In vitro imaging of bacteria using 18F-fluorodeoxyglucose micro positron emission tomography

Marjolein Heuker1, Jürgen W A Sijbesma2, Rocío Aguilar Suárez1

  • 1Department of Medical Microbiology, University of Groningen, University Medical Center Groningen, Hanzeplein 1, PO Box 30001, 9700 RB, Groningen, The Netherlands.

Scientific Reports
|July 12, 2017
PubMed

Insights

Bacterial pathogens actively accumulate fluorine-18-fluorodeoxyglucose (18F-FDG), a key component in PET imaging for infection detection. This uptake suggests bacteria may directly contribute to the PET signal in vivo.

Area of Science:

  • Nuclear medicine
  • Microbiology
  • Biochemistry

Background:

  • Fluorine-18-fluorodeoxyglucose (18F-FDG) Positron Emission Tomography (PET) is utilized for detecting infection and inflammation.
  • The contribution of bacterial pathogens to the 18F-FDG PET signal has not been fully elucidated.

Purpose of the Study:

  • To investigate the in vitro uptake of 18F-FDG by clinical bacterial pathogen isolates.
  • To determine if 18F-FDG inhibits bacterial growth, similar to 2-deoxy-glucose.

Main Methods:

  • Twenty-two Gram-positive and Gram-negative bacterial isolates were incubated with 18F-FDG.
  • 18F-FDG uptake was quantified using gamma-counting and microPET imaging.
  • Bacterial growth inhibition assays were performed with Staphylococcus aureus and Bacillus subtilis.

Main Results:

  • All tested bacterial isolates demonstrated active accumulation of 18F-FDG.
  • 18F-FDG uptake in B. subtilis was dependent on the phosphotransferase system (pts), indicating active transport.
  • 18F-FDG exhibited only minor growth inhibition in S. aureus and B. subtilis, which was abrogated in pts mutants.

Conclusions:

  • Bacteria actively take up 18F-FDG, suggesting they can contribute to the signal in clinical FDG-PET infection imaging.
  • The phosphotransferase system plays a crucial role in bacterial 18F-FDG uptake and susceptibility to growth inhibition by FDG.