Bashiri Roghayeh, Jahangiri Abolfazl, Masoomkhani Saeede, Rasooli Iraj
Department of Biology, Faculty of Basic Sciences, Shahed University, Tehran, Iran.
Applied Microbiology Research Center, Biomedicine Technologies Institute, Baqiyatallah University of Medical Sciences, Tehran, Iran.
Curr Microbiol. 2025 May 19;82(7):292. doi: 10.1007/s00284-025-04275-1.
The overuse of antibiotics has led to antibiotic-resistant Acinetobacter baumannii. This study evaluated the protective effect of a recombinant protein, derived from Omp34's loop 3 repeats, as a potential vaccine candidate against A. baumannii in a murine sepsis model. Recombinant Omp34 and L3 × 5 proteins were expressed in E. coli BL21 using the autoinduction method. The proteins were then purified and verified. To assess their protective efficacy, the proteins were injected into BALB/c mice, and the vaccine's effectiveness in both prevention and treatment stages was evaluated in a murine sepsis model against an infection caused by a clinical strain of A. baumannii. The study shows that recombinant proteins Omp34 and Omp34L3 × 5 have protective and immunogenic properties against A. baumannii. Using the immunogen loop 3, rather than the mature Omp34 protein, to stimulate the immune system yielded promising results. Omp34 offered superior protection, likely through B- and T-cell activation, while L3 × 5, though less protective, induced significant antibody production and recognized the clinical strain, warranting further research. The study highlights the potential of recombinant proteins Omp34 and Omp34L3 × 5 as vaccine candidates against A. baumannii. Omp34 provided stronger protection in mouse sepsis models, likely due to its activation of both B- and T-cell responses. While Omp34L3 × 5 was less protective, it still produced significant antibodies and recognized clinical strains. The results emphasize the need for further research into these proteins to develop vaccines or treatments against A. baumannii infections.
抗生素的过度使用已导致产生对多种抗生素耐药的鲍曼不动杆菌。本研究评估了一种源自Omp34的环3重复序列的重组蛋白作为抗鲍曼不动杆菌潜在疫苗候选物在小鼠败血症模型中的保护作用。使用自诱导方法在大肠杆菌BL21中表达重组Omp34和L3×5蛋白。然后对这些蛋白进行纯化和验证。为评估其保护效力,将这些蛋白注射到BALB/c小鼠体内,并在小鼠败血症模型中评估该疫苗在预防和治疗阶段针对临床分离的鲍曼不动杆菌感染的有效性。研究表明,重组蛋白Omp34和Omp34L3×5对鲍曼不动杆菌具有保护和免疫原性特性。使用免疫原性环3而非成熟的Omp34蛋白来刺激免疫系统产生了有前景的结果。Omp34可能通过激活B细胞和T细胞提供了更好的保护,而L3×5虽然保护作用较弱,但诱导产生了大量抗体并能识别临床菌株,值得进一步研究。该研究突出了重组蛋白Omp34和Omp34L3×5作为抗鲍曼不动杆菌疫苗候选物的潜力。Omp34在小鼠败血症模型中提供了更强的保护,可能是由于其激活了B细胞和T细胞反应。虽然Omp34L3×5的保护作用较弱,但它仍产生了大量抗体并能识别临床菌株。结果强调需要对这些蛋白进行进一步研究,以开发针对鲍曼不动杆菌感染的疫苗或治疗方法。