Evidence map›Paper›PMID 27690385›Full record

ArticleACS infectious diseases2016

Small-Molecule Probes Reveal Esterases with Persistent Activity in Dormant and Reactivating Mycobacterium tuberculosis.

Katie R Tallman, Samantha R Levine, Kimberly E Beatty

Open access · greenAbstract read
In one paragraph

Article in ACS infectious diseases, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
4.9field-weighted citation impact, top 5% 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

42 citing papers in PubMed, 79 citations in OpenAlex.

  1. Article
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  3. Review
  4. Article
  5. Article
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  7. Article
  8. Roles of Lipolytic enzymes inFrontiers in microbiology · 2024
    Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Target Identification in Anti-Tuberculosis Drug Discovery.International journal of molecular sciences · 2023
    Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Visual Identification ofAnalytical chemistry · 2022
    Article
  19. Article
  20. 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

3 authors at 1 institution in 1 country.

Katie R TallmanProgram in Chemical Biology and Department of Biomedical Engineering, Oregon Health & Science University , Mail Code CL3B, 2730 S.W. Moody Avenue, Portland, Oregon 97201, United States.
Samantha R LevineProgram in Chemical Biology and Department of Biomedical Engineering, Oregon Health & Science University , Mail Code CL3B, 2730 S.W. Moody Avenue, Portland, Oregon 97201, United States.
Kimberly E BeattyProgram in Chemical Biology and Department of Biomedical Engineering, Oregon Health & Science University , Mail Code CL3B, 2730 S.W. Moody Avenue, Portland, Oregon 97201, United States.
Oregon Health & Science University · US

Funding

INTERACTIONS AT THE MICROBE/HOST INTERFACET32AI007472 · NIAID · OREGON HEALTH & SCIENCE UNIVERSITY · PI LANDFEAR, SCOTT M · 1995 to 2019
$6.7M
NIAID NIH HHS T32 AI007472
6 · The paper itself

Abstract

Mycobacterium tuberculosis (Mtb) is the deadliest bacterial pathogen in the world. An estimated one-third of humans harbor Mtb in a dormant state. These asymptomatic, latent infections impede tuberculosis eradication due to the long-term potential for reactivation. Dormant Mtb has reduced enzymatic activity, but hydrolases that remain active facilitate pathogen survival. We targeted Mtb esterases, a diverse set of enzymes in the serine hydrolase family, and studied their activities using both activity-based probes (ABPs) and fluorogenic esterase substrates. These small-molecule probes revealed functional esterases in active, dormant, and reactivating cultures. Using ABPs, we identified five esterases that remained active in dormant Mtb, including LipM (Rv2284), LipN (Rv2970c), CaeA (Rv2224c), Rv0183, and Rv1683. Three of these, CaeA, Rv0183, and Rv1683, were catalytically active in all three culture conditions. Fluorogenic probes additionally revealed LipH (Rv1399c), Culp1 (Rv1984c), and Rv3036c esterase activity in dormant and active cultures. Esterases with persistent activity are potential diagnostic biomarkers or therapeutic targets for Mtb-infected individuals with latent or active tuberculosis.

Indexed as

Antitubercular AgentsBacterial ProteinsDrug Evaluation, PreclinicalEnzyme InhibitorsEsterasesHumansLatent TuberculosisMycobacterium tuberculosisTuberculosisAntitubercular AgentsBacterial ProteinsEnzyme InhibitorsEsteraseschemical biologyesterasefluorescentMycobacterium tuberculosisproteomics

Identifiers

PMID27690385
PMCPMC7880555
OpenAlexW2527718780

What OpenQuestion holds

Textmetadata
LicenceTDM
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.