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用于莫桑比克马普托即时检测的1小时无提取环介导等温扩增HPV DNA检测法

One-hour extraction-free loop-mediated isothermal amplification HPV DNA assay for point-of-care testing in Maputo, Mozambique.

作者信息

Barra Maria J, Wilkinson Alexis F, Ma Ariel E, Goli Karthik, Atif Hira, Osman Nafissa M R B, Lorenzoni Cesaltina, Tivir Guilhermina, Lathrop Eva H, Castle Philip E, Guo Ming, Montealegre Jane R, Baker Ellen S, Salcedo Mila P, Schmeler Kathleen M, Richards-Kortum Rebecca R

机构信息

Department of Bioengineering, Rice University, Houston, TX, USA.

Universidade Eduardo Mondlane (UEM), Maputo, Mozambique.

出版信息

Nat Commun. 2025 Aug 7;16(1):7295. doi: 10.1038/s41467-025-62454-x.

Abstract

Human papillomavirus (HPV) is responsible for nearly all cases of cervical cancer. Affordable point-of-care DNA testing is needed for cervical cancer screening in low- and middle-income countries, where most cervical cancer cases occur. HPV DNA testing typically requires complex lab infrastructure and trained personnel. In this work, we develop a loop-mediated isothermal amplification (LAMP)-based HPV DNA test, which targets three of the most oncogenic HPV types (HPV16, HPV18, HPV45) and a cellular control and achieves analytical sensitivity comparable to gold standard methods. Our extraction-free sample preparation strategy permits adding sample lysate directly to the LAMP reaction. We utilize a low-cost benchtop heater/fluorimeter, delivering results in less than one hour. We analytically evaluate our assay with clinical samples in Houston, Texas (n = 38) and Maputo, Mozambique (n = 191). Results show 100% and 93% concordance, respectively, with a reference test widely used in low-resource settings. This sensitive and specific four-step assay can potentially expand cervical cancer screening in resource-limited settings.

摘要

人乳头瘤病毒(HPV)几乎导致了所有宫颈癌病例。在大多数宫颈癌病例发生的低收入和中等收入国家,宫颈癌筛查需要价格可承受的即时DNA检测。HPV DNA检测通常需要复杂的实验室基础设施和经过培训的人员。在这项工作中,我们开发了一种基于环介导等温扩增(LAMP)的HPV DNA检测方法,该方法针对三种最具致癌性的HPV类型(HPV16、HPV18、HPV45)以及一种细胞对照,其分析灵敏度与金标准方法相当。我们无需提取的样品制备策略允许将样品裂解液直接添加到LAMP反应中。我们使用低成本的台式加热器/荧光计,在不到一小时内得出结果。我们在德克萨斯州休斯顿(n = 38)和莫桑比克马普托(n = 191)用临床样品对我们的检测方法进行了分析评估。结果分别显示与在资源有限环境中广泛使用的参考检测方法的一致性为100%和93%。这种灵敏且特异的四步法检测方法有可能在资源有限的环境中扩大宫颈癌筛查范围。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/122a/12331945/0c57d434eba7/41467_2025_62454_Fig1_HTML.jpg

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