The results demonstrate that iModulons provide a genome-scale framework for comparing transcriptional regulation across closely related organisms, revealing regulatory innovations that are not apparent from genome comparisons alone.
Abstract
The genus Pseudomonas consists of diverse and ecologically significant species that form close associations with both plants and animals. This genus is widely studied due to the clinically relevant Pseudomonas aeruginosa, model plant pathogen Pseudomonas syringae, and non-pathogenic, industrially relevant Pseudomonas putida. The different metabolic and physiological capabilities of these species are enabled by their unique genetic makeup as well as varying regulatory mechanisms. To study the transcriptional basis for the diversity of the three species, we applied independent component analysis to strain-specific RNA-seq datasets to identify independently modulated gene sets (iModulons) and their condition-specific activity levels. We then mapped iModulons across strains based on their similarity in orthologous gene membership. Through comparison of iModulon gene membership and activities, we find that: (i) iModulons reveal shared and unique regulatory modalities across strains; (ii) unique adaptations in common functions, such as translation and pyoverdine production/uptake, manifest through both differential iModulon gene membership and condition-specific activation states in each strain; (iii) iModulons facilitate comparison of stress responses at the systems level; and (iv) iModulons highlight unique virulence factor enrichment and host-specific adaptations in human and plant pathogens. Altogether, comparing the modularized transcriptomes of the three strains provides unique and comprehensive insights into their differential evolution. Importance Closely related bacterial species often have vastly different metabolic and physiological capabilities, yet the regulatory mechanisms underlying these adaptations remain poorly understood. Here, we compare the transcriptional regulatory networks of three representative Pseudomonas strains through cross-strain iModulon analysis. By comparing both iModulon gene composition and activity across strains, we identify conserved regulatory modules alongside lineage-specific adaptations in functions associated with virulence, translation, iron acquisition, motility, and stress responses. Our results demonstrate that iModulons provide a genome-scale framework for comparing transcriptional regulation across closely related organisms, revealing regulatory innovations that are not apparent from genome comparisons alone. This work establishes a scalable approach for studying the evolution of bacterial transcriptional regulatory networks and the regulatory basis of niche specialization.
Understanding of the metabolic capabilities and genomic landscape of the P. fluorescens species is enhanced, providing a foundation for natural product discovery using bioinformatic approaches.
Sajid Iqbal, Farida Begum· Discover Genetics and Evolut...· 0 citations
Rec reconstructed genome-scale metabolic models of 44 Pseudomonas strains from various environments and investigated their capabilities to metabolize different carbon sources and metabolic intermediaries, demonstrating how GEM-predicted capabilities can differentiate between strains and that high metabolic versatility is associated with the predicted ability of the strains to remove toxic compounds while maintaining core functionalities.
C. Fócil-Espinosa, Christopher Dalldorf, Diego Martinez et al.· Computational and Structural...· 0 citations
This study reveals that persister cells retain active metabolism and exhibit a metabolic program distinct from that of untreated cells, and integrated transcriptomics, metabolomics, and genome-scale metabolic modeling to identify specific metabolic pathways that are critical for persister survival.
Joseph M. Ficarrotta, Anna S. Blazier, Aline Métris et al.· Journal of Bacteriology· 0 citations
ABSTRACT The accelerating deposition of RNAseq data over the past decade has motivated the development of advanced transcriptomic data analytics that can operate on a large number of samples. One successful approach is to apply independent component analysis (ICA) to large prokaryotic transcriptomic compendia to decompose them into independently modulated gene sets, called iModulons. Here, we review the data science principles underlying ICA-based transcriptome decomposition, computational workflows that support its routine application, and iModulonDB infrastructure that hosts and disseminates the resulting decompositions. We present iModulonDB 3.0 that contains 53 species and 71 ICA decompositions across 33,062 RNA-seq samples, with several well-sampled species (e.g., Escherichia coli, Bacillus subtilis, Staphylococcus aureus, Pseudomonas aeruginosa) represented by more than one compendium. With 71 standardized decompositions, we demonstrate systematic cross-species comparison of species-specific iModulon structures. This comparison identifies a shared “regulatory toolkit” of 13 modules conserved across distantly related bacteria, alongside a long tail of lineage-specific programs. We assess the design principles and limitations governing iModulon reconstruction and computation. Together, these advances position the iModulon framework as an accessible, community-driven approach for reading accumulating public transcriptomes as reusable regulatory programs, enabling biological discovery and module-level design in synthetic biology.
Kangsan Kim, E. Catoiu, Yongjae Lee et al.· mSystems· 0 citations
Pseudomonas sp. MUP55, isolated from rainfall water in Western Australia, was characterized by polyphasic taxonomy and functional assays. Whole-genome and 16S rRNA phylogeny placed Pseudomonas sp. MUP55 in the Pseudomonas fluorescens species group. Massetolide A/D was identified as the leading candidate bioactive compound(s), consistent with its biosynthetic gene cluster, GNPS library matching, and loss of activity in regulatory mutants. The strain showed broad-spectrum antimicrobial activity against bacterial (Escherichia coli and Xanthomonas campestris) and fungal (Fusarium oxysporum and Rhizoctonia solani) plant pathogens. GacA regulates Massetolide production: a P58L mutation abolished synthesis and reduced biocontrol efficacy. Metabolomic and transcriptomic analysis of a ΔpvfC mutant revealed that the pvf cluster regulates specialized metabolism while also contributing to secreted growth-inhibitory activity. The pvf cluster differentially regulates dual siderophore systems and uncouples the co-regulated small RNAs rsmY and rsmZ in the Gac/Rsm cascade. Deletion of pvfC partially reduced the growth-inhibitory activity of Pseudomonas sp. MUP55 supernatants against bacterial pathogens, indicating that pvfC also influences secreted antimicrobial activity beyond its global regulatory role. These findings establish Pseudomonas sp. MUP55 as a taxonomically novel, mechanistically characterized biocontrol agent with potential for sustainable agriculture.
Hussain Alattas, Samuele Sala, Joseph Boctor et al.· International Journal of Mol...· 0 citations