计算机科学
背景(考古学)
计算生物学
数据挖掘
基因组学
数据整理
遗传程序设计
基因组
人工智能
接口(物质)
数据集成
计算模型
参考数据
机器学习
生物
封面(代数)
作者
Gioele Lazzari,Giovanna E. Felis,Elisa Salvetti,Matteo Calgaro,Francesca Di Cesare,Bas Teusink,Nicola Vitulo
出处
期刊:MSystems
[American Society for Microbiology]
日期:2025-12-12
卷期号:11 (1): e0100725-e0100725
标识
DOI:10.1128/msystems.01007-25
摘要
Genome-scale metabolic models (GSMMs) can mechanistically explain phenotypic differences among closely related bacterial strains. However, high-throughput multi-strain reconstructions of GSMMs are still challenging: reference-based methods inherit curated information while missing new contents; alternatively (universe-based), reference-free methods could cover strain-specific reactions, but they disregard curated information. Ideally, references should be curated pan-GSMMs for species (or genus), but their reconstruction is extremely demanding, making them still rare in the literature. Here, Gempipe is presented, a computational tool streamlining the multi-strain reconstruction and analysis of GSMMs, going through the production of a pan-GSMM. Its reconstruction method is hybrid; as an optional reference, GSMM is automatically expanded with extra reactions taken from a reference-free reconstruction. Gempipe also downloads, filters, and annotates genomes; performs in-depth gene recovery; annotates models' contents; and predicts strain-specific capabilities. The companion programming interface includes functions ranging from the (pan-)GSMMs' curation to the multi-strain analysis. Gempipe was validated using multi-strain data sets, showing improved accuracy when compared with state-of-the-art tools. Moreover, metabolic diversities within Limosilactobacillus reuteri were explored, grouping strains into metabolically coherent clusters and systematically predicting health-related metabolites' biosynthesis.IMPORTANCEAvailable genome-scale metabolic model (GSMM) reconstruction tools present major limitations in the context of multi-strain modeling. Gempipe surpasses these limitations by implementing a novel, hybrid reconstruction strategy. Not only does it produce more accurate strain-specific GSMMs, but it also produces pan-GSMMs when the only available reference is a manually curated model for a single strain, which is currently the most common case. With the vast availability of genome sequences, the high-throughput, multi-strain GSMM reconstruction and analysis approach provided by Gempipe will facilitate large-scale studies of exploration and bioprospecting of strain-level bacterial metabolic diversity, moving a step forward in strains' screening and rational selection.
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