bioRxiv ScienceSearch

bioRxiv · 10.64898/2026.09.01.748571

A configuration-resolved benchmark of differential abundance analysis methods for human gut 16S rRNA microbiome data

Abstract

Tools for differential abundance testing of 16S rRNA data are conventionally treated as discrete methods, and benchmarks have accordingly sought to determine which tool performs best. However, each tool offers an array of configurations based on different normalisation, transformation, reference choice, and sensitivity filtering methods, and the specific impact of these configurations on performance has rarely been systematically investigated. We benchmarked five widely used tools (MaAsLin 2, MaAsLin 3, edgeR, ALDEx2, and ANCOM-BC2) across 18 configurations, using simulated communities and human gut profiles with implanted signals, at two taxonomic resolutions and across several design factors. Configuration accounted for as much performance variation as the choice of tool itself, with the ranking of two tools depending on which of their settings are compared. Individual parameters behaved as switches between opposite error regimes rather than as graded adjustments, and the settings carrying this weight are identifiable in advance. These behaviours were reproducible across data sources and resolutions. Our results define a configuration-aware framework for matching a tool and its settings to the cohort, study design, and feature resolution, establishing that a differential abundance result is interpretable only if the configuration used for the analysis is reported.

Explore related subjects

Keep this discovery

BibTeXRIS

Abdelmalek, N., Di Meo, C., Fiorito, G., Uzzau, S., Tanca, A.. 2026-09-03. A configuration-resolved benchmark of differential abundance analysis methods for human gut 16S rRNA microbiome data. https://doi.org/10.64898/2026.09.01.748571

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

Discover connections

Connections use source metadata and explicit phrase matches, not verified experimental comparisons.

KEEP EXPLORING

Related preprints

Understanding the physiological alterations of Vibrio cholerae upon exposure to L-ascorbic acid

The scourge of cholera remains a major global public health threat. It affects up to 4 million people worldwide and causes tens of thousands of deaths each year. The disease is experiencing a concerning resurgence in many parts of Africa, the Middle East, and Asia. To effectively tackle cholera and circumvent rising antimicrobial resistance, targeted biological and preventive approaches, complementing traditional rehydration, are urgently needed. In this regard, our group has demonstrated the efficacy of L-ascorbic acid in controlling the growth and pathogenesis of Vibrio cholerae in vitro. The present work further provides a mechanistic elucidation of the L-ascorbic acid-mediated physiological changes in V. cholerae and also bolsters such a non-antibiotic approach to control cholera.

microbiology

Motile bacteria collectively transport soil water during host colonisation

Nutrient availability in soil is temporally and spatially heterogeneous, and, as a result, microbial migration is critical for many species. The nature of microbial movement in soil, however, is unknown due to a lack of observations and experimental data. We developed live-imaging and image-analysis techniques to track the movement of single cells through soil to elucidate how Bacillus subtilis utilises pore space during the early root colonisation. The study reveals that the bacterium can modify fluid pathways to create streams, even at low bulk cell density. The phenomenon was influenced by pore structure, distance from the root and the viscosity of the soil solution. By generating macroscopic fluid motion, bacteria may also be able to travel faster and farther than individually, while limiting energy expenditure.

microbiology

Mechanism-based prediction of insertion-driven high pathogenicity avian influenza virus emergence

High pathogenicity avian influenza viruses (HPAIVs) emerge from H5 and H7 low-pathogenicity avian influenza virus progenitors through mutations that introduce a multibasic cleavage site in haemagglutinin. Although nucleotide insertions recurrently generate this motif, the molecular determinants of insertion and whether particular HA sequences are genetically predisposed to evolve toward HPAIV remain unknown. Combining experimental virology and thermodynamic modelling, we show that insertions arise through polymerase slippage controlled by local product-template duplex thermodynamics within the viral polymerase catalytic site. Predicted RNA secondary structures outside the polymerase are not required for high-frequency insertions and only modestly modulate insertion rates. We formalize this mechanism in HPAIVpredict, which predicts insertion profiles, recapitulates intermediates associated with documented HPAIV emergence events and identifies H5 and H7 sequence backgrounds predisposed to acquire functional multibasic cleavage sites.

microbiology