Chromosomal "stress-response" domains govern the spatiotemporal expression of the bacterial virulence program

• Published in: mBio 2015-04, Vol.6 (3), p.e00353-e00315
• Main Authors: Jiang, Xuejiao, Sobetzko, Patrick, Nasser, William, Reverchon, Sylvie, Muskhelishvili, Georgi
• Format: Article
• Language: English
• Subjects: bacterial infections; Bacterial Proteins - genetics; Bacterial Proteins - metabolism; Bacteriology; chromosomes; Chromosomes, Bacterial; couplings; Dickeya dadantii; DNA; DNA, Bacterial - chemistry; DNA, Bacterial - genetics; DNA, Superhelical; Erwinia chrysanthemi; gene expression; Gene Expression Regulation, Bacterial; Genes, Bacterial; Lamiales - microbiology; Life Sciences; microbial growth; Microbiology and Parasitology; nucleotide sequences; pathogens; Pectobacterium chrysanthemi - genetics; Pectobacterium chrysanthemi - pathogenicity; Pectobacterium chrysanthemi - physiology; physicochemical properties; proteins; stress response; Stress, Physiological; thermodynamics; Transcriptome; Virulence; Virulence Factors - genetics; Virulence Factors - metabolism
• ISSN: 2161-2129; 2150-7511; 2150-7511
• DOI: 10.1128/mBio.00353-15

Recent studies strongly suggest that the gene expression sustaining both normal and pathogenic bacterial growth is governed by the structural dynamics of the chromosome. However, the mechanistic device coordinating the chromosomal configuration with selective expression of the adaptive traits remains largely unknown. We used a holistic approach exploring the inherent relationships between the physicochemical properties of the DNA and the expression of adaptive traits, including virulence factors, in the pathogen Dickeya dadantii (formerly Erwinia chrysanthemi). In the transcriptomes obtained under adverse conditions encountered during bacterial infection, we explored the patterns of chromosomal DNA sequence organization, supercoil dynamics, and gene expression densities, together with the long-range regulatory impacts of the abundant DNA architectural proteins implicated in pathogenicity control. By integrating these data, we identified transient chromosomal domains of coherent gene expression featuring distinct couplings between DNA thermodynamic stability, supercoil dynamics, and virulence traits. We infer that the organization of transient chromosomal domains serving specific functions acts as a fundamental device for versatile adjustment of the pathogen to environmental stress. We believe that the identification of chromosomal "stress-response" domains harboring distinct virulence traits and mediating the cellular adaptive behavior provides a breakthrough in understanding the control mechanisms of bacterial pathogenicity.