A smartphone-based diagnostic platform for rapid detection of Zika, chikungunya, and dengue viruses

被引:224
作者
Priye, Aashish [1 ]
Bird, Sara W. [1 ]
Light, Yooli K. [2 ]
Ball, Cameron S. [1 ]
Negrete, Oscar A. [1 ]
Meagher, Robert J. [1 ]
机构
[1] Sandia Natl Labs, Dept Biotechnol & Bioengn, Livermore, CA 94550 USA
[2] Sandia Natl Labs, Dept Syst Biol, Livermore, CA 94550 USA
关键词
MEDIATED ISOTHERMAL AMPLIFICATION; COLORIMETRIC DETECTION; DNA; PCR;
D O I
10.1038/srep44778
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Current multiplexed diagnostics for Zika, dengue, and chikungunya viruses are situated outside the intersection of affordability, high performance, and suitability for use at the point-of-care in resourcelimited settings. Consequently, insufficient diagnostic capabilities are a key limitation facing current Zika outbreak management strategies. Here we demonstrate highly sensitive and specific detection of Zika, chikungunya, and dengue viruses by coupling reverse-transcription loop-mediated isothermal amplification (RT-LAMP) with our recently developed quenching of unincorporated amplification signal reporters (QUASR) technique. We conduct reactions in a simple, inexpensive and portable "LAMP box" supplemented with a consumer class smartphone. The entire assembly can be powered by a 5 V USB source such as a USB power bank or solar panel. Our smartphone employs a novel algorithm utilizing chromaticity to analyze fluorescence signals, which improves the discrimination of positive/ negative signals by 5-fold when compared to detection with traditional RGB intensity sensors or the naked eye. The ability to detect ZIKV directly from crude human sample matrices (blood, urine, and saliva) demonstrates our device's utility for widespread clinical deployment. Together, these advances enable our system to host the key components necessary to expand the use of nucleic acid amplification-based detection assays towards point-of-care settings where they are needed most.
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页数:11
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