Evidence map›Paper›PMID 35077930›Full record

ArticleTuberculosis (Edinburgh, Scotland)2022

Mycobacterium abscessus drug discovery using machine learning.

Alan A Schmalstig, Kimberley M Zorn, Sebastian Murcia, Andrew Robinson, Svetlana Savina, Elena Komarova, Vadim Makarov, Miriam Braunstein, Sean Ekins

Open access · greenAbstract read
In one paragraph

Article in Tuberculosis (Edinburgh, Scotland), 2022. 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
0.9field-weighted citation impact, top 27% 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, 7 citations in OpenAlex.

  1. Antimicrobial Resistance: The Answers.British journal of biomedical science · 2026
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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

9 authors at 2 institutions in 1 country.

Alan A SchmalstigDepartment of Microbiology and Immunology, School of Medicine, University of North Carolina at Chapel Hill, North Carolina, 27599, USA.
Kimberley M ZornCollaborations Pharmaceuticals, Inc., 840 Main Campus Drive Lab 3510, Raleigh, NC, 27606, USA.
Sebastian MurciaDepartment of Microbiology and Immunology, School of Medicine, University of North Carolina at Chapel Hill, North Carolina, 27599, USA.
Andrew RobinsonDepartment of Microbiology and Immunology, School of Medicine, University of North Carolina at Chapel Hill, North Carolina, 27599, USA.
Svetlana SavinaResearch Center of Biotechnology RAS, Moscow, 119071, Russia.
Elena KomarovaResearch Center of Biotechnology RAS, Moscow, 119071, Russia.
Vadim MakarovResearch Center of Biotechnology RAS, Moscow, 119071, Russia.
Miriam BraunsteinDepartment of Microbiology and Immunology, School of Medicine, University of North Carolina at Chapel Hill, North Carolina, 27599, USA.
Sean EkinsCollaborations Pharmaceuticals, Inc., 840 Main Campus Drive Lab 3510, Raleigh, NC, 27606, USA. Electronic address: sean@collaborationspharma.com.
University of North Carolina at Chapel Hill · USCollaborations Pharmaceuticals (United States) · US

Funding

Centralized assay datasets for modelling support of small drug discovery organizationsR44GM122196 · NIGMS · COLLABORATIONS PHARMACEUTICALS, INC. · PI EKINS, SEAN · 2018 to 2022
$3.3M
NIGMS NIH HHS R44 GM122196
6 · The paper itself

Abstract

The prevalence of infections by nontuberculous mycobacteria is increasing, having surpassed tuberculosis in the United States and much of the developed world. Nontuberculous mycobacteria occur naturally in the environment and are a significant problem for patients with underlying lung diseases such as bronchiectasis, chronic obstructive pulmonary disease, and cystic fibrosis. Current treatment regimens are lengthy, complicated, toxic and they are often unsuccessful as seen by disease recurrence. Mycobacterium abscessus is one of the most commonly encountered organisms in nontuberculous mycobacteria disease and it is the most difficult to eradicate. There is currently no systematically proven regimen that is effective for treating M. abscessus infections. Our approach to drug discovery integrates machine learning, medicinal chemistry and in vitro testing and has been previously applied to Mycobacterium tuberculosis. We have now identified several novel 1-(phenylsulfonyl)-1H-benzimidazol-2-amines that have weak activity on M. abscessus in vitro but may represent a starting point for future further medicinal chemistry optimization. We also address limitations still to be overcome with the machine learning approach for M. abscessus.

Indexed as

Machine LearningAntitubercular AgentsBayes TheoremDrug DiscoveryHumansMycobacterium abscessusAntitubercular AgentsDrug discoveryMachine learningMycobacterium abscessusMycobacterium tuberculosisNontuberculous mycobacteria

Identifiers

PMID35077930
PMCPMC8855326
OpenAlexW4205718200

What OpenQuestion holds

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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.