Recombinant-attenuated Salmonella enterica serovar Choleraesuis vector expressing the PlpE protein of Pasteurella multocida protects mice from lethal challenge

被引:2
作者
Zhou, Guodong [1 ,2 ]
Tian, Jiashuo [1 ,2 ]
Tian, Yichen [1 ,2 ]
Ma, Qifeng [1 ,2 ]
Li, Quan [1 ,2 ]
Wang, Shifeng [3 ]
Shi, Huoying [1 ,2 ,4 ]
机构
[1] Yangzhou Univ, Coll Vet Med, Yangzhou 225009, Jiangsu, Peoples R China
[2] Jiangsu Coinnovat Ctr Prevent & Control Important, Yangzhou 225009, Peoples R China
[3] Univ Florida, Coll Vet Med, Dept Infect Dis & Immunol, Gainesville, FL 32611 USA
[4] Yangzhou Univ JIRLAAPS, Joint Int Res Lab Agr & Agriprod Safety, Yangzhou, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
Recombinant attenuated Salmonella vaccine; P; multocida; PlpE; Vaccine candidate; Immune responses; IMMUNE-RESPONSES; RESPIRATORY-DISEASE; LIPOPROTEIN-E; IMMUNOGENICITY; SWINE; PHAGOCYTOSIS; IMMUNIZATION; SEROGROUP; EFFICACY; VACCINES;
D O I
10.1186/s12917-023-03679-0
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
BackgroundBacterial surface proteins play key roles in pathogenicity and often contribute to microbial adhesion and invasion. Pasteurella lipoprotein E (PlpE), a Pasteurella multocida (P. multocida) surface protein, has recently been identified as a potential vaccine candidate. Live attenuated Salmonella strains have a number of potential advantages as vaccine vectors, including immunization with live vector can mimic natural infections by organisms, lead to the induction of mucosal, humoral, and cellular immune responses. In this study, a previously constructed recombinant attenuated Salmonella Choleraesuis (S. Choleraesuis) vector rSC0016 was used to synthesize and secrete the surface protein PlpE of P. multocida to form the vaccine candidate rSC0016(pS-PlpE). Subsequently, the immunogenicity of S. Choleraesuis rSC0016(pS-PlpE) as an oral vaccine to induce protective immunity against P. multocida in mice was evaluated.ResultsAfter immunization, the recombinant attenuated S. Choleraesuis vector can efficiently delivered P. multocida PlpE protein in vivo and induced a specific immune response against this heterologous antigen in mice. In addition, compared with the inactivated vaccine, empty vector (rSC0016(pYA3493)) and PBS immunized groups, the rSC0016(pS-PlpE) vaccine candidate group induced higher antigen-specific mucosal, humoral and mixed Th1/Th2 cellular immune responses. After intraperitoneal challenge, the rSC0016(pS-PlpE) immunized group had a markedly enhanced survival rate (80%), a better protection efficiency than 60% of the inactivated vaccine group, and significantly reduced tissue damage.ConclusionsIn conclusion, our study found that the rSC0016(pS-PlpE) vaccine candidate provided good protection against challenge with wild-type P. multocida serotype A in a mouse infection model, and may potentially be considered for use as a universal vaccine against multiple serotypes of P. multocida in livestock, including pigs.
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页数:13
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