SitA contributes to the virulence of Klebsiella pneumoniae in a mouse infection model |
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Affiliation: | 1. Medical University of Sofia, Medical Faculty, Department of Medical Microbiology, Bulgaria;2. Medical University of Varna, Department of Microbiology and Virology, University Multiprofile Hospital for Active Treatment (UMHAT), St Marina, Varna, Bulgaria;3. MICOER-Institute, Munich, Germany;4. Department of Clinical Microbiology, Medical Institute - Ministry of the Interior, Sofia, Bulgaria;5. Molecular Medicine Center, Medical University of Sofia, Sofia, Bulgaria;6. Medical University of Plovdiv, Department of Microbiology and Immunology, UMHAT, “St George”, Plovdiv, Bulgaria;7. Medical University of Pleven, Department of Microbiology and Virology, UMHAT “Georgi Stranski”, Pleven, Bulgaria;8. Emergency Medical Institute “Pirogov”, Sofia, Bulgaria;9. Second Multiprofile Hospital for Active Treatment, Sofia, Bulgaria;10. UMHAT “Prof. dr St Kirkovich” Stara Zagora, Thracian University, Stara Zagora, Bulgaria |
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Abstract: | Klebsiella pneumoniae is an opportunistic pathogen, which causes a wide range of nosocomial infections. Recently, antibiotic resistance makes K. pneumoniae infection difficult to deal with. Investigation on virulence determinants of K. pneumoniae can provide more information about pathogenesis and unveil new targets for treatment or vaccine development. In this study, SitA, a Fur-regulated divalent cation transporter, was found significantly increased when K. pneumoniae was cultured in a nutrient-limited condition. A sitA-deletion strain (ΔsitA) was created to characterize the importance of SitA in virulence. ΔsitA showed higher sensitivity toward hydroperoxide than its parental strain. In a mouse intraperitoneal infection model, the survival rate of mice infected with ΔsitA strain increased greatly when compared with that of mice infected with the parental strain, suggesting that sitA deletion attenuates the bacterial virulence in vivo. To test whether ΔsitA strain is a potential vaccine candidate, mice were immunized with inactivated bacteria and then challenged with the wild-type strain. The results showed that using ΔsitA mutant protected mice better than using the wild-type strain or the capsule-negative congenic bacteria. In summary, SitA was found being important for the growth of K. pneumoniae in vivo and deleting sitA might be a potential approach to generate vaccines against K. pneumoniae. |
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Keywords: | Virulence determinant SitA Vaccination Mouse intraperitoneal infection cfu" },{" #name" :" keyword" ," $" :{" id" :" kwrd0040" }," $$" :[{" #name" :" text" ," _" :" colony-forming unit CPS" },{" #name" :" keyword" ," $" :{" id" :" kwrd0050" }," $$" :[{" #name" :" text" ," _" :" capsule polysaccharide 2-D" },{" #name" :" keyword" ," $" :{" id" :" kwrd0060" }," $$" :[{" #name" :" text" ," _" :" two-dimensional DMEM" },{" #name" :" keyword" ," $" :{" id" :" kwrd0070" }," $$" :[{" #name" :" text" ," _" :" Dulbecco's Modified Eagle's Medium Kp K2044" },{" #name" :" keyword" ," $" :{" id" :" kwrd0080" }," $$" :[{" #name" :" text" ," $$" :[{" #name" :" italic" ," _" :" Klebsiella pneumoniae" },{" #name" :" __text__" ," _" :" strain NTUH-K2044 LB broth" },{" #name" :" keyword" ," $" :{" id" :" kwrd0090" }," $$" :[{" #name" :" text" ," _" :" Luria–Bertani broth OMVs" },{" #name" :" keyword" ," $" :{" id" :" kwrd0100" }," $$" :[{" #name" :" text" ," _" :" outer membrane vesicles Q-TOF" },{" #name" :" keyword" ," $" :{" id" :" kwrd0110" }," $$" :[{" #name" :" text" ," _" :" quadrupole time-of-flight |
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