q2-metnet: QIIME2 package to analyse 16S rRNA data via high-quality metabolic reconstructions of the human gut microbiota
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Balzerani, Francesco; Blasco, Telmo; Pèrez-Burillo, Sergio; Francino Puget, María Pilar; Rufián-Henares, José Ángel; Valcárcel, Luis V.; Planes, Francisco J.Editorial
Oxford University Press
Date
2024-07-17Referencia bibliográfica
Balzerani, F. et. al. Bioinformatics, 2024, 40(11), btae455. [https://doi.org/10.1093/bioinformatics/btae455]
Sponsorship
European Union’s Horizon 2020 research and innovation programme through the STANCE4HEALTH project (Grant No. 816303); postdoctoral grant Juan de la Cierva— Formacion, awarded by the Spanish Ministry of Science and Innovation (Ref.: FJC2020-046252 I)Abstract
Motivation: 16S rRNA gene sequencing is the most frequent approach for the characterization of the human gut microbiota. Despite different
efforts in the literature, the inference of functional and metabolic interpretations from 16S rRNA gene sequencing data is still a challenging task.
High-quality metabolic reconstructions of the human gut microbiota, such as AGORA and AGREDA, constitute a curated resource to improve
functional inference from 16S rRNA data, but they are not typically integrated into standard bioinformatics tools.
Results: Here, we present q2-metnet, a QIIME2 plugin that enables the contextualization of 16S rRNA gene sequencing data into AGORA and
AGREDA. In particular, based on relative abundances of taxa, q2-metnet determines normalized activity scores for the reactions and subsystems
involved in the selected metabolic reconstruction. Using these scores, q2-metnet allows the user to conduct differential activity analysis
for reactions and subsystems, as well as exploratory analysis using PCA and hierarchical clustering. We apply q2-metnet to a dataset from our
group that involves 16S rRNA data from stool samples from lean, allergic to cow’s milk, obese and celiac children, and the Belgian Flemish Gut
Flora Project cohort, which includes faecal 16S rRNA data from obese and normal-weight adult individuals. In the first case, q2-metnet outperforms
existing algorithms in separating different clinical conditions based on predicted pathway abundances and subsystem scores. In the second
case, q2-metnet complements competing approaches in predicting functional alterations in the gut microbiota of obese individuals. Overall,
q2-metnet constitutes a powerful bioinformatics tool to provide metabolic context to 16S rRNA data from the human gut microbiota.