Title PoMeLo: a systematic computational approach to predicting metabolic loss in pathogen genomes /
Authors Glascock, Abigail ; Waltari, Eric ; Dudas, Gytis ; Wong, Joan ; Ahyong, Vida
DOI 10.1186/s12859-024-05640-w
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Is Part of BMC Bioinformatics.. London : BioMed Central Ltd. 2024, vol. 25, iss. 1, art. no. 49, p. [1-13].. eISSN 1471-2105
Keywords [eng] genome streamlining ; metabolic profiling ; phylogenomics ; software
Abstract [eng] Background: Genome streamlining, the process by which genomes become smaller and encode fewer genes over time, is a common phenomenon among pathogenic bacteria. This reduction is driven by selection for minimized energy expenditure in a nutrient-rich environment. As pathogens evolve to become more reliant on the host, metabolic genes and resulting capabilities are lost in favor of siphoning metabolites from the host. Characterizing genome streamlining, gene loss, and metabolic pathway degradation can be useful in assessing pathogen dependency on host metabolism and identifying potential targets for host-directed therapeutics. Results: PoMeLo (Predictor of M etabolic L oss) is a novel evolutionary genomics-guided computational approach for identifying metabolic gaps in the genomes of pathogenic bacteria. PoMeLo leverages a centralized public database of high-quality genomes and annotations and allows the user to compare an unlimited number of genomes across individual genes and pathways. PoMeLo runs locally using user-friendly prompts in a matter of minutes and generates tabular and visual outputs for users to compare predicted metabolic capacity between groups of bacteria and individual species. Each pathway is assigned a Predicted Metabolic Loss (PML) score to assess the magnitude of genome streamlining. Optionally, PoMeLo places the results in an evolutionary context by including phylogenetic relationships in visual outputs. It can also initially compute phylogenetically-weighted mean genome sizes to identify genome streamlining events. Here, we describe PoMeLo and demonstrate its use in identifying metabolic gaps in genomes of pathogenic Treponema species. Conclusions: PoMeLo represents an advance over existing methods for identifying metabolic gaps in genomic data, allowing comparison across large numbers of genomes and placing the resulting data in a phylogenetic context. PoMeLo is freely available for academic and non-academic use at https://github.com/czbiohub-sf/pomelo .
Published London : BioMed Central Ltd
Type Journal article
Language English
Publication date 2024
CC license CC license description