Niu Mengya, Zhao Luo, Gong Shuang, Liu Xinxin, Zheng Cuixia, Jiao Jiannan, Wang Fangfang, Wang Lei
School of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, 450001, China.
Henan Key Laboratory of Nanomedicine for Targeting Diagnosis and Treatment, Zhengzhou, 450001, China.
J Nanobiotechnology. 2025 May 26;23(1):378. doi: 10.1186/s12951-025-03468-x.
Salmonella Typhimurium (S. Tm), a Gram-negative pathogenic bacterium, is one of the most common causes of invasive bacterial diseases. Antibiotic therapy remains the principal therapeutic modality for treating S. Tm infection. However, due to the difficulty in precisely targeted pathogenic bacteria after oral administration, the therapeutic effect remains unsatisfactory. Here, we developed an oral probiotic spores-based biohybrid delivery system (BCs@PME-Au) to treat S. Tm-induced colitis. By employing a one-pot metal deposition method, Polymyxin E (PME) acted as a reducing agent to promote the Au rapid nucleation and growth into PME-capped Au NPs (PME-Au NPs). By forming Au-S and Au-N bonds with the active sites (-SH, -NH) of Bacillus coagulans spores (BCs), PME-Au NPs were anchored onto the surface of BCs to construct the biohybrid system BCs@PME-Au. Following oral administration, BCs@PME-Au successfully passed through the gastric acid barrier. After absorbed water and nutrients, BCs germinated into Bacillus coagulans (BC) in the gut and PME-Au NPs were released. Based on the BC's targeting pathogen infection site and PME-Au NPs' targeting Gram-negative bacteria, the biohybrid system achieved significantly antibacterial effect of S. Tm. Mechanistically, by blocked the LPS-induced inflammatory pathway TLR4/MyD88/NF-κB, BCs@PME-Au exerted a powerful anti-inflammatory effect. With its robust antibacterial efficacy, targeted delivery, and excellent safety profile demonstrated both in vitro and in vivo, the biohybrid system BCs@PME-Au offers significant promise in treating bacterial colitis.
鼠伤寒沙门氏菌(S. Tm)是一种革兰氏阴性病原菌,是侵袭性细菌疾病最常见的病因之一。抗生素治疗仍然是治疗鼠伤寒沙门氏菌感染的主要治疗方式。然而,由于口服给药后难以精确靶向病原菌,治疗效果仍不尽人意。在此,我们开发了一种基于口服益生菌孢子的生物杂交递送系统(BCs@PME-Au)来治疗鼠伤寒沙门氏菌诱导的结肠炎。通过采用一锅法金属沉积方法,多粘菌素E(PME)作为还原剂促进金快速成核并生长为PME包覆的金纳米颗粒(PME-Au NPs)。通过与凝结芽孢杆菌孢子(BCs)的活性位点(-SH,-NH)形成Au-S和Au-N键,PME-Au NPs锚定在BCs表面以构建生物杂交系统BCs@PME-Au。口服给药后,BCs@PME-Au成功穿过胃酸屏障。吸收水分和营养后,BCs在肠道中萌发为凝结芽孢杆菌(BC)并释放出PME-Au NPs。基于BC对病原体感染部位的靶向作用以及PME-Au NPs对革兰氏阴性菌的靶向作用,该生物杂交系统对鼠伤寒沙门氏菌具有显著的抗菌效果。从机制上讲,通过阻断LPS诱导的炎症途径TLR4/MyD88/NF-κB,BCs@PME-Au发挥了强大的抗炎作用。凭借其强大的抗菌功效、靶向递送以及在体外和体内均表现出的优异安全性,生物杂交系统BCs@PME-Au在治疗细菌性结肠炎方面具有巨大的潜力。