Metabolic effects of influenza virus infection in cultured animal cells: Intra- and extracellular metabolite profiling

BackgroundMany details in cell culture-derived influenza vaccine production are still poorly understood and approaches for process optimization mainly remain empirical. More insights on mammalian cell metabolism after a viral infection could give hints on limitations and cell-specific virus production capacities. A detailed metabolic characterization of an influenza infected adherent cell line (MDCK) was carried out based on extracellular and intracellular measurements of metabolite concentrations.ResultsFor most metabolites the comparison of infected (human influenza A/PR/8/34) and mock-infected cells showed a very similar behavior during the first 10-12 h post infection (pi). Significant changes were observed after about 12 h pi: (1) uptake of extracellular glucose and lactate release into the cell culture supernatant were clearly increased in infected cells compared to mock-infected cells. At the same time (12 h pi) intracellular metabolite concentrations of the upper part of glycolysis were significantly increased. On the contrary, nucleoside triphosphate concentrations of infected cells dropped clearly after 12 h pi. This behaviour was observed for two different human influenza A/PR/8/34 strains at slightly different time points.ConclusionsComparing these results with literature values for the time course of infection with same influenza strains, underline the hypothesis that influenza infection only represents a minor additional burden for host cell metabolism. The metabolic changes observed after12 h pi are most probably caused by the onset of apoptosis in infected cells. The comparison of experimental data from two variants of the A/PR/8/34 virus strain (RKI versus NIBSC) with different productivities and infection dynamics showed comparable metabolic patterns but a clearly different timely behavior. Thus, infection dynamics are obviously reflected in host cell metabolism.

[1]  Harry Greenberg,et al.  Novel generations of influenza vaccines. , 2003, Vaccine.

[2]  V. Cristofalo,et al.  Metabolism of rubella virus-infected BHK21 cells Enhanced glycolysis and late cellular inhibition , 2005, Archiv für die gesamte Virusforschung.

[3]  J. August,et al.  Alterations in glucose metabolism in chick-embryo cells transformed by Rous sarcoma virus: intracellular levels of glycolytic intermediates. , 1974, Proceedings of the National Academy of Sciences of the United States of America.

[4]  M. Essex,et al.  Glycolysis During Early Infection of Feline and Human Cells with Feline Leukemia Virus , 1974, Infection and immunity.

[5]  R. Lowy,et al.  INFLUENZA VIRUS INDUCTION OF APOPTOSIS BY INTRINSIC AND EXTRINSIC MECHANISMS , 2003, International reviews of immunology.

[6]  Jan B Hoek,et al.  Hexokinase II: the integration of energy metabolism and control of apoptosis. , 2003, Current medicinal chemistry.

[7]  M. Dauner,et al.  Comparison of Metabolic Flux Distributions for MDCK Cell Growth in Glutamine‐ and Pyruvate‐Containing Media , 2008, Biotechnology progress.

[8]  J. Kasir,et al.  On the mechanism of the glucose-induced ATP catabolism in ascites tumour cells and its reversal by pyruvate. , 1980, The Biochemical journal.

[9]  A. Lehninger Principles of Biochemistry , 1984 .

[10]  Johannes H. de Winde,et al.  Dynamics of Glycolytic Regulation during Adaptation of Saccharomyces cerevisiae to Fermentative Metabolism , 2008, Applied and Environmental Microbiology.

[11]  Udo Reichl,et al.  Monitoring influenza virus content in vaccine production: precise assays for the quantitation of hemagglutination and neuraminidase activity. , 2008, Biologicals : journal of the International Association of Biological Standardization.

[12]  J. E. Felíu,et al.  Interconvertible forms of class A pyruvate kinase from Ehrlich ascites tumour cells. , 1975, FEBS letters.

[13]  Juan E. Feli´u,et al.  Interconvertible forms of class a pyruvate kinase from Ehrlich ascites tumour cells , 1975 .

[14]  Udo Reichl,et al.  Influenza Vaccines : Challenges in Mammalian Cell Culture Technology , 2007 .

[15]  Tatiana El-Bacha,et al.  Mayaro virus infection alters glucose metabolism in cultured cells through activation of the enzyme 6-phosphofructo 1-kinase , 2004, Molecular and Cellular Biochemistry.

[16]  U Reichl,et al.  Wave microcarrier cultivation of MDCK cells for influenza virus production in serum containing and serum-free media. , 2006, Vaccine.

[17]  M. Butler,et al.  Intracellular ATP and total adenylate concentrations are critical predictors of reovirus productivity from Vero cells , 2006, Biotechnology and bioengineering.

[18]  Xiao-Jiang Feng,et al.  Systems-level metabolic flux profiling identifies fatty acid synthesis as a target for antiviral therapy , 2008, Nature Biotechnology.

[19]  S BARON,et al.  The effect of animal viruses on host cell metabolism. II. Effect of poliomyelitis virus on glycolysis and uptake of glycine by monkey kidney tissue cultures. , 1957, The Journal of infectious diseases.

[20]  G. Tannock,et al.  Cell-based influenza vaccines: progress to date. , 2008, Drugs.

[21]  Udo Reichl,et al.  Segregated Mathematical Model for Growth of Anchorage‐Dependent MDCK Cells in Microcarrier Culture , 2008, Biotechnology progress.

[22]  M. Dauner,et al.  Metabolic flux model for an anchorage‐dependent MDCK cell line: Characteristic growth phases and minimum substrate consumption flux distribution , 2008, Biotechnology and bioengineering.

