Oral vaccination with LcrV from Yersinia pestis KIM delivered by live attenuated Salmonella enterica serovar Typhimurium elicits a protective immune response against challenge with Yersinia pseudotuberculosis and Yersinia enterocolitica
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Branger, Christine G.
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Ctr Infect Dis & Vaccinol, Biodesign Inst, Tempe, AZ 85287 USA
Sch Life Sci, Tempe, AZ 85287 USACtr Infect Dis & Vaccinol, Biodesign Inst, Tempe, AZ 85287 USA
Branger, Christine G.
[1
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Torres-Escobar, Ascencion
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Ctr Infect Dis & Vaccinol, Biodesign Inst, Tempe, AZ 85287 USA
Sch Life Sci, Tempe, AZ 85287 USACtr Infect Dis & Vaccinol, Biodesign Inst, Tempe, AZ 85287 USA
Torres-Escobar, Ascencion
[1
,2
]
Sun, Wei
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Ctr Infect Dis & Vaccinol, Biodesign Inst, Tempe, AZ 85287 USA
Sch Life Sci, Tempe, AZ 85287 USACtr Infect Dis & Vaccinol, Biodesign Inst, Tempe, AZ 85287 USA
Sun, Wei
[1
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]
Perry, Robert
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Univ Kentucky, Dept Microbiol Mol Genet & Immunol, Lexington, KY 40536 USACtr Infect Dis & Vaccinol, Biodesign Inst, Tempe, AZ 85287 USA
Perry, Robert
[3
]
Fetherston, Jacqueline
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Univ Kentucky, Dept Microbiol Mol Genet & Immunol, Lexington, KY 40536 USACtr Infect Dis & Vaccinol, Biodesign Inst, Tempe, AZ 85287 USA
Fetherston, Jacqueline
[3
]
Roland, Kenneth L.
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Ctr Infect Dis & Vaccinol, Biodesign Inst, Tempe, AZ 85287 USA
Sch Life Sci, Tempe, AZ 85287 USACtr Infect Dis & Vaccinol, Biodesign Inst, Tempe, AZ 85287 USA
Roland, Kenneth L.
[1
,2
]
Curtiss, Roy, III
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Ctr Infect Dis & Vaccinol, Biodesign Inst, Tempe, AZ 85287 USA
Sch Life Sci, Tempe, AZ 85287 USACtr Infect Dis & Vaccinol, Biodesign Inst, Tempe, AZ 85287 USA
Curtiss, Roy, III
[1
,2
]
机构:
[1] Ctr Infect Dis & Vaccinol, Biodesign Inst, Tempe, AZ 85287 USA
[2] Sch Life Sci, Tempe, AZ 85287 USA
[3] Univ Kentucky, Dept Microbiol Mol Genet & Immunol, Lexington, KY 40536 USA
The use of live recombinant attenuated Salmonella vaccines (RASV) synthesizing Yersinia proteins is a promising approach for controlling infection by Yersinia species. In this study, we constructed attenuated Salmonella strains which synthesize a truncated form of LcrV, LcrV196 and evaluated the immune response and protective efficacy elicited by these strains in mice against two other major species of Yersinia: Yersinia pseudotuberculosis and Yersinia enterocolitica. Surprisingly, we found that the RASV strain alone was sufficient to afford nearly full protection against challenge with Y. pseudotuberculosis, indicating the likelihood that Salmonella produces immunogenic cross-protective antigens. In contrast, IcrV196 expression was required for protection against challenge with Y. enterocolitica strain 8081, but was not sufficient to achieve significant protection against challenge with Y enterocolitica strain WA, which expressed a divergent form of IcrV. Nevertheless, we are encouraged by these findings to continue pursuing our long-term goal of developing a single vaccine to protect against all three human pathogenic species of Yersinia. (C) 2009 Elsevier Ltd. All rights reserved.