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Updated: Apr 26, 2026

A Delayed Inoculation Model of Chronic Pseudomonas aeruginosa Wound Infection
Published on: February 20, 2020
Requirements for Pseudomonas aeruginosa acute burn and chronic surgical wound infection
Keith H Turner1, Jake Everett2, Urvish Trivedi2
1Department of Molecular Biosciences, Institute of Cellular and Molecular Biology, Center for Infectious Disease, The University of Texas at Austin, Austin, Texas, United States of America.
Abstract:
Opportunistic infections caused by Pseudomonas aeruginosa can be acute or chronic. While acute infections often spread rapidly and can cause tissue damage and sepsis with high mortality rates, chronic infections can persist for weeks, months, or years in the face of intensive clinical intervention. Remarkably, this diverse infectious capability is not accompanied by extensive variation in genomic content, suggesting that the genetic capacity to be an acute or a chronic pathogen is present in most P. aeruginosa strains. To investigate the genetic requirements for acute and chronic pathogenesis in P. aeruginosa infections, we combined high-throughput sequencing-mediated transcriptome profiling (RNA-seq) and genome-wide insertion mutant fitness profiling (Tn-seq) to characterize gene expression and fitness determinants in murine models of burn and non-diabetic chronic wound infection. Generally we discovered that expression of a gene in vivo is not correlated with its importance for fitness, with the exception of metabolic genes. By combining metabolic models generated from in vivo gene expression data with mutant fitness profiles, we determined the nutritional requirements for colonization and persistence in these infections. Specifically, we found that long-chain fatty acids represent a major carbon source in both chronic and acute wounds, and P. aeruginosa must biosynthesize purines, several amino acids, and most cofactors during infection. In addition, we determined that P. aeruginosa requires chemotactic flagellar motility for fitness and virulence in acute burn wound infections, but not in non-diabetic chronic wound infections. Our results provide novel insight into the genetic requirements for acute and chronic P. aeruginosa wound infections and demonstrate the power of using both gene expression and fitness profiling for probing bacterial virulence.
Insights
Pseudomonas aeruginosa can cause acute or chronic infections. This study reveals key genetic factors and nutritional needs, like fatty acids, for its virulence in wound infections, differentiating acute vs. chronic disease.
Area of Science:
- Microbiology
- Bacterial Pathogenesis
- Genomics
Background:
- Pseudomonas aeruginosa causes severe acute and persistent chronic infections.
- Most strains possess the genetic capability for both acute and chronic pathogenesis.
- Understanding these differences is crucial for effective treatment.
Purpose of the Study:
- To investigate the genetic requirements for acute and chronic pathogenesis in P. aeruginosa wound infections.
- To identify key genes and metabolic pathways essential for virulence in different infection types.
- To compare gene expression and fitness determinants in vivo.
Main Methods:
- Utilized high-throughput sequencing for transcriptome profiling (RNA-seq).
- Employed genome-wide insertion mutant fitness profiling (Tn-seq).
- Combined transcriptomic data with metabolic models and fitness profiles in murine wound models.
Main Results:
- Gene expression in vivo does not always correlate with fitness importance, except for metabolic genes.
- Long-chain fatty acids are a primary carbon source in both acute and chronic wounds.
- P. aeruginosa requires de novo biosynthesis of purines, amino acids, and cofactors.
- Chemotactic flagellar motility is vital for acute, but not chronic, wound infections.
Conclusions:
- Identified specific genetic requirements differentiating acute and chronic P. aeruginosa wound infections.
- Demonstrated the utility of integrating gene expression and fitness profiling for virulence studies.
- Provided novel insights into P. aeruginosa virulence mechanisms and host-pathogen interactions.
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