[23]  G Bardeletti,et al.  Respiration and ATP level in BHK21/13S cells during the earlist stages of rubella virus replication. , 1977, Intervirology.

[24]  H. Temin,et al.  Studies on carcinogenesis by avian sarcoma viruses: VIII. Glycolysis and cell multiplication , 1968 .

[25]  Udo Reichl,et al.  Substitution of Glutamine by Pyruvate To Reduce Ammonia Formation and Growth Inhibition of Mammalian Cells , 2008, Biotechnology progress.

[26]  D. Nelson,et al.  Lehninger Principles of Biochemistry (5th edition) , 2008 .

[27]  M. Reuss,et al.  In vivo analysis of metabolic dynamics in Saccharomyces cerevisiae : I. Experimental observations. , 1997, Biotechnology and bioengineering.

[28]  P. L. Collins,et al.  Virus Replication in Engineered Human Cells That Do Not Respond to Interferons , 2003, Journal of Virology.

[29]  G. Stephanopoulos,et al.  Intracellular flux analysis applied to the effect of dissolved oxygen on hybridomas , 1995, Applied Microbiology and Biotechnology.

[30]  Emma Saavedra,et al.  Energy metabolism in tumor cells , 2007, The FEBS journal.

[31]  U. Reichl,et al.  Structured model of influenza virus replication in MDCK cells , 2004, Biotechnology and bioengineering.

[32]  H. Klemperer,et al.  Glucose breakdown in chick embryo cells infected with influenza virus. , 1961, Virology.

[33]  Udo Reichl,et al.  Simultaneous extraction of several metabolites of energy metabolism and related substances in mammalian cells: optimization using experimental design. , 2008, Analytical biochemistry.

[34]  M. Landini,et al.  Early enhanced glucose uptake in human cytomegalovirus-infected cells. , 1984, The Journal of general virology.

[35]  U Reichl,et al.  Infection dynamics and virus-induced apoptosis in cell culture-based influenza vaccine production-Flow cytometry and mathematical modeling. , 2009, Vaccine.

[36]  U Reichl,et al.  Serum-free influenza virus production avoiding washing steps and medium exchange in large-scale microcarrier culture. , 2006, Vaccine.

[37]  Hansjörg Hauser,et al.  Mammalian Cell Biotechnology in Protein Production , 1997 .

[38]  Roland Wagner 2.1 Metabolic Control of Animal Cell Culture Processes , 1997 .

[39]  H. Hanafusa,et al.  Analysis of a functional change in membrane in the process of cell transformation by Rous sarcoma virus; alteration in the characteristics of sugar transport. , 1970, Virology.

[40]  U Reichl,et al.  Metabolism of MDCK cells during cell growth and influenza virus production in large-scale microcarrier culture. , 2004, Vaccine.

[41]  Chi V Dang,et al.  Multifaceted roles of glycolytic enzymes. , 2005, Trends in biochemical sciences.

[42]  T N FISHER,et al.  The reaction of influenza viruses with guinea pig polymorphonuclear leucocytes. II. The reduction of white blood cell glycolysis by influenza viruses and receptor-destroying enzyme (RDE). , 1956, Virology.

[43]  Thomas Shenk,et al.  Dynamics of the Cellular Metabolome during Human Cytomegalovirus Infection , 2006, PLoS pathogens.

[44]  M. Betenbaugh,et al.  Links between metabolism and apoptosis in mammalian cells: applications for anti-apoptosis engineering. , 2007, Metabolic engineering.

[45]  Udo Reichl,et al.  High-performance anion-exchange chromatography using on-line electrolytic eluent generation for the determination of more than 25 intermediates from energy metabolism of mammalian cells in culture. , 2006, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

[46]  B. Berkhout,et al.  Increased virus replication in mammalian cells by blocking intracellular innate defense responses , 2008, Gene Therapy.

[47]  S. Baron,et al.  Some Metabolic Effects of Poliomyelitis Virus on Tissue Culture , 1956, Nature.

[48]  Thorsten Wolff,et al.  Ringing the alarm bells: signalling and apoptosis in influenza virus infected cells , 2006, Cellular microbiology.

[49]  Udo Reichl,et al.  Mathematical model of influenza A virus production in large-scale microcarrier culture. , 2005, Biotechnology and bioengineering.

[50]  Chris Janson Biochemistry, 4th Edition , 1995, The Yale Journal of Biology and Medicine.

[51]  Udo Reichl,et al.  Amino acid analysis in mammalian cell culture media containing serum and high glucose concentrations by anion exchange chromatography and integrated pulsed amperometric detection. , 2004, Analytical biochemistry.

[52]  N. Salzman,et al.  Alterations in HeLa cell metabolism resulting from poliovirus infection. , 1959, Virology.

[53]  Tatiana El-Bacha,et al.  Mitochondrial and bioenergetic dysfunction in human hepatic cells infected with dengue 2 virus. , 2007, Biochimica et biophysica acta.

[54]  G. Bardeletti,et al.  Primary effects of the rubella virus on the metabolism of BHK-21 cells grown in suspension cultures , 2005, Archiv für die gesamte Virusforschung.

[55]  H. Krebs,et al.  The redox state of free nicotinamide-adenine dinucleotide in the cytoplasm and mitochondria of rat liver. , 1967, The Biochemical journal.

[56]  G. Henle,et al.  Respiration and glycolysis of human cells grown in tissue culture. , 1958, Virology.