Evidence map›Paper›PMID 22760036›Full record

ArticleJournal of clinical microbiology2012

Phylogenetic distribution of CTX-M- and non-extended-spectrum-β-lactamase-producing Escherichia coli isolates: group B2 isolates, except clone ST131, rarely produce CTX-M enzymes.

Sylvain Brisse, Laure Diancourt, Cédric Laouénan, Marie Vigan, Valérie Caro, Guillaume Arlet, Laurence Drieux, Véronique Leflon-Guibout, France Mentré, Vincent Jarlier and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of clinical microbiology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 2 pooled it
3.3field-weighted citation impact, top 7% 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

33 citing papers in PubMed, 2 syntheses or guidelines pooled it, 63 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Article
  5. Whole-Genome Analysis ofAntibiotics (Basel, Switzerland) · 2025
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  6. A First Report on Multidrug-ResistantAntibiotics (Basel, Switzerland) · 2025
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  7. Genotypic Characteristics and Antimicrobial Resistance ofAntibiotics (Basel, Switzerland) · 2023
    Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. High Prevalence of ST131 Subclades C2-Frontiers in cellular and infection microbiology · 2020
    Article
  13. Infection and drug resistance · 2019
    Article
  14. Article
  15. Article
  16. Article
  17. Clonal Diversity of ESBL-Producing Escherichia coli Isolated from Environmental, Human and Food Samples.International journal of environmental research and public health · 2017
    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

12 authors at 6 institutions in 1 country.

Sylvain BrisseInstitut Pasteur, Genotyping of Pathogens and Public Health, Paris, France. sylvain.brisse@pasteur.fr
Laure Diancourt
Cédric Laouénan
Marie Vigan
Valérie Caro
Guillaume Arlet
Laurence Drieux
Véronique Leflon-Guibout
France Mentré
Vincent Jarlier
Marie-Hélène Nicolas-Chanoine
Coli β Study Group
Assistance Publique – Hôpitaux de Paris · FRInstitut Pasteur · FRUniversité Paris Cité · FRHôpital Charles-Foix · FRInserm · FRSorbonne Paris Cité · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Escherichia coli is the species most frequently associated with clinical infections by extended-spectrum-β-lactamase (ESBL)-producing isolates, with the CTX-M ESBL enzymes being predominant and found in genetically diverse E. coli isolates. The main objective of this study was to compare, on the basis of a case-control design, the phylogenetic diversity of 152 CTX-M-producing and 152 non-ESBL-producing clinical E. coli isolates. Multilocus sequence typing revealed that even though CTX-M enzymes were largely disseminated across the diversity of E. coli isolates, phylogenetic group B2 showed a particularly heterogeneous situation. First, clone ST131 of group B2 was strongly associated with CTX-M production (55 [79%] of 70 isolates), with CTX-M-15 being predominant. Second, the remaining members of group B2 were significantly less frequently associated with CTX-M production (9 [12%] of 75) than E. coli phylogenetic groups A, B1, and D (88 [55%] of 159). CTX-M-producing ST131 E. coli isolates were significantly more frequent in patients hospitalized in geriatric wards or long-term care facilities. Besides, the non-ESBL ST131 isolates significantly more frequently showed resistance to penicillins than the non-ESBL, non-ST131 isolates did. In conclusion, the present study emphasizes the particular antimicrobial resistance and epidemiologic characteristics of clone ST131 within group B2, which could result from the higher antibiotic exposure of this clone, as it is the predominant clone of group B2 carried in the human gut.

Indexed as

Genetic VariationPhylogenybeta-LactamasesCluster AnalysisDrug Resistance, BacterialEscherichia coliEscherichia coli InfectionsHumansMolecular EpidemiologyMultilocus Sequence TypingPrevalencebeta-Lactamases

Identifiers

PMID22760036
PMCPMC3421780
OpenAlexW2077147594

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.