Vaccination against Bacterial Mastitis in Sheep
Abstract
:1. Introduction
2. General Principles of Vaccination against Mastitis in Sheep
3. Application of Anti-Mastitis Vaccination in Sheep
3.1. Vaccines against Staphylococcal Mastitis
3.2. Vaccines against Mastitis Caused by Other Pathogens
4. Application of Anti-Mastitis Vaccination within the Frame of Flock Health Management
- 1.
- Improved mastitis control, i.e., reduced incidence risk of clinical and subclinical mastitis. In this respect, the clinical studies (field and experimental work) carried out for licencing a vaccine, as well as any evidence becoming available will subsequently present data regarding the efficacy of a vaccine.
- 2.
- Improved milk quality: low somatic cell counts, optimum chemical composition, absence of staphylococci therein. In this respect, an association of the vaccination with a vaccine licenced against staphylococcal mastitis (Vimco®) with a reduced recovery of staphylococci from the farm bulk-tank raw milk was found in an extensive field study carried out in dairy sheep flocks (n = 325) in Greece. Among the 126 flocks in which sheep had been vaccinated against staphylococcal mastitis, staphylococci were recovered from 64 (50.8%), whilst among the 199 unvaccinated flocks, the bacteria were recovered from 142 (71.4%) (p = 0.0002) [45] (Figure 1).
- 3.
- Increased milk production, as the result of reduced incidence risk of the disease. In this respect, during the study referred to hereabove, it was found that milk production in flocks in which anti-staphylococcal mastitis vaccination was applied was higher than in which it was not performed: 231 ± 7 mL versus 193 ± 6 mL per ewe annually (p = 0.0001) [45] (Figure 2).
- 4.
- Reduced dissemination of mastitis-causing pathogens in the farm environment. In this respect, in an extensive field study carried out in dairy sheep flocks (n = 255) [46], an association was found between the vaccination with the same licenced vaccine against staphylococcal mastitis and the proportion of milking clusters from which staphylococci were isolated. From the 459 clusters sampled in sheep flocks where vaccination was performed, staphylococci were recovered from the upper part of 13.9% and the lower part of 4.8% of clusters; in contrast, higher recovery rates were seen among the 656 clusters sampled in sheep flocks where vaccination was not performed: 19.2% and 9.1%, respectively (p < 0.022) [46] (Figure 3).
- 5..
- Reduction of antibiotic use in flocks, as cases of mastitis would be reduced and, consequently, the need for using antibiotics for their treatment would decrease. In this respect, animal vaccination is considered to be a valid and useful strategy for controlling diseases, recommended by guidelines for the prudent use of antibiotics in veterinary work [47] (Table 1).
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Conflicts of Interest
References
- Lacasta, D.; Ferrer, L.M.; Ramos, J.J.; Gonzalez, J.M.; Ortin, A.; Fthenakis, G.C. Vaccination schedules in small ruminant farms. Vet. Microbiol. 2015, 181, 34–46. [Google Scholar] [CrossRef] [PubMed]
- Scott, P.R.; Sargison, N.D.; Wilson, D.J. The potential for improving welfare standards and productivity in United Kingdom sheep flocks using veterinary flock health plans. Vet. J. 2007, 173, 522–531. [Google Scholar] [CrossRef]
- Kyriakis, S.C. Tomorrow’s vaccines for small ruminants. Vet. Microbiol. 2015, 181, 47–52. [Google Scholar] [CrossRef] [PubMed]
