Metabolically Specific In Situ Fluorescent Visualization of Bacterial Infection on Wound Tissues

• Published in: ACS applied materials & interfaces Vol. 14; no. 35; pp. 39808 - 39818
• Main Authors: Zhong, Chen-Jian, Hu, Xi-Le, Yang, Xiao-Lan, Gan, Hui-Qi, Yan, Kai-Cheng, Shu, Fu-Ting, Wei, Pei, Gong, Teng, Luo, Peng-Fei, James, Tony D., Chen, Zhao-Hong, Zheng, Yong-Jun, He, Xiao-Peng, Xia, Zhao-Fan
• Format: Journal Article
• Language: English
• Published: American Chemical Society 07.09.2022
• Subjects: bacterial infections; Biological and Medical Applications of Materials and Interfaces; fluorescence; fluorescent dyes; folic acid; graphene oxide; humans; hydrogels; metabolism; p-aminobenzoic acid; folate; metabolism; wound infection; bacteria; fluorescence imaging
• ISSN: 1944-8244; 1944-8252; 1944-8252
• DOI: 10.1021/acsami.2c10115

The ability to effectively detect bacterial infection in human tissues is important for the timely treatment of the infection. However, traditional techniques fail to visualize bacterial species adhered to host cells in situ in a target-specific manner. Dihydropteroate synthase (DHPS) exclusively exists in bacterial species and metabolically converts p-aminobenzoic acid (PABA) to folic acid (FA). By targeting this bacterium-specific metabolism, we have developed a fluorescent imaging probe, PABA-DCM, based on the conjugation of PABA with a long-wavelength fluorophore, dicyanomethylene 4H-pyran (DCM). We confirmed that the probe can be used in the synthetic pathway of a broad spectrum of Gram-positive and negative bacteria, resulting in a significantly extended retention time in bacterial over mammalian cells. We validated that DHPS catalytically introduces a dihydropteridine group to the amino end of the PABA motif of PABA-DCM, and the resulting adduct leads to an increase in the FA levels of bacteria. We also constructed a hydrogel dressing containing PABA-DCM and graphene oxide (GO), termed PABA-DCM@GO, that achieves target-specific fluorescence visualization of bacterial infection on the wounded tissues of mice. Our research paves the way for the development of fluorescent imaging agents that target species-conserved metabolic pathways of microorganisms for the in situ monitoring of infections in human tissues.