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Updated: May 13, 2025

Murine Oropharyngeal Aspiration Model of Ventilator-associated and Hospital-acquired Bacterial Pneumonia
Published on: June 28, 2018
The pathogenesis of ventilator-associated pneumonia: old and new mechanisms
Arnau Ulsamer1,2, Sergio Bonilla3, Xosé Pérez-Fernández1,2
1Institut d'Investigació Biomèdica de Bellvitge (IDIBELL), Barcelona, Spain.
Introduction:
Ventilator-associated pneumonia (VAP), defined as a lung infection that occurs in patients after 48 hours on mechanical ventilation, is among the most frequently found nosocomial infections in intensive care units around the world and is associated with increased morbidity, mortality, and economic burden.
Areas Covered:
We review the classical mechanisms of VAP development and explore more recent ones, such as dysbiosis, which has changed our view of the pathogenesis of the disease; whereas in the past the lower respiratory tract was classically considered a sterile organ, the use of new diagnostic techniques has shown that the lungs of healthy humans are inhabited by a large, dynamic ecosystem of microorganisms. Dysbiosis is the disruption of this ecosystem and is a key factor in the development of VAP. Recent findings have demonstrated that host immunity is microbiome-regulated and, consequently, is profoundly affected by dysbiosis. In this paper the significance of the microbiome-immunity crosstalk in the pathophysiology of VAP will be discussed.
Expert Opinion:
A deeper understanding of mechanisms of VAP pathogenesis should help to devise new preventive, diagnostic and therapeutic strategies for reducing the incidence of this condition and for improving patient prognosis.
Insights
Ventilator-associated pneumonia (VAP) is a common intensive care unit infection. Recent research highlights how disruption of the lung microbiome (dysbiosis) significantly impacts VAP development and host immunity.
Area of Science:
- Microbiology
- Immunology
- Critical Care Medicine
Background:
- Ventilator-associated pneumonia (VAP) is a frequent nosocomial infection in ICUs, increasing patient morbidity, mortality, and healthcare costs.
- Traditionally, the lower respiratory tract was considered sterile, but new diagnostics reveal a complex microbial ecosystem.
- Dysbiosis, or disruption of this ecosystem, is now recognized as a critical factor in VAP pathogenesis.
Purpose of the Study:
- To review classical and emerging mechanisms of VAP development.
- To explore the role of the lung microbiome and dysbiosis in VAP.
- To discuss the significance of microbiome-immunity interactions in VAP pathophysiology.
Main Methods:
- Literature review of VAP pathogenesis.
- Analysis of recent findings on lung microbiome dynamics.
- Examination of host immunity regulation by the microbiome.
Main Results:
- Dysbiosis is a key factor in VAP development, challenging the sterile lung paradigm.
- Host immunity is regulated by the microbiome and is profoundly affected by dysbiosis.
- Microbiome-immunity crosstalk plays a significant role in VAP pathophysiology.
Conclusions:
- Understanding VAP pathogenesis requires acknowledging the lung microbiome.
- Dysbiosis and its impact on host immunity are central to VAP.
- Further research into microbiome-immunity interactions can lead to improved VAP prevention and treatment strategies.
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