Viral infections (like different types of influenza virus) are becoming alarmingly common often leading to epidemics. Since Viruses can multiply from genomic materials it can spread the infection quickly as well as cause other complications like birth defects, autoimmune disease and even cancer. Diagnostics of viral infection traditionally is performed using antigen-antibody reaction, which is time consuming and labor intensive. Also, viral infections can be latent or show false negative results when antibody reaction is tested. In-situ direct hybridization detection is possible by expensive, long and difficult radiation-based methods. Our group has developed a Carbon Nanotube (CNT) & Graphene based Bionanosensor (BNS) for rapid and direct detection of specific DNA sequences. In this technique, single-stranded (ss) DNA probe (known as priming) is immobilized on a substrate. This recognizes a specific complementary target DNA in a sample solution and gets hybridized leading to a detectable electrical signal. In this study we have expanded the scope of this BNS by using it to detect quick in-situ RNA hybridization. A sample of RNA was tested simultaneously in an array of 4 biosensors (each primed by the complementary sequence). The resistance across each of the biosensors was measured with a self-designed, feed-back controlled, balanced Wheatstone bridge circuit with an Arduino interface. A specific pattern related to hybridization was observed and a weighted average performed over 30 experiments. The sensors primed with the forward RNA was able to detect the complementary sequence in a mixed sample in 10 minutes from the starting time.

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