A1 Refereed original research article in a scientific journal
Identifying viral infections through analysis of head space volatile organic compounds
Authors: Sanmark, E; Marjanen, P; Virtanen, J; Aaltonen, K; Tauriainen, S; Österlund, P; Mäkelä, M; Saari, S; Roine, A; Rönkkö, T; Vartiainen, V. A.
Publisher: IOP Publishing
Publication year: 2024
Journal: Journal of Breath Research
Journal name in source: Journal of Breath Research
Article number: 016004
Volume: 19
ISSN: 1752-7155
eISSN: 1752-7163
DOI: https://doi.org/10.1088/1752-7163/ad89f0
Web address : http://doi.org/10.1088/1752-7163/ad89f0
Self-archived copy’s web address: https://research.utu.fi/converis/portal/detail/Publication/459084988
Volatile organic compounds (VOCs) produced by human respiratory cells reflect metabolic and pathophysiological processes which can be detected with the use of modern technology. Analysis of exhaled breath or indoor air may potentially play an important role in screening of upper respiratory tract infections such as COVID-19 or influenza in the future. In this experimental study, air samples were collected and analyzed from the headspace of an in vitro cell culture infected by selected pathogens (influenza A H1N1 and seasonal coronaviruses OC43 and NL63). VOCs were measured with a real-time proton-transfer-reaction time-of-flight mass spectrometer and a differential mobility spectrometer. Measurements were performed every 12 h for 7 d. Non-infected cells and cell culture media served as references. In H1N1 and OC43 we observed four different VOCs which peaked during the infection. Different, individual VOCs were also observed in both infections. Activity began to clearly increase after 2 d in all analyses. We did not see increased VOC production in cells infected with NL63. VOC analysis seems to be suitable to differentiate the infected cells from those which are not infected as well as different viruses, from another. In the future, this could have practical value in both individual diagnostics and indoor environment screening.
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Funding information in the publication:
This work was funded by Business Finland Co-Innovation funding (all), Finnish Medical Foundation (V.V.), Finska Läkaresäälskapet funding (E.S.), Tampereen tuberkuloosisäätiö (E.S) and Tuberkuloosin vastustamissäätiö (E.S).