Electrochemical Sensors for Detections of Influenza Viruses: Fundamentals and Applications

Avian influenza viruses (AIVs) could cause severe diseases and, as the consequence, serious economic losses as well as a risk for potential transmission to humans. Therefore, the detection of viruses and their fragments or specific DNA sequences becomes an important approach in molecular diagnosis. Here, we present electrochemical genosensors devoted for detection of influenza virus H5N1 gene sequence. We focus our attention on ion-channel mechanism, E-DNA sensors, and genosensors based on redox-active layer. The novel dual DNA electrochemical sensor with “signal-off” and “signal-on” architecture for simultaneous detection of two different sequences of DNA derived from avian influenza virus type H5N1 by means of one electrode is presented. Immunosensors are also adequate analytical devices for detection of pathogens since antibodies are natural receptors responsible for binding of antigens. Thus, the binding selectivity and efficiency are naturally high. The immunosensors presented could be divided into two main groups: ion-channel mimetic and based on redox-active monolayer

A highly sensitive electrochemical genosensor based on Co-porphyrin-labelled DNA

We report the use of Co-porphyrins as electrochemical tags for a highly sensitive and selective genosensor. An avian influenza virus-based DNA sequence characteristic of H5N1 was detected at femtomolar levels from competing non-complementary sequences through hybridisation with the labeled DNA

Electrochemical genosensor based on disc and screen printed goldelectrodes for detection of specific DNA and RNA sequences derivedfrom Avian Influenza Virus H5N1

tThe genosensors based on thiolated ssDNA probe deposited on the two types of gold electrodes: screen-printed (miniaturized) and disc electrodes destined for determination of specific sequences of DNA andRNA derived from Avian Influenza Virus H5N1 have been proposed. The working principle of genosensor isbased on the ion-channel mechanism. The analytical signals generated upon hybridization processes wererecorded using electrochemical technique – Osteryoung square wave voltammetry in the presence of aredox active marker [Fe(CN)6]3−/4−in the sample solution. The miniaturized genosensor based on screenprinted gold electrodes was able to detect the 20-mer complementary DNA oligonucleotide sequence aswell as ∼280-mer RNA sequences containing the complementary 20-mer sequence in various positions:at 3�-terminus, at 5�-terminus and in the middle of the RNA transcript at the 1 pM concentration. Themeasuring systems were selective. Non-complementary 20-mer oligonucleotide sequence as well asRNA transcript without complementary region generated weak response. The RNA transcripts were alsotested with gold disc electrodes modified in the same manner. This device was able to detect ∼280-mer RNA sequences, but at higher concentration of 10 pM. The good discrimination of the position ofcomplementary part in the ∼280-mer RNA sequences was observed with using both types of modifiedelectrodes

Ultrasensitive electrochemical genosensor for direct detection of specific RNA sequences derived from avian influenza viruses present in biological samples

An electrochemical genosensor based on an epoxyphenanthroline–Fe(III)–NH2-ssDNA layer for the detection of RNA derived from Avian Influenza is presented. The biosensor preparation consists of: (I) modification of gold electrodes with aminoethanethiol, (II) modification of the self-assembled monolayer of aminoethanethiol with 5,6-epoxy-5,6-dihydro-[1,10]-phenanthroline using “click” chemistry, (III) a first step of complexation of Fe(III) by 5,6-epoxy-5,6-dihydro-[1,10]-phenanthroline, (IV) a second step of complexation of Fe(III) by 5,6-epoxy-5,6-dihydro-[1,10]-phenanthroline, (V) immobilization of the single stranded amino-DNA probe via “click” chemistry between epoxy and amino groups. The interactions between the ssDNA probe and RNA targets were explored with Osteryoung Square Wave Voltammetry. The genosensor showed a remarkable detection limit of 3 copies/μL (5 aM) for RNA extracted from A/swan/Poland/305/06 (H5N1) containing a fully complementary sequence. A linear dynamic range for this sequence was observed from 3.0×103 to 3.0×105 [copies/μl]. RNA extracted from A/mallard/Poland/446/09 (H7N7), containing a non-complementary sequence, generated a much weaker response. Moreover, the developed genosensor allows to distinguish RNA present in biological samples having 2, 3 and 4 mismatches. This biosensing approach can become a potential alternative tool for detecting RNA samples in biomedical research and early clinical diagnosis of avian influenza viruses

An electrochemical immunosensor based on a 4,4′-thiobisbenzenethiol self-assembled monolayer for the detection of hemagglutinin from avian influenza virus H5N1

An electrochemical immunosensor for the detection of hemagglutinin from avian influenza virus H5N1 is presented in this paper. The following steps lead up to the construction of immunosensor: (i) modification of gold electrodes with 4,4′-thiobisbenzenethiol, (ii) modification of self-assembled monolayer of 4,4′-thiobisbenzenethiol with gold colloidal nanoparticles, (iii) immobilization of single chain variable fragments of antibodies (scFv) against hemagglutinin H5 via Ssingle bondAu covalent bonds, (iv) blocking of the remaining free space with bovine serum albumin. The interactions between the scFv and hemagglutinin variants have been explored with electrochemical impedance spectroscopy in the presence of [Fe(CN)6]3−/4− as an electroactive marker. The immunosensor was able to detect two different His-tagged variants of recombinant hemagglutinin from H5N1 viruses: the short fragment (17–340 residues) of A/swan/Poland/305-135V08/2006 and the long (17–530 residues) of A/Bar-headed Goose/Qinghai/12/2005. The strongest response has been observed for the long variant with a detection limit of 0.6 pg/mL and a dynamic range from 4.0 to 20.0 pg/mL. The recombinant hemagglutinin (17–527 residues) from A/chicken/Netherlands/1/03 (H7N7), used as the negative control generated a weak response. This confirms the selectivity of the immunsensor proposed. A miniaturized version of the immunosensor, based on screen-printed gold electrodes, was tested with the same set of recombinant hemagglutinins and it achieved a linear range from 1 to 8 pg/mL with a detection limit of 0.9 pg/mL for the long fragment of hemagglutinin