Evidence map›Paper›PMID 30135466›Full record

ArticleScientific reports2018

Bioengineering of bacterial pathogens for noninvasive imaging and in vivo evaluation of therapeutics.

Sathish Rajamani, Kyle Kuszpit, Jennifer M Scarff, Linnea Lundh, Maisha Khan, Jennifer Brown, Robert Stafford, Lisa H Cazares, Rekha G Panchal, Thomas Bocan

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.8field-weighted citation impact, top 35% of its field
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

8 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
  2. Genetically Engineered Microorganisms and Their Impact on Human Health.International journal of clinical practice · 2024
    Review
  3. Pathophysiology and Molecular Imaging of Diabetic Foot Infections.International journal of molecular sciences · 2021
    Review
  4. Review
  5. Molecular Imaging of Diabetic Foot Infections: New Tools for Old Questions.International journal of molecular sciences · 2019
    Review
  6. Article
  7. Review
  8. 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

10 authors at 1 institution in 1 country.

Sathish RajamaniMolecular & Translational Sciences Division, US Army Medical Research Institute of Infectious Diseases, 1425 Porter Street, Frederick, MD, 21702, United States. Sathish.rajamani.ctr@mail.mil.
Kyle KuszpitMolecular & Translational Sciences Division, US Army Medical Research Institute of Infectious Diseases, 1425 Porter Street, Frederick, MD, 21702, United States.
Jennifer M ScarffMolecular & Translational Sciences Division, US Army Medical Research Institute of Infectious Diseases, 1425 Porter Street, Frederick, MD, 21702, United States.
Linnea LundhMolecular & Translational Sciences Division, US Army Medical Research Institute of Infectious Diseases, 1425 Porter Street, Frederick, MD, 21702, United States.
Maisha KhanMolecular & Translational Sciences Division, US Army Medical Research Institute of Infectious Diseases, 1425 Porter Street, Frederick, MD, 21702, United States.
Jennifer BrownMolecular & Translational Sciences Division, US Army Medical Research Institute of Infectious Diseases, 1425 Porter Street, Frederick, MD, 21702, United States.
Robert StaffordMolecular & Translational Sciences Division, US Army Medical Research Institute of Infectious Diseases, 1425 Porter Street, Frederick, MD, 21702, United States.
Lisa H CazaresMolecular & Translational Sciences Division, US Army Medical Research Institute of Infectious Diseases, 1425 Porter Street, Frederick, MD, 21702, United States.
Rekha G PanchalMolecular & Translational Sciences Division, US Army Medical Research Institute of Infectious Diseases, 1425 Porter Street, Frederick, MD, 21702, United States.
Thomas BocanMolecular & Translational Sciences Division, US Army Medical Research Institute of Infectious Diseases, 1425 Porter Street, Frederick, MD, 21702, United States. Thomas.m.bocan.ctr@mail.mil.
United States Army Medical Research Institute of Infectious Diseases · US

Funding

DOD | Defense Threat Reduction Agency (DTRA) 13267645
6 · The paper itself

Abstract

Critical bacterial pathogens of public health and biodefense concerns were engineered to constitutively express Escherichia coli enzyme thymidine kinase (TK) that allows for noninvasive nuclear imaging via phosphorylation and entrapment of radiolabeled nucleoside analog 1-(2'deoxy-2'-fluoro-β-D-arabinofuranosyl)-5-iodouracil (FIAU). Expression of functional TK was established using a nucleoside analog Zidovudine that impeded the growth of tk-engineered bacteria. Significantly, no observable growth differences were detected for FIAU. High resolution mass spectrometry with Pseudomonas aeruginosa PAO1 and its tk variant (PAO1TK) confirmed FIAU phosphorylation and retention only in PAO1TK. In vitro gamma counting with wild-type PAO1, Acinetobacter baumannii and Burkholderia pseudomallei Bp82 and their tk derivatives with [

Indexed as

Acinetobacter baumanniiAnimalsArabinofuranosyluracilBacteriaBioengineeringBiomedical EngineeringBurkholderia pseudomalleiEscherichia coliEscherichia coli ProteinsIodine RadioisotopesMiceNucleosidesPositron Emission Tomography Computed TomographyPseudomonas aeruginosaThymidine KinaseTomography, X-Ray ComputedArabinofuranosyluracilEscherichia coli ProteinsfialuridineIodine RadioisotopesNucleosidesThymidine KinaseZidovudine

Identifiers

PMID30135466
PMCPMC6105664
OpenAlexW2887418501

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.