Quantitation of influenza virus using field flow fractionation and multi-angle light scattering for quantifying influenza A particles

被引:41
作者
Bousse, Tatiana [1 ]
Shore, David A. [1 ]
Goldsmith, Cynthia S. [2 ]
Hossain, M. Jaber [1 ]
Jang, Yunho [1 ]
Davis, Charles T. [1 ]
Donis, Ruben O. [1 ]
Stevens, James [1 ]
机构
[1] Ctr Dis Control & Prevent, Natl Ctr Immunizat & Resp Dis, Influenza Div, Atlanta, GA 30333 USA
[2] Ctr Dis Control & Prevent, Natl Ctr Emerging & Zoonot Infect Dis, Div High Consequence Pathogens & Pathol, Infect Dis Pathol Branch, Atlanta, GA 30333 USA
关键词
Influenza virus; Vaccine; Field flow fractionation; Multiangle light scattering; MDCK CELLS; PROTEIN; GENERATION; VACCINES; GROWTH; SIZE; LIVE; DNA;
D O I
10.1016/j.jviromet.2013.07.026
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Recent advances in instrumentation and data analysis in field flow fractionation and multi-angle light scattering (FFF-MALS) have enabled greater use of this technique to characterize and quantitate viruses. In this study, the FFF-MALS technique was applied to the characterization and quantitation of type A influenza virus particles to assess its usefulness for vaccine preparation. The use of FFF-MALS for quantitation and measurement of control particles provided data accurate to within 5% of known values, reproducible with a coefficient of variation of 1.9%. The methods, sensitivity and limit of detection were established by analyzing different volumes of purified virus, which produced a linear regression with fitting value R-2 of 0.99. FFF-MALS was further applied to detect and quantitate influenza virus in the supernatant of infected MDCK cells and allantoic fluids of infected eggs. FFF fractograms of the virus present in these different fluids revealed similar distribution of monomeric and oligomeric virions. However, the monomer fraction of cell grown virus had greater size variety. Notably, beta-propialactone (BPL) inactivation of influenza viruses did not influence any of the FFF-MALS measurements. Quantitation analysis by FFF-MALS was compared to infectivity assays and real-time RT-PCR (qRT-PCR) and the limitations of each assay were discussed. Published by Elsevier B.V.
引用
收藏
页码:589 / 596
页数:8
相关论文
共 41 条
[31]   Flow cytometric monitoring of influenza A virus infection in MDCK cells during vaccine production [J].
Schulze-Horsel, Josef ;
Genzel, Yvonne ;
Reichl, Udo .
BMC BIOTECHNOLOGY, 2008, 8 (1)
[32]   THE SIZE OF INFLUENZA VIRUS [J].
Stanley, W. M. .
JOURNAL OF EXPERIMENTAL MEDICINE, 1944, 79 (03) :267-283
[33]   Comparison of large-scale mammalian cell culture systems with egg culture for the production of influenza virus A vaccine strains [J].
Tree, JA ;
Richardson, C ;
Fooks, AR ;
Clegg, JC ;
Looby, D .
VACCINE, 2001, 19 (25-26) :3444-3450
[34]  
U.S. Environmental Protection Agency, 2003, EPAHQOW200300020110
[35]   Characterization of high-growth reassortant influenza A viruses generated in MDCK cells cultured in serum-free medium [J].
Voeten, JTM ;
Brands, R ;
Palache, AM ;
van Scharrenburg, GJM ;
Rimmelzwaan, GF ;
Osterhaus, ADME ;
Claas, ECJ .
VACCINE, 1999, 17 (15-16) :1942-1950
[36]   Biophysical characterization of influenza virus subpopulations using field flow fractionation and multiangle light scattering: Correlation of particle counts, size distribution and infectivity [J].
Wei, Ziping ;
Mcevoy, Matt ;
Razinkov, Vladimir ;
Polozova, Alla ;
Li, Elizabeth ;
Casas-Finet, Jose ;
Tous, Guillermo I. ;
Balu, Palani ;
Pan, Alfred A. ;
Mehta, Harshvardhan ;
Schenerman, Mark A. .
JOURNAL OF VIROLOGICAL METHODS, 2007, 144 (1-2) :122-132
[37]  
World Health Organisation, 2006, REV PROD TECHN INFL
[38]  
World Health Organization, 2011, MAN LAB DIAGN VIR SU
[39]  
World Health Organization, 2009, PAND INFL VACC MAN P
[40]  
Wyatt P. J., 2004, Method and Apparatus for Determining Absolute Number Densities of Particles in Suspension, Patent No. [6,774,994B1, 6774994, 6,774,994 B1]