Evidence map›Paper›PMID 33911082›Full record

ArticleNature communications2021

Rapid evolution and host immunity drive the rise and fall of carbapenem resistance during an acute Pseudomonas aeruginosa infection.

Rachel Wheatley, Julio Diaz Caballero, Natalia Kapel, Fien H R de Winter, Pramod Jangir, Angus Quinn, Ester Del Barrio-Tofiño, Carla López-Causapé, Jessica Hedge, Gabriel Torrens and 16 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
4.4field-weighted citation impact, top 4% 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

52 citing papers in PubMed, 76 citations in OpenAlex.

  1. Review
  2. Climate change and antimicrobial resistance.Nature reviews. Microbiology · 2026
    Review
  3. Review
  4. Beyond Resistance Genes:Life (Basel, Switzerland) · 2026
    Review
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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

26 authors at 7 institutions in 5 countries.

Rachel Wheatley *University of Oxford, Department of Zoology, Oxford, UK.ORCID http://orcid.org/0000-0003-1212-2286
Julio Diaz Caballero *University of Oxford, Department of Zoology, Oxford, UK.
Natalia KapelUniversity of Oxford, Department of Zoology, Oxford, UK.
Fien H R de WinterLaboratory of Medical Microbiology, Vaccine and Infectious Disease Institute, University of Antwerp, Wilrijk, Belgium.ORCID http://orcid.org/0000-0003-3803-7813
Pramod JangirUniversity of Oxford, Department of Zoology, Oxford, UK.
Angus QuinnUniversity of Oxford, Department of Zoology, Oxford, UK.ORCID http://orcid.org/0000-0003-1210-3894
Ester Del Barrio-TofiñoHospital Universitario Son Espases, Palma de Mallorca, Spain.
Carla López-CausapéHospital Universitario Son Espases, Palma de Mallorca, Spain.
Jessica HedgeUniversity of Oxford, Department of Zoology, Oxford, UK.ORCID http://orcid.org/0000-0002-4343-4146
Gabriel TorrensHospital Universitario Son Espases, Palma de Mallorca, Spain.
Thomas Van der SchalkLaboratory of Medical Microbiology, Vaccine and Infectious Disease Institute, University of Antwerp, Wilrijk, Belgium.ORCID http://orcid.org/0000-0001-7493-4082
Basil Britto XavierLaboratory of Medical Microbiology, Vaccine and Infectious Disease Institute, University of Antwerp, Wilrijk, Belgium.ORCID http://orcid.org/0000-0002-5897-0240
Felipe Fernández-CuencaDepartamento de Medicina, Universidad de Sevilla, Seville, Spain.
Angel ArenzanaDepartamento de Medicina, Universidad de Sevilla, Seville, Spain.
Claudia RecanatiniJulius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.ORCID http://orcid.org/0000-0003-0643-7599
Leen TimbermontLaboratory of Medical Microbiology, Vaccine and Infectious Disease Institute, University of Antwerp, Wilrijk, Belgium.ORCID http://orcid.org/0000-0002-9543-9205
Frangiscos SifakisBoehringer Ingelheim Pharmaceuticals, Inc, Ridgefield, CT, USA.
Alexey RuzinMicrobial Sciences, BioPharmaceuticals R&D, AstraZeneca, Gaithersburg, MD, USA.
Omar AliMicrobial Sciences, BioPharmaceuticals R&D, AstraZeneca, Gaithersburg, MD, USA.
Christine LammensLaboratory of Medical Microbiology, Vaccine and Infectious Disease Institute, University of Antwerp, Wilrijk, Belgium.
Herman GoossensLaboratory of Medical Microbiology, Vaccine and Infectious Disease Institute, University of Antwerp, Wilrijk, Belgium.
Jan KluytmansJulius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.
Samir Kumar-SinghLaboratory of Medical Microbiology, Vaccine and Infectious Disease Institute, University of Antwerp, Wilrijk, Belgium.
Antonio OliverHospital Universitario Son Espases, Palma de Mallorca, Spain.
Surbhi Malhotra-KumarLaboratory of Medical Microbiology, Vaccine and Infectious Disease Institute, University of Antwerp, Wilrijk, Belgium.ORCID http://orcid.org/0000-0001-8699-8905
Craig MacLeanUniversity of Oxford, Department of Zoology, Oxford, UK. craig.maclean@zoo.ox.ac.uk.ORCID http://orcid.org/0000-0002-7941-813X
University of Antwerp · BEUniversity of Oxford · GBHospital Universitario Son Espases · ESAstraZeneca (United States) · USUniversidad de Sevilla · ESUtrecht University · NLBoehringer Ingelheim (United States) · US

Funding

Wellcome TrustWellcome Trust 106918/Z/15/ZWellcome Trust 203141/Z/16/Z
6 · The paper itself

Abstract

It is well established that antibiotic treatment selects for resistance, but the dynamics of this process during infections are poorly understood. Here we map the responses of Pseudomonas aeruginosa to treatment in high definition during a lung infection of a single ICU patient. Host immunity and antibiotic therapy with meropenem suppressed P. aeruginosa, but a second wave of infection emerged due to the growth of oprD and wbpM meropenem resistant mutants that evolved in situ. Selection then led to a loss of resistance by decreasing the prevalence of low fitness oprD mutants, increasing the frequency of high fitness mutants lacking the MexAB-OprM efflux pump, and decreasing the copy number of a multidrug resistance plasmid. Ultimately, host immunity suppressed wbpM mutants with high meropenem resistance and fitness. Our study highlights how natural selection and host immunity interact to drive both the rapid rise, and fall, of resistance during infection.

Indexed as

Anti-Bacterial AgentsBacterial Outer Membrane ProteinsBacterial ProteinsDrug Resistance, Multiple, BacterialHumansHydro-LyasesMembrane Transport ProteinsMeropenemMicrobial Sensitivity TestsMiddle AgedPlasmidsPorinsPseudomonas aeruginosaPseudomonas InfectionsRespiratory Tract InfectionsSelection, GeneticAnti-Bacterial AgentsBacterial Outer Membrane ProteinsBacterial ProteinsHydro-LyasesMembrane Transport ProteinsMeropenemMexA protein, Pseudomonas aeruginosaMexB protein, Pseudomonas aeruginosaOprD protein, Pseudomonas aeruginosaOprM protein, Pseudomonas aeruginosaPorinswbpM protein, Pseudomonas aeruginosa

Identifiers

PMID33911082
PMCPMC8080559
OpenAlexW3159421822

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.