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Imaging sensitive and drug-resistant bacterial infection with [(11)C]-trimethoprim
BACKGROUND: Several molecular imaging strategies can identify bacterial infections in humans. PET affords the potential for sensitive infection detection deep within the body. Among PET-based approaches, antibiotic-based radiotracers, which often target key bacterial-specific enzymes, have considera...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Clinical Investigation
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9479701/ https://www.ncbi.nlm.nih.gov/pubmed/36106638 http://dx.doi.org/10.1172/JCI156679 |
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author | Lee, Iris K. Jacome, Daniel A. Cho, Joshua K. Tu, Vincent Young, Anthony J. Dominguez, Tiffany Northrup, Justin D. Etersque, Jean M. Lee, Hsiaoju S. Ruff, Andrew Aklilu, Ouniol Bittinger, Kyle Glaser, Laurel J. Dorgan, Daniel Hadjiliadis, Denis Kohli, Rahul M. Mach, Robert H. Mankoff, David A. Doot, Robert K. Sellmyer, Mark A. |
author_facet | Lee, Iris K. Jacome, Daniel A. Cho, Joshua K. Tu, Vincent Young, Anthony J. Dominguez, Tiffany Northrup, Justin D. Etersque, Jean M. Lee, Hsiaoju S. Ruff, Andrew Aklilu, Ouniol Bittinger, Kyle Glaser, Laurel J. Dorgan, Daniel Hadjiliadis, Denis Kohli, Rahul M. Mach, Robert H. Mankoff, David A. Doot, Robert K. Sellmyer, Mark A. |
author_sort | Lee, Iris K. |
collection | PubMed |
description | BACKGROUND: Several molecular imaging strategies can identify bacterial infections in humans. PET affords the potential for sensitive infection detection deep within the body. Among PET-based approaches, antibiotic-based radiotracers, which often target key bacterial-specific enzymes, have considerable promise. One question for antibiotic radiotracers is whether antimicrobial resistance (AMR) reduces specific accumulation within bacteria, diminishing the predictive value of the diagnostic test. METHODS: Using a PET radiotracer based on the antibiotic trimethoprim (TMP), [(11)C]-TMP, we performed in vitro uptake studies in susceptible and drug-resistant bacterial strains and whole-genome sequencing (WGS) in selected strains to identify TMP resistance mechanisms. Next, we queried the NCBI database of annotated bacterial genomes for WT and resistant dihydrofolate reductase (DHFR) genes. Finally, we initiated a first-in-human protocol of [(11)C]-TMP in patients infected with both TMP-sensitive and TMP-resistant organisms to demonstrate the clinical feasibility of the tool. RESULTS: We observed robust [(11)C]-TMP uptake in our panel of TMP-sensitive and -resistant bacteria, noting relatively variable and decreased uptake in a few strains of P. aeruginosa and E. coli. WGS showed that the vast majority of clinically relevant bacteria harbor a WT copy of DHFR, targetable by [(11)C]-TMP, and that despite the AMR, these strains should be “imageable.” Clinical imaging of patients with [(11)C]-TMP demonstrated focal radiotracer uptake in areas of infectious lesions. CONCLUSION: This work highlights an approach to imaging bacterial infection in patients, which could affect our understanding of bacterial pathogenesis as well as our ability to better diagnose infections and monitor response to therapy. TRIAL REGISTRATION: ClinicalTrials.gov NCT03424525. FUNDING: Institute for Translational Medicine and Therapeutics, Burroughs Wellcome Fund, NIH Office of the Director Early Independence Award (DP5-OD26386), and University of Pennsylvania NIH T32 Radiology Research Training Grant (5T32EB004311-12). |
format | Online Article Text |
id | pubmed-9479701 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Society for Clinical Investigation |
record_format | MEDLINE/PubMed |
