Paper-based nucleic acid testing system for simple and early diagnosis of mosquito-borne RNA viruses from human serum

被引:66
作者
Batule, Bhagwan S. [1 ]
Seok, Youngung [1 ]
Kim, Min-Gon [1 ]
机构
[1] Gwangju Inst Sci & Technol, Sch Phys & Chem, Dept Chem, 261 Cheomdan Gwagiro, Gwangju 61005, South Korea
基金
新加坡国家研究基金会;
关键词
Nucleic acid testing; Paper microfluidics; Mosquito-borne diseases; Viral RNA extraction; RT-LAMP; Point-of-care diagnostics; RECOMBINASE POLYMERASE AMPLIFICATION; DNA EXTRACTION METHOD; INFECTIOUS-DISEASES; POINT; DEVICE; BLOOD; ASSAY; CHIP;
D O I
10.1016/j.bios.2019.111998
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The recent outbreaks of mosquito-borne diseases (e.g., zika, dengue, and chikungunya) increased public health burden in developing countries. To control the spread of these infectious diseases, a simple, economic, reliable, sensitive, and selective diagnostic platform is required. Considering demand for affordable and accessible methods, we have demonstrated a two-step strategy for extraction and detection of viral RNAs of infectious diseases within 1 h. Ready-to-use devices for viral RNA extraction and detection were successfully fabricated using paper as a substrate. Viral RNA (e.g., zika, dengue, and chikungunya) was captured and eluted using a handheld RNA extraction paper-strip device, and another paper-chip device was used for reverse transcription loop-mediated isothermal amplification (RT-LAMP) assay with a detection limit of a single copy and 10 copies of viral RNA in phosphate buffer solution (PBS) and serum, respectively. With these proposed devices, we have detected viral RNAs of zika and dengue in clinical human serum samples. The proposed paper-based extraction and detection platforms could be employed for detection of infectious viral diseases from complex clinical samples in resource-limited settings.
引用
收藏
页数:7
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