J Vet Sci.  2017 Aug;18(S1):315-322. 10.4142/jvs.2017.18.S1.315.

Influence of vaccine potency and booster administration of foot-and-mouth disease vaccines on the antibody response in calves with maternal antibodies

Affiliations
  • 1Institute of Foot and Mouth Disease (SAP), Ministry of Food, Agriculture and Livestock, Ankara 06044, Turkey. cancokcaliskan@gmail.com
  • 2Directorate-General for Agriculture and Rural Development, Ministry of Food, Agriculture and Livestock, Ankara 06044, Turkey.
  • 3Directorate-General for State Farms, Ministry of Food, Agriculture and Livestock, Ankara 06044, Turkey.

Abstract

Foot-and-mouth disease is one of the most important viral diseases of cloven-hoofed animals. Mass vaccination is an effective method to control the disease and is frequently utilized in endemic regions. Sufficient protection of young animals is important in mass vaccination campaigns. Maternal antibodies negatively affect the success of vaccination. Hence, determination of the optimal vaccination age is crucial for the uninterrupted protection of young animals. This study was performed to identify the effect of vaccine potency and booster administration on serum neutralizing antibody titers of calves with different levels of maternal antibodies. Calves (n = 111) on a state farm were used in this study. Oil adjuvant foot-and-mouth disease vaccines with 3 PDâ‚…â‚€ and 6 PDâ‚…â‚€ potencies were used with or without booster administration. Serum samples were collected each month up to day 120 postvaccination. Virus neutralization tests were used to measure the serum neutralizing antibody titers and estimate the protection period by using pre-determined cut-off values for protection. The results revealed that a vaccination with a 6 PDâ‚…â‚€ potency vaccine, preferably followed by a booster dose, should be used to overcome maternal immunity for incessant protection.

Keyword

calf; foot-and-mouth disease; high potency vaccine; maternal antibody; virus neutralization

MeSH Terms

Animals
Antibody Formation/immunology
Cattle
Cattle Diseases/immunology/*prevention & control/virology
Foot-and-Mouth Disease/immunology/*prevention & control
*Foot-and-Mouth Disease Virus/immunology
Neutralization Tests/veterinary
Viral Vaccines/administration & dosage/immunology/*therapeutic use
Viral Vaccines

Figure

  • Fig. 1 (A) Individual serum virus neutralizing antibody titers of calves according to calf age on day 0 of the experiment. Horizontal red line indicates the cut-off level of antibody titers for estimated protection. (B) Geometric means of neutralizing antibodies for calves grouped by 10-day intervals based on calf age at day 0 of the experiment. A linear slope was drawn using these titer values. Horizontal red line indicates the cut-off level of antibody titers for estimated protection. Green color filled area indicates the estimated protection period. (C) Geometric means of neutralizing maternal antibody levels of unvaccinated group. A linear slope was drawn with these titer values. Horizontal red lines indicate the cut-off level of antibody titers for estimated protection. Green color filled area indicates the estimated protection period.

  • Fig. 2 Arithmetic means of serum virus neutralizing antibody titers of calves vaccinated with 3 PD50 vaccine. (A) 3 PD50 single < 1.50, (B) 3 PD50 single 1.50–1.80, (C) 3 PD50 single > 1.80, (D) 3 PD50 booster < 1.50, (E) 3 PD50 booster 1.50–1.80, (F) 3 PD50 booster > 1.80. Arrows indicate the time of vaccination. Serum samples were collected before vaccination as day 0 and additional blood samples were obtained on days 28, 60, 90, and 120 postvaccination and analyzed via virus neutralization test. Horizontal red lines indicate the cut-off level of antibody titers for estimated protection.

  • Fig. 3 Arithmetic means of serum virus neutralizing antibody titers of calves vaccinated with 6 PD50 vaccine. (A) 6 PD50 single < 1.50, (B) 6 PD50 single 1.50–1.80, (C) 6 PD50 single > 1.80, (D) 6 PD50 booster < 1.50, (E) 6 PD50 booster 1.50–1.80, (F) 6 PD50 booster > 1.80. Arrows indicate the time of vaccination. Serum samples were collected before vaccination as day 0 and additional blood samples were obtained on days 28, 60, 90, and 120 postvaccination and analyzed via virus neutralization test. Horizontal red lines indicate the cut-off level of antibody titers for estimated protection.


