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Abstract
<p class="first" id="d1485947e150">Hepatitis A virus (HAV) infection has caused substantial
morbidity and economic losses
to human society, presenting a major public health problem in many parts of the world.
Despite the capability for low-concentration detection, current PCR-based techniques
are limited by the requirement of specialized lab equipment, trained personnel and
a relatively large time-commitment. The need for a prompt in-field quantitative identification
of HAV in real samples has led us to develop a chemiluminescent fibre optic genosensor
system. In this study, a two-probe sandwich-type hybridization process was implemented
on the tip of a fibre optic with an area of 0.12mm2. After optimization of the probes
and the working conditions, we showed that the biosensor was able to work for both
cDNA and RNA with a relatively large signal/noise ratio and a good sensitivity. An
excellent specificity was also confirmed by screening with a broad range of other
pathogen samples. The nucleic acid probes method was validated by optimized PCR and
qPCR, and may thus be used when field testing would be required.
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