- European Food Safety Authority. Scientific opinion on the welfare risks related to the farming of sheep for wool, meat and milk production. EFSA J. 2014, 12, 3933–4060. [Google Scholar]
- Vasileiou, N.G.C.; Cripps, P.J.; Ioannidi, K.S.; Chatzopoulos, D.C.; Gougoulis, D.A.; Sarrou, S.; Orfanou, D.C.; Politis, A.P.; Calvo Gonzalez-Valerio, T.; Argyros, S.; et al. Extensive countrywide field investigation of subclinical mastitis in sheep in Greece. J. Dairy Sci. 2018, 101, 7297–7310. [Google Scholar] [CrossRef] [Green Version]
- Gelasakis, A.I.; Mavrogianni, V.S.; Petridis, I.G.; Vasileiou, N.G.C.; Fthenakis, G.C. Mastitis in sheep—The last 10 years and the future of research. Vet. Microbiol. 2015, 185, 136–146. [Google Scholar] [CrossRef]
- Ergun, Y.; Aslantas, O.; Dogruer, G.; Kirecci, E.; Saribay, M.K.; Ates, C.T.; Ulku, A.; Demir, C. Prevalence and etiology of subclinical mastitis in Awassi dairy ewes in southern Turkey. Turk. J. Vet. Anim. Sci. 2009, 33, 477–483. [Google Scholar] [CrossRef]
- Las Heras, A.; Dominguez, L.; Fernandez-Garayzabal, J.F. Prevalence and aetiology of subclinical mastitis in dairy ewes of the Madrid region. Small Rumin. Res. 1999, 32, 21–29. [Google Scholar] [CrossRef]
- Mørk, T.; Tollersrud, T.; Kvitle, B.; Jorgensen, H.J.; Waage, S. Genetic diversity of Staphylococcus aureus isolated from ovine intramammary infections in Norway. Vet. Microbiol. 2005, 106, 265–273. [Google Scholar] [CrossRef]
- Bergonier, D.; de Cremoux, R.; Rupp, R.; Lagriffoul, G.; Berthelot, X. Mastitis of dairy small ruminants. Vet. Res. 2003, 34, 689–716. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Fthenakis, G.C.; Jones, J.E.T. Incidence and aetiology of clinical ovine mastitis in flocks in Central Macedonia, Greece. Bull. Hell. Vet. Med. Soc. 1990, 41, 133–141. [Google Scholar]
- Mørk, T.; Waage, S.; Tollersrud, T.; Kvitle, B.; Sviland, S. Clinical mastitis in ewes; bacteriology, epidemiology and clinical features. Acta Vet. Scand. 2007, 49, 23. [Google Scholar] [CrossRef] [PubMed]
- Koop, G.; Rietman, J.F.; Pieterse, M.C. Staphylococcus aureus mastitis in Texel sheep associated with suckling twins. Vet. Rec. 2010, 167, 868–869. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Fthenakis, G.C. Prevalence and aetiology of subclinical mastitis in ewes of southern Greece. Small Rumin. Res. 1994, 13, 293–300. [Google Scholar] [CrossRef]
- Mavrogianni, V.S.; Cripps, P.J.; Fthenakis, G.C. Bacterial flora and risk of infection of the ovine teat duct and mammary gland throughout lactation. Prev. Vet. Med. 2007, 79, 163–173. [Google Scholar] [CrossRef]
- Vasileiou, N.G.C.; Mavrogianni, V.S.; Petinaki, E.; Fthenakis, G.C. Predisposing factors for bacterial mastitis in ewes. Reprod. Dom. Anim. 2019, 54, 1424–1431. [Google Scholar] [CrossRef]
- Bridre, J. La mammite gangreneuse des brebis laitieres: Pathogenie et vaccination. Bull. Soc. Cent. Med. Vet. 1907, 61, 500–506. [Google Scholar]
- Azara, E.; Longheu, C.; Sanna, G.; Tola, S. Biofilm formation and virulence factor analysis of Staphylococcus aureus isolates collected from ovine mastitis. J. Appl. Microbiol. 2017, 123, 372–379. [Google Scholar] [CrossRef]
- Katsafadou, A.I.; Politis, A.P.; Mavrogianni, V.S.; Barbagianni, M.S.; Vasileiou, N.G.C.; Fthenakis, G.C.; Fragkou, I.A. Mammary defences and immunity against mastitis in sheep. Animals 2019, 9, 726. [Google Scholar] [CrossRef] [Green Version]