Reference

1. Bielefeldt-Ohmann H, Prow NA, Wang W, Tan CS, Coyle M, Douma A, Hobson-Peters J, Kidd L, Hall RA, Petrovsky N. Safety and immunogenicity of a delta inulin-adjuvanted inactivated Japanese encephalitis virus vaccine in pregnant mares and foals. Vet Res. 2014; 45:130.
Article
2. Bucafusco D, Di Giacomo S, Pega J, Juncos MS, Schammas JM, Pérez-Filgueira M, Capozzo AV. Influence of antibodies transferred by colostrum in the immune responses of calves to current foot-and-mouth disease vaccines. Vaccine. 2014; 32:6576–6582.
Article
3. Chase CC, Hurley DJ, Reber AJ. Neonatal immune development in the calf and its impact on vaccine response. Vet Clin North Am Food Anim Pract. 2008; 24:87–104.
Article
4. Council of Europe, European Pharmacopoeia Commission, European Directorate for the Quality of Medicines & Healthcare. European Pharmacopoeia. 8th ed. Strasbourg: Council of Europe, European Directorate for the Quality of Medicines and Healthcare;2013.
5. Davis EG, Bello NM, Bryan AJ, Hankins K, Wilkerson M. Characterisation of immune responses in healthy foals when a multivalent vaccine protocol was initiated at age 90 or 180 days. Equine Vet J. 2015; 47:667–674.
Article
6. Dekker A, Eblé P, Stockhofe N, Chénard G. Intratypic heterologous vaccination of calves can induce an antibody response in presence of maternal antibodies against foot-and-mouth disease virus. BMC Vet Res. 2014; 10:127.
Article
7. Downey ED, Tait RG Jr, Mayes MS, Garrick DJ, Ridpath J, Reecy JM. Effects of calf age and dam age on circulating BVDV II antibody levels prior to vaccination in Angus weanling calves. Reports No. 214. Ames: Iowa State Research Farm Progress Reports (US);2011.
8. Ellis J, Gow S, Bolton M, Burdett W, Nordstrom S. Inhibition of priming for bovine respiratory syncytial virus-specific protective immune responses following parenteral vaccination of passively immune calves. Can Vet J. 2014; 55:1180–1185.
9. Elnekave E, Zamir L, Hamd F, Even Tov B, Klement E. Risk factors for foot and mouth disease outbreaks in grazing beef cattle herds. Prev Vet Med. 2015; 120:236–240.
Article
10. Endsley JJ, Roth JA, Ridpath J, Neill J. Maternal antibody blocks humoral but not T cell responses to BVDV. Biologicals. 2003; 31:123–125.
Article
11. Foote MR, Nonnecke BJ, Beitz DC, Waters WR. Antigen-specific B-cell responses by neonatal calves after early vaccination. J Dairy Sci. 2007; 90:5208–5217.
Article
12. Guzman E, Taylor G, Charleston B, Ellis SA. Induction of a cross-reactive CD8+ T cell response following foot-and-mouth disease virus vaccination. J Virol. 2010; 84:12375–12384.
Article
13. Hodgins DC, Shewen PE, Dewey CE. Influence of age and maternal antibodies on antibody responses of neonatal piglets vaccinated against Mycoplasma hyopneumoniae. J Swine Health Prod. 2004; 12:10–16.
14. Jamal SM, Bouma A, van den Broek J, Stegeman A, Chénard G, Dekker A. Foot-and-mouth disease vaccine potency testing: the influence of serotype, type of adjuvant, valency, fractionation method, and virus culture on the dose-response curve in cattle. Vaccine. 2008; 26:6317–6321.
Article
15. Knight-Jones TJ, Bulut AN, Gubbins S, Stärk KD, Pfeiffer DU, Sumption KJ, Paton DJ. Retrospective evaluation of foot-and-mouth disease vaccine effectiveness in Turkey. Vaccine. 2014; 32:1848–1855.
Article
16. Knight-Jones TJ, Gubbins S, Bulut AN, Stärk KD, Pfeiffer DU, Sumption KJ, Paton DJ. Mass vaccination, immunity and coverage: modelling population protection against foot-and-mouth disease in Turkish cattle. Sci Rep. 2016; 6:22121.
Article
17. Lee HS, Lee NH, Seo MG, Ko YJ, Kim B, Lee JB, Kim JS, Park S, Shin YK. Serological responses after vaccination of growing pigs with foot-and-mouth disease trivalent (type O, A and Asia1) vaccine. Vet Microbiol. 2013; 164:239–245.
Article
18. Murphy JM, Hagey JV, Chigerwe M. Comparison of serum immunoglobulin G half-life in dairy calves fed colostrum, colostrum replacer or administered with intravenous bovine plasma. Vet Immunol Immunopathol. 2014; 158:233–237.
Article
19. Nicholls MJ, Black L, Rweyemamu MM, Genovese J, Ferrari R, Hammant CA, de Silva E, Umehara O. The effect of maternally derived antibodies on the response of calves to vaccination against foot and mouth disease. J Hyg (Lond). 1984; 92:105–116.
Article
20. Niewiesk S. Maternal antibodies: clinical significance, mechanism of interference with immune responses, and possible vaccination strategies. Front Immunol. 2014; 5:446.
Article
21. Patil PK, Sajjanar CM, Natarajan C, Bayry J. Neutralizing antibody responses to foot-and-mouth disease quadrivalent (type O, A, C and Asia 1) vaccines in growing calves with pre-existing maternal antibodies. Vet Microbiol. 2014; 169:233–235.
Article
22. Polewicz M, Gracia A, Buchanan R, Strom S, Halperin SA, Potter AA, Babiuk LA, Gerdts V. Influence of maternal antibodies on active pertussis toxoid immunization of neonatal mice and piglets. Vaccine. 2011; 29:7718–7726.
Article
23. Sadir AM, Schudel AA, Laporte O, Braun M, Margni RA. Response to foot-and-mouth disease vaccines in newborn calves. Influence of age, colostral antibodies and adjuvants. Epidemiol Infect. 1988; 100:135–144.
Article
24. Shankar H, Uppal PK. Immune response of newborn calves to vaccination with foot-and-mouth disease vaccine. Rev Sci Tech Off Int Epiz. 1982; 1:403–414.
Article
25. Späth EJ, Smitsaart E, Casaro AP, Fondevila N, Fernández F, Leunda MR, Compaired D, Buffarini M, Pessi H. Immune response of calves to foot-and-mouth disease virus vaccine emulsified with oil adjuvant. Strategies of vaccination. Vaccine. 1995; 13:909–914.
Article
26. Vidor E. Vaccination of newborns against hepatitis A in the presence of maternally derived antibodies. J Comp Pathol. 2007; 137:Suppl 1. S42–S45.
Article
27. World Organisation for Animal Health (OIE). Foot and mouth disease. OIE. Terrestrial Animal Health Code. 20th ed. Paris: OIE;2011. p. 437–463.
Full Text Links
  • JVS
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr