Chronic obstructive pulmonary disease (COPD) will soon become the third leading cause of death in the world. COPD is caused by multiple factors including environmental exposures, infections, inflammation, and genetic predisposition. Several lines of investigation have indicated that, in advanced disease, increased bacterial colonization leads to airway inflammation and accelerated airway obstruction. However, in early COPD, culture-dependent techniques commonly failed to isolate bacteria. Thus, the role of microbes in COPD has been difficult to study. We hypothesize that microbes are part of the pathogenesis of early COPD, contributing to inflammatory processes. This proposal will use culture independent techniques to evaluate the contribution of the microbiome to airway inflammation in early COPD. It will also investigate the microbial genomic potential (metagenome) and metabolic profile (metabolome) to better understand functional aspects of the lung microbiome.
Aim 1 will assess lung microbiome and inflammation in smokers with and without COPD. We will perform research bronchoscopy in 48 subjects with mild-moderate COPD and 48 matched smoker controls to measure lung inflammation with multiplexed cytokine assays of bronchoalveolar lavage and lower airway bacteria by 16S rRNA gene sequencing.
Aim 2 will investigate active bacterial metabolic pathways in the lower airways using metagenomics and metabolomics by using the samples obtained in AIM 1. We will test whether differences in genomic potential of the lower airway microbiome accounts for variation in the lung metabolome. Presence of correlation between operons encoding synthetic pathways and the metabolic products of those pathways would support that the lung microbiome is metabolically active, thus composed by live microorganisms.
Aim 3 will assess relationships among different inter-omic datasets (microbiome, metagenome, metabolome and host immune responses) in COPD and controls with the goal of integrating information from vastly different platforms to achieve a multidimensional model of disease. Under the mentorship of Drs. Blaser, Weiden and with the collaboration of Dr. Virgin, Fiehn, and Clemente this research plan will serve as the foundation of a training plan that uses state-of-the-art molecular and bio-informatic methods to improve our understanding of complex bacterial community networks and their association with host immune response in COPD.

Public Health Relevance

Chronic obstructive pulmonary disease (COPD) will become the third leading cause of death in the world by 2020. There are no pharmacological therapies today that will prevent disease progression or reduce mortality once COPD is established. In advanced disease, increased bacterial colonization of the airways has been associated with disease progression. However, the study of the role of microbes in the initiation of the inflammation and consequent lung destruction has been limited by reliance on culture methods. This investigation will use novel culture-independent methods to explore the contribution of microbes to airway inflammation in early disease.

Agency
National Institute of Health (NIH)
Type
Mentored Patient-Oriented Research Career Development Award (K23)
Project #
1K23AI102970-01A1
Application #
8767264
Study Section
Microbiology and Infectious Diseases Research Committee (MID)
Program Officer
Prograis, Lawrence J
Project Start
Project End
Budget Start
Budget End
Support Year
1
Fiscal Year
2014
Total Cost
Indirect Cost
Name
New York University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
City
New York
State
NY
Country
United States
Zip Code
10016