Pseudomonas aeruginosa elongation factor-Tu (EF-Tu) is an immunogenic protective protein antigen

被引:0
|
作者
Moustafa, Dina A. [1 ]
Lou, Emma [2 ]
Schafer-Kestenman, Morgan E. [1 ]
Mateu-Borras, Margalida [3 ]
Domenech-Sanchez, Antonio [3 ]
Alberti, Sebastian [3 ]
Goldberg, Joanna B. [1 ]
机构
[1] Emory Univ, Emory Childrens Cyst Fibrosis Ctr, Dept Pediat, Div Pulm Asthma Cyst Fibrosis & Sleep,Sch Med, Atlanta, GA USA
[2] Emory Univ, Dept Biol, Atlanta, GA USA
[3] Univ Islas Baleares, Inst Univ Invest Ciencias Salud IUNICS, Palma De Mallorca, Spain
基金
美国国家卫生研究院;
关键词
Pseudomonas aeruginosa; Elongation factor-Tu; Vaccine candidate; Passive immunotherapy; Acute pneumonia; IMMUNOREACTIVE PROTEINS; FACTOR-H; IDENTIFICATION; ACTIVATION; MEMBRANE; BINDING; INTERACTS; VECTORS; LONG;
D O I
10.1016/j.vaccine.2024.126476
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 a Gram-negative, opportunistic pathogen that infects immunocompromised individuals, especially in the hospital setting. This bacterium is an important pathogen in people with weakened immune systems, injuries, and other underlying physiologic dysfunctions. P. aeruginosa is responsible for up to 20 % of all hospital-acquired pneumonias. It is one of the major causes of nosocomial infections and has been noted to be one of the most common bacteria co-infecting patients with COVID-19 or causing super-infections following COVID-19 infections. Despite improvements in antimicrobial therapy and hospital care, P. aeruginosa bacteremia and pneumonia remain fatal in about 30 % of cases. P. aeruginosa is also the leading cause of chronic life-threatening lung infections in cystic fibrosis patients. This bacterium is naturally antibiotic resistant, and infections are notoriously difficult to treat once established, with no vaccine available. We have previously shown that elongation factor-Tu (EF-Tu), a protein best known for its role in protein synthesis, is surface exposed on P. aeruginosa. As this protein is highly expressed, evolutionally conserved, and essential, we hypothesized it would make a good vaccine target. In this study, we found that P. aeruginosa EF-Tu is immunogenic in people, and that mice can develop an immune response following immunization with recombinant P. aeruginosa EF-Tu. Furthermore, immunized mice were protected from subsequent P. aeruginosa pneumonia and transfer of this vaccine antisera to na & iuml;ve mice resulted in decreased colonization. Altogether these findings support the consideration of EF-Tu as a new vaccine candidate against P. aeruginosa.
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页数:9
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