The innate immune system is our first line of defense against pathogenic challenge. These responses include cell-intrinsic mechanisms to combat these invaders in infected cells. Autophagy, the mechanism by which cells engulf cytoplasmic components, has been shown to have antimicrobial properties against intracellular bacteria. This process leads to the destruction of these cytoplasmic microorganisms. It has been proposed that such a mechanism may play an important role in controlling viral infection. Our preliminary data support this in that loss of this conserved pathway leads to an increase in viral replication in Drosophila. This suggests that autophagy plays an important antiviral role. In this proposal we seek to establish the mechanism by which the autophagic pathway affects viral propagation and pathogenesis, and the mechanisms whereby this process is activated to clear the viral invader. By taking advantage of the powerful tools available in this model system, including genetics and functional genomics, to investigate these questions in a variety of contexts we will be uniquely situated to identify conserved intrinsic mechanisms by which all organisms fight viruses. The identification of new host factors amenable to inhibition may lead to targets for much-needed antiviral therapeutics. ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI074951-02
Application #
7448509
Study Section
Immunity and Host Defense Study Section (IHD)
Program Officer
Palker, Thomas J
Project Start
2007-07-01
Project End
2012-06-30
Budget Start
2008-07-01
Budget End
2009-06-30
Support Year
2
Fiscal Year
2008
Total Cost
$372,910
Indirect Cost
Name
University of Pennsylvania
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
042250712
City
Philadelphia
State
PA
Country
United States
Zip Code
19104
Liu, Yuan; Gordesky-Gold, Beth; Leney-Greene, Michael et al. (2018) Inflammation-Induced, STING-Dependent Autophagy Restricts Zika Virus Infection in the Drosophila Brain. Cell Host Microbe 24:57-68.e3
Hackett, Brent A; Cherry, Sara (2018) Flavivirus internalization is regulated by a size-dependent endocytic pathway. Proc Natl Acad Sci U S A 115:4246-4251
Molleston, Jerome M; Cherry, Sara (2017) Attacked from All Sides: RNA Decay in Antiviral Defense. Viruses 9:
Aguado, Lauren C; Schmid, Sonja; May, Jared et al. (2017) RNase III nucleases from diverse kingdoms serve as antiviral effectors. Nature 547:114-117
Rausch, Keiko; Hackett, Brent A; Weinbren, Nathan L et al. (2017) Screening Bioactives Reveals Nanchangmycin as a Broad Spectrum Antiviral Active against Zika Virus. Cell Rep 18:804-815
Bayer, Avraham; Lennemann, Nicholas J; Ouyang, Yingshi et al. (2016) Type III Interferons Produced by Human Placental Trophoblasts Confer Protection against Zika Virus Infection. Cell Host Microbe 19:705-12
Molleston, Jerome M; Sabin, Leah R; Moy, Ryan H et al. (2016) A conserved virus-induced cytoplasmic TRAMP-like complex recruits the exosome to target viral RNA for degradation. Genes Dev 30:1658-70
Zhang, Rong; Miner, Jonathan J; Gorman, Matthew J et al. (2016) A CRISPR screen defines a signal peptide processing pathway required by flaviviruses. Nature 535:164-8
Sansone, Christine L; Cohen, Jonathan; Yasunaga, Ari et al. (2015) Microbiota-Dependent Priming of Antiviral Intestinal Immunity in Drosophila. Cell Host Microbe 18:571-81
Hackett, Brent A; Yasunaga, Ari; Panda, Debasis et al. (2015) RNASEK is required for internalization of diverse acid-dependent viruses. Proc Natl Acad Sci U S A 112:7797-802

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