parsons TD. Financial evaluation of vaccination and testing alternatives for control of parvovirus-induced reproductive failure in swine.. J Am Vet Med Assoc 1996 Mar 15;208(6):863-9.
      pubmed: 8617643
    89. Elliott H. Blue tongue disease: background to the outbreak in N W Europe.. The Goat Veterinary Society 2007;23:31–39.
    90. Meiswinkel R, van Rijn P, Leijs P, Goffredo M. Potential new Culicoides vector of bluetongue virus in northern Europe.. Vet Rec 2007 Oct 20;161(16):564-5.
      pubmed: 17951565doi: 10.1136/vr.161.16.564google scholar: lookup
    91. Erasmus B.J. In: Virus infections of ruminants. Dinter Z., Morein B., editors. Elsevier Science Publications; 1990. pp. 227–232.
    92. Menzies FD, McCullough SJ, McKeown IM, Forster JL, Jess S, Batten C, Murchie AK, Gloster J, Fallows JG, Pelgrim W, Mellor PS, Oura CA. Evidence for transplacental and contact transmission of bluetongue virus in cattle.. Vet Rec 2008 Aug 16;163(7):203-9.
      pubmed: 18708653doi: 10.1136/vr.163.7.203google scholar: lookup
    93. Roy P. From genes to complex structures of bluetongue virus and their efficacy as vaccines.. Vet Microbiol 1992 Nov;33(1-4):155-68.
      pubmed: 1336237doi: 10.1016/0378-1135(92)90043-sgoogle scholar: lookup
    94. Ngichabe CK, Wamwayi HM, Ndungu EK, Mirangi PK, Bostock CJ, Black DN, Barrett T. Long term immunity in African cattle vaccinated with a recombinant capripox-rinderpest virus vaccine.. Epidemiol Infect 2002 Apr;128(2):343-9.
      pmc: PMC2869829pubmed: 12002554doi: 10.1017/s0950268801006513google scholar: lookup
    95. Reid H.W. Epidemiology of louping-ill.. Tick vectors in virus biology 1984. pp. 161–178.
    96. Shaw B, Reid HW. Immune responses of sheep to louping-ill virus vaccine.. Vet Rec 1981 Dec 12;109(24):529-31.
      pubmed: 6280367
    97. Dory D, Fischer T, Béven V, Cariolet R, Rziha HJ, Jestin A. Prime-boost immunization using DNA vaccine and recombinant Orf virus protects pigs against Pseudorabies virus (Herpes suid 1).. Vaccine 2006 Sep 11;24(37-39):6256-63.
      pubmed: 16814432doi: 10.1016/j.vaccine.2006.05.078google scholar: lookup
    98. Capua I, Alexander DJ. The challenge of avian influenza to the veterinary community.. Avian Pathol 2006 Jun;35(3):189-205.
      pubmed: 16753610doi: 10.1080/03079450600717174google scholar: lookup
    99. Webster R.G, Campitelli L, Krauss S, Shortridge K, Fioretti A, Guan Y. Are chickens playing an increasing role in the ecology of influenza viruses?. Proceedings of the 5th international congress of the European society for veterinary virology 2000. pp. 34–37.
    100. Kilbourne ED. Future influenza vaccines and the use of genetic recombinants.. Bull World Health Organ 1969;41(3):643-5.
      pmc: PMC2427719pubmed: 5309489
    101. Wood JS, Robertson JS. Reference viruses for seasonal and pandemic influenza vaccine preparation.. Influenza Other Respir Viruses 2007 Jan;1(1):5-9.
    102. Swayne DE, Lee CW, Spackman E. Inactivated North American and European H5N2 avian influenza virus vaccines protect chickens from Asian H5N1 high pathogenicity avian influenza virus.. Avian Pathol 2006 Apr;35(2):141-6.
      pubmed: 16595307doi: 10.1080/03079450600597956google scholar: lookup
    103. Webster RG, Taylor J, Pearson J, Rivera E, Paoletti E. Immunity to Mexican H5N2 avian influenza viruses induced by a fowl pox-H5 recombinant.. Avian Dis 1996 Apr-Jun;40(2):461-5.
      pubmed: 8790900
    104. Veits J, Wiesner D, Fuchs W, Hoffmann B, Granzow H, Starick E, Mundt E, Schirrmeier H, Mebatsion T, Mettenleiter TC, Römer-Oberdörfer A. Newcastle disease virus expressing H5 hemagglutinin gene protects chickens against Newcastle disease and avian influenza.. Proc Natl Acad Sci U S A 2006 May 23;103(21):8197-202.
