PT - JOURNAL ARTICLE AU - Yuan Yuan AU - Yara Seif AU - Kevin Rychel AU - Reo Yoo AU - Siddharth Chauhan AU - Saugat Poudel AU - Tahani Al-bulushi AU - Bernhard O. Palsson AU - Anand Sastry TI - Pan-genomic analysis of transcriptional modules across <em>Salmonella</em> Typhimurium reveals the regulatory landscape of different strains AID - 10.1101/2022.01.11.475931 DP - 2022 Jan 01 TA - bioRxiv PG - 2022.01.11.475931 4099 - http://biorxiv.org/content/early/2022/01/11/2022.01.11.475931.short 4100 - http://biorxiv.org/content/early/2022/01/11/2022.01.11.475931.full AB - Salmonella enterica Typhimurium is a serious pathogen that is involved in human nontyphoidal infections. Tackling Typhimurium infections is difficult due to the species’ dynamic adaptation to its environment, which is dictated by a complex transcriptional regulatory network (TRN). While traditional biomolecular methods provide characterizations of specific regulators, it is laborious to construct the global TRN structure from this bottom-up approach. Here, we used a machine learning technique to understand the transcriptional signatures of S. enterica Typhimurium from the top down, as a whole and in individual strains. Furthermore, we conducted cross-strain comparison of 6 strains in serovar Typhimurium to investigate similarities and differences in their TRNs with pan-genomic analysis. By decomposing all the publicly available RNA-Seq data of Typhimurium with independent component analysis (ICA), we obtained over 400 independently modulated sets of genes, called iModulons. Through analysis of these iModulons, we 1) discover three transport iModulons linked to antibiotic resistance, 2) describe concerted responses to cationic antimicrobial peptides (CAMPs), 3) uncover evidence towards new regulons, and 4) identify two iModulons linked to bile responses in strain ST4/74. We extend this analysis across the pan-genome to show that strain-specific iModulons 5) reveal different genetic signatures in pathogenicity islands that explain phenotypes and 6) capture the activity of different phages in the studied strains. Using all high-quality publicly-available RNA-Seq data to date, we present a comprehensive, data-driven Typhimurium TRN. It is conceivable that with more high-quality datasets from more strains, the approach used in this study will continue to guide our investigation in understanding the pan-transcriptome of Typhimurium. Interactive dashboards for all gene modules in this project are available at https://imodulondb.org/ under the “Salmonella Typhimurium” page to enable browsing for interested researchers.Competing Interest StatementThe authors have declared no competing interest.