Positron Emission Tomography Imaging of Bacterial Infections With an Enterobactin Analog to Monitor Treatment Efficacy With a Catechol Antibiotic

M M. Andrey Joaqui‐Joaqui (Department of Chemistry University of Wisconsin – Madison Madison Wisconsin USA) P Phuong Nguyen Tran (Department of Chemistry University of Wisconsin – Madison Madison Wisconsin USA) A Axia Marlin (Department of Chemistry, University of Wisconsin-Madison, 1101 University Avenue, Madison, Wisconsin 53705, United States) F Fiona Armstrong‐Pavlik (Department of Chemistry University of Minnesota Minneapolis Minnesota USA) M Minhua Cao (Department of Chemistry, University of Wisconsin-Madison, 1101 University Avenue, Madison, Wisconsin 53705, United States) V Valérie C. Pierre (Department of Chemistry) E Eszter Boros (Department of Chemistry)

Abstract

ABSTRACT Positron emission tomography (PET) is an emerging tool under clinical investigation for the detection of bacterial infections. The ability to identify the site of infection and the pathogen's potential susceptibility to subsequent treatment approaches can streamline treatment and prevent misuse of antibiotics. Previous studies identified TREN‐CAM as a promising scaffold for radiometal labeling using the positron‐emitting radionuclide 68 Ga. Here, we investigate the suitability of 67/68 Ga‐labeled TREN‐CAM and enterobactin for the noninvasive imaging of an Escherichia coli infection. In vitro uptake experiments with [ 67 Ga]Ga III ‐TREN‐CAM demonstrate superior uptake in E. coli K12 and Pseudomonas aeruginosa PAO1 when compared with [ 67 Ga]Ga III ‐DFO, a compound currently under clinical investigation for infection imaging. Selectivity experiments indicate that [ 67 Ga]Ga III ‐TREN‐CAM is recognized by the active transmembrane transport machinery for nat Fe III ‐Ent. Using a soft tissue E. coli infection model, we demonstrate that [ 68 Ga]Ga III ‐TREN‐CAM selectively accumulates in infected tissue. Notably, [ 68 Ga]Ga III ‐TREN‐CAM provides better infection‐to‐inflammation contrast, accelerated blood clearance, and lower off‐target accumulation compared to [ 68 Ga]Ga III ‐Ent and [ 68 Ga]Ga III ‐citrate. The potential of [ 68 Ga]Ga III ‐TREN‐CAM to serve as a tool to monitor the therapeutic efficacy of cefiderocol is also evaluated, offering insight into its utility in guiding antibiotic treatment.

Article Details

Volume / Issue Vol. 65, Issue 17
Published April 20, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (7)

M

M. Andrey Joaqui‐Joaqui

Department of Chemistry University of Wisconsin – Madison Madison Wisconsin USA

P

Phuong Nguyen Tran

Department of Chemistry University of Wisconsin – Madison Madison Wisconsin USA

A

Axia Marlin

Department of Chemistry, University of Wisconsin-Madison, 1101 University Avenue, Madison, Wisconsin 53705, United States

F

Fiona Armstrong‐Pavlik

Department of Chemistry University of Minnesota Minneapolis Minnesota USA

M

Minhua Cao

Department of Chemistry, University of Wisconsin-Madison, 1101 University Avenue, Madison, Wisconsin 53705, United States

V

Valérie C. Pierre

Department of Chemistry

E

Eszter Boros

Department of Chemistry