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Generation of In-Frame Gene Deletion Mutants in Pseudomonas aeruginosa and Testing for Virulence Attenuation in a Simple Mouse Model of Infection
Published on: January 8, 2020
Pseudomonas aeruginosa virulence expression is directly activated by morphine and is capable of causing lethal
Trissa Babrowski1, Christopher Holbrook, Jonathan Moss
1Center of Surgical Infection Research and Therapeutics, Department of Surgery, Pritzker School of Medicine, University of Chicago, Chicago, IL 60637, USA.
Objective:
This study was designed to examine the effect of morphine administration on the intestinal mucus barrier and determine its direct effect on the virulence and lethality of Pseudomonas aeruginosa, one of the most frequent pathogens to colonize the gut of critically ill patients.
Background Data:
Surgical injury is associated with significant exposure of host tissues to morphine from both endogenous release and its use as a potent analgesic agent. Morphine use in surgical patients exposed to extreme physiologic stress is well established to result in increased infection risk. Although morphine is a known immunosuppressant, whether it directly induces virulence expression and lethality in microbes that colonize the human gut remains unknown.
Methods:
Mice were implanted with a slow release morphine or placebo pellet with and without intestinal inoculation of P. aeruginosa created by direct cecal injection. Mucus production and epithelial integrity was assessed in cecal tissue via Alcian blue staining and histologic analysis. In vivo and in vitro P. aeruginosa virulence expression was examined using reporter strains tagged to the epithelial barrier disrupting protein PA-I lectin. P. aeruginosa chemotaxis toward morphine was also assayed in vitro. Finally, the direct effect of morphine to induce PA-I lectin expression was determined in the absence and presence of methylnaltrexone, a micro opioid receptor antagonist.
Results:
Mice intestinally inoculated with P. aeruginosa and implanted with a morphine pellet demonstrated significant suppression of intestinal mucus, disrupted intestinal epithelium, and enhanced mortality; whereas exposure of mice to either systemic morphine or intestinal P. aeruginosa alone enhanced intestinal mucus without mortality, suggesting a shift in P. aeruginosa during morphine exposure to a mucus suppressing, barrier disrupting, and lethal phenotype. Direct exposure of P. aeruginosa to morphine in vitro confirmed that morphine can transform P. aeruginosa to a more virulent phenotype that is attenuated in part by methylnaltrexone.
Conclusions:
Morphine administration shifts intestinal P. aeruginosa to express a virulent phenotype and may play a role in its ability to causes lethal gut-derived sepsis in a susceptible host.
Insights
Morphine use in critically ill patients can increase the virulence of Pseudomonas aeruginosa, a common gut pathogen. This shift in the bacteria
Area of Science:
- Microbiology and Immunology
- Gastroenterology
- Pharmacology
Background:
- Surgical patients often receive morphine, leading to host tissue exposure.
- Morphine is a known immunosuppressant, and its role in increasing infection risk is established.
- The direct impact of morphine on microbial virulence in the gut remains unclear.
Purpose of the Study:
- To investigate morphine's effect on the intestinal mucus barrier.
- To determine morphine's direct influence on Pseudomonas aeruginosa virulence and lethality.
- To explore the mechanism of morphine-induced bacterial changes.
Main Methods:
- Mice received morphine or placebo pellets and were inoculated with P. aeruginosa.
- Intestinal mucus production and epithelial integrity were assessed.
- P. aeruginosa virulence, including PA-I lectin expression and chemotaxis toward morphine, was evaluated in vitro and in vivo.
Main Results:
- Morphine administration suppressed intestinal mucus and disrupted the epithelium in P. aeruginosa-infected mice, increasing mortality.
- Morphine exposure shifted P. aeruginosa to a mucus-suppressing, barrier-disrupting, and lethal phenotype.
- In vitro studies confirmed morphine enhances P. aeruginosa virulence, partly blocked by methylnaltrexone.
Conclusions:
- Morphine administration promotes a virulent phenotype in intestinal P. aeruginosa.
- This morphine-induced bacterial shift may contribute to lethal gut-derived sepsis in susceptible individuals.
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