基于核酸的电化学生物传感器,利用金纳米粒子检测乙型流感。

IF 2.3 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Isar Yahyavi, Fahime Edalat, Neda Pirbonyeh, Arash Letafati, Naghmeh Sattarahmady, Hossein Heli, Afagh Moattari
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引用次数: 0

摘要

流感病毒是一种普遍存在的病原体,在寒冷季节的流行率会增加,导致每年出现大量感染病例。值得注意的是,对甲型流感病毒株有效的药物干预措施往往对乙型流感病毒变种的疗效有限。在这种背景下,显然需要采用创新方法来准确、迅速地区分和检测乙型流感。生物传感器在这一检测过程中发挥着关键作用,可快速、特异、灵敏地识别病毒,便于及时干预和遏制。我们设计了针对保守的 B/Victoria/2/87 流感病毒 NP 区的寡核苷酸序列。从疑似感染流感病毒的患者身上采集鼻咽拭子,提取病毒 RNA。使用随机六聚体进行 cDNA 合成,并通过实时 PCR 对流感基因组进行定量。金纳米粒子被固定在一个表面上,以固定特异性 DNA 探针,并进行电化学杂交。该生物传感器具有高选择性,能有效区分互补序列、错配序列和流感病毒 cDNA 基因组。该生物传感器成功检测了真实样本中的乙型流感病毒基因组。非流感样本没有产生明显的杂交信号。对生物传感器和实时 PCR 的结果进行比较后发现,这两种方法的结果完全一致。该生物传感器利用电化学方法检测杂交,被证明能有效地检测乙型流感病毒基因组,具有高度的特异性、灵敏度和选择性。与实时 PCR 的比较分析表明,该生物传感器在快速和特异性病毒检测方面具有准确性和潜在的适用性。这种创新方法为未来检测乙型流感病毒和其他病原体的诊断和流行病学应用带来了希望。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Nucleic acid-based electrochemical biosensor for detection of influenza B by gold nanoparticles

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.

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来源期刊
Journal of Molecular Recognition
Journal of Molecular Recognition 生物-生化与分子生物学
CiteScore
4.60
自引率
3.70%
发文量
68
审稿时长
2.7 months
期刊介绍: Journal of Molecular Recognition (JMR) publishes original research papers and reviews describing substantial advances in our understanding of molecular recognition phenomena in life sciences, covering all aspects from biochemistry, molecular biology, medicine, and biophysics. The research may employ experimental, theoretical and/or computational approaches. The focus of the journal is on recognition phenomena involving biomolecules and their biological / biochemical partners rather than on the recognition of metal ions or inorganic compounds. Molecular recognition involves non-covalent specific interactions between two or more biological molecules, molecular aggregates, cellular modules or organelles, as exemplified by receptor-ligand, antigen-antibody, nucleic acid-protein, sugar-lectin, to mention just a few of the possible interactions. The journal invites manuscripts that aim to achieve a complete description of molecular recognition mechanisms between well-characterized biomolecules in terms of structure, dynamics and biological activity. Such studies may help the future development of new drugs and vaccines, although the experimental testing of new drugs and vaccines falls outside the scope of the journal. Manuscripts that describe the application of standard approaches and techniques to design or model new molecular entities or to describe interactions between biomolecules, but do not provide new insights into molecular recognition processes will not be considered. Similarly, manuscripts involving biomolecules uncharacterized at the sequence level (e.g. calf thymus DNA) will not be considered.
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