Effects of Contagious Respiratory Pathogens on Breath Biomarkers

• Main Authors: Nele Kemnitz (Author), Patricia Fuchs (Author), Rasmus Remy (Author), Leo Ruehrmund (Author), Julia Bartels (Author), Ann-Christin Klemenz (Author), Phillip Trefz (Author), Wolfram Miekisch (Author), Jochen K. Schubert (Author), Pritam Sukul (Author)
• Format: Book
• Published: MDPI AG, 2024-01-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.
• Notes: 10.3390/antiox13020172; 2076-3921
• Keywords: metabolic profiling; respiratory virus; pulmonary bacteria; breathomics; volatile biomarkers; real-time mass spectrometry; Therapeutics. Pharmacology; RM1-950
• Source: Antioxidants, Vol 13, Iss 2, p 172 (2024)

Due to their immediate exhalation after generation at the cellular/microbiome levels, exhaled volatile organic compounds (VOCs) may provide real-time information on pathophysiological mechanisms and the host response to infection. In recent years, the metabolic profiling of the most frequent respiratory infections has gained interest as it holds potential for the early, non-invasive detection of pathogens and the monitoring of disease progression and the response to therapy. Using previously unpublished data, randomly selected individuals from a COVID-19 test center were included in the study. Based on multiplex PCR results (non-SARS-CoV-2 respiratory pathogens), the breath profiles of 479 subjects with the presence or absence of flu-like symptoms were obtained using proton-transfer-reaction time-of-flight mass spectrometry. Among 223 individuals, one respiratory pathogen was detected in 171 cases, and more than one pathogen in 52 cases. A total of 256 subjects had negative PCR test results and had no symptoms. The exhaled VOC profiles were affected by the presence of <i>Haemophilus influenzae</i>, <i>Streptococcus pneumoniae,</i> and Rhinovirus. The endogenous ketone, short-chain fatty acid, organosulfur, aldehyde, and terpene concentrations changed, but only a few compounds exhibited concentration changes above inter-individual physiological variations. Based on the VOC origins, the observed concentration changes may be attributed to oxidative stress and antioxidative defense, energy metabolism, systemic microbial immune homeostasis, and inflammation. In contrast to previous studies with pre-selected patient groups, the results of this study demonstrate the broad inter-individual variations in VOC profiles in real-life screening conditions. As no unique infection markers exist, only concentration changes clearly above the mentioned variations can be regarded as indicative of infection or colonization.