期刊论文详细信息
BMC Veterinary Research
Immunogenicity and protective efficacy of Salmonella enterica serovar Pullorum pathogenicity island 2 mutant as a live attenuated vaccine candidate
Xinan Jiao1  Zhiming Pan1  Shizhong Geng1  Qiuchun Li1  Lijuan Xu1  Zhao Cheng1  Junlei Yin1 
[1]Jiangsu Key Laboratory of Zoonosis, Jiangsu Co-innovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonoses, Yangzhou University, Yangzhou 225009, Jiangsu, P R China
关键词: live attenuated vaccine;    Salmonella pathogenicity island 2;    Pullorum disease;    Salmonella enterica serovar Pullorum;   
Others  :  1224422
DOI  :  10.1186/s12917-015-0497-3
 received in 2015-03-30, accepted in 2015-07-16,  发布年份 2015
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【 摘 要 】

Background

Salmonella enterica serovar Pullorum (S. Pullorum) causes Pullorum disease (PD), a severe systemic disease of poultry and results in considerable economic losses in developing countries. In order to develop a safe and immunogenic vaccine, the immunogenicity and protective efficacy of S06004ΔSPI2, a Salmonella pathogenicity island 2 (SPI2) deleted mutant of S. Pullorum was evaluated in 2-day old chickens.

Results

Single intramuscular vaccination with S06004ΔSPI2 (2 × 10 7  CFU) of chickens revealed no differences in body weight or clinical symptoms compared to control group. S06004ΔSPI2 bacteria can colonize and persistent in liver and spleen of vaccinated chickens approximately 14 days, and specific humoral and cellular immune responses were significantly induced. Vaccination of chickens offered efficient protection against S. Pullorum strain S06004 and S. Gallinarum strain SG9 challenge, respectively, at 10 days post vaccination (dpv) based on mortality and clinical symptoms compared to control group.

Conclusions

These findings suggest that S06004ΔSPI2 appears to be a highly immunogenic and efficient live attenuated vaccine candidate.

