Evidence map›Paper›PMID 35733912›Full record

ArticleJAC-antimicrobial resistance2022

Synthetic oxepanoprolinamide iboxamycin is active against

Tetiana Brodiazhenko, Kathryn Jane Turnbull, Kelvin J Y Wu, Hiraku Takada, Ben I C Tresco, Tanel Tenson, Andrew G Myers, Vasili Hauryliuk

Open access · goldAbstract read
In one paragraph

Article in JAC-antimicrobial resistance, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.7field-weighted citation impact, top 40% 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

7 citing papers in PubMed, 9 citations in OpenAlex.

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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

8 authors at 5 institutions in 5 countries.

Tetiana BrodiazhenkoUniversity of Tartu, Institute of Technology, 50411 Tartu, Estonia.
Kathryn Jane TurnbullDepartment of Clinical Microbiology, Rigshospitalet, 2200 Copenhagen, Denmark.
Kelvin J Y WuDepartment of Chemistry and Chemical Biology, Harvard University, Cambridge, MA, USA.
Hiraku TakadaDepartment of Experimental Medicine, University of Lund, 221 84 Lund, Sweden.
Ben I C TrescoDepartment of Chemistry and Chemical Biology, Harvard University, Cambridge, MA, USA.
Tanel TensonUniversity of Tartu, Institute of Technology, 50411 Tartu, Estonia.
Andrew G MyersDepartment of Chemistry and Chemical Biology, Harvard University, Cambridge, MA, USA.
Vasili HauryliukUniversity of Tartu, Institute of Technology, 50411 Tartu, Estonia.ORCID https://orcid.org/0000-0003-2389-5057
Harvard University · USUniversity of Tartu · EEKyoto Sangyo University · JPLund University · SERigshospitalet · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Listeriosis is a food-borne disease caused by the Gram-positive Bacillota (Firmicute) bacterium Objectives: We have established newly developed lincosamide iboxamycin as a potential novel antilisterial agent. Methods: We determined MICs of the lincosamides lincomycin, clindamycin and iboxamycin for Results: We show that the synthetic lincosamide iboxamycin is highly active against Conclusions: While iboxamycin is a promising new antilisterial agent, our findings suggest that emergence and spread of ABCF ARE variants capable of defeating next-generation lincosamides in the clinic is possible and should be closely monitored.

Identifiers

PMID35733912
PMCPMC9204466
OpenAlexW4283026857

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.