Evidence map›Paper›PMID 38849863›Full record

ArticleGenome medicine2024

Keeping up with the pathogens: improved antimicrobial resistance detection and prediction from Pseudomonas aeruginosa genomes.

Danielle E Madden, Timothy Baird, Scott C Bell, Kate L McCarthy, Erin P Price, Derek S Sarovich

Abstract read
In one paragraph

Article in Genome medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Article
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  5. Antimicrobial agents and chemotherapy · 2026
    Article
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  9. Review
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  11. Antibiotic resistance inFrontiers in microbiology · 2026
    Review
  12. Article
  13. Prediction of antimicrobial resistance inMicrobiology spectrum · 2025
    Article
  14. Article
  15. Article
  16. 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

6 authors.

Danielle E MaddenCentre for Bioinnovation, University of the Sunshine Coast, Sippy Downs, QLD, Australia.
Timothy BairdCentre for Bioinnovation, University of the Sunshine Coast, Sippy Downs, QLD, Australia.
Scott C BellAdult Cystic Fibrosis Centre, The Prince Charles Hospital, Chermside, Queensland, Australia.
Kate L McCarthyUniversity of Queensland Medical School, Herston, QLD, Australia.
Erin P Price *Centre for Bioinnovation, University of the Sunshine Coast, Sippy Downs, QLD, Australia.
Derek S Sarovich *Centre for Bioinnovation, University of the Sunshine Coast, Sippy Downs, QLD, Australia. dsarovich@usc.edu.au.ORCID 0000-0002-6944-3980

Funding

Advance Queensland AQIRF0362018Advance Queensland AQRF13016-17RD2National Health and Medical Research Council GNT455919Wishlist 2019-14
6 · The paper itself

Abstract

backgroundAntimicrobial resistance (AMR) is an intensifying threat that requires urgent mitigation to avoid a post-antibiotic era. Pseudomonas aeruginosa represents one of the greatest AMR concerns due to increasing multi- and pan-drug resistance rates. Shotgun sequencing is gaining traction for in silico AMR profiling due to its unambiguity and transferability; however, accurate and comprehensive AMR prediction from P. aeruginosa genomes remains an unsolved problem.

methodsWe first curated the most comprehensive database yet of known P. aeruginosa AMR variants. Next, we performed comparative genomics and microbial genome-wide association study analysis across a Global isolate Dataset (n = 1877) with paired antimicrobial phenotype and genomic data to identify novel AMR variants. Finally, the performance of our P. aeruginosa AMR database, implemented in our AMR detection and prediction tool, ARDaP, was compared with three previously published in silico AMR gene detection or phenotype prediction tools-abritAMR, AMRFinderPlus, ResFinder-across both the Global Dataset and an analysis-naïve Validation Dataset (n = 102).

resultsOur AMR database comprises 3639 mobile AMR genes and 728 chromosomal variants, including 75 previously unreported chromosomal AMR variants, 10 variants associated with unusual antimicrobial susceptibility, and 281 chromosomal variants that we show are unlikely to confer AMR. Our pipeline achieved a genotype-phenotype balanced accuracy (bACC) of 85% and 81% across 10 clinically relevant antibiotics when tested against the Global and Validation Datasets, respectively, vs. just 56% and 54% with abritAMR, 58% and 54% with AMRFinderPlus, and 60% and 53% with ResFinder. ARDaP's superior performance was predominantly due to the inclusion of chromosomal AMR variants, which are generally not identified with most AMR identification tools.

conclusionsOur ARDaP software and associated AMR variant database provides an accurate tool for predicting AMR phenotypes in P. aeruginosa, far surpassing the performance of current tools. Implementation of ARDaP for routine AMR prediction from P. aeruginosa genomes and metagenomes will improve AMR identification, addressing a critical facet in combatting this treatment-refractory pathogen. However, knowledge gaps remain in our understanding of the P. aeruginosa resistome, particularly the basis of colistin AMR.

Indexed as

Genome, BacterialPseudomonas aeruginosaAnti-Bacterial AgentsDatabases, GeneticDrug Resistance, BacterialGenomicsHumansMicrobial Sensitivity TestsPhenotypePseudomonas InfectionsAnti-Bacterial AgentsAMR databaseAMR predictionAMR softwareAntibioticBioinformaticsGenomicsHigh-throughput sequencingMetagenomicsWhole-genome sequencing

Identifiers

PMID38849863
PMCPMC11157771

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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.