Evidence map›Paper›PMID 36719135›Full record

ReviewThe Journal of antimicrobial chemotherapy2023

Transiently silent acquired antimicrobial resistance: an emerging challenge in susceptibility testing.

Theresa Maria Wagner, Benjamin Peter Howden, Arnfinn Sundsfjord, Kristin Hegstad

Abstract readReview
In one paragraph

Review in The Journal of antimicrobial chemotherapy, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Within-patient carbapenem heteroresistance inCurrent research in microbial sciences · 2026
    Article
  2. Article
  3. Article
  4. Review
  5. Resistome Profiling of a Large Collection ofInternational journal of molecular sciences · 2026
    Article
  6. Genomic and clinical characteristics ofMicrobiology spectrum · 2026
    Article
  7. Plasmid-linked virulence genes and high-level gentamicin resistance inJournal of conservative dentistry and endodontics · 2026
    Article
  8. Article
  9. Article
  10. Article
  11. Antimicrobial and Phylogenomic Characterization ofAntibiotics (Basel, Switzerland) · 2024
    Article
  12. Review
  13. Genetic analysis of vancomycin-variable Enterococcus faecium clinical isolates in Italy.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2024
    Article
  14. Antibiotic Resistance/Susceptibility Profiles ofInternational journal of molecular sciences · 2023
    Article
  15. 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

4 authors.

Theresa Maria WagnerResearch Group for Host-Microbe Interactions, Department of Medical Biology, Faculty of Health Sciences, UiT the Arctic University of Norway, Tromsø, Norway.ORCID 0000-0002-8605-6296
Benjamin Peter HowdenMicrobiological Diagnostic Unit Public Health Laboratory, The Department of Microbiology and Immunology, The University of Melbourne at The Peter Doherty Institute for Infection and Immunity, Melbourne, Australia.ORCID 0000-0003-0237-1473
Arnfinn SundsfjordResearch Group for Host-Microbe Interactions, Department of Medical Biology, Faculty of Health Sciences, UiT the Arctic University of Norway, Tromsø, Norway.
Kristin HegstadResearch Group for Host-Microbe Interactions, Department of Medical Biology, Faculty of Health Sciences, UiT the Arctic University of Norway, Tromsø, Norway.ORCID 0000-0002-1314-0497

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acquisition and expression of antimicrobial resistance (AMR) mechanisms in bacteria are often associated with a fitness cost. Thus, evolutionary adaptation and fitness cost compensation may support the advance of subpopulations with a silent resistance phenotype when the antibiotic selection pressure is absent. However, reports are emerging on the transient nature of silent acquired AMR, describing genetic alterations that can change the expression of these determinants to a clinically relevant level of resistance, and the association with breakthrough infections causing treatment failures. This phenomenon of transiently silent acquired AMR (tsaAMR) is likely to increase, considering the overall expansion of acquired AMR in bacterial pathogens. Moreover, the augmented use of genotypic methods in combination with conventional phenotypic antimicrobial susceptibility testing (AST) will increasingly enable the detection of genotype and phenotype discrepancy. This review defines tsaAMR as acquired antimicrobial resistance genes with a corresponding phenotype within the wild-type distribution or below the clinical breakpoint for susceptibility for which genetic alterations can mediate expression to a clinically relevant level of resistance. References to in vivo resistance development and therapeutic failures caused by selected resistant subpopulations of tsaAMR in Gram-positive and Gram-negative pathogens are given. We also describe the underlying molecular mechanisms, including alterations in the expression, reading frame or copy number of AMR determinants, and discuss the clinical relevance concerning challenges for conventional AST.

Indexed as

Anti-Bacterial AgentsAnti-Infective AgentsBacteriaDrug Resistance, BacterialMicrobial Sensitivity TestsPhenotypeAnti-Bacterial AgentsAnti-Infective Agents

Identifiers

PMID36719135
PMCPMC9978586

What OpenQuestion holds

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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.