Label-free, multiplexed virus detection using spectral reflectance imaging

被引:47
作者
Lopez, Carlos A. [1 ]
Daaboul, George G. [2 ]
Vedula, Rahul S. [1 ]
Oezkumur, Emre [3 ]
Bergstein, David A. [4 ]
Geisbert, Thomas W. [5 ,6 ,8 ]
Fawcett, Helen E. [7 ]
Goldberg, Bennett B. [1 ,2 ,9 ]
Connor, John H. [7 ,8 ]
Uenlue, M. Selim [1 ,2 ,9 ]
机构
[1] Boston Univ, Dept Elect & Comp Engn, Boston, MA 02215 USA
[2] Boston Univ, Dept Biomed Engn, Boston, MA 02215 USA
[3] Harvard Univ, Massachusetts Gen Hosp, Ctr Canc, Ctr Engn Med, Boston, MA 02114 USA
[4] Zoiray Technol Inc, Boston, MA USA
[5] Univ Texas Galveston, Med Branch, Galveston Natl Lab, Galveston, TX 77550 USA
[6] Univ Texas Galveston, Med Branch, Dept Microbiol & Immunol, Galveston, TX 77550 USA
[7] Boston Univ, Photon Ctr, Boston, MA 02215 USA
[8] Boston Univ, Sch Med, Dept Microbiol, Boston, MA 02118 USA
[9] Boston Univ, Dept Phys, Boston, MA 02215 USA
基金
美国国家卫生研究院;
关键词
Virus detection; Label-free; Interferometry; Biosensor; High-throughput; Microarray; Quantitative sensing; VESICULAR STOMATITIS-VIRUS; MICROARRAY APPLICATIONS; ELECTRON-MICROSCOPY; INFLUENZA-VIRUS; MOUTH-DISEASE; BIOSENSORS; DIAGNOSIS; DNA; FUTURE; AGENTS;
D O I
10.1016/j.bios.2011.01.019
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
We demonstrate detection of whole viruses and viral proteins with a new label-free platform based on spectral reflectance imaging. The Interferometric Reflectance Imaging Sensor (IRIS) has been shown to be capable of sensitive protein and DNA detection in a real time and high-throughput format. Vesicular stomatitis virus (VSV) was used as the target for detection as it is well-characterized for protein composition and can be modified to express viral coat proteins from other dangerous, highly pathogenic agents for surrogate detection while remaining a biosafety level 2 agent. We demonstrate specific detection of intact VSV virions achieved with surface-immobilized antibodies acting as capture probes which is confirmed using fluorescence imaging. The limit of detection is confirmed down to 3.5 x 10(5) plaque-forming units/mL (PFUs/mL). To increase specificity in a clinical scenario, both the external glycoprotein and internal viral proteins were simultaneously detected with the same antibody arrays with detergent-disrupted purified VSV and infected cell lysate solutions. Our results show sensitive and specific virus detection with a simple surface chemistry and minimal sample preparation on a quantitative label-free interferometric platform. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:3432 / 3437
页数:6
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