Evidence map›Paper›PMID 34027898›Full record

ArticleJCI insight2021

Leveraging copper import by yersiniabactin siderophore system for targeted PET imaging of bacteria.

Nabil A Siddiqui, Hailey A Houson, Nitin S Kamble, Jose R Blanco, Robert E O'Donnell, Daniel J Hassett, Suzanne E Lapi, Nalinikanth Kotagiri

Abstract read
In one paragraph

Article in JCI insight, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed.

  1. Review
  2. Article
  3. Microbial medicines: Unlocking the therapeutic potential of the microbiome in cancer treatment.Journal of controlled release : official journal of the Controlled Release Society · 2026
    Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Review
  10. Radiometal chelators for infection diagnostics.Frontiers in nuclear medicine · 2023
    Article
  11. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Nabil A SiddiquiDivision of Pharmaceutical Sciences, James L. Winkle College of Pharmacy, University of Cincinnati, Cincinnati, Ohio, USA.
Hailey A HousonDivision of Advanced Medical Imaging Research, Department of Radiology and Chemistry, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Nitin S KambleDivision of Pharmaceutical Sciences, James L. Winkle College of Pharmacy, University of Cincinnati, Cincinnati, Ohio, USA.
Jose R BlancoDivision of Advanced Medical Imaging Research, Department of Radiology and Chemistry, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Robert E O'DonnellDepartment of Internal Medicine, Heart, Lung and Vascular Institute, and.
Daniel J HassettDepartment of Molecular Genetics, Biochemistry and Microbiology, College of Medicine, University of Cincinnati, Cincinnati, Ohio, USA.
Suzanne E LapiDivision of Advanced Medical Imaging Research, Department of Radiology and Chemistry, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Nalinikanth KotagiriDivision of Pharmaceutical Sciences, James L. Winkle College of Pharmacy, University of Cincinnati, Cincinnati, Ohio, USA.

Funding

LCenter for Clinical and Translational Science and TrainingUL1TR001425 · NCATS · UNIVERSITY OF CINCINNATI · PI HEUBI, JAMES E., KISSELA, BRETT M · 2015 to 2024
$37.5M
A Synthetic Approach for Bacterial-Mammalian Cell BindingR21GM137321 · NIGMS · UNIVERSITY OF CINCINNATI · PI KOTAGIRI, NALINIKANTH · 2020 to 2021
$450k
American Heart Association-American Stroke Association 18IPA34170157NCATS NIH HHS UL1 TR001425NIGMS NIH HHS R21 GM137321
6 · The paper itself

Abstract

There is an emerging need for accurate and rapid identification of bacteria in the human body to achieve diverse biomedical objectives. Copper homeostasis is vital for the survival of bacterial species owing to the roles of the metal as a nutrient, respiratory enzyme cofactor, and a toxin. Here, we report the development of a copper-64-labeled bacterial metal chelator, yersiniabactin, to exploit a highly conserved metal acquisition pathway for noninvasive and selective imaging of bacteria. Compared with traditional techniques used to manufacture probes, our strategy simplifies the process considerably by combining the function of metal attachment and cell recognition to the same molecule. We demonstrate, for the first time to our knowledge, how a copper-64 PET probe can be used to identify specific bacterial populations, monitor antibiotic treatment outcomes, and track bacteria in diverse niches in vivo.

Indexed as

Bacterial InfectionsPhenolsSiderophoresThiazolesAnimalsBacteriaCopperDisease Models, AnimalEchocardiographyFemaleMiceMice, Inbred BALB CMolecular ImagingPositron-Emission TomographyCopperPhenolsSiderophoresThiazolesyersiniabactinBacterial infectionsDiagnostic imagingInfectious disease

Identifiers

PMID34027898
PMCPMC8262292

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.