Humoral antibody response of 10 horses after vaccination against African horse sickness with an inactivated vaccine containing all 9 serotypes in one injection.


Journal

Equine veterinary journal
ISSN: 2042-3306
Titre abrégé: Equine Vet J
Pays: United States
ID NLM: 0173320

Informations de publication

Date de publication:
Jul 2021
Historique:
revised: 02 09 2020
received: 20 07 2020
accepted: 20 09 2020
pubmed: 5 10 2020
medline: 22 6 2021
entrez: 4 10 2020
Statut: ppublish

Résumé

African horse sickness (AHS) is a devastating viral disease of equids that was first recorded in 1327. Currently, prevention and control of the disease are based on attenuated vaccines and midge control. It has been shown that attenuated Orbivirus vaccines are not always safe as they may reverse to virulence. In the Emirate of Dubai, a vaccination experiment was carried out with an inactivated AHS vaccine produced at the Central Veterinary Research Laboratory (CVRL), Dubai, UAE to investigate the humoral antibody response of AHS-naïve horses to this vaccine. Our vaccination experiment was performed to establish an AHS vaccine bank in the UAE to protect horses from the disease in case of an outbreak. Therefore, CVRL established an inactivated AHS vaccine containing all nine serotypes which induce high neutralising antibodies. A total of 10 horses kept in a desert isolation area were subcutaneously and intramuscularly vaccinated with an inactivated vaccine containing all nine AHS serotypes previously isolated from Kenyan horse fatalities. Primary immunisation was followed by two booster immunisations 4 weeks and 6 months apart. After 13 months, an annual booster was administered. Blood samples were regularly withdrawn for ELISA and virus neutralisation testing. Additionally, EDTA blood was tested every second day for 14 days post each vaccination for the presence of AHS virus or its RNA. Results show that ELISA and virus neutralising antibodies appeared after the first booster, declined after 4-6 months and therefore three vaccinations and an annual vaccination are necessary to achieve high protective virus neutralising antibodies. No challenge infection was carried out due to the lack of a safe facility in the UAE. Before more advanced AHS vaccines become a reality, inactivated vaccines containing all nine serotypes should be used as they produce high ELISA and neutralising antibodies.

Sections du résumé

BACKGROUND BACKGROUND
African horse sickness (AHS) is a devastating viral disease of equids that was first recorded in 1327. Currently, prevention and control of the disease are based on attenuated vaccines and midge control. It has been shown that attenuated Orbivirus vaccines are not always safe as they may reverse to virulence.
OBJECTIVES OBJECTIVE
In the Emirate of Dubai, a vaccination experiment was carried out with an inactivated AHS vaccine produced at the Central Veterinary Research Laboratory (CVRL), Dubai, UAE to investigate the humoral antibody response of AHS-naïve horses to this vaccine. Our vaccination experiment was performed to establish an AHS vaccine bank in the UAE to protect horses from the disease in case of an outbreak. Therefore, CVRL established an inactivated AHS vaccine containing all nine serotypes which induce high neutralising antibodies.
STUDY DESIGN METHODS
A total of 10 horses kept in a desert isolation area were subcutaneously and intramuscularly vaccinated with an inactivated vaccine containing all nine AHS serotypes previously isolated from Kenyan horse fatalities. Primary immunisation was followed by two booster immunisations 4 weeks and 6 months apart. After 13 months, an annual booster was administered.
METHODS METHODS
Blood samples were regularly withdrawn for ELISA and virus neutralisation testing. Additionally, EDTA blood was tested every second day for 14 days post each vaccination for the presence of AHS virus or its RNA.
RESULTS RESULTS
Results show that ELISA and virus neutralising antibodies appeared after the first booster, declined after 4-6 months and therefore three vaccinations and an annual vaccination are necessary to achieve high protective virus neutralising antibodies.
MAIN LIMITATIONS CONCLUSIONS
No challenge infection was carried out due to the lack of a safe facility in the UAE.
CONCLUSION CONCLUSIONS
Before more advanced AHS vaccines become a reality, inactivated vaccines containing all nine serotypes should be used as they produce high ELISA and neutralising antibodies.

