Abstract | BACKGROUND: Mycobacterium tuberculosis (TB) infection is one of the deadliest infectious diseases worldwide and is responsible for 1.7 million deaths per year. The increase in multidrug-resistant TB poses formidable challenges to the global control of tuberculosis. TB infection could easily yield false-positive results in fluorine-18-fluorodeoxyglucose ([F]FDG) PET imaging for cancer detection because of its high [F]FDG uptake. We describe the combined [F]FDG PET with fluorine-18-fluoroacetate ([F]FAC), a promising analog of carbon-11-acetate, for targeting glycolysis and de novo lipogenesis, respectively, to determine the metabolic differences between chronic TB infection and acute infection. MATERIALS AND METHODS: Six-month-old BALB/c mice were inoculated with Mycobacterium bovis to induce chronic TB infection, and Escherichia coli as well as Staphylococcus aureus to induce acute infection for an in-vivo imaging study. Eighteen days after inoculation for chronic TB infection and 5 days for acute infection, both [F]FDG and [F]FAC micro-PET were performed on the infected mice. Analysis of variance and the Tukey honest ad-hoc test were carried out to determine differences among treatment with different bacterial infections. RESULTS: CONCLUSION: The marked metabolic differences in de novo lipogenesis and glycolysis in [F]FDG and [F]FAC uptakes in micro-PET imaging, respectively, help to differentiate chronic TB infection from acute infection.
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Authors | Chin-Ho Tsao, Chun-Yi Wu, Chi-Wei Chang, Hsin-Ell Wang, Bing-Fu Shih, Ren-Shyan Liu |
Journal | Nuclear medicine communications
(Nucl Med Commun)
Vol. 40
Issue 6
Pg. 639-644
(Jun 2019)
ISSN: 1473-5628 [Electronic] England |
PMID | 30932968
(Publication Type: Journal Article)
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Chemical References |
- Fluoroacetates
- Fluorodeoxyglucose F18
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Topics |
- Acute Disease
- Animals
- Chronic Disease
- Diagnosis, Differential
- Disease Models, Animal
- Fluoroacetates
- Fluorodeoxyglucose F18
- Glycolysis
- Mice
- Mice, Inbred BALB C
- Mycobacterium tuberculosis
(physiology)
- Positron-Emission Tomography
- Tuberculosis
(diagnostic imaging, metabolism)
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