KbvR mutant of Klebsiella pneumoniae affects the synthesis of type 1 fimbriae and provides protection to mice as a live attenuated vaccine

Klebsiella pneumoniae is a leading cause of severe infections in humans and animals, and the emergence of multidrug-resistant strains highlights the need to develop effective vaccines for preventing such infections. Live attenuated vaccines are attractive vaccine candidates available in the veterinary field. We recently characterized that the K. pneumoniae kbvR ( K lebsiella biofilm and virulence regulator) mutant was a highly attenuated strain in the mice model. In the present study, the characterization, safety, and protective efficacy of Δ kbvR strain as a live attenuated vaccine were evaluated. The synthesis and activity of type 1 fimbriae were increased in the Δ kbvR strain. All mice inoculated by the subcutaneous route with 10 5 , 10 6 , and 10 7 colony-forming units (CFU) doses of the Δ kbvR strain survived. Subcutaneous immunization with two doses of 10 5 or 10 7 CFU Δ kbvR elicited a robust humoral immune response, and provided protection against the following K. pneumoniae intraperitoneal infection. The antisera of mice immunized with 10 5 CFU dose improved the opsonophagocytic ability and complement-mediated lysis not only to the same serotype strain but also to the different serotype strain. The passive transfer of antisera from 10 5 CFU dose-immunized mice provided protection against K. pneumoniae infection. Overall, our results suggest the great potential of the Δ kbvR strain as a novel vaccine candidate against K. pneumoniae infections in herds or humans.