Rapid, targeted and culture-free viral infectivity assay in drop-based microfluidics

被引:52
作者
Tao, Ye [1 ,2 ]
Rotem, Assaf [1 ]
Zhang, Huidan [1 ,3 ,4 ]
Chang, Connie B. [1 ,5 ]
Basu, Anindita [1 ,6 ]
Kolawole, Abimbola O. [7 ]
Koehler, Stephan A. [1 ]
Ren, Yukun [2 ]
Lin, Jeffrey S. [8 ]
Pipas, James M. [9 ]
Feldman, Andrew B. [8 ]
Wobus, Christiane E. [7 ]
Weitz, David A. [1 ,10 ]
机构
[1] Harvard Univ, Sch Engn & Appl Sci, Cambridge, MA 02138 USA
[2] Harbin Inst Technol, Sch Mech Engn, Harbin 150001, Peoples R China
[3] China Med Univ, Minist Publ Hlth, Dept Cell Biol, Key Lab Cell Biol, Shenyang 110001, Peoples R China
[4] China Med Univ, Minist Educ, Key Lab Med Cell Biol, Shenyang 110001, Peoples R China
[5] Montana State Univ, Dept Chem & Biol Engn, Bozeman, MT 59717 USA
[6] Broad Inst MIT & Harvard, Cambridge Ctr 7, Cambridge, MA 02142 USA
[7] Univ Michigan, Dept Microbiol & Immunol, Ann Arbor, MI 48109 USA
[8] Johns Hopkins Univ, Appl Phys Lab, Laurel, MD 20723 USA
[9] Univ Pittsburgh, Dept Biol Sci, Pittsburgh, PA 15260 USA
[10] Harvard Univ, Dept Phys, Cambridge, MA 02138 USA
基金
美国国家科学基金会; 中国国家自然科学基金;
关键词
MURINE NOROVIRUSES; ATTACHMENT RECEPTORS; ENTERIC VIRUSES; NEUTRALIZATION; QUANTITATION; SAMPLES; RNA;
D O I
10.1039/c5lc00556f
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A key viral property is infectivity, and its accurate measurement is crucial for the understanding of viral evolution, disease and treatment. Currently viral infectivity is measured using plaque assays, which involve prolonged culturing of host cells, and whose measurement is unable to differentiate between specific strains and is prone to low number fluctuation. We developed a rapid, targeted and culture-free infectivity assay using high-throughput drop-based microfluidics. Single infectious viruses are incubated in a large number of picoliter drops with host cells for one viral replication cycle followed by in-drop gene-specific amplification to detect infection events. Using murine noroviruses (MNV) as a model system, we measure their infectivity and determine the efficacy of a neutralizing antibody for different variants of MNV. Our results are comparable to traditional plaque-based assays and plaque reduction neutralization tests. However, the fast, low-cost, highly accurate genomic-based assay promises to be a superior method for drug screening and isolation of resistant viral strains. Moreover our technique can be adapted to measuring the infectivity of other pathogens, such as bacteria and fungi.
引用
收藏
页码:3934 / 3940
页数:7
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