- Craven, N.; Williams, M.R. Defences of the bovine mammary gland against infection and prospects for their enhancement. Vet. Immunol. Immunopathol. 1985, 10, 71–127. [Google Scholar] [CrossRef]
- Norcross, N.L. Specific defence mechanisms of the udder. Flem. Vet. J. 1991, 62, 129–139. [Google Scholar]
- Oestensson, K.; Lun, S. Transfer of immunoglobulins through the mammary endothelium and epithelium and in the local lymph node of cows during the initial response after intramammary challenge with E. coli endotoxin. Acta Vet. Scand. 2008, 50, 26. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Wellnitz, O.; Zbinden, C.; Lüttgenau, J.; Bollwein, H.; Bruckmaier, R.M. Different chronological patterns of appearance of blood derived milk components during mastitis indicate different mechanisms of transfer from blood into milk. J. Dairy Res. 2015, 82, 322–327. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Hine, B.C.; Hunt, P.W.; Beasley, A.M.; Windon, R.G.; Glover, S.A.; Colditz, I.G. Selective transport of IgE into ovine mammary secretions. Res. Vet. Sci. 2010, 89, 184–190. [Google Scholar] [CrossRef] [PubMed]
- Barrio, M.B.; Rainard, P.; Poutrel, B. Milk complement and the opsonophagocytosis and killing of Staphylococcus aureus mastitis isolates by bovine neutrophils. Microb. Pathogen. 2003, 34, 1–9. [Google Scholar] [CrossRef]
- DiCarlo, A.; Paape, M. Comparison of C3b binding to bovine peripheral blood and mammary gland neutrophils (PMN). Am. J. Vet. Res. 1996, 57, 151–156. [Google Scholar]
- Cunnion, K.M.; Lee, J.C.; Frank, M.M. Capsule production and growth phase influence binding of complement to Staphylococcus aureus. Infect. Immun. 2001, 69, 6796–6803. [Google Scholar] [CrossRef] [Green Version]
- Rainard, P. The complement in milk and defense of the bovine mammary gland against infections. Vet. Res. 2003, 34, 647–670. [Google Scholar] [CrossRef] [Green Version]
- Rainard, P.; Gilbert, F.B.; Martins, R.P.; Germon, P.; Foucras, G. Progress towards the elusive mastitis vaccines. Vaccines 2022, 10, 296. [Google Scholar] [CrossRef]
- Belkaid, Y.; Harrison, O.J. Homeostatic immunity and the microbiota. Immunity 2017, 46, 562–576. [Google Scholar] [CrossRef] [Green Version]
- Watson, D.L. Vaccination against experimental staphylococcal mastitis in ewes. Res. Vet. Sci. 1988, 45, 16–21. [Google Scholar] [CrossRef]
- Amorena, B.; Baselga, R.; Albizu, I. Use of liposome-immunopotentiated exopolysaccharide as a component of an ovine mastitis staphylococcal vaccine. Vaccine 1994, 12, 243–249. [Google Scholar] [CrossRef]
- Tollersrud, T.; Norstebo, P.E.; Engvik, J.P.; Andersen, S.R.; Reitan, L.J.; Lund, A. Antibody responses in sheep vaccinated against Staphylococcus aureus mastitis: A comparison of two experimental vaccines containing different adjuvants. Vet. Res. Comm. 2002, 26, 587–600. [Google Scholar] [CrossRef]
- Hadimli, H.H.; Erganis, O.; Kav, K.; Sayin, Z. Evaluation of a combined vaccine against staphylococcal mastitis in ewes. Bull. Vet. Inst. Pulawy 2005, 49, 179–182. [Google Scholar]
- Perez, M.M.; Prenafeta, A.; Valle, J.; Penades, J.; Rota, C.; Solano, C.; Marco, J.; Grillo, M.J.; Lasa, I.; Irache, J.M.; et al. Protection from Staphylococcus aureus mastitis associated with poly-N-acetyl beta-1,6 glucosamine specific antibody production using biofilm-embedded bacteria. Vaccine 2009, 27, 2379–2386. [Google Scholar] [CrossRef] [Green Version]
