A high-throughput drop microfluidic system for virus culture and analysis

Audrey E. Fischer, Susan K. Wu, Jody B G Proescher, Assaf Rotem, Connie B. Chang, Huidan Zhang, Ye Tao, Thomas S. Mehoke, Peter M. Thielen, Abimbola O. Kolawole, Thomas Smith, Christiane E. Wobus, David A. Weitz, Jeffrey S. Lin, Andrew B. Feldman, Joshua T. Wolfe

Research output: Contribution to journalArticle

14 Citations (Scopus)

Abstract

High mutation rates and short replication times lead to rapid evolution in RNA viruses. New tools for high-throughput culture and analysis of viral phenotypes will enable more effective studies of viral evolutionary processes. A water-in-oil drop microfluidic system to study virus-cell interactions at the single event level on a massively parallel scale is described here. Murine norovirus (MNV-1) particles were co-encapsulated with individual RAW 264.7 cells in 65. pL aqueous drops formed by flow focusing in 50. μm microchannels. At low multiplicity of infection (MOI), viral titers increased greatly, reaching a maximum 18. h post-encapsulation. This system was employed to evaluate MNV-1 escape from a neutralizing monoclonal antibody (clone A6.2). Further, the system was validated as a means for testing escape from antibody neutralization using a series of viral point mutants. Finally, the replicative capacity of single viral particles in drops under antibody stress was tested. Under standard conditions, many RNA virus stocks harbor minority populations of genotypic and phenotypic variants, resulting in quasispecies. These data show that when single cells are encapsulated with single viral particles under antibody stress without competition from other virions, the number of resulting infectious particles is nearly equivalent to the number of viral genomes present. These findings suggest that lower fitness virions can infect cells successfully and replicate, indicating that the microfluidics system may serve as an effective tool for isolating mutants that escape evolutionary stressors.

Original languageEnglish (US)
Pages (from-to)111-117
Number of pages7
JournalJournal of Virological Methods
Volume213
DOIs
StatePublished - Mar 1 2015

Fingerprint

Microfluidics
Virion
Viruses
RNA Viruses
Antibodies
Norovirus
Viral Genome
Virus Diseases
Mutation Rate
Neutralizing Antibodies
Cell Communication
Oils
Clone Cells
Monoclonal Antibodies
Phenotype
Water
Population

Keywords

  • Antibody neutralization
  • Evolution
  • Microfluidics
  • Murine norovirus

ASJC Scopus subject areas

  • Virology

Cite this

Fischer, A. E., Wu, S. K., Proescher, J. B. G., Rotem, A., Chang, C. B., Zhang, H., ... Wolfe, J. T. (2015). A high-throughput drop microfluidic system for virus culture and analysis. Journal of Virological Methods, 213, 111-117. https://doi.org/10.1016/j.jviromet.2014.12.003

A high-throughput drop microfluidic system for virus culture and analysis. / Fischer, Audrey E.; Wu, Susan K.; Proescher, Jody B G; Rotem, Assaf; Chang, Connie B.; Zhang, Huidan; Tao, Ye; Mehoke, Thomas S.; Thielen, Peter M.; Kolawole, Abimbola O.; Smith, Thomas; Wobus, Christiane E.; Weitz, David A.; Lin, Jeffrey S.; Feldman, Andrew B.; Wolfe, Joshua T.

In: Journal of Virological Methods, Vol. 213, 01.03.2015, p. 111-117.

Research output: Contribution to journalArticle

Fischer, AE, Wu, SK, Proescher, JBG, Rotem, A, Chang, CB, Zhang, H, Tao, Y, Mehoke, TS, Thielen, PM, Kolawole, AO, Smith, T, Wobus, CE, Weitz, DA, Lin, JS, Feldman, AB & Wolfe, JT 2015, 'A high-throughput drop microfluidic system for virus culture and analysis', Journal of Virological Methods, vol. 213, pp. 111-117. https://doi.org/10.1016/j.jviromet.2014.12.003
Fischer, Audrey E. ; Wu, Susan K. ; Proescher, Jody B G ; Rotem, Assaf ; Chang, Connie B. ; Zhang, Huidan ; Tao, Ye ; Mehoke, Thomas S. ; Thielen, Peter M. ; Kolawole, Abimbola O. ; Smith, Thomas ; Wobus, Christiane E. ; Weitz, David A. ; Lin, Jeffrey S. ; Feldman, Andrew B. ; Wolfe, Joshua T. / A high-throughput drop microfluidic system for virus culture and analysis. In: Journal of Virological Methods. 2015 ; Vol. 213. pp. 111-117.
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