Search bioRxiv⌕ Search

bioRxiv · 10.64898/2026.10.19.760091

The impact of strain heterogeneity on genomic profiling accuracy in mixed-strain Escherichia coli metagenomes

Abstract

Metagenomic sequencing is increasingly used for surveillance of bacterial populations, enabling simultaneous characterisation of antimicrobial resistance, virulence, and epidemiologically relevant strain markers. However, the ability of commonly used bioinformatic tools to recover these features from heterogeneous populations remains incompletely understood. Here, we developed a controlled benchmarking framework based on simulated single-species Escherichia coli metagenomes generated from genomes with PCR-determined annotations. Assembly-based and read-based tools were evaluated for antimicrobial resistance gene (ARG) detection, virulence gene (VG) detection, multilocus sequence typing (MLST), and serotype prediction. In addition, datasets with varying strain compositions were used to assess the effect of population complexity on strain-level characterisation. We found that recovery of individual genetic determinants of interest (7 ARGs, 3 VGs) was consistently more successful than recovery of strain-level markers. ARG detection achieved high recovery rates across all evaluated tools (84.3-90.0%), while short read sequencing typer SRST2 achieved the highest virulence gene recovery rate (100.0%). In contrast, MLST and serotype prediction were strongly affected by strain composition. None of the evaluated MLST tools correctly assigned the dominant sequence type in the multi-strain log-normal dataset, despite successful partial recovery of MLST alleles, while complete serotype recovery remained uncommon across all methods. Decreasing the complexity of the simulated metagenome by increasing the abundance of the dominant strain improved both MLST and serotype prediction performance, while long-read analyses indicated that increased read length was insufficient to overcome the challenges associated with mixed-strain communities. These findings demonstrate that performance estimates derived from gene detection do not necessarily translate to strain-level characterisation. While individual resistance and virulence determinants could often be recovered reliably, accurate reconstruction of sequence types and serotypes remained strongly constrained by strain heterogeneity. More broadly, the results highlight current limitations in resolving strain composition from metagenomic data and provide a framework for investigating the abundance thresholds and population structures required for reliable strain-resolved surveillance.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Shridar, V. D., Engblom, S.. 2026-10-20. The impact of strain heterogeneity on genomic profiling accuracy in mixed-strain Escherichia coli metagenomes. https://doi.org/10.64898/2026.10.19.760091

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

Carrier-Limited Release Risk in Electrospun Nanofibers for Regenerative Endodontics: Constraint Discovery from 25 Formulations

Regenerative endodontics needs an intracanal carrier that keeps disinfecting across a dressing interval that clinicians schedule at one to four weeks, without harming the stem cells that rebuild the pulp. We ask what one completed 25-formulation electrospinning campaign of poly(vinylpyrrolidone) (PVP) fibers carrying metronidazole, ciprofloxacin, minocycline and Ca(OH)2 can decide, and use machine learning for constraint discovery and decision support rather than as a new predictor. After an audit against the source thesis, logistic regression predicts fine-fiber formation at 96% leave-one-out accuracy, but a one-threshold rule does as well, the gain over the 80% majority baseline is not significant (exact McNemar p = 0.125), and accuracy falls to 84% when mixture loading is encoded per component. Diameter models interpolate within formulation families (ridge MAE 193 nm, 95% CI 96 to 317 nm) and fail across them (R^2 < 0). Because the campaign never measured release, we assemble a same-drug, cross-carrier evidence table: 17 bounded metronidazole and ciprofloxacin observations from seven studies, with two-sided censoring. Water-soluble carriers (PVP, PVA) completed release within 80 h (PVP within 8 h); no water-insoluble monolithic carrier reached 90% within its observation window, releasing 1.5 to 50%; both within-study comparisons separate at matched loading; and blend, core-shell and thick-mat architectures released over 3 to 28 days. The PVP mats therefore carry a carrier-limited release risk, not a proven ceiling, and one dissolution experiment can confirm or overturn it. A censoring-aware screen keeps three necessarily and one possibly nondominated formulation, and fixed-budget replays show that uncertainty sampling finds failed formulations sooner, except the one it is confidently wrong about.

bioinformatics↗

CellMethMarker provides an integrated database of human cell- and tissue-type-specific DNA methylation markers

Cell- and tissue-type-specific DNA methylation markers provide epigenetic signatures of cellular identity and are widely used to infer cellular origin from bulk and single-cell methylomes. Existing resources mainly emphasize disease-associated biomarkers, methylome atlases, genomic annotations or RNA-based cell markers, leaving an unmet need for an integrated region-level resource dedicated to such markers. Here we present CellMethMarker (http://gu-zhanglab.hfcas.ac.cn/CellMethMarker), a curated database integrating 347,514 de novo markers derived from uniformly processed whole-genome and reduced-representation bisulfite sequencing datasets, 2,203,507 literature-derived marker records and harmonized metadata for 2,810 samples. CellMethMarker enables cell- and tissue-centered marker retrieval, coordinate-based search, genome-browser visualization, interactive methylation analysis and data download. In an independent single-cell methylome atlas, these markers recover the expected cell-type-associated methylation patterns, and a platform-matched reference built from them lowers the mean deconvolution error from 0.365 to 0.144. CellMethMarker therefore links region-level DNA methylation variation to cellular identity and supports methylome-based cell-type annotation and deconvolution.

bioinformatics↗

IG-28 enables identification and quantification of high-confidence isoforms from large bulk and single-cell full-length cDNA datasets

The technology to sequence full-length transcriptomes from bulk and single-cell samples has rapidly advanced. As a result, full-length cDNA datasets now reach billions of reads in size which is beyond the capability of most established isoform identification tools. Here, we introduce IG-28 which addresses this challenge with its capability to process and analyze large fl-cDNA datasets fast and using minimal computational resources. In contrast to its predecessor Mandalorion, IG-28 is not limited to bulk fl-cDNA but is capable of parsing, processing, and analyzing single-cell fl-cDNA datasets. It does so in a lightweight, flexible manner, integrating seamlessly with established scRNA-seq analysis workflows. We benchmarked IG-28 against a variety of established and new isoform identification tools using several bulk and a complex single-cell fl-cDNA dataset and found that IG-28 consistently outperformed the other tools by identifying high-confidence public isoforms.

bioinformatics↗