Zhu Xinchao, Zhao Jun, Hu Anzhong, Pan Jingyu, Deng Guoqing, Hua Changyi, Zhu Cancan, Liu Yong, Yang Ke, Zhu Ling
Optoelectronic Application Technology Research Center, Institute of Applied Technology, Hefei Institutes of Physical Science, Chinese Academy of Science, Hefei 230031, China.
University of Science and Technology of China, Hefei 230026, China.
Micromachines (Basel). 2020 Feb 11;11(2):186. doi: 10.3390/mi11020186.
The outbreak of Zika virus (ZIKV) has posed a great challenge to public health in recent years. To address the urgent need of ZIKV RNA assays, we integrate the microfluidic chip embedded with chitosan-modified silicon dioxide capillaries, smartphone-based detection unit to be a C3-system for the rapid extraction and detection of ZIKV RNA. The C3-system is characterized by: (1) four chitosan-modified silicon dioxide capillaries integrated in the microfluidic chip for target ZIKV RNA enrichment and "in situ PCR" (polymerase chain reaction) amplification; (2) smartphone-based point of care (POC) device consisting of a pneumatic subsystem for controlling the nucleic acid extraction processes in the microfluidic chip, a heating subsystem for sample lysis and PCR amplification, and an optical subsystem for signal acquisition. The entire detection processes including sample lysis, ZIKV RNA enrichment, and reverse-transcription polymerase chain reaction (RT-PCR) is achieved in the microfluidic chip. Moreover, PCR buffers can be directly loaded into the chitosan-modified silicon dioxide capillaries for "in situ PCR", in which the captured ZIKV RNA is directly used for downstream PCR without any loss. ZIKV RNA extracted by the C3-system can be successfully recovered at very low concentrations of 50 transducing units (TU)/mL from crude human saliva. This means that our method of detecting viremia in patients infected with ZIKV is reliable.
近年来,寨卡病毒(ZIKV)的爆发对公共卫生构成了巨大挑战。为满足对寨卡病毒RNA检测的迫切需求,我们将嵌入壳聚糖修饰二氧化硅毛细管的微流控芯片与基于智能手机的检测单元集成,构建了一个用于快速提取和检测寨卡病毒RNA的C3系统。该C3系统的特点包括:(1)微流控芯片中集成了四个壳聚糖修饰的二氧化硅毛细管,用于富集目标寨卡病毒RNA并进行“原位PCR”(聚合酶链反应)扩增;(2)基于智能手机的即时检测(POC)设备,由一个用于控制微流控芯片中核酸提取过程的气动子系统、一个用于样品裂解和PCR扩增的加热子系统以及一个用于信号采集的光学子系统组成。整个检测过程,包括样品裂解、寨卡病毒RNA富集和逆转录聚合酶链反应(RT-PCR),均在微流控芯片中完成。此外,PCR缓冲液可直接加载到壳聚糖修饰的二氧化硅毛细管中进行“原位PCR”,其中捕获的寨卡病毒RNA可直接用于下游PCR,无任何损失。通过C3系统从粗制人唾液中以50转导单位(TU)/mL的极低浓度成功回收了寨卡病毒RNA。这意味着我们检测寨卡病毒感染患者病毒血症的方法是可靠的。