4.5 Article

PET Imaging of Active Invasive Fungal Infections with D-[5-11C]- Glutamine

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ACS INFECTIOUS DISEASES
卷 -, 期 -, 页码 -

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsinfecdis.2c00249

关键词

d-amino acid; metabolic imaging; glutamine; fungal infection; positron emission tomography

资金

  1. Cancer Prevention and Research Institute of Texas [CPRIT RP1706638, RP110771]
  2. National Heart, Lung, and Blood Institute [NIH T32 HL134613]
  3. Dr. Jack Krohmer Professorship Funds in Radiation Physics
  4. Robert W. Parkey, M.D. Distinguished Professorship in Radiology

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The increasing prevalence of invasive fungal infections (IFIs) has led to a greater need for rapid diagnosis. A radiotracer derived from D-amino acids (DAAs) shows promise as a more accurate way to detect bacterial and fungal pathogens. This study demonstrates the potential of D-[5-11C]-glutamine as a radiotracer for noninvasive PET imaging of IFIs.
The increasing prevalence and severity of invasive fungal infections (IFIs), especially in immunocompromised populations, has amplified the need for rapid diagnosis of fungal pathogens. Radiotracers derived from D-amino acids (DAAs) show promise as bacterial-specific positron emission tomography (PET) imaging agents due to their preferential consumption by bacteria and largely nonutilization by hosts. Unlike mammals, fungi can utilize external DAAs including D-glutamine for their growth by rapidly upregulating DAA oxidases. Additionally, glutamine is essential for fungal nitrogen assimilation, survival, and virulence. We previously validated D-[5-11C]-glutamine (D-[5-11C]-Gln) as an efficient radiotracer targeting live bacterial soft-tissue infections. Here, we further expanded this investigation to evaluate its translational potential for PET imaging of IFIs in immunocompetent mouse models subcutaneously (SubQ) and intramuscularly (IM) infected with Candida albicans (C. albicans), using its L-isomer counterpart (L-[5-11C]-Gln) as a control. Comparative studies between pathogens showed significantly (p < 0.05) higher uptake in fungi (C. albicans and C. tropicalis) versus tested bacterial species for D-[5-11C]-Gln, suggesting that it could potentially serve as a more sensitive radiotracer for detection of fungal infections. Additionally, comparative PET imaging studies in immunocompetent infected mice demonstrated significantly higher infection-to-background ratios for D- versus L-[5-11C]-Gln in both SubQ (ratio = 1.97, p = 0.043) and IM (ratio = 1.97, p = 0.028) infections. Fungal infection imaging specificity was confirmed with no significant difference observed between localized inflammation sites versus untreated muscle background (heat-killed injection site/untreated muscle: similar to 1.1). Taken together, this work demonstrates the translational potential of D-[5-11C]-Gln for noninvasive PET imaging of IFIs.

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