Skip to main content
Log in

Continued expression of plant-made vaccines following long-term cryopreservation of antigen-expressing tobacco cell cultures

  • Molecular farming
  • Published:
In Vitro Cellular & Developmental Biology - Plant Aims and scope Submit manuscript

Abstract

Production of vaccines in plant cells provides an alternative system that has several advantages when compared to current vaccine production methods. Establishment of stable seed stocks for a continuous supply of a vaccine is a critical part of production systems. Therefore, a vitrification method for cryopreservation was applied to non-transgenic and three different antigen-expressing transgenic Nicotiana tabacum (NT-1) lines. Preculture of the suspension cultures 1 d prior to vitrification was sufficient for cell survival through the cryopreservation process. Inclusion of 0.3 M mannitol in the preculture medium was necessary for maintenance of cell viability. Cultures were also treated with and without heat shock prior to vitrification, and it was found that heat shock was unnecessary for growth recovery post cryopreservation. All cultures survived storage in liquid nitrogen at intervals ranging from 1 h to 1 yr. Antigen expression was measured by enzyme-linked immunosorbent assay for cultures that grew post cryopreservation and those that had never been cryopreserved. Expression levels in cultures derived from cryopreserved material were comparable to cultures that had not been cryopreserved. Transmission electron microscopy showed that the integrity of the cell structure was maintained post cryopreservation.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Figure 1
Figure 2

Similar content being viewed by others

References

  • Bradford M. M. A rapid and sensitive method for the quantitation of microgram quantities of proteins utilizing the principle of protein-dye binding. Anal. Biochem. 72: 248–254; 1976.

    Article  CAS  PubMed  Google Scholar 

  • Cho J.-S.; Hong S.-M.; Joo S.-Y.; Yoo J.-S.; Kim D.-I. Cryopreservation of transgenic rice suspension cells producing recombinant hCTLA4Ig. Appl. Microbiol. Biotechnol. 73: 1470–1476; 2007.

    Article  CAS  PubMed  Google Scholar 

  • Dodds J. H.; Roberts L. W. Experiments in Plant Tissue Culture. Cambridge University Press, New York, pp 35–53; 1988.

    Google Scholar 

  • Elleuch H.; Gazeau C.; David H.; David A. Cryopreservation does not affect the expression of a foreign sam gene in transgenic Papaver somniferum cells. Plant Cell Rep. 18: 94–98; 1998.

    Article  CAS  Google Scholar 

  • Fretz A.; Lörz H. Cryopreservation of in vitro cultures of barley (Hordeum vulgare L. and H. murinum L.) and transgenic cells of wheat (Triticum aestivum L.). J. Plant Physiol. 146: 489–496; 1995.

    CAS  Google Scholar 

  • Huang Z.; Panda A.; Elankumaran S.; Govindarajan D.; Rockemann D. D.; Samal S. K. The hemagglutinin-neuramnidase protein of Newcastle disease virus determines tropism and virulence. J. Virol. 78: 4176–4184; 2004.

    Article  CAS  PubMed  Google Scholar 

  • Leunufna S.; Keller E. R. J. Investigating a new cryopreservation protocol for yams (Dioscorea spp.). Plant Cell Rep. 21: 1159–1166; 2003.

    Article  CAS  PubMed  Google Scholar 

  • Linsmaier E. M.; Skoog F. Organic growth factor requirements of tobacco tissue cultures. Physiol. Plant. 18: 100–127; 1965.

    Article  CAS  Google Scholar 

  • Menges M.; Murray J. A. H. Cryopreservation of transformed and wild-type Arabidopsis and tobacco cell suspension cultures. Plant J. 37: 635–644; 2004.

    Article  CAS  PubMed  Google Scholar 

  • Murashige T.; Skoog F. A revised medium for rapid growth and bioassays with tobacco tissue cultures. Physiol. Plant. 15: 473–497; 1962.

