Patients in intensive care units are at high risk for long-term health threats including cognitive impairment. The correlation was only recently revealed after large-scale follow-up cognitive assessments on intensive patient survivors after their discharge from the hospital. There are testimonials, reviews and calls-to-action on many critical care websites and in journal issues over the last 2-3 years on this public health crisis. However, the causative mechanisms that lead to abrupt cognitive impairment are unclear?they are not attributable to age, gender, relative brain hypoxia, anesthetics and sedatives. Nosocomial bacteria such as Pseudomonas aeruginosa impair endothelial cell function during the course of infection that culminates in acute lung injury. Recent studies implicate that after P. aeruginosa infection, endothelial cells produces and releases cytotoxic amyloids that are transmissible among cells. Having access to the endothelium of whole blood circulation, these cytotoxic amyloids likely propagate. In fact, the amyloids are detectable in the blood and cerebrospinal fluid of nosocomial pneumonia patients in intensive care units. Further, when applied to brain slices, the cytotoxic amyloids derived from endothelium impair neural activity and synaptic information transfer. This project takes advantage of vertically integrated approaches, ranging from the use of different bacteria stains and cultured cells, to in vitro brain slice recordings and in vivo animal behavior studies. The studies are designs to test the hypothesis that nosocomial pneumonias induce amyloid protein accumulation in CSF, resulting in LTP suppression and learning deficit. Altogether, studies systematically examine a possible lung-brain axis, where a primary lung infection induces production of cytotoxic amyloids that spread to the cerebrospinal fluid and contribute to cognitive impairment. This work addresses a novel mechanism underlying the end organ dysfunction that is evident during, and in the aftermath of, critical illness. Mechanistic insight into endothelium-derived cytotoxicity to brain function will reveal novel therapeutic approaches to prevent cognitive decline.

Public Health Relevance

Many intensive care unit survivors suffer from pervasive cognitive impairment. While the causative mechanisms that lead to abrupt cognitive impairment are unclear, recent studies show that lung vascular endothelium produces cytotoxins after nosocomial bacteria infection. This application tests the hypothesis that lung infection induces amyloid accumulation and impairs neural function in critically ill patients with pneumonia infection.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL140182-02
Application #
9677041
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Caler, Elisabet V
Project Start
2018-04-01
Project End
2022-03-31
Budget Start
2019-04-01
Budget End
2020-03-31
Support Year
2
Fiscal Year
2019
Total Cost
Indirect Cost
Name
University of South Alabama
Department
Physiology
Type
Schools of Medicine
DUNS #
172750234
City
Mobile
State
AL
Country
United States
Zip Code
36688
Lin, Mike T; Balczon, Ron; Pittet, Jean-Francois et al. (2018) Nosocomial Pneumonia Elicits an Endothelial Proteinopathy: Evidence for a Source of Neurotoxic Amyloids in Critically Ill Patients. Am J Respir Crit Care Med :