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Murine Oropharyngeal Aspiration Model of Ventilator-associated and Hospital-acquired Bacterial Pneumonia
Published on: June 28, 2018
Novel toxin assays implicate Mycoplasma pneumoniae in prolonged ventilator course and hypoxemia
Mark T Muir1, Stephen M Cohn1, Christopher Louden2
1Department of Surgery, University of Texas Health Science Center at San Antonio, San Antonio, TX.
Background:
Community-acquired respiratory distress syndrome (CARDS) toxin is a unique Mycoplasma pneumoniae virulence factor. Molecular assays targeting this toxin are more sensitive than existing diagnostics, but these assays have not been used to investigate the role of M pneumoniae as a nosocomial infection in critical illness. We sought to determine the incidence of M pneumoniae among mechanically ventilated subjects using these novel assays and to investigate the impact of this pathogen on pulmonary outcomes.
Methods:
We conducted a prospective observational study enrolling subjects with suspected ventilator-associated pneumonia (VAP) undergoing BAL in the surgical trauma ICU at a level I trauma center. Lavage fluid and serum samples were tested for M pneumoniae using assays to detect CARDS toxin gene sequences, protein, or antitoxin antibodies.
Results:
We collected samples from 37 subjects, with 41% (15 of 37) testing positive using these assays. The positive and negative groups did not differ significantly in baseline demographic characteristics, including age, sex, injury severity, or number of ventilator days before bronchoscopy. The positive group had significantly fewer ventilator-free days (P = .04) and lower average oxygenation (P = .02). These differences were most pronounced among subjects with ARDS.
Conclusions:
Evidence is provided that M pneumoniae is present in a substantial number of subjects with suspected VAP. Subjects testing positive experience a significantly longer ventilator course and worse oxygenation compared with subjects testing negative.
Insights
Mycoplasma pneumoniae, detected by novel assays, was found in 41% of mechanically ventilated patients. This pathogen is linked to longer ventilator use and poorer oxygenation, especially in ARDS patients.
Area of Science:
- Critical Care Medicine
- Infectious Diseases
- Pulmonary Medicine
Background:
- Community-acquired respiratory distress syndrome (CARDS) toxin is a key Mycoplasma pneumoniae virulence factor.
- Novel molecular assays offer higher sensitivity for M. pneumoniae detection.
- The role of M. pneumoniae as a nosocomial infection in critical illness requires further investigation.
Purpose of the Study:
- To determine the incidence of M. pneumoniae in mechanically ventilated subjects using advanced molecular assays.
- To investigate the impact of M. pneumoniae infection on pulmonary outcomes in critically ill patients.
Main Methods:
- Prospective observational study in a surgical trauma ICU.
- Enrollment of subjects with suspected ventilator-associated pneumonia (VAP) undergoing bronchoalveolar lavage (BAL).
- Testing of lavage fluid and serum for M. pneumoniae via CARDS toxin gene, protein, or antitoxin antibodies.
Main Results:
- 41% (15 of 37) of subjects tested positive for M. pneumoniae.
- No significant differences in baseline demographics between positive and negative groups.
- M. pneumoniae-positive subjects had fewer ventilator-free days (P=.04) and worse oxygenation (P=.02), particularly those with ARDS.
Conclusions:
- M. pneumoniae is present in a significant proportion of mechanically ventilated patients with suspected VAP.
- M. pneumoniae infection is associated with prolonged mechanical ventilation and impaired oxygenation.
- Novel assays confirm M. pneumoniae as a relevant pathogen in critical care settings.
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