期刊
SCIENCE ADVANCES
卷 7, 期 39, 页码 -出版社
AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/sciadv.abh2848
关键词
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资金
- National Science Foundation [CBET 20-29215]
- Institute for Sustainability, Energy, and Environment at University of Illinois at Urbana-Champaign
- Illinois-JITRI Institute [JITRI 23965]
- PEW Latin American Fellowship
- CONICET [PIP0370]
- ANPCyT [PICT-2016-1680, PICT-2017-1523]
A new method has been developed for direct detection and differentiation of infectious viruses, including human adenovirus and SARS-CoV-2, from noninfectious ones without the need for sample pretreatment. This method utilizes DNA aptamers to bind intact infectious viruses and incorporates them into a solid-state nanopore for enhanced sensitivity. Applications of this sensor have been demonstrated in various types of samples, making it generally applicable for detecting emerging viruses of environmental and public health concern.
Viral infections are a major global health issue, but no current method allows rapid, direct, and ultrasensitive quantification of intact viruses with the ability to inform infectivity, causing misdiagnoses and spread of the viruses. Here, we report a method for direct detection and differentiation of infectious from noninfectious human adenovirus and SARS-CoV-2, as well as from other virus types, without any sample pretreatment. DNA aptamers are selected from a DNA library to bind intact infectious, but not noninfectious, virus and then incorporated into a solid-state nanopore, which allows strong confinement of the virus to enhance sensitivity down to 1 pfu/ml for human adenovirus and 1 x 10(4) copies/ml for SARS-CoV-2. Applications of the aptamer-nanopore sensors in different types of water samples, saliva, and serum are demonstrated for both enveloped and nonenveloped viruses, making the sensor generally applicable for detecting these and other emerging viruses of environmental and public health concern.
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