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Published on: March 17, 2014
Clinical outcomes of type III Pseudomonas aeruginosa bacteremia
Ali A El-Solh1, Angela Hattemer, Alan R Hauser
1Veterans Affairs Western New York Healthcare System, Western New York Respiratory Research Center, Division of Pulmonary, Critical Care, and Sleep Medicine, Buffalo, NY, USA. solh@buffalo.edu
Background:
Pseudomonas aeruginosa bacteremia is a serious and life-threatening infection associated with high mortality. Among the multitude of virulence determinants possessed by P. aeruginosa, the type 3 secretion system has been implicated with more acute and invasive infection in respiratory diseases. However, the relationship between the type 3 secretion system and clinical outcomes in P. aeruginosa bacteremia has not been investigated.
Objectives:
To determine the association between the type 3 secretion system virulence factor in P. aeruginosa bloodstream infection and 30-day mortality.
Design:
Retrospective analysis of 85 cases of P. aeruginosa bacteremia.
Setting:
Tertiary care hospital.
Interventions:
Bacterial isolates were assayed in vitro for secretion of type 3 exotoxins (ExoU, ExoT, and ExoS). Strain relatedness was analyzed using randomly amplified polymorphic DNA polymerase chain reaction genotyping. Antimicrobial susceptibilities were determined by means of the Kirby-Bauer disk-diffusion test.
Measurements And Main Results:
At least one of the type 3 secretion system proteins was detected in 37 out of the 85 isolates (44%). Septic shock was identified in 43% of bacteremic patients with type 3 secretion system+ isolates compared to 23% of patients with type 3 secretion system- isolates (p = .12). A high frequency of resistance in the type 3 secretion system+ isolates was observed to ciprofloxacin (59%), cefepime (35%), and gentamicin (38%). There was a significant difference in the 30-day cumulative probability of death after bacteremia between secretors and nonsecretors (p = .02). None of the type 3 secretion system+ patients who survived the first 30 days had a P. aeruginosa isolate which exhibited ExoU phenotype.
Conclusions:
The expression of type 3 secretion system exotoxins in bacteremic isolates of P. aeruginosa confers poor clinical outcomes independent of antibiotic susceptibility profile.
Insights
The type 3 secretion system in Pseudomonas aeruginosa bacteremia is linked to increased mortality. This virulence factor predicts poor outcomes, regardless of antibiotic resistance, highlighting its clinical significance.
Area of Science:
- Microbiology
- Infectious Diseases
- Clinical Medicine
Background:
- Pseudomonas aeruginosa bacteremia is a severe infection with high mortality.
- The type 3 secretion system (T3SS) is a key virulence factor implicated in invasive infections.
- The association between T3SS and clinical outcomes in P. aeruginosa bacteremia remains understudied.
Purpose of the Study:
- To investigate the relationship between T3SS virulence factors in P. aeruginosa bloodstream infections and 30-day mortality.
- To determine if T3SS expression impacts patient outcomes independently of antimicrobial susceptibility.
Main Methods:
- Retrospective analysis of 85 P. aeruginosa bacteremia cases from a tertiary care hospital.
- In vitro assays to detect type 3 exotoxins (ExoU, ExoT, ExoS) in bacterial isolates.
- Randomly amplified polymorphic DNA genotyping for strain relatedness and Kirby-Bauer disk diffusion for antimicrobial susceptibility testing.
Main Results:
- T3SS proteins were detected in 44% of P. aeruginosa isolates.
- Patients with T3SS-positive isolates showed a trend towards higher rates of septic shock (43% vs. 23%).
- A significant increase in 30-day mortality was observed in patients with T3SS-positive isolates (p = .02).
- T3SS-positive isolates exhibited high resistance rates to ciprofloxacin, cefepime, and gentamicin.
Conclusions:
- Expression of type 3 secretion system exotoxins in P. aeruginosa bacteremia is associated with poor clinical outcomes.
- The T3SS appears to confer a worse prognosis independent of antibiotic susceptibility.
- The absence of ExoU phenotype in survivors of T3SS-positive bacteremia warrants further investigation.
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