Molecular Detection of Salmonella pullorum from Poultry Ceca and Vaccine Preparation
DOI:
https://doi.org/10.3923/ijps.2018.71.77Keywords:
Broiler and layer production, Genus Salmonella, PCR, poultry cecum, Salmonella pullorum, vaccineAbstract
Objective: Isolation of Salmonella pullorum (S. pullorum) from chicken ceca and confirmation by PCR after a trial to prepare a vaccine from this isolate by using the freezing and thawing method. Materials and Methods: A total of 69 samples were isolated from chicken ceca. Biochemical tests were performed and diagnoses were made. Twenty-one Salmonella positive samples were found, 12 of which were S. pullorum, which were confirmed by differential biochemical tests (glucose, sucrose, lactose, mannitol and maltose) and additionally confirmed by PCR. The second part of the study was to determine the LD50 of S. pullorum at doses up to 2×10–7 after isolate exposure to slow freezing and after thawing, which effected isolation effectiveness. The third part of the study included the 28 day a challenge-dose test. Results: Mortality in the control group (n = 15) was 20%, with clinical signs. On the third day of challenge via oral inoculation with S. pullorum (0.5 mL of 2×10–7 CFU mL–1), there were two cases of lameness that improved in the vaccinated group. Over 2-3 days, signs of respiratory symptoms were minimal and nonspecific, with animals in the control group showing a dull appearance, depressed activity and a loss of appetite. Non-significant signs were noted 5 days after experimental infection in the vaccinated group. Conclusion: The isolation and characterization of S. pullorum from infected blisters and attempts to prepare a vaccine using a freezing and thawing method showed protective results after the challenge test with the same isolated strain compared to results in non-vaccinated chickens.
References
Bidhendi, M., P.S. Khaki and N. Cheraghchi, 2015. Study on phenotypic characteristics of Salmonella gallinarum and Sallmonella pullorum isolates based on biochemical and antimicrobial susceptibility tests in Iran. Arch. Razi Inst., 70: 171-177.
Kabir, S.M.L., 2010. Avian colibacillosis and salmonellosis: A closer look at epidemiology, pathogenesis, diagnosis, control and public health concerns. Int. J. Environ. Res. Public Health, 7: 89-114.
OIE., 2012. Fowl typhoid and pullorum disease, Chapter 2.3.11. Office International des Epizooties Terrestrial Manual 2012.
Li, Q., Y. Hu, J. Chen, Z. Liu, J. Han, L. Sun and X. Jiao, 2013. Identification of Salmonella enteric serovar Pullorum antigenic determinants expressed in vivo. Infect. Immun., 81: 3119-3127.
Ribeiro, S.A.M., J.B. de Paiva, F. Zotesso, M.V.F. Lemos and A. Berchieri, Jr., 2009. Molecular differentiation between Salmonella enteric subsp. enteric serovar Pullorum and Salmonella enteric subsp enteric serovar Gallinarum. Braz. J. Microbiol., 40: 184-188.
Priyantha, M.A.R., 2009. An overview: Vaccination to control fowl typhoid in commercial layers, Sri Lanka. Wayamba J. Anim. Sci., 1: 23-25.
Davies, R. and M. Breslin, 2003. Effects of vaccination and other preventive methods for Salmonella enteritidis on commercial laying chicken farms. Vet. Rec., 153: 673-677.
Anonymous, 2010. Applied biosystems. Taqman Salmonella enteritidis detection kit protocol for drag swabs: Protocol for real-time PCR detection of SE in environmental samples. Life Technologies, Carlsbad, CA., pp: 18.
Thomas, D., A. Rodrigo, M. Hernandez and M.A. Ferrus, 2009. Validation of real-time PCR and enzyme-linked fluorescent assay-based methods for detection of Salmonella spp. in chicken faces samples. Food Anal. Methods, 2: 180-189.
Sunar, N.M., E.I. Stentiford, D.I. Stewart and L.A. Fletcher, 2014. Molecular techniques to characterize the invA genes of Salmonella spp. for pathogen inactivation study in composting. https://arxiv.org/abs/1404.5208.
Reed, L.J. and H. Muench, 1938. A simple method of estimating fifty percent endpoints. Am. J. Epidemiol., 27: 493-497.
Calcott, P.H. and R.A. MacLeod, 1974. Survival of Escherichia coli from freeze-thaw damage: A theoretical and practical study. Can. J. Microbiol., 20: 671-681.
Gast, R.K., J. Guard-Petter and P.S. Holt, 2003. Effect of prior serial in vivo passage on the frequency of Salmonella enteritidis contamination in eggs from experimentally infected laying hens. Avian Dis., 47: 633-639.
Hannon, R., 2013. [Detecting the prevalence of Salmonella in the giblets of the broiler carcass in the poultry slaughter houses in the Southern region of Syria]. Damascus Univ. J. Agirc. Sci., 29: 137-151.
Al-Matar, A.H., K. Al-Shawabkeh and H. Zakaria, 2010. Prevalence of Salmonella in broiler chicken carcasses in Jordan. Agric. Sci., 32: 267-277.
Al-Abadi, I.K.M. and A.A.S. Al-Mayah, 2011. Isolation and identification of Salmonella spp. from chicken and chicken environment in Basrah province. Afr. J. Biol. Sci., 7: 33-43.
Rodriguez, J.M., I.S. Rondon and N. Verjan, 2015. Serotypes of Salmonella in broiler carcasses marketed at Ibague, Colombia. Brazil. J. Poult. Sci., 17: 545-552.
Yin, J., Z. Cheng, X. Wang, L. Xu, Q. Li, S. Geng and X. Jiao, 2015. Evaluation of the Salmonella enteric serovar Pullorum pathogenicity island 2 mutant as a candidate live attenuated oral vaccine. Clin. Vaccine Immunol., 22: 706-710.
Obafemi, A. and R. Davies, 1986. The destruction of Salmonella typhimurium in chicken exudate by different freeze‐thaw treatments. J. Applied Microbiol., 60: 381-387.
Saleem, G., R. Ramzaan, F. Khattak and R. Akhtar, 2016. Effects of acetic acid supplementation in broiler chickens orally challenged with Salmonella pullorum. Turk. J. Vet. Anim. Sci., 40: 434-443.
Barman, T.K., V.D. Sharma and S. Kumar, 2005. Protective efficacy of maternal antibodies induced by Salmonella toxoid (vaccine). Indian J. Exp. Biol., 43: 163-166.
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