Skip to main content
Log in

A novel chimeric influenza virosome containing Vesicular stomatitis G protein as a more efficient gene delivery system

  • Original Research Paper
  • Published:
Biotechnology Letters Aims and scope Submit manuscript

    We’re sorry, something doesn't seem to be working properly.

    Please try refreshing the page. If that doesn't work, please contact support so we can address the problem.

Abstract

Objectives

To enhance the efficiency of influenza virosome-mediated gene delivery by engineering this virosome.

Results

A novel chimeric influenza virosome was constructed containing the glycoprotein of Vesicular stomatitis virus (VSV-G), along with its own hemagglutinin protein. To optimize the transfection efficiency of both chimeric and influenza cationic virosomes, HEK cells were transfected with plasmid DNA and virosomes and the transfection efficiency was assessed by FACS analysis. The chimeric virosome was significantly more efficient in mediating transfection for all amounts of DNA and virosomes compared to the influenza virosome.

Conclusions

Chimeric influenza virosome, including VSV-G, is superior to the conventional influenza virosome for gene delivery.

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.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6
Fig. 7

Similar content being viewed by others

References

  • Barsoum J, Brown R, McKee M, Boyce FM (1997) Efficient transduction of mammalian cells by a recombinant baculovirus having the vesicular stomatitis virus G glycoprotein. Hum Gene Ther 8:2011–2018

    Article  CAS  PubMed  Google Scholar 

  • Carneiro FA, Bianconi ML, Weissmüller G et al (2002) Membrane recognition by vesicular stomatitis virus involves enthalpy-driven protein-lipid interactions. J Virol 76:3756–3764

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • De Jonge J, Holtrop M, Wilschut J, Huckriede A (2006a) Reconstituted influenza virus envelopes as an efficient carrier system for cellular delivery of small-interfering RNAs. Gene Ther 13:400–411

    Article  PubMed  Google Scholar 

  • De Jonge J, Schoen P, terVeer W et al (2006b) Use of a dialyzable short-chain phospholipid for efficient solubilization and reconstitution of influenza virus envelopes. Biochim Biophys Acta 1758:527–536

    Article  PubMed  Google Scholar 

  • De Jonge J, Leenhouts JM, Holtrop M et al (2007) Cellular gene transfer mediated by influenza virosomes with encapsulated plasmid DNA. Biochem J 405:41–49

    Article  PubMed  PubMed Central  Google Scholar 

  • Gaudin Y, Tuffereau C, Segretain D et al (1991) Reversible conformational changes and fusion activity of rabies virus glycoprotein. J Virol 65:4853–4859

    CAS  PubMed  PubMed Central  Google Scholar 

  • Gurusinghe S, Young P, Michelsen J, Strappe P (2015) Suppression of dedifferentiation and hypertrophy in canine chondrocytes through lentiviral vector expression of Sox9 and induced pluripotency stem cell factors. Biotechnol Lett 37:1495–1504

    Article  CAS  PubMed  Google Scholar 

  • Irvine DJ, Swartz MA, Szeto GL (2013) Engineering synthetic vaccines using cues from natural immunity. Nat Mater 12:978–990

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Machida K, Imataka H (2015) Production methods for viral particles. Biotechnol Lett 37:753–760

    Article  CAS  PubMed  Google Scholar 

  • Mizuarai S, Ono K, Yamaguchi K et al (2001) Production of transgenic quails with high frequency of germ-line transmission using VSV-G pseudotyped retroviral vector. Biochem Biophys Res Commun 286:456–463

    Article  CAS  PubMed  Google Scholar 

  • Ohkuma S, Poole B (1978) Fluorescence probe measurement of the intralysosomal pH in living cells and the perturbation of pH by various agents. Proc Natl Acad Sci USA 75:3327–3331

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Park S, Pyo C-W, Choi S-Y (2014) High-efficiency lentiviral transduction of primary human CD34+ hematopoietic cells with low-dose viral inocula. Biotechnol Lett 37:1–8

    Google Scholar 

  • Paternostre MT, Lowy RJ, Blumenthal R (1989) pH-dependent fusion of reconstituted vesicular stomatitis virus envelopes with vero cells: measurement by dequenching of fluorescence. FEBS Lett 243:251–258

    Article  CAS  PubMed  Google Scholar 

  • Puri A, Booy FP, Doms RW et al (1990) Conformational changes and fusion activity of influenza virus hemagglutinin of the H2 and H3 subtypes: effects of acid pretreatment. J Virol 64:3824–3832

    CAS  PubMed  PubMed Central  Google Scholar 

  • Schoen P, Chonn A, Cullis PR et al (1999) Gene transfer mediated by fusion protein hemagglutinin reconstituted in cationic lipid vesicles. Gene Ther 6:823–832

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgment

This work was supported by a grant from Pasteur Institute, Tehran, Iran.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Abbas Jamali.

Ethics declarations

Conflict of Interest

The authors declare that there are no conflicts of interest

Additional information

Yahya Mohammadzadeh and Narges Rasouli are equal first authors.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Mohammadzadeh, Y., Rasouli, N., Aref, M.H.S. et al. A novel chimeric influenza virosome containing Vesicular stomatitis G protein as a more efficient gene delivery system. Biotechnol Lett 38, 1321–1329 (2016). https://doi.org/10.1007/s10529-016-2108-1

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10529-016-2108-1

Keywords

Navigation