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近红外二区荧光成像体内动态监测细菌感染

In Vivo Dynamic Monitoring of Bacterial Infection by NIR-II Fluorescence Imaging.

机构信息

Institute of Sports Medicine of Fudan University, Department of Orthopaedic Sports Medicine, Huashan Hospital, Fudan University, Shanghai, 200040, China.

Institute of Antibiotics, Huashan Hospital, Key Laboratory of Clinical Pharmacology of Antibiotics, National Health Commission, Fudan University, Shanghai, 200040, China.

出版信息

Small. 2020 Aug;16(34):e2002054. doi: 10.1002/smll.202002054. Epub 2020 Jul 26.

Abstract

Time window of antibiotic administration is a critical but long-neglected point in the treatment of bacterial infection, as unnecessary prolonged antibiotics are increasingly causing catastrophic drug-resistance. Here, a second near-infrared (NIR-II) fluorescence imaging strategy based on lead sulfide quantum dots (PbS QDs) is presented to dynamically monitor bacterial infection in vivo in a real-time manner. The prepared PbS QDs not only provide a low detection limit (10 CFU mL ) of four typical bacteria strains in vitro but also show a particularly high labeling efficiency with Escherichia coli (E. coli). The NIR-II in vivo imaging results reveal that the number of invading bacteria first decreases after post-injection, then increases from 1 d to 1 week and drop again over time in infected mouse models. Meanwhile, there is a simultaneous variation of dendritic cells, neutrophils, macrophages, and CD8+ T lymphocytes against bacterial infection at the same time points. Notably, the infected mouse self-heals eventually without antibiotic treatment, as a robust immune system can successfully prevent further health deterioration. The NIR-II imaging approach enables real-time monitoring of bacterial infection in vivo, thus facilitating spatiotemporal deciphering of time window for antibiotic treatment.

摘要

抗生素给药时间窗是治疗细菌感染的一个关键但长期被忽视的要点,因为不必要的抗生素延长使用正导致灾难性的耐药性越来越严重。在这里,提出了一种基于硫化铅量子点(PbS QDs)的第二种近红外二区(NIR-II)荧光成像策略,以实时动态监测体内细菌感染。所制备的 PbS QDs 不仅在体外对四种典型细菌菌株的检测下限低(10 CFU mL ),而且对大肠杆菌(E. coli)具有特别高的标记效率。体内 NIR-II 成像结果表明,在感染的小鼠模型中,注入后入侵细菌的数量先减少,然后在 1 天到 1 周之间增加,随着时间的推移再次下降。同时,树突状细胞、嗜中性粒细胞、巨噬细胞和 CD8+T 淋巴细胞针对细菌感染的数量也同时发生变化。值得注意的是,受感染的小鼠最终无需抗生素治疗即可自行治愈,因为强大的免疫系统可以成功防止病情进一步恶化。该 NIR-II 成像方法能够实时监测体内细菌感染,从而有助于对抗生素治疗时间窗进行时空解析。

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