Identifiants

pubmed: 33011979
doi: 10.1111/evj.13363
doi:

Substances chimiques

Antibodies, Neutralizing 0
Antibodies, Viral 0
Vaccines, Inactivated 0
Viral Vaccines 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

826-833

Subventions

Organisme : Central Veterinary Research Laboratory (CVRL)

Informations de copyright

© 2020 EVJ Ltd.

Références

Coetzer J, Guthrie AJ. African horse sickness. In: Coetzer J, Tustin RC, editors. Infectious diseases of livestock. 2nd ed. England: Oxford University. Volume 2; 2004:1231-46.
St Zientara X. African horse sickness. In: Lefèvre P-C, Blancou J, Chermette R, Uilenberg G, editors. Infectious and parasitic diseases of livestock. Volume 1. Lavoisier; 2010; p. 689-704.
Fernández PJ, White WR. African horse sickness. In: Fernández PJ, White WR, editors. Atlas of transboundary animal diseases. OIE, 2010; p. 11-8.
Wernery U, Joseph S, Rodriguez M, Raghavan R, Dyer B, Spendrup S. African horse sickness fever in vaccinated horses. Short communication. J Equine Vet Sci. 2020;88:102967.
Crafford JE, Lourens CW, Smit TK, Gardner IA, MacLachlan NJ, Guthrie AJ. Serological response of foals to polyvalent and monovalent live-attenuated African horse sickness virus vaccines. Vaccine. 2014;32(29):3611-6.
Guthrie AJ, Quan M. African horse sickness. In: Mair TS, Hutchinson RE, editors. Infectious diseases of the horse. Cambridgeshire, UK: A peer-reviewed publication, 2009; p. 72-82.
Aiello SE, Moses MA, Allen DG. Merck veterinary manual. Kenilworth, USA: Merck and Co., Inc., Bluetongue, 2016; p. 738-41.
Salama SA, El Husseini MM, Abdalla SK. 3rd and 4th Ann. Rep. US AHS Project 169, Cairo 1979 and 1980; 55-69: 91-98.
Diouf ND, Etter E, Lo MM, Lo M, Akakpo AJ. Outbreaks of African horse sickness in Senegal and methods of control of the 2007 epidemic. Vet Rec. 2013;172(6):152-9.
OIE. Manual of diagnostic tests and vaccines for terrestrial animals. African horse sickness. 8th ed. OIE, 2018:1237-52.
van Vuuren M, Penzhorn BL. Geographic range of vector-borne infections and their vectors: the role of African wildlife. Rev Sci Tech Off Int Epiz. 2015;34(1):139-49.
OIE WAHIS (World Animal Health Information System). 2019. https://www.oie.int/wahis_2/public/wahid.php/Reviewreport/Review?page_refer=MapFullEventReport&reportid=30236
OIE WAHIS (World Animal Health Information System). 2020. https://www.oie.int/wahis_2/public/wahid.php/Reviewreport/Review?page_refer=MapEventSummary&reportid=33912
Attoui H, Mohd JF. Zoonotic and emerging orbivirus infections. Rev Sci Tech Off Int Epiz. 2015;34(2):353-61.
Zientara S, Weyer CT, Lecollinet S. African horse sickness. Rev Sci Tech Off Int Epiz. 2015;34(2):315-27.
Lubroth J. African horse sickness and the epizootic in Spain in 1987. Equine Pract. 1988;10:26-33.
Oura CA. Possible role for domestic dogs in the spread of African horse sickness virus. Vet Rec. 2018;713-4.
O'Dell N, Arnot L, Janisch CE, Steyl JCA. Clinical presentation and pathology of suspected vector transmitted African horse sickness in South African domestic dogs from 2006 to 2017. Vet Rec. 2018;182(25):715.
Weyer CT, Grewar JD, Burger P, Rossouw E, Lourens C, Joone C, et al. African Horse Sickness caused by genome reassortment and reversion to virulence of live, attenuated vaccine viruses, South Africa, 2004-2014. Emerg Infect Dis. 2016;22(12):2087-96.
