In Situ Photoacoustic Visualization of Pneumonia Induced by MRSA and Specific Identifying Tumor-Homing Bacteria

Optical imaging holds great promise for monitoring Bacterial infectious processes and drug resistance with high temporal-spatial resolution. Currently, the diagnosis of deep-seated Bacterial infections in vivo with fluorescence imaging, including near-infrared (NIR) fluorescence imaging technology, remains a significant challenge due to its limited tissue penetration depth. In this study, we developed a highly specific targeting probe, Cy7-Neo-NO₂, by conjugating a Bacterial 16S rRNA-targeted moiety, neomycin, with a Bacterial nitroreductase (NTR)-activated NIR photoacoustic (PA) scaffold using our previously developed caged photoinduced electron transfer (a-PeT) approach. This conjugation effectively resolved probe aggregation issues in physiological conditions and substantially enhanced its reactivity toward Bacterial NTR. Notably, Cy7-Neo-NO₂ enabled the first in situ photoacoustic imaging of pneumonia induced by methicillin-resistant Staphylococcus aureus (MRSA), as well as the detection of bacteria within tumors. Furthermore, upon NIR irradiation, Cy7-Neo-NO₂ successfully inhibited MRSA growth through a synergistic effect combining photothermal therapy and photodynamic therapy. Our results provided an effective tool for obtaining exceptional PA agents for accurate diagnosis, therapeutic evaluation of deep-seated Bacterial infections in vivo, and intratumoral bacteria-specific recognition.

MRSA-induced pneumonia; deep-seated bacterial infection; nitroreductase (NTR) response; photoacoustic imaging; phototherapy; tumor-homing bacteria.