A chimeric vaccine targeting Pseudomonas aeruginosa virulence factors protects mice against lethal infection

被引:9
作者
Korpi, Fatemeh [1 ]
Irajian, Gholamreza [1 ,2 ]
Forouhi, Fatemeh [1 ]
Mohammadian, Taher [1 ]
机构
[1] Islamic Azad Univ, Fac Basic Sci, Dept Cell & Mol Biol, Shahre Qods Branch, Tehran, Iran
[2] Iran Univ Med Sci, Sch Med, Dept Microbiol, Tehran, Iran
关键词
Pseudomonas aeruginosa; OprF; PcrV; Flagellin; Acute pneumonia; LUNG INFECTION; ACUTE PNEUMONIA; B FLAGELLIN; IMMUNIZATION; ADJUVANT; IMMUNOTHERAPY; PATHOGENESIS; CELLS; OPRF; LIPOPOLYSACCHARIDE;
D O I
10.1016/j.micpath.2023.106033
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Pseudomonas aeruginosa is an important and hazardous nosocomial pathogen in respiratory tract infections and rapidly achieves antibiotic resistance, so it is necessary to develop an effective vaccine to combat the infection. The Type III secretion system (T3SS) protein P. aeruginosa V-antigen (PcrV), outer membrane protein F (OprF), and two kinds of flagellins (FlaA and FlaB) all play important roles in the pathogenesis of P. aeruginosa lung infection and its spread into deeper tissues. In a mouse acute pneumonia model, the protective effects of a chimer vaccine including PcrV, FlaA, FlaB, and OprF (PABF) protein were investigated. PABF immunization prompted robust opsonophagocytic titer of IgG antibodies and decreased bacterial burden, and improved survival after-ward intranasal challenge with ten times 50% lethal doses (LD50) of P. aeruginosa strains, indicating its broad-spectrum immunity. Moreover, these findings showed a promise chimeric vaccine candidate to treat and control P. aeruginosa infections.
引用
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页数:10
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