Otieno OGE, Amimo JO. Molecular epidemiology of African Horse Sickness in Kenya. African Horse Sickness Conf., Proc. Abstract, Nairobi Kenya. 2018;33-4.
Dennis SJ, Meyers AE, Hitzeroth J, Rybicki EP. African Horse Sickness: a review of current understanding and vaccine development. Viruses. 2019;11(9):844.
Wernery U, Joseph S, Elizabeth ShK, Patteril NG, Wernery R, Spendrup S. Production of an African Horse Sickness killed vaccine containing all 9 serotypes. J Equine Vet Sci. 2016;39:S101-S102.
Dubourget P, Preaud JM, Detraz N, Lacoste F. Production and quality control of an industrial inactivated vaccine against AHS type IV. In: Walton TE, Osburn BI, editors. Bluetongue, african horse sickness and related orbiviruses. Boca Raton, Florida: CRC Press, 1993;874-86.
House J, Lombard M, Dubourget P, House C, Mebus C. Efficacy of an inactivated African horse sickness serotype 4 vaccine. In: Walton TE, Osburn BI, editors. Bluetongue, African horse sickness and related orbivirus. Proc. Of the Sec. Int. Symposium. Boca Raton, Florida, USA: CRC Press, 1992; p. 891-5.
Ronchi GF, Ulisse S, Rossi E, Franchi P, Armillotta G, Capista S, et al. Immunogenicity of two adjuvant formulations of an inactivated African horse sickness vaccine in guinea-pigs and target animals. Vet Ital. 2012;48(1):55-76.
OIE. Manual of Diagnostic Tests and Vaccines for Terrestrial Animals. Tests for sterility and freedom from contamination of biological materials intended for veterinary use. 8th ed; Paris, France: OIE; p. 109-122.
Mirchamsy H, Taslimi H. Inactivated African Horse Sickness virus cell culture vaccine. Immunology. 1968;14(1):81-8.
Bahnemann HG. The inactivation of foot-and-mouth disesase virus by ethylenimine and propylenimine. Zentralbl Veterinarmed B. 1972;20(5):356-60.
Bahnemann HG. Inactivation of viral antigens for vaccine preparation with particular reference to the application of binary ethylenimine. Vaccine. 1990;8(4):299-303.
Rodriguez M, Joseph S, Pfeffer M, Raghavan R, Wernery U. Immune response of horses to inactivated African horse sickness vaccine. BMC Vet Res. In press. 2020;16(1):1-13.
Hamblin C, Graham SD, Anderson EC, Crowther JR. A competitive ELISA for the detection of group-specific antibodies to African horse sickness virus. Epidemiol Infect. 1990;104:303-12.
Lelli R, Molini U, Ronchi GF, Rossi E, Franchi P, Ulisse S, et al. Inactivated and ajuvanated vaccine for the control of the African horse sickness virus serotype 9 infection: evaluation of efficacy in horses and guinea-pig model. Vet Ital. 2013;49(1):89-98.
Guthrie AJ, MacLachlan NJ, Joone C, Lourens CW, Weyer CT, Quan M, et al. Diagnostic accuracy of a duplex real-time reverse transcription quantitative PCR assay for detection of African horse sickness virus. J Virol Methods. 2013;189:30-5.
Maree S, Paweska JT. Preparation of recombinant African horse sickenss virus Vp7 antigen via a simple method and validation of a VP7 based indirect ELISA for the detection of group-specific IgG antibodies in horse sera. J Virol Methods. 2005;125:155-65.