【 授权许可】

   
2015 Yin et al.

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【 参考文献 】
  • [1]Rettger LF. Further Studies on fatal Septicemia in Young Chickens, or "White Diarrhea.". J Med Res. 1909; 21:115-23.
  • [2]Barrow PA, Freitas Neto OC. Pullorum disease and fowl typhoid--new thoughts on old diseases: a review. Avian Pathol. 2011; 40:1-13.
  • [3]Li J, Smith NH, Nelson K, Crichton PB, Old DC, Whittam TS, Selander RK. Evolutionary origin and radiation of the avian-adapted non-motile salmonellae. J Med Microbiol. 1993; 38:129-39.
  • [4]Baumler AJ, Tsolis RM, Ficht TA, Adams LG. Evolution of host adaptation in Salmonella enterica. Infect Immun. 1998; 66:4579-487.
  • [5]Wigley P, Berchieri A, Page KL, Smith AL, Barrow PA. Salmonella enterica serovar Pullorum persists in splenic macrophages and in the reproductive tract during persistent, disease-free carriage in chickens. Infect Immun. 2001; 69:7873-9.
  • [6]Mastroeni P, Chabalgoity JA, Dunstan SJ, Maskell DJ, Dougan G. Salmonella: immune responses and vaccines. Vet J. 2001; 161:132-64.
  • [7]Galan JE. Salmonella interactions with host cells: type III secretion at work. Annu Rev Cell Dev Bi. 2001; 17:53-86.
  • [8]Waterman SR, Holden DW. Functions and effectors of the Salmonella pathogenicity island 2 type III secretion system. Cell Microbiol. 2003; 5:501-11.
  • [9]Matulova M, Havlickova H, Sisak F, Rychlik I. Vaccination of chickens with Salmonella Pathogenicity Island (SPI) 1 and SPI2 defective mutants of Salmonella enterica serovar Enteritidis. Vaccine. 2012; 30:2090-7.
  • [10]Khan SA, Stratford R, Wu T, McKelvie N, Bellaby T, Hindle Z et al.. Salmonella typhi and S. typhimurium derivatives harbouring deletions in aromatic biosynthesis and Salmonella Pathogenicity Island-2 (SPI-2) genes as vaccines and vectors. Vaccine. 2003; 21:538-48.
  • [11]Boyen F, Pasmans F, Van Immerseel F, Morgan E, Botteldoorn N, Heyndrickx M et al.. A limited role for SsrA/B in persistent Salmonella Typhimurium infections in pigs. Vet Microbiol. 2008; 128:364-73.
  • [12]Coombes BK, Coburn BA, Potter AA, Gomis S, Mirakhur K, Li Y, Finlay BB. Analysis of the contribution of Salmonella pathogenicity islands 1 and 2 to enteric disease progression using a novel bovine ileal loop model and a murine model of infectious enterocolitis. Infect Immun. 2005; 73:7161-9.
  • [13]Dieye Y, Ameiss K, Mellata M, Curtiss R. The Salmonella Pathogenicity Island (SPI) 1 contributes more than SPI2 to the colonization of the chicken by Salmonella enterica serovar Typhimurium. BMC Microbiol. 2009; 9:3. BioMed Central Full Text
  • [14]Karasova D, Sebkova A, Havlickova H, Sisak F, Volf J, Faldyna M et al.. Influence of 5 major Salmonella pathogenicity islands on NK cell depletion in mice infected with Salmonella enterica serovar Enteritidis. BMC Microbiol. 2010; 10:75. BioMed Central Full Text
  • [15]Geng S, Jiao X, Barrow PA, Pan Z, Chen X. Virulence determinants of Salmonella Gallinarum biovar Pullorum identified by PCR signature-tagged mutagenesis and the spiC mutant as a candidate live attenuated vaccine. Vet Microbiol. 2014; 168:388-94.
  • [16]Jones MA, Wigley P, Page KL, Hulme SD, Barrow PA. Salmonella enterica serovar Gallinarum requires the Salmonella pathogenicity island 2 type III secretion system but not the Salmonella pathogenicity island 1 type III secretion system for virulence in chickens. Infect Immun. 2001; 69:5471-6.
  • [17]Datsenko KA, Wanner BL. One-step inactivation of chromosomal genes in Escherichia coli K-12 using PCR products. Proc Natl Acad Sci U S A. 2000; 97:6640-5.
  • [18]Yin J, Wu Y, Lin Z, Wang X, Hu Y, Li Q, et al. Construction and characterization of SPI-2 deletion mutant of Salmonella Pullorum S06004. Wei Sheng Wu Xue Bao. 2015;. 10. 13343/j.cnki.wsxb.20140621 webcite
  • [19]Haneda T, Okada N, Kikuchi Y, Takagi M, Kurotaki T, Miki T et al.. Evaluation of Salmonella enterica serovar Typhimurium and Choleraesuis slyA mutant strains for use in live attenuated oral vaccines. Comp Immunol Microbiol. 2011; 34:399-409.
  • [20]Rana N, Kulshreshtha RC. Cell-mediated and humoral immune responses to a virulent plasmid-cured mutant strain of Salmonella enterica serotype gallinarum in broiler chickens. Vet Microbiol. 2006; 115:156-62.
  • [21]Song H, Yan R, Xu L, Song X, Shah MA, Zhu H, Li X. Efficacy of DNA vaccines carrying Eimeria acervulina lactate dehydrogenase antigen gene against coccidiosis. Exp Parasitol. 2010; 126:224-31.
  • [22]Cirillo DM, Valdivia RH, Monack DM, Falkow S. Macrophage-dependent induction of the Salmonella pathogenicity island 2 type III secretion system and its role in intracellular survival. Mol Microbiol. 1998; 30:175-88.
  • [23]Collins FM, Scott MT. Effect of Corynebacterium parvum treatment on the growth of Salmonella enteritidis in mice. Infect Immun. 1974; 9:863-9.
  • [24]Matsuda K, Chaudhari AA, Lee JH. Evaluation of safety and protection efficacy on cpxR and lon deleted mutant of Salmonella Gallinarum as a live vaccine candidate for fowl typhoid. Vaccine. 2011; 29:668-74.
  • [25]Wigley P, Jones MA, Barrow PA. Salmonella enterica serovar Pullorum requires the Salmonella pathogenicity island 2 type III secretion system for virulence and carriage in the chicken. Avian Pathol. 2002; 31:501-6.
  • [26]Heithoff DM, House JK, Thomson PC, Mahan MJ. Development of a Salmonella cross-protective vaccine for food animal production systems. Vaccine. 2015; 33:100-7.
  • [27]Nandre RM, Lee D, Lee JH. Cross-protection against Salmonella Typhimurium infection conferred by a live attenuated Salmonella Enteritidis vaccine. Can J Vet Res. 2015; 79:16-21.
  • [28]Yin J, Cheng Z, Wang X, Xu L, Li Q, Geng S, Jiao X. Evaluation of Salmonella enterica serovar Pullorum pathogenicity island 2 mutant as a candidate live attenuated oral vaccine. Clin Vaccine Immunol. 2015; 22:706-10.
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