Single
virus particle detections using a solid-state nanopore. Courtesy: Osaka
University
Scientists
at Osaka University develop a label-free method for identifying respiratory
viruses based on changes in electrical current when they pass through silicon
nanopores, which may lead to new rapid COVID-19 tests.
The
ongoing global pandemic has created an urgent need for rapid tests that can
diagnose the presence of the SARS-CoV-2 virus, the pathogen that causes
COVID-19, and distinguish it from other respiratory viruses. Now, researchers
from Japan have demonstrated a new system for single-virion identification of
common respiratory pathogens using a machine learning algorithm trained on
changes in current across silicon nanopores. This work may lead to fast and
accurate screening tests for diseases like COVID-19 and influenza.
In a study
published this month in ACS Sensors scientists at Osaka University have
introduced a new system using silicon nanopores sensitive enough to detect even
a single virus particle when coupled with a machine learning algorithm.
In this
method, a silicon nitride layer just 50 nm thick suspended on a silicon wafer
has tiny nanopores added, which are themselves only 300 nm in diameter. When a
voltage difference is applied to the solution on either side of the wafer, ions
travel through the nanopores in a process called electrophoresis.
The motion
of the ions can be monitored by the current they generate, and when a viral
particle enters a nanopore, it blocks some of the ions from passing through,
leading to a transient dip in current. Each dip reflects the physical
properties of the particle, such as volume, surface charge, and shape, so they
can be used to identify the kind of virus.
The
natural variation in the physical properties of virus particles had previously
hindered implementation of this approach, however, using machine learning, the
team built a classification algorithm trained with signals from known viruses
to determine the identity of new samples. “By combining single-particle
nanopore sensing with artificial intelligence, we were able to achieve highly
accurate identification of multiple viral species,” explains senior author
Makusu Tsutsui.
The
computer can discriminate the differences in electrical current waveforms that
cannot be identified by human eyes, which enables highly accurate virus
classification. In addition to coronavirus, the system was tested with similar
pathogens — respiratory syncytial virus, adenovirus, influenza A, and influenza
B.
The team
believes that coronaviruses are especially well suited for this technique since
their spiky outer proteins may even allow different strains to be classified
separately. “This work will help with the development of a virus test kit that
outperforms conventional viral inspection methods,” says last author Tomoji
Kawai.
Compared
with other rapid viral tests like polymerase chain reaction or antibody-based
screens, the new method is much faster and does not require costly reagents,
which may lead to improved diagnostic tests for emerging viral particles that
cause infectious diseases such as COVID-19.