Evidence map›Paper›PMID 38526049›Full record

ArticleAntimicrobial agents and chemotherapy2024

Role of amino acid 159 in carbapenem and temocillin hydrolysis of OXA-933, a novel OXA-48 variant.

Mariam Rima, Saoussen Oueslati, Garance Cotelon, Elodie Creton, Rémy A Bonnin, Laurent Dortet, Bogdan I Iorga, Thierry Naas

Abstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Characterization of GUA-1, a chromosomally encoded ESBL fromAntimicrobial agents and chemotherapy · 2026
    Article
  2. 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

8 authors.

Mariam RimaTeam ReSIST, INSERM U1184, School of Medicine Université Paris-Saclay, LabEx LERMIT, Le Kremlin-Bicêtre, France.
Saoussen OueslatiTeam ReSIST, INSERM U1184, School of Medicine Université Paris-Saclay, LabEx LERMIT, Le Kremlin-Bicêtre, France.
Garance CotelonFrench National Reference Center for Antibiotic Resistance: Carbapenemase-Producing Enterobacterales, Le Kremlin-Bicêtre, France.
Elodie CretonFrench National Reference Center for Antibiotic Resistance: Carbapenemase-Producing Enterobacterales, Le Kremlin-Bicêtre, France.
Rémy A BonninTeam ReSIST, INSERM U1184, School of Medicine Université Paris-Saclay, LabEx LERMIT, Le Kremlin-Bicêtre, France.
Laurent DortetTeam ReSIST, INSERM U1184, School of Medicine Université Paris-Saclay, LabEx LERMIT, Le Kremlin-Bicêtre, France.ORCID 0000-0001-6596-7384
Bogdan I IorgaUniversité Paris-Saclay, CNRS UPR 2301, Institut de Chimie des Substances Naturelles, Gif-sur-Yvette, France.ORCID 0000-0003-0392-1350
Thierry NaasTeam ReSIST, INSERM U1184, School of Medicine Université Paris-Saclay, LabEx LERMIT, Le Kremlin-Bicêtre, France.ORCID 0000-0001-9937-9572

Funding

Agence Nationale de la Recherche (ANR) ANR-19-AMRB-0004Agence Nationale de la Recherche (ANR) ANR-20-PAMR-0010Assistance Publique - Hôpitaux de Paris (AP-HP)Institut National de la Santé et de la Recherche Médicale (Inserm) 1184Université Paris-Saclay (University of Paris-Saclay) 1184
6 · The paper itself

Abstract

OXA-48 has rapidly disseminated worldwide and become one of the most common carbapenemases in many countries with more than 45 variants reported with, in some cases, significant differences in their hydrolysis profiles. The R214 residue, located in the ß5-ß6 loop, is crucial for the carbapenemase activity, as it stabilizes carbapenems in the active site and maintains the shape of the active site through interactions with D159. In this study, we have characterized a novel variant of OXA-48, OXA-933 with a single D159N change. To evaluate the importance of this residue, point mutations were generated (D159A, D159G, D159K, and D159W), kinetic parameters of OXA-933, OXA-48 D159G, and OXA-48 D159K were determined and compared to those of OXA-48 and OXA-244. The

Indexed as

Anti-Bacterial Agentsbeta-LactamasesCarbapenemsEscherichia coliMicrobial Sensitivity TestsPenicillinsBacterial ProteinsCatalytic DomainDNA Transposable ElementsEscherichia coli ProteinsHydrolysisKineticsPoint MutationAnti-Bacterial AgentsBacterial Proteinsbeta-lactamase OXA-48, E colibeta-LactamasescarbapenemaseCarbapenemsDNA Transposable ElementsEscherichia coli ProteinsPenicillinstemocillincarbapenemaseenterobacterales carbapenemase producerOXA-48-likeresistance carbapenems

Identifiers

PMID38526049
PMCPMC11064584

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Registered trials

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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.