Oral Delivery of Novel Recombinant Lactobacillus Elicit High Protection against Staphylococcus aureus Pulmonary and Skin Infections
Open Access
Abstract
Staphylococcus aureus is a leading cause of nosocomial and community-associated infection worldwide; however, there is no licensed vaccine available. S. aureus initiates infection via the mucosa; therefore, a mucosal vaccine is likely to be a promising approach against S. aureus infection. Lactobacilli, a non-pathogenic bacterium, has gained increasing interest as a mucosal delivery vehicle. Hence, we attempted to develop an oral S. aureus vaccine based on lactobacilli to cushion the stress of drug resistance and vaccine needs. In this study, we designed, constructed, and evaluated recombinant Lactobacillus strains synthesizing S. aureus nontoxic mutated α-hemolysins (HlaH35L). The results from animal clinical trials showed that recombinant Lactobacillus can persist for at least 72 h and can stably express heterologous protein in vivo. Recombinant L. plantarum WXD234 (pNZ8148-Hla) could induce robust mucosal immunity in the GALT, as evidenced by a significant increase in IgA and IL-17 production and the strong proliferation of T-lymphocytes derived from Peyer’s patches. WXD234 (pNZ8148-Hla) conferred up to 83% protection against S. aureus pulmonary infection and significantly reduced the abscess size in a S. aureus skin infection model. Of particular interest is the sharp reduction of the protective effect offered by WXD234 (pNZ8148-Hla) vaccination in γδ T cell-deficient or IL-17-deficient mice. In conclusion, for the first time, genetically engineered Lactobacillus WXD234 (pNZ8148-Hla) as an oral vaccine induced superior mucosal immunity, which was associated with high protection against pulmonary and skin infections caused by S. aureus. Taken together, our findings suggest the great potential for a delivery system based on lactobacilli and provide experimental data for the development of mucosal vaccines for S. aureus.Keywords
Funding Information
- National Natural Science Foundation of China (32060800, 31660706)
- Research Program of Science and Technology at Universities of Inner Mongolia Autonomous Region (2019ZD031, zdzx2018065)
This publication has 80 references indexed in Scilit:
- Th17 Cells in Immunity and AutoimmunityJournal of Immunology Research, 2013
- Role of gamma-delta T cells in host response against Staphylococcus aureus-induced pneumoniaBMC Immunology, 2012
- Targeting of Alpha‐Hemolysin by Active or Passive Immunization Decreases Severity of USA300 Skin Infection in a Mouse ModelThe Journal of Infectious Diseases, 2010
- IL-17 is essential for host defense against cutaneous Staphylococcus aureus infection in miceJournal of Clinical Investigation, 2010
- Differentiation of Effector CD4 T Cell PopulationsAnnual Review of Immunology, 2010
- Dendritic cell targeting ofBacillus anthracisprotective antigen expressed byLactobacillus acidophilusprotects mice from lethal challengeProceedings of the National Academy of Sciences, 2009
- Basis for the barrier abnormality in atopic dermatitis: Outside-inside-outside pathogenic mechanismsJournal of Allergy and Clinical Immunology, 2008
- Vaccine protection againstStaphylococcus aureuspneumoniaJournal of Experimental Medicine, 2008
- Controlling Endemic Cholera with Oral VaccinesPLOS Medicine, 2007
- Reciprocal developmental pathways for the generation of pathogenic effector TH17 and regulatory T cellsNature, 2006