    Article  CAS  Google Scholar 

  • Paszty C.; Lurquin P. F. Improved plant protoplast plating/selection technique for quantitation of transformation frequencies. Bio Techniques 5: 716–718; 1987.

    Google Scholar 

  • Reinhoud P. J.; Schrijnemakers E. W. M.; van Iren F.; Kijne J. W. Vitrification and a heat-shock treatment improve cryopreservation of tobacco cell suspensions compared to two-step freezing. Plant Cell Tissue Organ Cult. 42: 261–267; 1995.

    Article  Google Scholar 

  • Sarkar D.; Naik P. S. Cryopreservation of shoot tips of tetraploid potato (Solanum tuberosum L.) clones by vitrification. Ann. Bot. 82: 455–461; 1998.

    Article  Google Scholar 

  • Sixma T. K.; Pronk S. E.; Kalk K. H.; Wartna E. S.; van Zanten B. A. M.; Witholt B.; Hol W. G. J. Crystal structure of a cholera toxin-related heat-labile enterotoxin from E. coli. Nature 351: 371–377; 1991.

    Article  CAS  PubMed  Google Scholar 

  • Smith, M. L. Hepatitis B surface antigen expression in plant cell culture: characterization of the production system, the antigen and its stabilization upon extraction. Ph.D. Thesis, Cornell University; 2002.

  • Smith M. L.; Mason H. S.; Shuler M. L. Hepatitis B surface antigen (HBsAg) expression in plant cell culture: kinetics of antigen accumulation in batch culture and its intracellular form. Biotechnol. Bioeng. 80: 812–822; 2002.

    Article  CAS  PubMed  Google Scholar 

  • Spangler B. D. Structure and function of cholera toxin and the related Escherichia coli heat-labile enterotoxin. Microbiological Rev. 56: 622–647; 1992.

    CAS  Google Scholar 

  • Verdaguer B.; de Kochko A.; Beachy R. N.; Fauquet C. Isolation and expression in transgenic tobacco and rice plants, of the cassava vein mosaic virus (CVMV) promoter. Plant Mol. Biol. 31: 1129–1139; 1996.

    Article  CAS  PubMed  Google Scholar 

  • Wohlleben W.; Arnold W.; Broer I.; Hillemann D.; Strauch E.; Pühler A. Nucleotide sequence of the phosphinothricin N-acetyltransferase gene from Streptomyces viridochromogenes Tü494 and its expression in Nicotiana tabacum. Gene 70: 25–37; 1988.

    Article  CAS  PubMed  Google Scholar 

  • Zhang Y.-X.; Wang J.-H.; Bian H.-W.; Zhu M. Y. Pregrowth-desiccation: a simple and efficient procedure for the cryopreservation of rice (Oryza sativa L.) embryogenic suspension cells. Cryo-Lett. 22: 221–228; 2001.

    Google Scholar 

  • Ziemienowicz A. Plant selectable markers and reporter genes. Acta Physiol. Plant. 23: 363–374; 2001.

    Article  CAS  Google Scholar 

Download references

Acknowledgements

This work was supported under collaborative research efforts with Dow AgroSciences LLC. We thank Dr. Mandayam V. Parthasarathy and Shannon Caldwell from Cornell Integrated Microscopy Center for the transmission electron microscopy. The authors also thank Benchmark Biolabs, Dr. Frank van Iren from the Institute of Molecular Sciences, Leiden University, The Netherlands for his advice on the design of our experiments.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Joyce Van Eck.

Additional information

Editor: Gregory C. Phillips

Rights and permissions

Reprints and permissions

About this article

Cite this article

Van Eck, J., Keen, P. Continued expression of plant-made vaccines following long-term cryopreservation of antigen-expressing tobacco cell cultures. In Vitro Cell.Dev.Biol.-Plant 45, 750–757 (2009). https://doi.org/10.1007/s11627-009-9231-9

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11627-009-9231-9

Keywords

Navigation