- Prenafeta, A.; March, R.; Foix, A.; Casals, I.; Costa, L. Study of the humoral immunological response after vaccination with a Staphylococcus aureus biofilm-embedded bacterin in dairy cows: Possible role of the exopolysaccharide specific antibody production in the protection from Staphylococcus aureus induced mastitis. Vet. Immunol. Immunopathol. 2010, 134, 208–217. [Google Scholar]
- Vasileiou, N.G.C.; Chatzopoulos, D.C.; Cripps, P.J.; Ioannidi, K.S.; Gougoulis, D.A.; Chouzouris, T.M.; Lianou, D.T.; Calvo Gonzalez-Valerio, T.; Guix Vallverdu, R.; Argyros, S.; et al. Evaluation of efficacy of a biofilm-embedded bacteria-based vaccine against staphylococcal mastitis in sheep—A randomized, placebo-controlled field study. J. Dairy Sci. 2019, 102, 9328–9344. [Google Scholar] [CrossRef] [PubMed]
- Vasileiou, N.G.C.; Cripps, P.J.; Ioannidi, K.S.; Katsafadou, A.I.; Chatzopoulos, D.C.; Barbagianni, M.S.; Tsioli, V.; Dermisiadou, E.; Karavanis, E.; Papadopoulos, N.; et al. Experimental study for evaluation of the efficacy of a biofilm-embedded bacteria-based vaccine against Staphylococcus chromogenes-associated mastitis in sheep. Vet. Microbiol. 2019, 239, 108480. [Google Scholar] [CrossRef] [PubMed]
- Vasileiou, N.G.C.; Gougoulis, D.A.; Katsafadou, A.I.; Mavrogianni, V.S.; Petinaki, E.; Fthenakis, G.C. Anti-staphylococcal biofilm antibodies in ewes and association with subclinical mastitis. Small Rumin. Res. 2019, 178, 117–122. [Google Scholar] [CrossRef]
- Alekish, M.O.; Ismail, Z.B.; Hammouri, H.M.; Daradka, M.H.; Al Taha, S.; Olymat, I. Bacteriological cure rate and changes in milk composition in mastitis vaccinated ewes affected with subclinical mastitis. Vet. World 2018, 11, 125–129. [Google Scholar] [CrossRef] [Green Version]
- Longheu, C.M.; Azara, E.; Marogna, G.; Addis, M.F.; Tola, S. Identification of secreted and cellular antigens of Staphylococcus aureus causing dairy sheep mastitis and their potential for vaccine development. Vet. Immunol. Immunopathol. 2020, 230, 110149. [Google Scholar] [CrossRef] [PubMed]
- Kabay, M.J.; Ellis, T.M. Intraperitoneal inoculation of ewes with an autogenous vaccine to prevent mastitis due to Pasteurella haemolytica. Aust. Vet. J. 1989, 66, 342–343. [Google Scholar] [CrossRef] [PubMed]
- Tassi, R.; Schiavo, M.; Filipe, J.; Todd, H.; Ewing, D.; Ballingall, K.T. Intramammary immunisation provides short term protection against Mannheimia haemolytica mastitis in sheep. Front. Vet. Sci. 2021, 8, 659803. [Google Scholar] [CrossRef] [PubMed]
- Leitner, G.; Krifucks, O. Pseudomonas aeruginosa mastitis outbreaks in sheep and goat flocks: Antibody production and vaccination in a mouse model. Vet. Immunol. Immunopathol. 2007, 119, 198–203. [Google Scholar] [CrossRef] [PubMed]
- Lianou, D.T.; Michael, C.K.; Petinaki, E.; Mavrogianni, V.S.; Fthenakis, G.C. Administration of vaccines in dairy sheep and goat farms: Patterns of vaccination, associations with health and production parameters, predictors. Vaccines 2022, 10, 1372. [Google Scholar] [CrossRef] [PubMed]
- Michael, C.K.; Lianou, C.K.; Vasileiou, N.G.C.; Tsilipounidaki, K.; Katsafadou, A.I.; Politis, A.P.; Kordalis, N.G.; Ioannidi, K.S.; Gougoulis, D.A.; Trikalinou, C.; et al. Association of staphylococcal populations on teatcups of milking parlours with vaccination against staphylococcal mastitis in sheep and goat farms. Pathogens 2021, 10, 385. [Google Scholar] [CrossRef] [PubMed]
- European Commission. Guidelines for the Prudent Use of Antimicrobials in Veterinary Medicine (2015/C 299/04); European Union: Brussels, Belgium, 2015; 26p.
