Evidence map›Paper›PMID 37122541›Full record

ReviewRSC medicinal chemistry2023

Ribosome-targeting antibiotics and resistance

Learnmore Jeremia, Benjamin E Deprez, Debayan Dey, Graeme L Conn, William M Wuest

Open access · greenAbstract readReview
In one paragraph

Review in RSC medicinal chemistry, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.5field-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

22 citing papers in PubMed, 37 citations in OpenAlex.

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  19. Complete list of canonical post-transcriptional modifications in thebioRxiv : the preprint server for biology · 2024
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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

5 authors at 1 institution in 1 country.

Learnmore JeremiaDepartment of Chemistry, Emory University 1515 Dickey Dr. Atlanta GA 30322 USA wwuest@emory.edu.
Benjamin E DeprezDepartment of Chemistry, Emory University 1515 Dickey Dr. Atlanta GA 30322 USA wwuest@emory.edu.
Debayan DeyDepartment of Biochemistry, Emory University School of Medicine 1510 Clifton Rd. Atlanta GA 30322 USA gconn@emory.edu.ORCID https://orcid.org/0000-0002-0222-6092
Graeme L ConnDepartment of Biochemistry, Emory University School of Medicine 1510 Clifton Rd. Atlanta GA 30322 USA gconn@emory.edu.ORCID https://orcid.org/0000-0002-2419-380X
William M WuestDepartment of Chemistry, Emory University 1515 Dickey Dr. Atlanta GA 30322 USA wwuest@emory.edu.ORCID https://orcid.org/0000-0002-5198-7744
Emory University · US

Funding

RNA modification and antibiotic resistanceR01AI088025 · NIAID · EMORY UNIVERSITY · PI Graeme L Conn, Christine M Dunham · 2010 to 2026
$7.9M
Emory/Georgia TB Research Advancement Center (TRAC)P30AI168386 · NIAID · EMORY UNIVERSITY · PI Neel Rajnikant Gandhi, Jyothi Rengarajan · 2022 to 2026
$5.8M
Natural Product-Inspired Approaches Toward The Development Of Antivirulence And Species-Specific InhibitorsR35GM119426 · NIGMS · TEMPLE UNIV OF THE COMMONWEALTH · PI William M Wuest · 2016 to 2026
$4.8M
NIAID NIH HHS P30 AI168386NIAID NIH HHS R01 AI088025NIGMS NIH HHS R35 GM119426
6 · The paper itself

Abstract

The rise of multidrug-resistant bacterial infections is a cause of global concern. There is an urgent need to both revitalize antibacterial agents that are ineffective due to resistance while concurrently developing new antibiotics with novel targets and mechanisms of action. Pathogen associated resistance-conferring ribosomal RNA (rRNA) methyltransferases are a growing threat that, as a group, collectively render a total of seven clinically-relevant ribosome-targeting antibiotic classes ineffective. Increasing frequency of identification and their growing prevalence relative to other resistance mechanisms suggests that these resistance determinants are rapidly spreading among human pathogens and could contribute significantly to the increased likelihood of a post-antibiotic era. Herein, with a view toward stimulating future studies to counter the effects of these rRNA methyltransferases, we summarize their prevalence, the fitness cost(s) to bacteria of their acquisition and expression, and current efforts toward targeting clinically relevant enzymes of this class.

Identifiers

PMID37122541
PMCPMC10131624
OpenAlexW4322749680

What OpenQuestion holds

Textmetadata
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.