Rapid detection and quantification of Enterovirus 71 by a portable surface plasmon resonance biosensor

• Published in: Biosensors & bioelectronics 2017-06, Vol.92, p.186-191
• Main Authors: Prabowo, Briliant Adhi, Wang, Robert Y.L., Secario, Muhammad Khari, Ou, Po-Ting, Alom, Azharul, Liu, Jia-Jung, Liu, Kou-Chen
• Format: Article
• Language: English
• Subjects: Capsid Proteins - analysis; Cell Line; Enterovirus A, Human - isolation & purification; Enterovirus Infections - diagnosis; Enterovirus Infections - virology; Equipment Design; EV71; Humans; Limit of Detection; Quantification method; Sensor; SPR; Surface Plasmon Resonance - instrumentation; Virus; VP1
• ISSN: 0956-5663; 1873-4235
• DOI: 10.1016/j.bios.2017.01.043

This study presents the first report on a label-free detection and rapid quantification method for human enterovirus 71 (EV71) using a portable surface plasmon resonance (SPR) system. The SPR sensor instrument was configured to run on low power in a miniaturized platform to improve the device portability for a wider application both in laboratories and in the field. A color tunable organic light emitting diode in red spectrum was attached on a trapezoidal prism for the disposable light source module. The SPR signal processing using integration area under the reflectivity curve is applied for optimum signal to noise ratio (SNR) enhancement. The major capsid protein VP1 of EV71 was selected as the biomarker target in the detection study. The experimental time required for the EV71 quantification was reduced from 6 days using the conventional viral plaque assay to several minutes using the proposed method. The study results establish a detection limit of approximately 67 virus particles per milliliter (vp/ml) of EV71 in a Dulbecco's modified Eagle's medium. The VP1 detection in the portable SPR biosensor had a detection limit of approximately 4.8pg/ml in the PBS buffer. Therefore, the proposed direct EV71 viral particle quantification method can be rapidly performed in real time, with high sensitivity and less labor and without assays or fluorescence. •Direct quantification of Enterovirus 71 particle using portable SPR biosensor.•The proposed method reduced the EV71 quantification time significantly compared to conventional viral plaque assay (VPA).•Label free detection of capsid protein VP1 of EV71 biomarker by SPR biosensor.