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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.
Abstract:
Positron emission tomography (PET) with fluorine-18-fluorodeoxyglucose (18F-FDG) can be applied to detect infection and inflammation. However, it was so far not known to what extent bacterial pathogens may contribute to the PET signal. Therefore, we investigated whether clinical isolates of frequently encountered bacterial pathogens take up 18F-FDG in vitro, and whether FDG inhibits bacterial growth as previously shown for 2-deoxy-glucose. 22 isolates of Gram-positive and Gram-negative bacterial pathogens implicated in fever and inflammation were incubated with 18F-FDG and uptake of 18F-FDG was assessed by gamma-counting and µPET imaging. Possible growth inhibition by FDG was assayed with Staphylococcus aureus and the Gram-positive model bacterium Bacillus subtilis. The results show that all tested isolates accumulated 18F-FDG actively. Further, 18F-FDG uptake was hampered in B. subtilis pts mutants impaired in glucose uptake. FDG inhibited growth of S. aureus and B. subtilis only to minor extents, and this effect was abrogated by pts mutations in B. subtilis. These observations imply that bacteria may contribute to the signals observed in FDG-PET infection imaging in vivo. Active bacterial FDG uptake is corroborated by the fact that the B. subtilis phosphotransferase system is needed for 18F-FDG uptake, while pts mutations protect against growth inhibition by FDG.
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.
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