Sphingosine Prevents Bacterial Adherence to Endotracheal Tubes: A Novel Mechanism to Prevent Ventilator-Associated Pneumonia

Abstract

Ventilator-associated pneumonia (VAP) is one of the most common nosocomial infections causing significant morbidity and mortality in critically ill patients. VAP prevention is an area that has received much attention. Bacteria responsible for VAP are diverse; however, 60 of causative agents are Gram-negative bacteria, most commonly Pseudomonas aeruginosa (PA) and Acine to bacter baumannii (AB). The cause of VAP is multifactorial, but is undeniably related to the presence of the endotracheal tube (ETT).Tracheal intubation inhibits the cough reflex, affects mucociliary clearance, provides direct access for bacteria from the upper to the lower respiratory system, and allows for the formation of biofilm, which can subsequently be a source of persistent infection. Thus, prevention of bacterial adherence on the surface of ETTs could have potential to significantly reduce rates of VAP. In this study, we used an in vitro bacterial adherence model to study the effectiveness and durability of sphingosine and phytosphingosine coating to reduce bacterial adherence of AB, PA, and Staphylococcus aureus to the surface of ETTs compared to standard plasticized polyvinylchloride and silver-coated ETTs. Our data show that sphingosine-coated and phytosphingosine-coated ETTs are highly efficacious at preventing bacterial adherence against three of the most common pathogens, AB, PA, and Staphylococcus aureus, associated with VAP when compared with standard plasticized polyvinyl chloride ETTs. Additionally, our data indicate our sphingolipid-coated tubes are equally efficacious as silver-coated ETTs. Future in vitro and animal studies are necessary to establish the safety of sphingolipid coatings, and future randomized clinical trials will be necessary to determine sphingosine or phytosphingosine s ability to provide a cost-effective preventative strategy to reduce rates of VAP.

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Document Details

Document Type
Technical Report
Publication Date
Jun 21, 2016
Accession Number
AD1012625

Entities

People

  • Aaron P. Seitz
  • Alex Lentsch
  • Bryce Robinson
  • Daniel Cox
  • Erich Gulbins
  • Richard D Branson

Organizations

  • University of Cincinnati

Tags

Communities of Interest

  • Biomedical

DTIC Thesaurus Topics

  • Adhesion
  • Air Force
  • Air Force Research Laboratories
  • Anti-Infective Agents
  • Bacteria
  • Chemistry
  • Chlorides
  • Electron Microscopy
  • Gram-Negative Bacteria
  • Health Services
  • Infection
  • Liquid Chromatography
  • Magnesium Compounds
  • Materials
  • Respiratory System
  • Standards
  • Staphylococcus Aureus

Readers

  • Aerial Delivery - Logistics and Supply Chain Management.
  • Trauma Surgery or Emergency Medicine.
  • Trauma or Military Medicine

Technology Areas

  • Biotechnology