Imaging of bacterial infection: Harnessing positron emission tomography and Cherenkov luminescence imaging with UBI‐derived octapeptide

Abstract

Noninvasive imaging techniques for the early detection of infections are in high demand. In this study, we present the development of an infection imaging agent consisting of the antimicrobial peptide fragment UBI (31–38) conjugated to the chelator 1,4,7‐triazacyclononane,1‐glutaric acid‐4,7‐acetic acid (NODAGA), which allows for labeling with the positron emitter Ga‐68. The preclinical evaluation of [68Ga]Ga–NODAGA–UBI (31–38) was conducted to investigate its potential for imaging bacterial infections caused by Staphylococcus aureus. The octapeptide derived from ubiquicidin, UBI (31–38), was synthesized and conjugated with the chelator NODAGA. The conjugate was then radiolabeled with Ga‐68. The radiolabeling process and the stability of the radio formulation were confirmed through chromatography. The study included both in vitro evaluations using S. aureus and in vivo evaluations in an animal model of infection and inflammation. Positron emission tomography (PET) and Cherenkov luminescence imaging (CLI) were performed to visualize the targeted localization of the radio formulation at the site of infection. Ex vivo biodistribution studies were carried out to quantify the uptake of the radio formulation in different organs and tissues. Additionally, the uptake of [18F]Fluorodeoxyglucose ([18F] FDG) in the animal model was also studied for comparison. The [68Ga]Ga–NODAGA–UBI (31–38) complex consistently exhibited high radiochemical purity (>90%) after formulation. The complex demonstrated stability in saline, phosphate‐buffered saline, and human serum for up to 3 h. Notably, the complex displayed significantly higher uptake in S. aureus, which was inhibited in the presence of unconjugated UBI (29–41) peptide, confirming the specificity of the formulation for bacterial membranes. Bacterial imaging capability was also observed in PET and CLI images. Biodistribution results indicated a substantial target‐to‐nontarget ratio of approximately 4 at 1 h postinjection of the radio formulation. Conversely, the uptake of [18F]FDG in the animal model did not allow for the discrimination of infected and inflamed sites. Our studies have demonstrated that [68Ga]Ga–NODAGA–UBI (31–38) holds promise as a radiotracer for imaging bacterial infections caused by S. aureus.