Evidence map›Paper›PMID 31268804›Full record

ArticleSLAS discovery : advancing life sciences R & D2019

A Whole-Cell Screen for Adjunctive and Direct Antimicrobials Active against Carbapenem-Resistant Enterobacteriaceae.

Kenneth P Smith, Matthew G Dowgiallo, Lucius Chiaraviglio, Prakash Parvatkar, Chungsik Kim, Roman Manetsch, James E Kirby

Open access · bronzeAbstract read
In one paragraph

Article in SLAS discovery : advancing life sciences R & D, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.4field-weighted citation impact, top 47% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Discovery of small-molecule inhibitors of multidrug-resistance plasmid maintenance using a high-throughput screening approach.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  5. New strategies and structural considerations in development of therapeutics for carbapenem-resistant Enterobacteriaceae.Translational research : the journal of laboratory and clinical medicine · 2020
    Review
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

7 authors at 2 institutions in 1 country.

Kenneth P Smith1 Department of Pathology, Beth Israel Deaconess Medical Center, Boston, MA, USA.
Matthew G Dowgiallo3 Department of Chemistry and Chemical Biology, Northeastern University, Boston, MA, USA.
Lucius Chiaraviglio1 Department of Pathology, Beth Israel Deaconess Medical Center, Boston, MA, USA.
Prakash Parvatkar3 Department of Chemistry and Chemical Biology, Northeastern University, Boston, MA, USA.
Chungsik Kim3 Department of Chemistry and Chemical Biology, Northeastern University, Boston, MA, USA.
Roman Manetsch3 Department of Chemistry and Chemical Biology, Northeastern University, Boston, MA, USA.
James E Kirby1 Department of Pathology, Beth Israel Deaconess Medical Center, Boston, MA, USA.
Northeastern University · USBeth Israel Deaconess Medical Center · US

Funding

Plasmid Eviction to Restore Susceptibility in Carbapenem-Resistant EnterobacteriaceaeR33AI119114 · NIAID · BETH ISRAEL DEACONESS MEDICAL CENTER · PI KIRBY, JAMES E · 2017 to 2019
$1.5M
Plasmid Eviction to Restore Susceptibility in Carbapenem-Resistant EnterobacteriaceaeR21AI119114 · NIAID · BETH ISRAEL DEACONESS MEDICAL CENTER · PI KIRBY, JAMES E · 2015 to 2016
$305k
Identification and Characterization of Novel Antimicrobial Adjunctives to Restore Susceptibility to Carbapenem Resistant EnterobacteriaceaeF32AI124590 · NIAID · BETH ISRAEL DEACONESS MEDICAL CENTER · PI SMITH, KENNETH PATRICK · 2017 to 2019
$175k
NIAID NIH HHS F32 AI124590NIAID NIH HHS R21 AI119114NIAID NIH HHS R33 AI119114
6 · The paper itself

Abstract

Carbapenem-resistant Enterobacteriaceae (CRE) are an emerging antimicrobial resistance threat for which few if any therapeutic options remain. Identification of new agents that either inhibit CRE or restore activity of existing antimicrobials is highly desirable. Therefore, a high-throughput screen of 182,427 commercially available compounds was used to identify small molecules which either enhanced activity of meropenem against a carbapenem-resistant

Indexed as

Drug Evaluation, PreclinicalMicrobial Sensitivity TestsAnti-Bacterial AgentsCarbapenem-Resistant EnterobacteriaceaeCheminformaticsHumansMolecular StructureSmall Molecule LibrariesSpectrum AnalysisAnti-Bacterial AgentsSmall Molecule Librariesantibiotic resistancecarbapenem-resistant EnterobactericeaeCREhigh-throughput screeningKPCmedicinal chemistrywhole-cell assay

Identifiers

PMID31268804
PMCPMC6702050
OpenAlexW2954382314

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.