      pmc: PMC1472452pubmed: 16717197doi: 10.1073/pnas.0602461103google scholar: lookup
    105. Swayne DE, Suarez DL, Schultz-Cherry S, Tumpey TM, King DJ, Nakaya T, Palese P, Garcia-Sastre A. Recombinant paramyxovirus type 1-avian influenza-H7 virus as a vaccine for protection of chickens against influenza and Newcastle disease.. Avian Dis 2003;47(3 Suppl):1047-50.
      pubmed: 14575108doi: 10.1637/0005-2086-47.s3.1047google scholar: lookup
    106. Bennett RS, LaRue R, Shaw D, Yu Q, Nagaraja KV, Halvorson DA, Njenga MK. A wild goose metapneumovirus containing a large attachment glycoprotein is avirulent but immunoprotective in domestic turkeys.. J Virol 2005 Dec;79(23):14834-42.
    107. Kapczynski DR, Sellers HS. Immunization of turkeys with a DNA vaccine expressing either the F or N gene of avian metapneumovirus.. Avian Dis 2003 Oct-Dec;47(4):1376-83.
      pubmed: 14708985doi: 10.1637/7033google scholar: lookup
    108. Calnek BW, Adldinger HK, Kahn DE. Feather follicle epithelium: a source of enveloped and infectious cell-free herpesvirus from Marek's disease.. Avian Dis 1970 May;14(2):219-33.
      pubmed: 4316765
    109. Baigent SJ, Smith LP, Currie RJW, Nair VK. Replication kinetics of Marek's disease vaccine virus in feathers and lymphoid tissues using PCR and virus isolation.. J Gen Virol 2005 Nov;86(Pt 11):2989-2998.
      pubmed: 16227220doi: 10.1099/vir.0.81299-0google scholar: lookup
    110. Rispens BH, van Vloten H, Mastenbroek N, Maas HJ, Schat KA. Control of Marek's disease in the Netherlands. I. Isolation of an avirulent Marek's disease virus (strain CVI 988) and its use in laboratory vaccination trials.. Avian Dis 1972 Apr;16(1):108-25.
      pubmed: 4337307
    111. de Boer GF, Groenendal JE, Boerrigter HM, Kok GL, Pol JM. Protective efficacy of Marek's disease virus (MDV) CVI-988 CEF65 clone C against challenge infection with three very virulent MDV strains.. Avian Dis 1986 Apr-Jun;30(2):276-83.
      pubmed: 3015113
    112. Witter RL. Induction of strong protection by vaccination with partially attenuated serotype 1 Marek's disease viruses.. Avian Dis 2002 Oct-Dec;46(4):925-37.
    113. Venugopal K. Marek's disease: an update on oncogenic mechanisms and control.. Res Vet Sci 2000 Aug;69(1):17-23.
      pubmed: 10924389doi: 10.1053/rvsc.2000.0396google scholar: lookup
    114. Witter RL, Calnek BW, Buscaglia C, Gimeno IM, Schat KA. Classification of Marek's disease viruses according to pathotype: philosophy and methodology.. Avian Pathol 2005 Apr;34(2):75-90.
      pubmed: 16191686doi: 10.1080/03079450500059255google scholar: lookup
    115. Johnson M, Jansen E, Morrissy C, Williamson M, Ignjatovic J, Pooley C. Porcine and fowl adenoviruses as cytokine delivery vectors.. Proceedings of the 5th international congress of the European society for veterinary virology 2000. pp. 119–120.
    116. Müller H, Schnitzler D, Bernstein F, Becht H, Cornelissen D, Lütticken DH. Infectious bursal disease of poultry: antigenic structure of the virus and control.. Vet Microbiol 1992 Nov;33(1-4):175-83.
      pubmed: 1336239doi: 10.1016/0378-1135(92)90045-ugoogle scholar: lookup
    117. Li S, Wang Y, Chou C.C. Field evaluation of flock production performance of in ovo injection of infectious bursal disease virus immune complex vaccine in commercial broiler farms.. Journal of Applied Poultry Research 2005;14:338–344.
