4.8 Article

The Lipid Mediator Protectin D1 Inhibits Influenza Virus Replication and Improves Severe Influenza

Journal

CELL
Volume 153, Issue 1, Pages 112-125

Publisher

CELL PRESS
DOI: 10.1016/j.cell.2013.02.027

Keywords

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Funding

  1. Funding Program for Next Generation World-Leading Researchers (NEXT Program, JSPS)
  2. Center of Education and Research for the Advanced Genome-Based Medicine-For Personalized Medicine and the Control of Worldwide Infectious Diseases
  3. Japan Initiative for Global Research Network on Infectious Diseases from the Ministry of Education, Culture, Sports, Science and Technology
  4. ERATO (Japan Science and Technology Agency)
  5. Public Health Service research grants from the National Institute of Allergy and Infectious Diseases
  6. Japan Science and Technology Agency Precursory Research for Embryonic Science and Technology (PRESTO)
  7. Ministry of Education, Culture, Sports, Science, and Technology of Japan
  8. IMBA
  9. Advanced ERC grant
  10. European Union
  11. Program for Promotion of Basic and Applied Research for Innovations in Bio-Oriented Industry
  12. Grants-in-Aid for Scientific Research [24591480, 24659482, 22116006, 24390021, 24657135, 23406033, 22116001, 24619007] Funding Source: KAKEN

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Influenza A viruses are a major cause of mortality. Given the potential for future lethal pandemics, effective drugs are needed for the treatment of severe influenza such as that caused by H5N1 viruses. Using mediator lipidomics and bioactive lipid screen, we report that the omega-3 polyunsaturated fatty acid (PUFA)-derived lipid mediator protectin D1 (PD1) markedly attenuated influenza virus replication via RNA export machinery. Production of PD1 was suppressed during severe influenza and PD1 levels inversely correlated with the pathogenicity of H5N1 viruses. Suppression of PD1 was genetically mapped to 12/15-lipoxygenase activity. Importantly, PD1 treatment improved the survival and pathology of severe influenza in mice, even under conditions where known antiviral drugs fail to protect from death. These results identify the endogenous lipid mediator PD1 as an innate suppressor of influenza virus replication that protects against lethal influenza virus infection.

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