基于纳米粒子的一步式快速生物传感器平台,用于在临床应用中同时鉴定乙型肝炎病毒和丙型肝炎病毒。

IF 4 2区 生物学 Q2 MICROBIOLOGY
Xu Chen, Yuanfang Shi, Qi Zhao, Yu Wang, Xinggui Yang, Yan Tan, Yi Wang, Shilei Dong, Zhenghua Xiao
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引用次数: 0

摘要

目标:由乙型肝炎病毒(HBV)和丙型肝炎病毒(HCV)感染引起的病毒性肝炎仍然是全球公共卫生的一大挑战,尤其是在中低收入国家。利用灵敏、特异、快速和用户友好的护理点(POC)检测平台来筛查和诊断这两种感染至关重要。在此,我们开发了一种新型分子诊断方法,它将多重环介导等温扩增与基于金纳米粒子的侧流生物传感器(mLAMP-AuNPs-LFB)结合在一起,用于一步、直观、快速、灵敏和特异性地鉴定 HBV 和 HCV:方法:设计并构建了基于 AuNPs 的 LFB,用于同时检测 HBV 和 HCV。HBV-LAMP和HCV-LAMP引物分别针对中国主要HBV基因型(B、C、D、B/C重组型和C/D重组型)和HCV亚型(1b、2a、3a、3b和6a)的S和5'-非翻译区(5'-UTR)基因设计。我们的检测条件、多重-LAMP 扩增温度和时间都经过了优化。结果表明,基于 AuNPs 的 LAMP 检测方法的灵敏度和特异性均优于传统方法:结果:基于 AuNPs 的 LFB 是根据我们的设计手册成功制造的。结果:基于 AuNPs 的 LFB 成功地按照我们的设计手册制造出来,并成功地设计出分别基于 S 和 5'-UTR 基因的两个独特的独立引物对。最佳的 mLAMP-AuNPs-LFB 检测过程包括快速核酸分离(10 分钟)、mLAMP(63 °C,35 分钟)和可视 AuNPs-LFB 解释(不到 2 分钟),可在 50 分钟内完成。HBV&HCV-mLAMP-AuNPs-LFB测定每次检测的质粒模板拷贝数低至20拷贝,即可检测到目标基因(HBV-S和HCV-5'-UTR),对实验病原体的特异性为100%:初步结果表明,我们的 mLAMP-AuNPs-LFB 检测方法是一种有价值的工具,作为 HBV 和 HCV 鉴定的 POC 检测方法具有巨大的潜力,尤其是在不发达地区。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
One-step, rapid, nanoparticle-based biosensor platform for the simultaneous identification of hepatitis B virus and hepatitis C virus in clinical applications.

Objectives: Viral hepatitis caused by hepatitis B virus (HBV) and hepatitis C virus (HCV) infections remain a major global public health challenge, particularly in low- and middle-income countries. It is crucial to utilize a pointof-care (POC) testing platform that is sensitive, specific, rapid, and user-friendly for screening and diagnosis of the two infections. Here, a novel molecular diagnostic assay, integrating multiplex loop-mediated isothermal amplification with a gold nanoparticle-based lateral flow biosensor (mLAMP-AuNPs-LFB) was developed and applied for one-step, visual, rapid, sensitive, and specific identification of HBV and HCV.

Methods: The AuNPs-based LFB was devised and constructed for the simultaneous detection of HBV and HCV. The HBV-LAMP and HCV-LAMP primers were designed against the S and 5'-untranslated region (5'-UTR) genes from the major HBV genotypes (B, C, D, B/C recombinant, and C/D recombinant) and HCV subtypes (1b, 2a, 3a, 3b, and 6a) in China, respectively. Our assay conditions, both multiplex-LAMP amplification temperature and time were optimized. The sensitivity and specificity of our assay were tested, and the feasibility of our assay was verified through clinical samples.

Results: The AuNPs-based LFB used here was successfully manufactured according to our devise manual. The two unique independent primer pairs were successfully designed based on the S and 5'-UTR genes, respectively. The optimal mLAMP-AuNPs-LFB detection process, involving rapid nucleic acid isolation (10 min), mLAMP (63 °C for 35 min), and visual AuNPs-LFB interpretation (less than 2 min), could be completed within 50 min. The HBV&HCV-mLAMP-AuNPs-LFB assay can detect the target genes (HBV-S and HCV-5'-UTR) with as low as 20 copies of plasmid template per test, and the specificity was 100% for the experimental pathogens.

Conclusions: The preliminary results manifested that our mLAMP-AuNPs-LFB assay is a valuable tool and has tremendous potential as a POC testing approach for HBV and HCV identification, especially in undeveloped regions.

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来源期刊
BMC Microbiology
BMC Microbiology 生物-微生物学
CiteScore
7.20
自引率
0.00%
发文量
280
审稿时长
3 months
期刊介绍: BMC Microbiology is an open access, peer-reviewed journal that considers articles on analytical and functional studies of prokaryotic and eukaryotic microorganisms, viruses and small parasites, as well as host and therapeutic responses to them and their interaction with the environment.
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