    118. McNulty MS. Chicken anaemia agent: a review.. Avian Pathol 1991 Jun;20(2):187-203.
      pubmed: 18680014doi: 10.1080/03079459108418756google scholar: lookup
    119. Adair BM. Immunopathogenesis of chicken anemia virus infection.. Dev Comp Immunol 2000 Mar-Apr;24(2-3):247-55.
      pubmed: 10717291doi: 10.1016/s0145-305x(99)00076-2google scholar: lookup
    120. Fries LF, Tartaglia J, Taylor J, Kauffman EK, Meignier B, Paoletti E, Plotkin S. Human safety and immunogenicity of a canarypox-rabies glycoprotein recombinant vaccine: an alternative poxvirus vector system.. Vaccine 1996 Apr;14(5):428-34.
      pubmed: 8735555doi: 10.1016/0264-410x(95)00171-vgoogle scholar: lookup
    121. Limbach KJ, Paoletti E. Non-replicating expression vectors: applications in vaccine development and gene therapy.. Epidemiol Infect 1996 Jun;116(3):241-56.
      pmc: PMC2271436pubmed: 8666067doi: 10.1017/s0950268800052547google scholar: lookup
    122. Stephensen CB, Welter J, Thaker SR, Taylor J, Tartaglia J, Paoletti E. Canine distemper virus (CDV) infection of ferrets as a model for testing Morbillivirus vaccine strategies: NYVAC- and ALVAC-based CDV recombinants protect against symptomatic infection.. J Virol 1997 Feb;71(2):1506-13.
    123. McMillen JK, Cochran MD, Junker DE, Reddy DN, Valencia DM. The safe and effective use of fowlpox virus as a vector for poultry vaccines.. Dev Biol Stand 1994;82:137-45.
      pubmed: 7958468
    124. Minke JM, Fischer L, Baudu P, Guigal PM, Sindle T, Mumford JA, Audonnet JC. Use of DNA and recombinant canarypox viral (ALVAC) vectors for equine herpes virus vaccination.. Vet Immunol Immunopathol 2006 May 15;111(1-2):47-57.
      pubmed: 16580075doi: 10.1016/j.vetimm.2006.01.008google scholar: lookup
    125. Mayr GA, Chinsangaram J, Grubman MJ. Development of replication-defective adenovirus serotype 5 containing the capsid and 3C protease coding regions of foot-and-mouth disease virus as a vaccine candidate.. Virology 1999 Oct 25;263(2):496-506.
      pubmed: 10544121doi: 10.1006/viro.1999.9940google scholar: lookup
    126. Reddy PS, Idamakanti N, Chen Y, Whale T, Babiuk LA, Mehtali M, Tikoo SK. Replication-defective bovine adenovirus type 3 as an expression vector.. J Virol 1999 Nov;73(11):9137-44.
    127. Ellis RW. New technologies for making vaccines.. Vaccine 1999 Mar 26;17(13-14):1596-604.
      pubmed: 10194811doi: 10.1016/s0264-410x(98)00416-2google scholar: lookup
    128. Veits J, Wiesner D, Fuchs W, Hoffmann B, Granzow H, Starick E, Mundt E, Schirrmeier H, Mebatsion T, Mettenleiter TC, Römer-Oberdörfer A. Newcastle disease virus expressing H5 hemagglutinin gene protects chickens against Newcastle disease and avian influenza.. Proc Natl Acad Sci U S A 2006 May 23;103(21):8197-202.
      pmc: PMC1472452pubmed: 16717197doi: 10.1073/pnas.0602461103google scholar: lookup
    129. Mebatsion T, Koolen MJ, de Vaan LT, de Haas N, Braber M, Römer-Oberdörfer A, van den Elzen P, van der Marel P. Newcastle disease virus (NDV) marker vaccine: an immunodominant epitope on the nucleoprotein gene of NDV can be deleted or replaced by a foreign epitope.. J Virol 2002 Oct;76(20):10138-46.
    130. Moormann RJ, van Gennip HG, Miedema GK, Hulst MM, van Rijn PA. Infectious RNA transcribed from an engineered full-length cDNA template of the genome of a pestivirus.. J Virol 1996 Feb;70(2):763-70.
      pmc: PMC189877pubmed: 8551613doi: 10.1128/jvi.70.2.763-770.1996google scholar: lookup
    131. Barrett AD. Current status of flavivirus vaccines.. Ann N Y Acad Sci 2001 Dec;951:262-71.
    132. Palese P, Zheng H, Engelhardt OG, Pleschka S, García-Sastre A. Negative-strand RNA viruses: genetic engineering and applications.. Proc Natl Acad Sci U S A 1996 Oct 15;93(21):11354-8.
      pmc: PMC38061pubmed: 8876139doi: 10.1073/pnas.93.21.11354google scholar: lookup
    133. Conzelmann KK. Genetic manipulation of non-segmented negative-strand RNA viruses.. J Gen Virol 1996 Mar;77 ( Pt 3):381-9.
