Evidence map›Paper›PMID 29698397›Full record

ArticlePloS one2018

Pathogen Box screening for hit identification against Mycobacterium abscessus.

Jinsun Jeong, Guehye Kim, Cheol Moon, Hyun Jung Kim, Tae Ho Kim, Jichan Jang

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

20 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Antimicrobial and Antibiofilm Effects of Bithionol againstAntibiotics (Basel, Switzerland) · 2024
    Article
  3. Article
  4. Exploring antibiotic resistance mechanisms inFrontiers in microbiology · 2024
    Review
  5. Article
  6. Microbiology spectrum · 2022
    Article
  7. Article
  8. Mycobacterium abscessus drug discovery using machine learning.Tuberculosis (Edinburgh, Scotland) · 2022
    Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Review
  14. Article
  15. Etamycin as a NovelInternational journal of molecular sciences · 2020
    Article
  16. Rifamycin O, An Alternative Anti-Molecules (Basel, Switzerland) · 2020
    Article
  17. Article
  18. 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

6 authors at 2 institutions in 1 country.

Jinsun JeongDivision of Applied Life Science (BK21plus Program), Gyeongsang National University, Jinju, South Korea.
Guehye KimDivision of Applied Life Science (BK21plus Program), Gyeongsang National University, Jinju, South Korea.
Cheol MoonDepartment of Clinical Laboratory Science, Semyung University, Jecheon, South Korea.
Hyun Jung KimDivision of Life Science, Research Institute of Life Science, Gyeongsang National University, Jinju, South Korea.
Tae Ho KimDivision of Life Science, Research Institute of Life Science, Gyeongsang National University, Jinju, South Korea.
Jichan JangDivision of Applied Life Science (BK21plus Program), Gyeongsang National University, Jinju, South Korea.ORCID 0000-0002-4598-5371
Gyeongsang National University · KRSemyung University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mycobacterium abscessus is a rapidly growing life-threatening mycobacterium with multiple drug-resistance mechanisms. However, there is no official regimen for M. abscessus therapy. In this study, we screened the Pathogen Box, which contains 400 drug-like molecules active against neglected diseases, to identify active molecules targeting Mycobacterium abscessus using resazurin live/dead assays. In this screening assay, the Z-factor was 0.7, as an indicator of the statistical confidence of the assay. A cut-off of 80% growth inhibition in the screening resulted in the identification of four different compounds at a single concentration (20 μM). Dose-response curves identified three different hit candidates, i.e., MMV688508, MMV688844, and MMV688845, which generated good inhibitory curves. All hit candidates were expected to have different molecular targets. Among them, MMV688844 showed the best minimum inhibitory concentration value for not only wild-type M. abscessus but also for nine different R and S morphotype clinical isolates. Thus, we found that MMV688844, identified from the Pathogen Box screen, may be a promising candidate in the M. abscessus drug discovery pipeline.

Indexed as

Anti-Bacterial AgentsDose-Response Relationship, DrugMicrobial Sensitivity TestsMycobacterium abscessusMycobacterium Infections, NontuberculousAnti-Bacterial Agents

Identifiers

PMID29698397
PMCPMC5919404
OpenAlexW2800337085

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.