This
work presents a sensitive and specific single-step RNA sensor
for Zika virus (ZIKV) in serum. Using AC electrokinetics (ACEK)-enhanced
capacitive sensing technology, ZIKV genomic RNA (gRNA) can be directly
detected from serum. The sensors are interdigitated electrodes modified
with oligonucleotide probes complementary to the conserved regions
of ZIKV gRNA. The ACEK capacitive sensing applies an optimized AC
excitation signal over the sensor, which induces ACEK microfluidic
enrichment of analytes and also simultaneously performs real-time
monitoring of hybridization of ZIKV gRNA on the sensor surface. Hence,
the sensing procedures are simple with rapid turn-around time and
good specificity and sensitivity. A series of experiments are conducted
to optimize the sensor performance. The performance of the sensor
is investigated for three different probes, two functionalization
buffers, and different hybridization buffers. With the optimized sensing
protocol, this method can detect spiked ZIKV gRNA from human serum
within 30 s and reach a limit of detection of 78.8 copies/μL
in analytical samples and as low as 287.5 copies/μL in neat
serum. The sensors can successfully differentiate between the RNAs
of the ZIKV and dengue virus, two viruses with similar transmission
paths and symptoms. The sensor is simple to use and requires no labeling
or sophisticated process typically involved in a polymerase chain
reaction, hybridization chain reaction, or nucleic acid sequence-based
amplification