Evidence map›Paper›PMID 25733512›Full record

ArticleAntimicrobial agents and chemotherapy2015

Impact of β-lactamase inhibition on the activity of ceftaroline against Mycobacterium tuberculosis and Mycobacterium abscessus.

Vincent Dubée, Daria Soroka, Mélanie Cortes, Anne-Laure Lefebvre, Laurent Gutmann, Jean-Emmanuel Hugonnet, Michel Arthur, Jean-Luc Mainardi

Abstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed.

  1. Article
  2. Durlobactam in combination with β-lactams to combatAntimicrobial agents and chemotherapy · 2025
    Article
  3. Review
  4. Microbiology spectrum · 2024
    Article
  5. Antimicrobial agents and chemotherapy · 2024
    Article
  6. Exploring antibiotic resistance mechanisms inFrontiers in microbiology · 2024
    Review
  7. Article
  8. Microorganisms · 2021
    Article
  9. "One-Two Punch": Synergistic ß-Lactam Combinations for Mycobacterium abscessus and Target Redundancy in the Inhibition of Peptidoglycan Synthesis Enzymes.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2021
    Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Looking beyond Typical Treatments for Atypical Mycobacteria.Antibiotics (Basel, Switzerland) · 2020
    Review
  15. New β-Lactamase Inhibitors Nacubactam and Zidebactam Improve theAntimicrobial agents and chemotherapy · 2019
    Article
  16. Select β-Lactam Combinations Exhibit Synergy againstAntimicrobial agents and chemotherapy · 2019
    Article
  17. Antimicrobial agents and chemotherapy · 2019
    Article
  18. Article
  19. Review
  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

8 authors.

Vincent DubéeINSERM, UMR_S 1138, Centre de Recherche des Cordeliers, LRMA, Equipe 12, Paris, France Sorbonne Universités, Université Pierre et Marie Curie-Paris 06, UMR_S 1138, Centre de Recherche des Cordeliers, Paris, France Université Paris Descartes, Sorbonne Paris Cité, UMR_S 1138, Centre de Recherche des Cordeliers, Paris, France Assistance Publique-Hôpitaux de Paris, Hôpital Saint-Antoine, Service de Réanimation Médicale, Paris, France.
Daria SorokaINSERM, UMR_S 1138, Centre de Recherche des Cordeliers, LRMA, Equipe 12, Paris, France Sorbonne Universités, Université Pierre et Marie Curie-Paris 06, UMR_S 1138, Centre de Recherche des Cordeliers, Paris, France Université Paris Descartes, Sorbonne Paris Cité, UMR_S 1138, Centre de Recherche des Cordeliers, Paris, France.
Mélanie CortesINSERM, UMR_S 1138, Centre de Recherche des Cordeliers, LRMA, Equipe 12, Paris, France Sorbonne Universités, Université Pierre et Marie Curie-Paris 06, UMR_S 1138, Centre de Recherche des Cordeliers, Paris, France Université Paris Descartes, Sorbonne Paris Cité, UMR_S 1138, Centre de Recherche des Cordeliers, Paris, France.
Anne-Laure LefebvreINSERM, UMR_S 1138, Centre de Recherche des Cordeliers, LRMA, Equipe 12, Paris, France Sorbonne Universités, Université Pierre et Marie Curie-Paris 06, UMR_S 1138, Centre de Recherche des Cordeliers, Paris, France Université Paris Descartes, Sorbonne Paris Cité, UMR_S 1138, Centre de Recherche des Cordeliers, Paris, France.
Laurent GutmannINSERM, UMR_S 1138, Centre de Recherche des Cordeliers, LRMA, Equipe 12, Paris, France Sorbonne Universités, Université Pierre et Marie Curie-Paris 06, UMR_S 1138, Centre de Recherche des Cordeliers, Paris, France Université Paris Descartes, Sorbonne Paris Cité, UMR_S 1138, Centre de Recherche des Cordeliers, Paris, France Assistance Publique-Hôpitaux de Paris, Hôpital Européen Georges Pompidou, Paris, France.
Jean-Emmanuel HugonnetINSERM, UMR_S 1138, Centre de Recherche des Cordeliers, LRMA, Equipe 12, Paris, France Sorbonne Universités, Université Pierre et Marie Curie-Paris 06, UMR_S 1138, Centre de Recherche des Cordeliers, Paris, France Université Paris Descartes, Sorbonne Paris Cité, UMR_S 1138, Centre de Recherche des Cordeliers, Paris, France.
Michel ArthurINSERM, UMR_S 1138, Centre de Recherche des Cordeliers, LRMA, Equipe 12, Paris, France Sorbonne Universités, Université Pierre et Marie Curie-Paris 06, UMR_S 1138, Centre de Recherche des Cordeliers, Paris, France Université Paris Descartes, Sorbonne Paris Cité, UMR_S 1138, Centre de Recherche des Cordeliers, Paris, France.
Jean-Luc MainardiINSERM, UMR_S 1138, Centre de Recherche des Cordeliers, LRMA, Equipe 12, Paris, France Sorbonne Universités, Université Pierre et Marie Curie-Paris 06, UMR_S 1138, Centre de Recherche des Cordeliers, Paris, France Université Paris Descartes, Sorbonne Paris Cité, UMR_S 1138, Centre de Recherche des Cordeliers, Paris, France Assistance Publique-Hôpitaux de Paris, Hôpital Européen Georges Pompidou, Paris, France jean-luc.mainardi@crc.jussieu.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The production of β-lactamases Bla(Mab) and BlaC contributes to β-lactam resistance in Mycobacterium abscessus and Mycobacterium tuberculosis, respectively. Ceftaroline was efficiently hydrolyzed by these enzymes. Inhibition of M. tuberculosis BlaC by clavulanate decreased the ceftaroline MIC from ≥ 256 to 16 to 64 μg/ml, but these values are clinically irrelevant. In contrast, the ceftaroline-avibactam combination should be evaluated against M. abscessus since it inhibited growth at lower and potentially achievable drug concentrations.

Indexed as

Azabicyclo Compoundsbeta-Lactamase Inhibitorsbeta-LactamasesCeftarolineCephalosporinsMycobacteriumMycobacterium tuberculosisavibactamAzabicyclo Compoundsbeta-Lactamase Inhibitorsbeta-LactamasesCeftarolineCephalosporins

Identifiers

PMID25733512
PMCPMC4394810

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.