[18F]FDG-6-P as a novel in vivo tool for imaging staphylococcal infections
Background Management of infection is a major clinical problem. Staphylococcus aureus is a Gram-positive bacterium which colonises approximately one third of the adult human population. Staphylococcal infections can be life-threatening and are frequently complicated by multi-antibiotic resistant st...
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| Format: | Article |
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BioMed Central
2015
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| Online Access: | https://eprints.nottingham.ac.uk/28818/ |
| _version_ | 1848793649933975552 |
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| author | Mills, Bethany Awais, Ramla Luckett, Jeni Turton, Dave Williams, Paul Perkins, A.C. Hill, P.J. |
| author_facet | Mills, Bethany Awais, Ramla Luckett, Jeni Turton, Dave Williams, Paul Perkins, A.C. Hill, P.J. |
| author_sort | Mills, Bethany |
| building | Nottingham Research Data Repository |
| collection | Online Access |
| description | Background
Management of infection is a major clinical problem. Staphylococcus aureus is a Gram-positive bacterium which colonises approximately one third of the adult human population. Staphylococcal infections can be life-threatening and are frequently complicated by multi-antibiotic resistant strains including methicillin-resistant S. aureus (MRSA). Fluorodeoxyglucose ([18F]FDG) imaging has been used to identify infection sites; however, it is unable to distinguish between sterile inflammation and bacterial load. We have modified [18F]FDG by phosphorylation, producing [18F]FDG-6-P to facilitate specific uptake and accumulation by S. aureus through hexose phosphate transporters, which are not present in mammalian cell membranes. This approach leads to the specific uptake of the radiopharmaceutical into the bacteria and not the sites of sterile inflammation.
Methods
[18F]FDG-6-P was synthesised from [18F]FDG. Yield, purity and stability were confirmed by RP-HPLC and iTLC. The specificity of [18F]FDG-6-P for the bacterial universal hexose phosphate transporter (UHPT) was confirmed with S. aureus and mammalian cell assays in vitro. Whole body biodistribution and accumulation of [18F]FDG-6-P at the sites of bioluminescent staphylococcal infection were established in a murine foreign body infection model.
Results
In vitro validation assays demonstrated that [18F]FDG-6-P was stable and specifically transported into S. aureus but not mammalian cells. [18F]FDG-6-P was elevated at the sites of S. aureus infection in vivo compared to uninfected controls; however, the increase in signal was not significant and unexpectedly, the whole-body biodistribution of [18F]FDG-6-P was similar to that of [18F]FDG.
Conclusions
Despite conclusive in vitro validation, [18F]FDG-6-P did not behave as predicted in vivo. However at the site of known infection, [18F]FDG-6-P levels were elevated compared with uninfected controls, providing a higher signal-to-noise ratio. The bacterial UHPT can transport hexose phosphates other than glucose, and therefore alternative sugars may show differential biodistribution and provide a means for specific bacterial detection. |
| first_indexed | 2025-11-14T19:03:40Z |
| format | Article |
| id | nottingham-28818 |
| institution | University of Nottingham Malaysia Campus |
| institution_category | Local University |
| last_indexed | 2025-11-14T19:03:40Z |
| publishDate | 2015 |
| publisher | BioMed Central |
| recordtype | eprints |
| repository_type | Digital Repository |
| spelling | nottingham-288182020-05-04T20:11:32Z https://eprints.nottingham.ac.uk/28818/ [18F]FDG-6-P as a novel in vivo tool for imaging staphylococcal infections Mills, Bethany Awais, Ramla Luckett, Jeni Turton, Dave Williams, Paul Perkins, A.C. Hill, P.J. Background Management of infection is a major clinical problem. Staphylococcus aureus is a Gram-positive bacterium which colonises approximately one third of the adult human population. Staphylococcal infections can be life-threatening and are frequently complicated by multi-antibiotic resistant strains including methicillin-resistant S. aureus (MRSA). Fluorodeoxyglucose ([18F]FDG) imaging has been used to identify infection sites; however, it is unable to distinguish between sterile inflammation and bacterial load. We have modified [18F]FDG by phosphorylation, producing [18F]FDG-6-P to facilitate specific uptake and accumulation by S. aureus through hexose phosphate transporters, which are not present in mammalian cell membranes. This approach leads to the specific uptake of the radiopharmaceutical into the bacteria and not the sites of sterile inflammation. Methods [18F]FDG-6-P was synthesised from [18F]FDG. Yield, purity and stability were confirmed by RP-HPLC and iTLC. The specificity of [18F]FDG-6-P for the bacterial universal hexose phosphate transporter (UHPT) was confirmed with S. aureus and mammalian cell assays in vitro. Whole body biodistribution and accumulation of [18F]FDG-6-P at the sites of bioluminescent staphylococcal infection were established in a murine foreign body infection model. Results In vitro validation assays demonstrated that [18F]FDG-6-P was stable and specifically transported into S. aureus but not mammalian cells. [18F]FDG-6-P was elevated at the sites of S. aureus infection in vivo compared to uninfected controls; however, the increase in signal was not significant and unexpectedly, the whole-body biodistribution of [18F]FDG-6-P was similar to that of [18F]FDG. Conclusions Despite conclusive in vitro validation, [18F]FDG-6-P did not behave as predicted in vivo. However at the site of known infection, [18F]FDG-6-P levels were elevated compared with uninfected controls, providing a higher signal-to-noise ratio. The bacterial UHPT can transport hexose phosphates other than glucose, and therefore alternative sugars may show differential biodistribution and provide a means for specific bacterial detection. BioMed Central 2015 Article PeerReviewed Mills, Bethany, Awais, Ramla, Luckett, Jeni, Turton, Dave, Williams, Paul, Perkins, A.C. and Hill, P.J. (2015) [18F]FDG-6-P as a novel in vivo tool for imaging staphylococcal infections. EJNMMI Research, 5 . 13/1-13/11. ISSN 2191-219X Pre-clinical; NanoPET-CT imaging; S. aureus; Infection diagnosis http://www.ejnmmires.com/content/5/1/13 doi:10.1186/s13550-015-0095-1 doi:10.1186/s13550-015-0095-1 |
| spellingShingle | Pre-clinical; NanoPET-CT imaging; S. aureus; Infection diagnosis Mills, Bethany Awais, Ramla Luckett, Jeni Turton, Dave Williams, Paul Perkins, A.C. Hill, P.J. [18F]FDG-6-P as a novel in vivo tool for imaging staphylococcal infections |
| title | [18F]FDG-6-P as a novel in vivo tool for imaging staphylococcal infections |
| title_full | [18F]FDG-6-P as a novel in vivo tool for imaging staphylococcal infections |
| title_fullStr | [18F]FDG-6-P as a novel in vivo tool for imaging staphylococcal infections |
| title_full_unstemmed | [18F]FDG-6-P as a novel in vivo tool for imaging staphylococcal infections |
| title_short | [18F]FDG-6-P as a novel in vivo tool for imaging staphylococcal infections |
| title_sort | [18f]fdg-6-p as a novel in vivo tool for imaging staphylococcal infections |
| topic | Pre-clinical; NanoPET-CT imaging; S. aureus; Infection diagnosis |
| url | https://eprints.nottingham.ac.uk/28818/ https://eprints.nottingham.ac.uk/28818/ https://eprints.nottingham.ac.uk/28818/ |