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Evaluation of a Salmonella strain lacking the secondary messenger c-di-GMP and RpoS as a live oral vaccine
- Source :
- Academica-e: Repositorio Institucional de la Universidad Pública de Navarra, Universidad Pública de Navarra, PLoS ONE, Vol 11, Iss 8, p e0161216 (2016), Digital.CSIC. Repositorio Institucional del CSIC, instname, Academica-e. Repositorio Institucional de la Universidad Pública de Navarra, PLoS ONE
- Publication Year :
- 2016
- Publisher :
- Public Library of Science, 2016.
-
Abstract
- Salmonellosis is one of the most important bacterial zoonotic diseases transmitted through the consumption of contaminated food, with chicken and pig related products being key reservoirs of infection. Although numerous studies on animal vaccination have been performed in order to reduce Salmonella prevalence, there is still a need for an ideal vaccine. Here, with the aim of constructing a novel live attenuated Salmonella vaccine candidate, we firstly analyzed the impact of the absence of cyclic-di-GMP (c-di-GMP) in Salmonella virulence. Cdi- GMP is an intracellular second messenger that controls a wide range of bacterial processes, including biofilm formation and synthesis of virulence factors, and also modulates the host innate immune response. Our results showed that a Salmonella multiple mutant in the twelve genes encoding diguanylate cyclase proteins that, as a consequence, cannot synthesize c-di-GMP, presents a moderate attenuation in a systemic murine infection model. An additional mutation of the rpoS gene resulted in a synergic attenuating effect that led to a highly attenuated strain, referred to as ΔXIII, immunogenic enough to protect mice against a lethal oral challenge of a S. Typhimurium virulent strain. ΔXIII immunogenicity relied on activation of both antibody and cell mediated immune responses characterized by the production of opsonizing antibodies and the induction of significant levels of IFN-γ, TNF-α, IL-2, IL-17 and IL-10. ΔXIII was unable to form a biofilm and did not survive under desiccation conditions, indicating that it could be easily eliminated from the environment. Moreover, ΔXIII shows DIVA features that allow differentiation of infected and vaccinated animals. Altogether, these results show ΔXIII as a safe and effective live DIVA vaccine.<br />SB is a predoctoral fellow from the Public University of Navarra. CG and BG are recipients of a postdoctoral contract under Grants IIM 13329.RI1 and BIO2011-30503-C02-02, respectively. This work was supported by grant IIM 13329.RI1 from the Departamento de Innovación, Empresa y Empleo, Government of Navarra and grants BIO2011-30503-C02-02 and BIO2014-53530-R from the Spanish Ministry of Economy and Competitiveness.
- Subjects :
- Bacterial Diseases
0301 basic medicine
Salmonella typhimurium
Salmonella
Salmonellosis
Physiology
Administration, Oral
lcsh:Medicine
Pathology and Laboratory Medicine
medicine.disease_cause
Mouse models
Biochemistry
Mice
Immune Physiology
Medicine and Health Sciences
Public and Occupational Health
Enzyme-linked immunoassays
lcsh:Science
Cyclic GMP
Mice, Inbred BALB C
Innate Immune System
Vaccines
Immune System Proteins
Multidisciplinary
Immunogenicity
Interleukin-17
Animal Models
Salmonella vaccine
Vaccination and Immunization
Interleukin-10
Bacterial Pathogens
Vaccination
Infectious Diseases
Medical Microbiology
Cytokines
Female
Pathogens
Research Article
Salmonella Vaccines
Immunology
030106 microbiology
Virulence
Sigma Factor
Vaccines, Attenuated
Research and Analysis Methods
Microbiology
Antibodies
Interferon-gamma
03 medical and health sciences
Model Organisms
Immune system
Bacterial Proteins
Enterobacteriaceae
medicine
Animals
Immunoassays
Microbial Pathogens
Salmonella Infections, Animal
Innate immune system
Bacteria
Tumor Necrosis Factor-alpha
business.industry
lcsh:R
Organisms
Biology and Life Sciences
Proteins
Molecular Development
Virology
030104 developmental biology
Immune System
Immunologic Techniques
Interleukin-2
lcsh:Q
Preventive Medicine
business
rpoS
Developmental Biology
Subjects
Details
- Database :
- OpenAIRE
- Journal :
- Academica-e: Repositorio Institucional de la Universidad Pública de Navarra, Universidad Pública de Navarra, PLoS ONE, Vol 11, Iss 8, p e0161216 (2016), Digital.CSIC. Repositorio Institucional del CSIC, instname, Academica-e. Repositorio Institucional de la Universidad Pública de Navarra, PLoS ONE
- Accession number :
- edsair.doi.dedup.....9bf24678f31b2e4ba66c282a75d2628a