Effects of Yersinia pseudotuberculosis outer membrane vesicles on Pseudomonas aeruginosa antigens immune response

Zhongxu Duan1,2, Jingqi Song1, Mingru Zhang1

  • 1Engineering Research Center of Bioreactor and Drug Development, Ministry of Education, College of Life Sciences, Jilin Agricultural University, Changchun, China.

Plos One
|December 20, 2024
PubMed

Insights

Outer membrane vesicles (OMVs) from Yersinia pseudotuberculosis carrying Pseudomonas aeruginosa antigens elicited balanced immune responses. Recombinant OMVs with PcrV antigen provided superior protection against Pseudomonas aeruginosa lung infection in mice.

Area of Science:

  • Bacteriology
  • Immunology
  • Vaccine Development

Background:

  • Outer membrane vesicles (OMVs) are self-adjuvanting, immunogenic nanoparticles produced by Gram-negative bacteria.
  • The immunomodulatory effects of OMVs when combined with specific antigens require further investigation.
  • Pseudomonas aeruginosa is an opportunistic pathogen causing severe infections, necessitating novel vaccine strategies.

Purpose of the Study:

  • To evaluate the immune response and protective efficacy of recombinant OMVs (rOMVs) derived from Yersinia pseudotuberculosis expressing Pseudomonas aeruginosa antigens.
  • To compare the efficacy of rOMVs carrying PcrV (rOMVyp2P) versus OprF/I (rOMVyp2F) against P. aeruginosa infection.

Main Methods:

  • Construction of a recombinant Yersinia pseudotuberculosis ΔlpxL strain expressing PcrV or OprF/I antigens.
  • Purification of ΔlpxL rOMVPcrV (rOMVyp2P) and ΔlpxL rOMVOprF/I (rOMVyp2F).
  • Analysis of humoral and cellular immune responses, and survival rates in a mouse model of P. aeruginosa PAO1 pulmonary infection.

Main Results:

  • Both rOMVyp2P and rOMVyp2F facilitated humoral immune responses against PcrV and OprF/I antigens, respectively.
  • rOMVs induced a balanced Th1/Th2 immune response, with elevated IgM and IgA antibody levels.
  • ΔlpxL rOMVPcrV demonstrated significantly better protection against P. aeruginosa pulmonary infection, with a 20% survival rate compared to the ΔlpxL rOMVOprF/I group.

Conclusions:

  • Recombinant Yersinia pseudotuberculosis OMVs can effectively present Pseudomonas aeruginosa antigens and elicit robust immune responses.
  • ΔlpxL rOMVPcrV shows enhanced efficacy in conferring pulmonary immune protection against Pseudomonas aeruginosa infection.
  • These findings suggest potential for developing OMV-based vaccines against P. aeruginosa.