spelling | pubmed-94797012022-09-19 Imaging sensitive and drug-resistant bacterial infection with [(11)C]-trimethoprim Lee, Iris K. Jacome, Daniel A. Cho, Joshua K. Tu, Vincent Young, Anthony J. Dominguez, Tiffany Northrup, Justin D. Etersque, Jean M. Lee, Hsiaoju S. Ruff, Andrew Aklilu, Ouniol Bittinger, Kyle Glaser, Laurel J. Dorgan, Daniel Hadjiliadis, Denis Kohli, Rahul M. Mach, Robert H. Mankoff, David A. Doot, Robert K. Sellmyer, Mark A. J Clin Invest Clinical Medicine BACKGROUND: Several molecular imaging strategies can identify bacterial infections in humans. PET affords the potential for sensitive infection detection deep within the body. Among PET-based approaches, antibiotic-based radiotracers, which often target key bacterial-specific enzymes, have considerable promise. One question for antibiotic radiotracers is whether antimicrobial resistance (AMR) reduces specific accumulation within bacteria, diminishing the predictive value of the diagnostic test. METHODS: Using a PET radiotracer based on the antibiotic trimethoprim (TMP), [(11)C]-TMP, we performed in vitro uptake studies in susceptible and drug-resistant bacterial strains and whole-genome sequencing (WGS) in selected strains to identify TMP resistance mechanisms. Next, we queried the NCBI database of annotated bacterial genomes for WT and resistant dihydrofolate reductase (DHFR) genes. Finally, we initiated a first-in-human protocol of [(11)C]-TMP in patients infected with both TMP-sensitive and TMP-resistant organisms to demonstrate the clinical feasibility of the tool. RESULTS: We observed robust [(11)C]-TMP uptake in our panel of TMP-sensitive and -resistant bacteria, noting relatively variable and decreased uptake in a few strains of P. aeruginosa and E. coli. WGS showed that the vast majority of clinically relevant bacteria harbor a WT copy of DHFR, targetable by [(11)C]-TMP, and that despite the AMR, these strains should be “imageable.” Clinical imaging of patients with [(11)C]-TMP demonstrated focal radiotracer uptake in areas of infectious lesions. CONCLUSION: This work highlights an approach to imaging bacterial infection in patients, which could affect our understanding of bacterial pathogenesis as well as our ability to better diagnose infections and monitor response to therapy. TRIAL REGISTRATION: ClinicalTrials.gov NCT03424525. FUNDING: Institute for Translational Medicine and Therapeutics, Burroughs Wellcome Fund, NIH Office of the Director Early Independence Award (DP5-OD26386), and University of Pennsylvania NIH T32 Radiology Research Training Grant (5T32EB004311-12). American Society for Clinical Investigation 2022-09-15 /pmc/articles/PMC9479701/ /pubmed/36106638 http://dx.doi.org/10.1172/JCI156679 Text en © 2022 Lee et al. https://creativecommons.org/licenses/by/4.0/This work is licensed under the Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Clinical Medicine Lee, Iris K. Jacome, Daniel A. Cho, Joshua K. Tu, Vincent Young, Anthony J. Dominguez, Tiffany Northrup, Justin D. Etersque, Jean M. Lee, Hsiaoju S. Ruff, Andrew Aklilu, Ouniol Bittinger, Kyle Glaser, Laurel J. Dorgan, Daniel Hadjiliadis, Denis Kohli, Rahul M. Mach, Robert H. Mankoff, David A. Doot, Robert K. Sellmyer, Mark A. Imaging sensitive and drug-resistant bacterial infection with [(11)C]-trimethoprim |
title | Imaging sensitive and drug-resistant bacterial infection with [(11)C]-trimethoprim |
title_full | Imaging sensitive and drug-resistant bacterial infection with [(11)C]-trimethoprim |
title_fullStr | Imaging sensitive and drug-resistant bacterial infection with [(11)C]-trimethoprim |
title_full_unstemmed | Imaging sensitive and drug-resistant bacterial infection with [(11)C]-trimethoprim |
title_short | Imaging sensitive and drug-resistant bacterial infection with [(11)C]-trimethoprim |
title_sort | imaging sensitive and drug-resistant bacterial infection with [(11)c]-trimethoprim |
topic | Clinical Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9479701/ https://www.ncbi.nlm.nih.gov/pubmed/36106638 http://dx.doi.org/10.1172/JCI156679 |
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