- Murphy, D.; Ricci, A.; Auce, Z.; Beechinor, J.G.; Bergendahl, H.; Breathnach, R.; Bureš, J.; Da Silva, D.; Pedro, J.; Hederová, J. EMA and EFSA Joint Scientific Opinion on measures to reduce the need to use antimicrobial agents in animal husbandry in the European Union, and the resulting impacts on food safety (RONAFA). EFSA J. 2017, 15, 4666. [Google Scholar]
- Hoelzer, K.; Bielke, L.; Blake, D.P.; Cox, E.; Cutting, S.M.; Devriendt, B.; Erlacher-Vindel, E.; Goossens, E.; Karaca, K.; Lemiere, S.; et al. Vaccines as alternatives to antibiotics for food producing animals. Part 1: Challenges and needs. Vet. Res. 2018, 49, 64. [Google Scholar] [CrossRef] [PubMed]
- Fthenakis, G.C.; Arsenos, G.; Brozos, C.; Fragkou, I.A.; Giadinis, N.D.; Giannenas, I.; Mavrogianni, V.S.; Papadopoulos, E.; Valasi, I. Health management of ewes during pregnancy. Anim. Reprod. Sci. 2012, 130, 198–212. [Google Scholar] [CrossRef] [PubMed]
Expected Benefits |
---|
Improved mastitis control (reduced incidence of mastitis) |
Improved milk quality (low somatic cell counts, absence of relevant bacteria) |
Increased milk production |
Reduced dissemination of mastitis pathogens (low excretion of staphylococci in milk) |
Reduction of antibiotic use in flocks |
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations. |
© 2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
Share and Cite
Vasileiou, N.G.C.; Lianou, D.T.; Michael, C.K.; Fthenakis, G.C.; Mavrogianni, V.S. Vaccination against Bacterial Mastitis in Sheep. Vaccines 2022, 10, 2088. https://doi.org/10.3390/vaccines10122088
Vasileiou NGC, Lianou DT, Michael CK, Fthenakis GC, Mavrogianni VS. Vaccination against Bacterial Mastitis in Sheep. Vaccines. 2022; 10(12):2088. https://doi.org/10.3390/vaccines10122088
Chicago/Turabian StyleVasileiou, Natalia G. C., Daphne T. Lianou, Charalambia K. Michael, George C. Fthenakis, and Vasia S. Mavrogianni. 2022. "Vaccination against Bacterial Mastitis in Sheep" Vaccines 10, no. 12: 2088. https://doi.org/10.3390/vaccines10122088
APA StyleVasileiou, N. G. C., Lianou, D. T., Michael, C. K., Fthenakis, G. C., & Mavrogianni, V. S. (2022). Vaccination against Bacterial Mastitis in Sheep. Vaccines, 10(12), 2088. https://doi.org/10.3390/vaccines10122088