Current clinical diagnostic methods for pneumonia typically take days or weeks and always require a sample from the patient, typically sputum. If sputum cannot be produced, it can sometimes be induced or lung lavage can be taken, both invasive techniques. Pneumonia is still one of the world's leading causes of death for children under the age of 5 according to the WHO and one of the top killers for adults in the USA, according to the CDC. Hence, there is a critical need for improved diagnostic tools to detect lung infections. Research groups at Dartmouth's Thayer School of engineering and the Vermont Lung Center have developed a technique allowing for rapid, non-invasive diagnosis of airway infections by analyzing infection-specific volatiles in the exhaled breath for singular infections, which can generate a diagnosis within minutes. The proposed work will complete the remaining experiments necessary before this technology is taken to a human population. The hypothesis is that that exhaled breath volatiles can be used to diagnose infections of the lung, and specifically, to distinguish between different pathogens, even during co-infection, for acute febrile illnesses. The hypothesis will be addressed in two specific aims: SA1: To determine whether breath volatile molecules can be used to distinguish between respiratory bacterial infections during clinical-relevant scenarios in a murine model. These experiments will demonstrate that a subset of breath molecules reflect infection etiology. The validity and specificity of the approach will be determined using confounding scenarios such as bacterial co-infection (in the lung and elsewhere) as well as during antibiotic treatment.
This aim will also demonstrate determination of antibiotic susceptibility using breath for two organisms of high clinical interest (K. pneumoniae and S. aureus). SA2: To establish the utility of breath volatile molecules to distinguish between viral and bacterial infections. It will be determined how bacterial and viral co-infection affects the diagnostic precision of the exhaled breath analysis. Using influenza A virus, adenovirus and respiratory syncytial virus, it will be demonstrated that the immune system response to viral infection leads to the generation of molecules that can be detected in the breath and are diagnostic of infection etiology. All bacterial and viral experiment will use known human pathogens and will take place in well-developed animal models. The research in this proposal is innovative because it utilizes the best tools currently available to measure breath molecules in a systematic series of clinically-relevant experimental scenarios. The outcomes will represent a robust and substantial step towards a novel conceptual system for respiratory pathogen detection. The data from this study is expected to support forthcoming studies in humans and the development of an analytical device for use in the clinic. Ultimately, the technology shows promise for radically improved patient diagnosis, monitoring, and prognosis.

Public Health Relevance

The proposed research is relevant to public health because it addresses one of the biggest concerns in childhood and adult pneumonia - the difficulty to get a quick and reliable diagnosis. Using a novel, comprehensive technique to identify the small volatile molecules in exhaled breath this research promises to eventually develop a technique that will give a diagnosis of respiratory infection in minutes. This will benefit the patient becaue the correct treatment depends on the correct diagnosis and thus, this work is relevant to the NIH core mission to protect and improve health and the mission of the NIAID to advance diagnostic options for infectious diseases.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Exploratory/Developmental Grants (R21)
Project #
1R21AI121076-01
Application #
9005094
Study Section
Special Emphasis Panel (ZRG1-IDM-V (12))
Program Officer
Taylor, Christopher E,
Project Start
2016-03-10
Project End
2018-02-28
Budget Start
2016-03-10
Budget End
2017-02-28
Support Year
1
Fiscal Year
2016
Total Cost
$252,372
Indirect Cost
$68,509
Name
Dartmouth College
Department
Type
Schools of Engineering
DUNS #
041027822
City
Hanover
State
NH
Country
United States
Zip Code
03755
Rees, Christiaan A; Burklund, Alison; Stefanuto, Pierre-Hugues et al. (2018) Comprehensive volatile metabolic fingerprinting of bacterial and fungal pathogen groups. J Breath Res 12:026001
Purcaro, Giorgia; Rees, Christiaan A; Wieland-Alter, Wendy F et al. (2018) Volatile fingerprinting of human respiratory viruses from cell culture. J Breath Res 12:026015
Rees, Christiaan A; Nasir, Mavra; Smolinska, Agnieszka et al. (2018) Detection of high-risk carbapenem-resistant Klebsiella pneumoniae and Enterobacter cloacae isolates using volatile molecular profiles. Sci Rep 8:13297
Purcaro, Giorgia; Stefanuto, Pierre-Hugues; Franchina, Flavio A et al. (2018) SPME-GC×GC-TOF MS fingerprint of virally-infected cell culture: Sample preparation optimization and data processing evaluation. Anal Chim Acta 1027:158-167
Purcaro, Giorgia; Rees, Christiaan A; Melvin, Jeffrey A et al. (2018) Volatile fingerprinting of Pseudomonas aeruginosa and respiratory syncytial virus infection in an in vitro cystic fibrosis co-infection model. J Breath Res 12:046001
Rees, Christiaan A; Nordick, Katherine V; Franchina, Flavio A et al. (2017) Volatile metabolic diversity of Klebsiella pneumoniae in nutrient-replete conditions. Metabolomics 13: