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基于斑点酶联免疫吸附试验和金纳米粒子的免疫层析试纸条对玉米褪绿斑驳病毒的可视化和超灵敏检测

Visual and Super-Sensitive Detection of Maize Chlorotic Mottle Virus by Dot-ELISA and Au Nanoparticle-Based Immunochromatographic Test Strip.

机构信息

State Key Laboratory of Rice Biology, Key Laboratory of Biology of Crop Pathogens and Insects of Zhejiang Province, Institute of Biotechnology, Zhejiang University, Hangzhou 310058, China.

Hainan Institute, Zhejiang University, Sanya 572025, China.

出版信息

Viruses. 2023 Jul 22;15(7):1607. doi: 10.3390/v15071607.

Abstract

Maize chlorotic mottle virus (MCMV) is the only species in the genus and is often co-infected with one or several viruses of the genus, posing a great threat to the global maize industry. Effective viral integrated management measures are dependent on the timely and proper detection of the causal agent of the disease. In this work, six super-sensitive and specific monoclonal antibodies (mAbs) against MCMV were first prepared using purified MCMV virions as the immunogen. Then, the Dot enzyme-linked immunosorbent assay (Dot-ELISA) was established based on the obtained mAbs, and it can detect MCMV in infected maize leaf crude extracts diluted up to 1:10,240-fold (/, g/mL). Furthermore, a rapid and user-friendly Au nanoparticle-based immunochromatographic test strip (AuNP-ICTS) based on paired mAbs 7B12 and 17C4 was created for monitoring MCMV in point-of-care tests, and it can detect the virus in a 25,600-fold dilution (/, g/mL) of MCMV-infected maize leaf crude extracts. The whole test process for ICTS was completed in 10 min. Compared with conventional reverse transcription-polymerase chain reaction (RT-PCR), the detection endpoint of both serological methods is higher than that of RT-PCR, especially the Dot-ELISA, which is 12.1 times more sensitive than that of RT-PCR. In addition, the detection results of 20 blinded maize samples by the two serological assays were consistent with those of RT-PCR. Therefore, the newly created Dot-ELISA and AuNP-ICTS exhibit favorable application potential for the detection of MCMV in plant samples.

摘要

玉米线条花叶病毒(MCMV)是该属中唯一的物种,通常与该属的一种或多种病毒共同感染,对全球玉米产业构成巨大威胁。有效的病毒综合管理措施依赖于及时、正确地检测疾病的病原体。在这项工作中,首先使用纯化的 MCMV 病毒粒子作为免疫原制备了针对 MCMV 的 6 种超敏和特异性单克隆抗体(mAb)。然后,基于获得的 mAb 建立了斑点酶联免疫吸附试验(Dot-ELISA),可检测感染玉米叶片粗提取物中稀释至 1:10,240 倍的 MCMV(/, g/mL)。此外,基于配对 mAb 7B12 和 17C4 创建了一种快速、用户友好的基于金纳米颗粒的免疫层析测试条(AuNP-ICTS),用于在即时护理测试中监测 MCMV,可检测感染玉米叶片粗提取物 25,600 倍稀释的病毒(/, g/mL)。整个 ICTS 测试过程在 10 分钟内完成。与常规逆转录聚合酶链反应(RT-PCR)相比,两种血清学方法的检测终点均高于 RT-PCR,尤其是 Dot-ELISA,比 RT-PCR 高 12.1 倍。此外,两种血清学检测方法对 20 个盲样玉米的检测结果与 RT-PCR 一致。因此,新创建的 Dot-ELISA 和 AuNP-ICTS 显示出在植物样品中检测 MCMV 的良好应用潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81c6/10383747/32b5373d6d9b/viruses-15-01607-g001.jpg

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