Environmental regulation of pathogenicity islands by nucleoid-associated proteins in bacteria
Pathogenicity islands (PAIs) are horizontally acquired genomic regions that encode virulence factors essential for bacterial pathogenicity. Their expression must be precisely regulated to avoid detrimental fitness costs outside the host and to ensure timely activation during infection. This review explores how environmental cues such as temperature, osmolarity, pH, and nutrient availability regulate PAI gene expression via nucleoid-associated proteins (NAPs). Molecular mechanisms by which key NAPs, including H-NS, Fis, IHF, and HU, modulate PAI activity in response to environmental changes are examined. H-NS functions as a central xenogeneic silencer by repressing AT-rich PAI genes under non-host conditions through oligomerization and DNA bridging. Its activity is modulated by environmental inputs and post-translational modifications. In contrast, Fis promotes virulence gene expression during early exponential growth. IHF and HU serve as architectural DNA-bending proteins that facilitate transcriptional activation by altering local DNA topology or counteracting H-NS repression. These proteins integrate environmental signals with chromosomal structure to fine-tune PAI expression. A cohesive model is proposed in which NAPs act as environmental interpreters of the genome, linking chromatin architecture with adaptive virulence gene regulation. Understanding these mechanisms provides valuable insight into bacterial pathogenesis and potential targets for antimicrobial intervention.
Authors
- Joydeep Chakraborty (ORCID: https://orcid.org/0000-0002-8804-2920)
- Harsh V. Purohit
Institutions
- Charotar University of Science and Technology (IN)
- Czech Academy of Sciences, Institute of Microbiology (CZ)
Publication Details
- Journal
- Critical Reviews in Microbiology
- Published
- 2026-06-16
- DOI
- https://doi.org/10.1080/1040841x.2026.2688089
- Primary Topic
- Bacterial Genetics and Biotechnology
- Type
- article
- Field-Weighted Citation Impact
- 0.00