An efficient isothermal PCR method for on-site detection of nucleic acid

Author:

Zhang Shiyin123,Wang Jin123,Zhuo Zhihao124,Su Xiaosong123,Chen Mengyuan123,Chen Wendi123,Li Tingdong123,Zhang Dongxu123,Min Xiaoping125,Ge Shengxiang123,Xia Ningshao123

Affiliation:

1. State Key Laboratory of Molecular Vaccinology & Molecular Diagnostics, Xiamen University, Xiamen, 361102, China

2. National Institute of Diagnostics & Vaccine Development in Infectious Diseases, Xiamen University, Xiamen, 361102, China

3. School of Public Health, Xiamen University, Xiamen, 361102, China

4. School of Life Science, Xiamen University, Xiamen, 361102, China

5. School of Information Science & Technology, Xiamen University, Xiamen, 361102, China

Abstract

Convective PCR (CPCR) is an isothermal nucleic acid amplification technology; however, natural convection exhibits a chaotic and multiplex flow state, resulting in low amplification efficiency and specificity. We placed a polycarbonate strip (p-strip) inside reaction tubes to induce circumfluence by blocking the inner ring that originally allowed fluid to flow at suboptimal temperatures. Moreover, we constructed a dual-temperature instrument to provide appropriate denaturing and annealing zones for CPCR. Tubes containing p-strips exhibited significantly improved efficiency, sensitivity and specificity. For real-time detection, the variation coefficients of three replicates having the same concentrations were less than 2% in more than half of the cases, indicating improved CPCR amplification and potential as a commercial on-site nucleic acid diagnosis tool.

Publisher

Future Science Ltd

Subject

General Biochemistry, Genetics and Molecular Biology,Biotechnology

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