tetano
Editor, Senior Moderator
J Mol Recognit
. 2023 Dec 21:e3073.
doi: 10.1002/jmr.3073. Online ahead of print. Nucleic acid-based electrochemical biosensor for detection of influenza B by gold nanoparticles
Isar Yahyavi[SUP] 1 2 [/SUP], Fahime Edalat[SUP] 1 [/SUP], Neda Pirbonyeh[SUP] 1 3 [/SUP], Arash Letafati[SUP] 4 [/SUP], Naghmeh Sattarahmady[SUP] 5 6 [/SUP], Hossein Heli[SUP] 6 [/SUP], Afagh Moattari[SUP] 1 [/SUP]
Affiliations
The influenza virus is a pervasive pathogen that exhibits increased prevalence during colder seasons, resulting in a significant annual occurrence of infections. Notably, pharmaceutical interventions effective against influenza A strains often exhibit limited efficacy against influenza B variants. Against this backdrop, the need for innovative approaches to accurately and swiftly differentiate and detect influenza B becomes evident. Biosensors play a pivotal role in this detection process, offering rapid, specific, and sensitive identification of the virus, facilitating timely intervention and containment efforts. Oligonucleotide sequences targeting the conserved B/Victoria/2/87 influenza virus NP region were designed. Nasopharyngeal swabs were collected from patients suspected of influenza virus infection, and viral RNA was extracted. RNA quality was assessed through one-step PCR. cDNA synthesis was performed using random hexamers, and real-time PCR quantified the influenza genome. Gold nanoparticles were immobilized on a surface to immobilize the specific DNA probe, and electrochemical hybridization was electrochemically followed. The biosensor exhibited high selectivity and effective distinction of complementary sequences from mismatches and influenza virus cDNA genome. The biosensor successfully detected the influenza B virus genome in real samples. Non-influenza samples yielded no significant hybridization signals. The comparison between the results obtained from the biosensor and real-time PCR revealed full agreement of these methods. The biosensor utilized electrochemical detection of hybridization and proved effective in detecting the influenza B virus genome with high specificity, sensitivity, and selectivity. Comparative analysis with real-time PCR underscored the accuracy and potential applicability of the biosensor in rapid and specific virus detection. This innovative approach holds promise for future diagnostic and epidemiological applications in detecting influenza B virus and other pathogens.
Keywords: AuNPs; c-DNA; electrochemical biosensor; flu B symptoms; genosensor.
. 2023 Dec 21:e3073.
doi: 10.1002/jmr.3073. Online ahead of print. Nucleic acid-based electrochemical biosensor for detection of influenza B by gold nanoparticles
Isar Yahyavi[SUP] 1 2 [/SUP], Fahime Edalat[SUP] 1 [/SUP], Neda Pirbonyeh[SUP] 1 3 [/SUP], Arash Letafati[SUP] 4 [/SUP], Naghmeh Sattarahmady[SUP] 5 6 [/SUP], Hossein Heli[SUP] 6 [/SUP], Afagh Moattari[SUP] 1 [/SUP]
Affiliations
- PMID: 38126612
- DOI: 10.1002/jmr.3073
The influenza virus is a pervasive pathogen that exhibits increased prevalence during colder seasons, resulting in a significant annual occurrence of infections. Notably, pharmaceutical interventions effective against influenza A strains often exhibit limited efficacy against influenza B variants. Against this backdrop, the need for innovative approaches to accurately and swiftly differentiate and detect influenza B becomes evident. Biosensors play a pivotal role in this detection process, offering rapid, specific, and sensitive identification of the virus, facilitating timely intervention and containment efforts. Oligonucleotide sequences targeting the conserved B/Victoria/2/87 influenza virus NP region were designed. Nasopharyngeal swabs were collected from patients suspected of influenza virus infection, and viral RNA was extracted. RNA quality was assessed through one-step PCR. cDNA synthesis was performed using random hexamers, and real-time PCR quantified the influenza genome. Gold nanoparticles were immobilized on a surface to immobilize the specific DNA probe, and electrochemical hybridization was electrochemically followed. The biosensor exhibited high selectivity and effective distinction of complementary sequences from mismatches and influenza virus cDNA genome. The biosensor successfully detected the influenza B virus genome in real samples. Non-influenza samples yielded no significant hybridization signals. The comparison between the results obtained from the biosensor and real-time PCR revealed full agreement of these methods. The biosensor utilized electrochemical detection of hybridization and proved effective in detecting the influenza B virus genome with high specificity, sensitivity, and selectivity. Comparative analysis with real-time PCR underscored the accuracy and potential applicability of the biosensor in rapid and specific virus detection. This innovative approach holds promise for future diagnostic and epidemiological applications in detecting influenza B virus and other pathogens.
Keywords: AuNPs; c-DNA; electrochemical biosensor; flu B symptoms; genosensor.