Label- free and amplification- free viral RNA quantification from primate biofluids using a trapping- assisted optofluidic nanopore platform

• 成果类型: Article
• 署名作者: Sampad, Mohammad Julker Neyen; Saiduzzaman, S. M.; Walker, Zach J.; Wells, Tanner N.; Wayment, Jesse X.; Ong, Ephraim M.; Mdaki, Stephanie D.; Tamhankar, Manasi A.; Yuzvinsky, Thomas D.; Patterson, Jean L.; Hawkins, Aaron R.; Schmidt, Holger
• 署名单位: University of California System; University of California Santa Cruz; Brigham Young University; Texas Biomedical Research Institute
• 刊物名称: PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
• ISSN/ISSBN: 0027-8636
• DOI: 10.1073/pnas.2400203121
• 发表日期: 2024-04-16
• 关键词: single-stranded-dna; zika virus; multiplexed detection; molecules; ebola; translocation; manipulation; sars-cov-2; infection; proteins

摘要

Viral outbreaks can cause widespread disruption, creating the need for diagnostic tools that provide high performance and sample versatility at the point of use with moderate complexity. Current gold standards such as PCR and rapid antigen tests fall short in one or more of these aspects. Here, we report a label - free and amplification - free nanopore sensor platform that overcomes these challenges via direct detection and quantification of viral RNA in clinical samples from a variety of biological fluids. The assay uses an optofluidic chip that combines optical waveguides with a fluidic channel and integrates a solid - state nanopore for sensing of individual biomolecules upon translocation through the pore. High specificity and low limit of detection are ensured by capturing RNA targets on microbeads and collecting them by optical trapping at the nanopore location where targets are released and rapidly detected. We use this device for longitudinal studies of the viral load progression for Zika and Severe Acute Respiratory Syndrome Coronavirus-2 (SARS- CoV-2) infections in marmoset and baboon animal models, respectively. The up to million - fold trapping - based target concentration enhancement enables amplification - free RNA quantification across the clinically relevant concentration range down to the assay limit of RT-qPCR as well as cases in which PCR failed. The assay operates across all relevant biofluids, including semen, urine, and whole blood for Zika and nasopharyngeal and throat swab, rectal swab, and bronchoalveolar lavage for SARS- CoV-2. The versatility, performance, simplicity, and potential for full microfluidic integration of the amplification - free nanopore assay points toward a unique approach to molecular diagnostics for nucleic acids, proteins, and other targets.