Detection
of viable viruses in the air is critical in
order to
determine the level of risk associated with the airborne diffusion
of viruses. Different methods have been developed for the isolation,
purification, and detection of viable airborne viruses, but they require
an extensive processing time and often present limitations including
low physical efficiency (i.e., the amount of collected viruses), low
biological efficiency (i.e., the number of viable viruses), or a combination
of all. To mitigate such limitations, we have employed an efficient
technique based on the magnetic levitation (Maglev) technique with
a paramagnetic solution and successfully identified distinct variations
in levitation and density characteristics among bacteria (Escherichia coli), phages (MS2), and human viruses
(SARS-CoV-2 and influenza H1N1). Notably, the Maglev approach enabled
a significant enrichment of viable airborne viruses in air samples.
Furthermore, the enriched viruses obtained through Maglev exhibited
high purity, rendering them suitable for direct utilization in subsequent
analyses such as reverse transcription-polymerase chain reaction (RT-PCR)
or colorimetric assays. The system is portable, easy to use, and cost-efficient
and can potentially provide proactive surveillance data for monitoring
future outbreaks of airborne infectious diseases and allow for the
induction of various preventative and mitigative measures.