Evidence map›Paper›PMID 20566877›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2010

Imaging tuberculosis with endogenous beta-lactamase reporter enzyme fluorescence in live mice.

Ying Kong, Hequan Yao, Hongjun Ren, Selvakumar Subbian, Suat L G Cirillo, James C Sacchettini, Jianghong Rao, Jeffrey D Cirillo

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed
6.1field-weighted citation impact, top 3% 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

68 citing papers in PubMed, 181 citations in OpenAlex.

  1. Article
  2. Article
  3. Expert review of respiratory medicine · 2026
    Review
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  5. Article
  6. Article
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  9. Article
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  14. Article
  15. Review
  16. Article
  17. Review
  18. Revisiting the methods for detectingAccess microbiology · 2021
    Review
  19. Review
  20. Review

8 more citing papers are in PubMed but not listed here.

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 at 3 institutions in 1 country.

Ying KongDepartment of Microbial and Molecular Pathogenesis, Texas A&M Health Sciences Center, College Station, TX 77843, USA.
Hequan Yao
Hongjun Ren
Selvakumar Subbian
Suat L G Cirillo
James C Sacchettini
Jianghong Rao
Jeffrey D Cirillo
Texas A&M Health Science Center · USStanford University · USTexas A&M University · US

Funding

Mycobacterial Dissemination and PersistenceR01AI047866 · NIAID · UNIVERSITY OF NEBRASKA LINCOLN · PI CIRILLO, JEFFREY D. · 2002 to 2010
$2.0M
NIAID NIH HHS AI47866NIAID NIH HHS R01 AI047866
6 · The paper itself

Abstract

The slow growth rate and genetic intractability of tubercle bacilli has hindered progress toward understanding tuberculosis, one of the most frequent causes of death worldwide. We overcame this roadblock through development of near-infrared (NIR) fluorogenic substrates for beta-lactamase, an enzyme expressed by tubercle bacilli, but not by their eukaryotic hosts, to allow real-time imaging of pulmonary infections and rapid quantification of bacteria in living animals by a strategy called reporter enzyme fluorescence (REF). This strategy has a detection limit of 6 +/- 2 x 10(2) colony-forming units (CFU) of bacteria with the NIR substrate CNIR5 in only 24 h of incubation in vitro, and as few as 10(4) CFU in the lungs of live mice. REF can also be used to differentiate infected from uninfected macrophages by using confocal microscopy and fluorescence activated cell sorting. Mycobacterium tuberculosis and the bacillus Calmette-Guérin can be tracked directly in the lungs of living mice without sacrificing the animals. Therapeutic efficacy can also be evaluated through loss of REF signal within 24 h posttreatment by using in vitro whole-bacteria assays directly in living mice. We expect that rapid quantification of bacteria within tissues of a living host and in the laboratory is potentially transformative for tuberculosis virulence studies, evaluation of therapeutics, and efficacy of vaccine candidates. This is a unique use of an endogenous bacterial enzyme probe to detect and image tubercle bacilli that demonstrates REF is likely to be useful for the study of many bacterial infections.

Indexed as

AnimalsBacterial Proteinsbeta-LactamasesCarbocyaninesCell LineDiagnostic ImagingFemaleFluorescence Resonance Energy TransferFluorescent DyesLactamsLungMiceMice, Inbred BALB CMicroscopy, ConfocalMycobacterium bovisMycobacterium tuberculosisBacterial Proteinsbeta-LactamasesCarbocyaninesCY5.5 cyanine dyecyanine dye 5Fluorescent DyesLactams

Identifiers

PMID20566877
PMCPMC2901431
OpenAlexW2121788831

What OpenQuestion holds

Textmetadata
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.