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

被引:23
作者
Heuker, Marjolein [1 ]
Sijbesma, Jurgen W. A. [2 ]
Suarez, Rocio Aguilar [1 ]
de Jong, Johan R. [2 ]
Boersma, Hendrikus H. [2 ,3 ]
Luurtsema, Gert [2 ]
Elsinga, Philip H. [2 ]
Glaudemans, Andor W. J. M. [2 ]
van Dam, Gooitzen M. [2 ,4 ]
van Dijl, Jan Maarten [1 ]
Slart, Riemer H. J. A. [2 ,5 ]
van Oosten, Marleen [1 ]
机构
[1] Univ Groningen, Univ Med Ctr Groningen, Dept Med Microbiol, Hanzepl 1,POB 30001, NL-9700 RB Groningen, Netherlands
[2] Univ Groningen, Univ Med Ctr Groningen, Dept Nucl Med & Mol Imaging, Hanzepl 1,POB 30001, NL-9700 RB Groningen, Netherlands
[3] Univ Groningen, Univ Med Ctr Groningen, Dept Clin Pharm & Pharmacol, Hanzepl 1,POB 30001, NL-9700 RB Groningen, Netherlands
[4] Univ Groningen, Univ Med Ctr Groningen, Div Surg Oncol & Intens Care, Dept Surg, Hanzepl 1,POB 30001, NL-9700 RB Groningen, Netherlands
[5] Univ Twente, Dept Biomed Photon Imaging, POB 217, NL-7500 AE Enschede, Netherlands
关键词
PHOSPHOTRANSFERASE SYSTEM; BACILLUS-SUBTILIS; INFECTION; GLUCOSE; PET;
D O I
10.1038/s41598-017-05403-z
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Positron emission tomography (PET) with fluorine-18-fluorodeoxyglucose (F-18-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 F-18-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 F-18-FDG and uptake of F-18-FDG was assessed by gamma-counting and mu PET 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 F-18-FDG actively. Further, F-18-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 F-18-FDG uptake, while pts mutations protect against growth inhibition by FDG.
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页数:9
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