Epigenetic cellular memory in Pseudomonas aeruginosa generates phenotypic variation in response to host environments

Phenotypic diversification within pathogen populations can enhance survival in stressful environments, broaden niche colonization, and expand the ecological range of infectious diseases due to emerging collective pathogenicity characteristics. We describe a gene regulatory network property in the op...

Full description

Saved in:
Bibliographic Details
Published inProceedings of the National Academy of Sciences - PNAS Vol. 122; no. 27; p. e2415345122
Main Authors Vatareck, Elisabeth, Rick, Tim, Oswaldo Gomez, Nicolas, Bandyopadhyay, Arnab, Kramer, Janina, Strunin, Dmytro, Erdmann, Jelena, Hartmann, Oliver, Alpers, Kathrin, Boedeker, Christian, Steffen, Anika, Sieben, Christian, Zhao, Gang, Tomasch, Jürgen, Häussler, Susanne
Format Journal Article
LanguageEnglish
Published United States National Academy of Sciences 08.07.2025
Subjects
Online AccessGet full text
ISSN0027-8424
1091-6490
1091-6490
DOI10.1073/pnas.2415345122

Cover

More Information
Summary:Phenotypic diversification within pathogen populations can enhance survival in stressful environments, broaden niche colonization, and expand the ecological range of infectious diseases due to emerging collective pathogenicity characteristics. We describe a gene regulatory network property in the opportunistic pathogen Pseudomonas aeruginosa that generates diversity of gene expression and pathogenicity behavior at the single-cell level and that is stabilized by epigenetic cellular memory. The resulting heterogeneity in the expression of the glpD gene—an indicator of host-derived glycerol metabolism and intra-host presence—shapes adaptive processes that are subject to natural selection. Our work on how epigenetics generates phenotypic variation in response to the environment and how these changes are inherited to the next generation provides insights into phenotypic diversity and the emergence of unique functionalities at higher levels of organization. These could be crucial for controlling infectious disease outcomes.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
ISSN:0027-8424
1091-6490
1091-6490
DOI:10.1073/pnas.2415345122