      pubmed: 8601771doi: 10.1099/0022-1317-77-3-381google scholar: lookup
    134. Mebatsion T, Schnell MJ, Cox JH, Finke S, Conzelmann KK. Highly stable expression of a foreign gene from rabies virus vectors.. Proc Natl Acad Sci U S A 1996 Jul 9;93(14):7310-4.
      pmc: PMC38980pubmed: 8692989doi: 10.1073/pnas.93.14.7310google scholar: lookup
    135. McKenna PM, McGettigan JP, Pomerantz RJ, Dietzschold B, Schnell MJ. Recombinant rhabdoviruses as potential vaccines for HIV-1 and other diseases.. Curr HIV Res 2003 Apr;1(2):229-37.
      pubmed: 15043205doi: 10.2174/1570162033485320google scholar: lookup
    136. Schlesinger S. Alphaviruses--vectors for the expression of heterologous genes.. Trends Biotechnol 1993 Jan;11(1):18-22.
      pmc: PMC7172487pubmed: 7764041doi: 10.1016/0167-7799(93)90070-pgoogle scholar: lookup
    137. Leitner WW, Ying H, Restifo NP. DNA and RNA-based vaccines: principles, progress and prospects.. Vaccine 1999 Dec 10;18(9-10):765-77.
    138. Johnson P.A, Liu H, O’Connell T, Phelps P, Bland M, Tyczkowski J. Applications in ovo technology.. Poultry Science 1997;76:165–178.
    139. Freytag LC, Clements JD. Bacterial toxins as mucosal adjuvants.. Curr Top Microbiol Immunol 1999;236:215-36.
      pubmed: 9893362doi: 10.1007/978-3-642-59951-4_11google scholar: lookup
    140. Lambert P.H. New vaccines for the world—needs and prospects.. The Immunologist 1993;1:50–55.
    141. Morein B. Iscoms.. Vet Microbiol 1990 Jun;23(1-4):79-84.
      pubmed: 2205974doi: 10.1016/0378-1135(90)90138-lgoogle scholar: lookup
    142. Bowersock TL, Martin S. Vaccine delivery to animals.. Adv Drug Deliv Rev 1999 Jul 26;38(2):167-194.
      pubmed: 10837755doi: 10.1016/s0169-409x(99)00015-0google scholar: lookup
    143. Frenkel H.S. La culture de la virus de la fievre aphteuse sur l’epithelium de la langue des bovides.. Bulletin Office International des Epizooties 1947;28:155–162.
    144. Enders JF, Weller TH, Robbins FC. Cultivation of the Lansing Strain of Poliomyelitis Virus in Cultures of Various Human Embryonic Tissues.. Science 1949 Jan 28;109(2822):85-7.
      pubmed: 17794160doi: 10.1126/science.109.2822.85google scholar: lookup

    Citations

    This article has been cited 5 times.
    1. Bernau M, Schwanitz S, Kreuzer LS, Scholz AM. Detection of Local Tissue Reactions after Anti-GnRF Injection in Male Pigs Assessed Using Magnetic Resonance Imaging. Animals (Basel) 2021 Mar 31;11(4).
      doi: 10.3390/ani11040968pubmed: 33807182google scholar: lookup
    2. Upadhaya SD, Kim YM, Shi H, Le Cour Grandmaison J, Blanchard A, Kim IH. Standardized Plant Extract Alleviates the Negative Effects of FMD Vaccination on Animal Performance. Animals (Basel) 2020 Mar 9;10(3).
      doi: 10.3390/ani10030455pubmed: 32182817google scholar: lookup
    3. Bernau M, Kremer-Rücker PV, Kreuzer LS, Schwanitz S, Cussler K, Hoffmann A, Scholz AM. Magnetic resonance imaging to detect local tissue reactions after vaccination in sheep in vivo. Vet Rec Open 2017;4(1):e000200.
      doi: 10.1136/vetreco-2016-000200pubmed: 29018531google scholar: lookup
    4. Patel JR, Heldens JG, Bakonyi T, Rusvai M. Important mammalian veterinary viral immunodiseases and their control. Vaccine 2012 Feb 27;30(10):1767-81.
      doi: 10.1016/j.vaccine.2012.01.014pubmed: 22261411google scholar: lookup
    5. Patel JR, Heldens JG. Review of companion animal viral diseases and immunoprophylaxis. Vaccine 2009 Jan 22;27(4):491-504.
      doi: 10.1016/j.vaccine.2008.11.027pubmed: 19041354google scholar: lookup