Van Dijk AA. African Horse Sickness vaccine development. In: Wernery U, Wade JF, Mumford JA, Kaaden O-R, editors. Equine infectious diseases, 8th edn. Newmarket, UK: R and W Publications; 1999; p. 261-5.
Dennis SJ, O’Kennedy MM, Rutkowska D, Tsekoa T, Lourens CW, Hitzeroth II, et al. Safety and immunogenicity of plant-produced African horse sickness virus-like particles in horses. Vet Res. 2018;49(1). https://doi.org/10.1186/s13567-018-0600-4
Wernery U, Joseph S, Raghavan R, Spendrup S, Dyer B. Serological evidence on the role of the Onderstepoort attenuated African horse sickness vaccine by induction of antibody response to a nine serotype containing CVRL inactivated African horse sickness vaccine. East African Journal of Veterinary and Animal Science 2020; (in press).
Hamblin C, Mellor PS, Graham SD, Hooghuis H, Montejano RC, Cubillo MA, et al. Antibodies in horses, mules and donkeys following monovalent vaccination against African horse sickness. Epidemiol Infect. 1991;106:365-71.
De la Poza F, Marin Lopez A, Castillo-Olivares J, Calvo-Pinilla E, Ortego J. Identification of CD8T cell epitopes in VP2 and NS1 proteins of African horse sickness virus in IFNAR (-/-) mice. Virus Res. 2015;210: 149-53.
Pretorius A, Van Kleef M, Van Wyngaarft W, Health J. Virus-specific CD8 + T-cells detected in PBMC from horses vaccinated against African horse sickness virus. Vet Immunol Immunopathol. 2012;146:81-6.
Mellor PS, Hamblin C. African horse sickness. Vet Res. 2004;35:445-66.
Lefèvre P-C, Mellor PH, Saegerman Cl. (2010). Bluetongue. In: Lefèvre P-C, Blancou J, Chermette R, Uilenberg G, editors. Infectious and parasitic diseases of livestock. Corsica, France: Lavoisier; p. 663-88, 1.
European Medicines Agency. mail@emea.europa.eu. 2009. https://www.ema.europa.eu/en/medicines/veterinary/EPAR/bluevac-btv8#authorisation-details-section. Accessed March 6, 2018
Alberca B, Bachanek-Bankowska K, Cabana M, Calvo-Pinilla E, Viaplana E, Frost L, et al. Vaccination of horses with a recombinant modified vaccinia Ankara virus (MVA) expressing African horse sickness (AHS) virus major capsid protein VP2 provides complete clinical protection against challenge. Vaccine. 2014;32:3670-4.
Guthrie AJ, Quan M, Lourens CW, Audonet J-C, Minke JM, Yao J, et al. Protective immunization of horses with a recombinant canarypox virus vectored vaccine co-expressing genes encoding the outer capsid proteins of African horse sickness virus. Vaccine. 2009;27:4434-8.

Auteurs

Ulrich Wernery (U)

Central Veterinary Research Laboratory, Dubai, UAE.

Marina Rodriguez (M)

Central Veterinary Research Laboratory, Dubai, UAE.

Rekha Raghavan (R)

Central Veterinary Research Laboratory, Dubai, UAE.

Ginu Syriac (G)

Central Veterinary Research Laboratory, Dubai, UAE.

Shruti Miriam Thomas M (S)

Central Veterinary Research Laboratory, Dubai, UAE.

Shyna K Elizabeth (SK)

Central Veterinary Research Laboratory, Dubai, UAE.

Gaetano Federico Ronchi (G)

Istituto Zooprofilattico Sperimentale, dell'Abruzzo e del Molise "G. Caporale", Teramo, Italy.

Rubeena Muhammed (R)

Central Veterinary Research Laboratory, Dubai, UAE.

Nissy A Patteril (NA)

Central Veterinary Research Laboratory, Dubai, UAE.

Sunitha Joseph (S)

Central Veterinary Research Laboratory, Dubai, UAE.

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