Evidence map›Paper›PMID 42443941›Full record

ArticleGenome biology2026

Long-read metagenomics and methylation-based binning support the discovery of antibiotic resistance gene-host associations in complex communities.

Melina Markkanen, Heidi Putkuri, Dovydas Kičiatovas, Ville Mustonen, Marko Virta, Antti Karkman

Abstract read
In one paragraph

Article in Genome biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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.

Melina MarkkanenDepartment of Microbiology, University of Helsinki, Helsinki, Finland. melina.markkanen@helsinki.fi.ORCID https://orcid.org/0000-0003-2392-1729
Heidi PutkuriDepartment of Computer Science, Department of Organismal and Evolutionary Biology, University of Helsinki, Helsinki, Finland.
Dovydas KičiatovasMultidisciplinary Center of Excellence in Antimicrobial Resistance Research, University of Helsinki, Helsinki, Finland.
Ville MustonenMultidisciplinary Center of Excellence in Antimicrobial Resistance Research, University of Helsinki, Helsinki, Finland.
Marko VirtaDepartment of Microbiology, University of Helsinki, Helsinki, Finland.
Antti KarkmanDepartment of Microbiology, University of Helsinki, Helsinki, Finland. antti.karkman@helsinki.fi.

Funding

Research Council of Finland funding for the Multidisciplinary Center of Excellence in Antimicrobial Resistance Research 364231Research Council of Finland funding for the Multidisciplinary Center of Excellence in Antimicrobial Resistance Research 364234
6 · The paper itself

Abstract

backgroundAntibiotic resistance genes (ARGs) circulating among clinically relevant bacteria pose serious challenges to public health. Given the ancient and environmental bacterial origins of ARGs, a better understanding of the carriers of ARGs beyond the clinically most relevant species is urgently needed for longer-term resistance monitoring and intervention measures. While the risks of emerging ARGs from environmental sources have been recognized, the identification bottlenecks stem from the limitations of shotgun metagenomic sequencing and bioinformatic methods.

resultsWe use long-read metagenomic sequencing and bacteria-specific methylation profiles to re-establish the links between established (well-described) or latent (absent in databases) ARGs and their bacterial and genetic contexts in wastewater. We analyze base modification data produced by PacBio SMRT sequencing using an in-house pipeline utilizing position weight matrices and UMAP visualizations, which we validate by a synthetic community with known bacterial composition. Our analysis reveals several previously unreported ARGs and ARG-host linkages in wastewater. For instance, we find that Arcobacter, a key wastewater associated taxon and emerging pathogen, carries a latent beta-lactamase gene with high predicted mobility potential. Of the other understudied beta-lactamases, we describe blaMCA within pdif-modules across highly varying contexts suggesting its recent acquisition events. Additionally, we uncover the wastewater resident taxa mediated carriage of clinically important ARGs.

conclusionsBy linking ARGs to their wider genetic contexts and hosts, our findings shed light on the previously unrecognized carriers of resistance genes in wastewater. The presented approach provides a valuable methodology for early identification of newly arising ARGs and their hosts.

Indexed as

BacteriaDNA MethylationDrug Resistance, BacterialDrug Resistance, MicrobialGenes, BacterialMetagenomicsMetagenomeWastewaterWastewaterAntibiotic resistanceDNA methylationLong-read metagenomic sequencingPdif-modulesWastewater

Identifiers

PMID42443941
PMCPMC13644095

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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.