4.7 Article

Elastase Activity From Pseudomonas aeruginosa Respiratory Isolates and ICU Mortality

Journal

CHEST
Volume 160, Issue 5, Pages 1624-1633

Publisher

ELSEVIER
DOI: 10.1016/j.chest.2021.04.015

Keywords

critical illness; pneumonia; Pseudomonas aeruginosa; pseudomonas elastase activity

Funding

  1. National Heart, Lung, And Blood Institute of the National Institutes of Health [F32 HL152504, R01 HL136143, R01 HL142084, K24 HL143285]
  2. United States Department of Veterans Affairs Biomedical Laboratory R&D (BLRD) Service [IK2 BX004886]
  3. Cystic Fibrosis Foundation [K22 AI127473, JORTH17F5, RDP BOMBER19RO]
  4. University of Pittsburgh from the Burroughs Wellcome Fund

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The study found that elastase activity of Pseudomonas aeruginosa (PA) was associated with increased 30-day mortality in ICU patients. Mice infected with a high elastase producer showed increased lung bacterial burden and inflammatory profile compared to those infected with a low elastase producer.
BACKGROUND: Pseudomonas aeruginosa (PA) is a common cause of respiratory infection and morbidity. Pseudomonas elastase is an important virulence factor regulated by the lasR gene. Whether PA elastase activity is associated with worse clinical outcomes in ICU patients is unknown. RESEARCH QUESTION: Is there an association between PA elastase activity and worse host outcomes in a cohort of ICU patients? METHODS: PA respiratory isolates from 238 unique ICU patients from two tertiary-care centers within the University of Pittsburgh Medical Center health system were prospectively collected and screened for total protease and elastase activity, biofilm production, antimicrobial resistance, and polymicrobial status. The association between pathogen characteristics and 30-day and 90-day mortality was calculated using logistic regression. For subgroup analysis, two patterns of early (#72 h) and late sample (>72 h) collection from the index ICU admission were distinguished using a finite mixture model. Lung inflammation and injury was evaluated in a mouse model using a PA high elastase vs low elastase producer. RESULTS: PA elastase activity was common in ICU respiratory isolates representing 75% of samples and was associated with increased 30-day mortality (adjusted OR [95% CI]: 1.39 [1.05-1.83]). Subgroup analysis demonstrated that elastase activity was a risk factor for 30and 90-day mortality in the early sample group, whereas antimicrobial resistance was a risk factor for 90-day mortality in the late sample group. Whole genome sequencing of high and low elastase producers showed that predicted loss-of-function lasR genotypes were less common among high elastase producers. Mice infected with a high elastase producer showed increased lung bacterial burden and inflammatory profile compared with mice infected with a low elastase producer. INTERPRETATION: Elastase activity is associated with 30-day ICU mortality. A high elastase producing clinical isolate confers increased lung tissue inflammation compared with a low elastase producer in vivo. CHEST 2021; 160(5):1624-1633

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