Abstract

The influenza pandemic of 1918/1919 was a unique event in recorded history, costing on the order of 50 million lives within the time span of only several months. The virus is extinct, but the advent of reverse genetics techniques for negative strand RNA viruses (a family of viruses which includes the influenza viruses) makes it possible to reconstruct infectious influenza viruses. Based on the nucleotide sequence that was obtained from RNA fragments present in lung samples of victims of the 1918 influenza virus, we succeeded in rebuilding the extinct pandemic virus entirely from commercially available oligonucleotides. This virus turned out to be highly virulent in the mouse model, more than any other human influenza virus strain tested. It also was shown to be highly pathogenic for chicken embryos and grew in human tissue culture cells to high titers and replicated in cells in the absence of trypsin (also indicative of high virulence). On the other hand, the 1918 virus was shown to be sensitive to the FDA-approved antivirals (amantadine as well as the neuraminidase inhibitors). We were also able to show that vaccines worked perfectly well in protecting mice against a challenge with a virus containing the 1918 hemagglutinin and neuraminidase genes. We also postulate that the human population, having experienced infections with currently circulating H1N1 viruses, is partially immune to a 1918 or 1918-like virus. Finally, we have recently developed a guinea pig transmission model for influenza which will help us to better understand the molecular basis of virulence and the mechanisms by which pandemic influenza viruses are transmitted. [1-3].

Highlights

  • 2006 International Meeting of The Institute of Human Virology Meeting abstracts

  • A single PDF containing all abstracts in this Supplement is available here http://www.biomedcentral.com/content/pdf/1742-4690-3-S1-info.pdf

  • Based on the nucleotide sequence that was obtained from RNA fragments present in lung samples of victims of the 1918 influenza virus, we succeeded in rebuilding the extinct pandemic virus entirely from commercially available oligonucleotides

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Summary

Introduction

Influenza pandemics: past and future Peter Palese* Address: Department of Microbiology, Mount Sinai School of Medicine, New York, New York, 10029, USA * Corresponding author from 2006 International Meeting of The Institute of Human Virology Baltimore, USA. 17–21 November, 2006 Published: 21 December 2006 Retrovirology 2006, 3(Suppl 1):S55 doi:10.1186/1742-4690-3-S1-S55

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