Viruses are potent cancer-inducing agents. While the clinical effects of cancer are obvious, its cellular and molecular causes are not fully understood. Here we propose to study the cellular entry mechanisms of polyomavirus (Py), a non-enveloped DNA tumor virus that induces cancer in mice. To infect cells, Py binds to a receptor at the plasma membrane and travels to the endoplasmic reticulum (ER) where it hijacks cellular machineries to cross the ER membrane and reach the cytosol. The virus is then transported into the nucleus where transcription and replication of the viral DNA ensue, leading to uncontrolled cell proliferation and cancer. How Py is transported across the ER membrane remains unclear and is a subject of intense interest. Using an in vitro biochemical approach, we propose to identify the ER factor(s) that facilitate the transport of Py from the ER into the cytosol and to clarify the molecular mechanism of this process. Next, we will employ an in vivo cell biological method to probe the physiological role of these ER factors in Py infection. Interactions between pathogens and their respective host cells expound on basic cellular events;thus, Py's engagement of cellular machineries to cross the ER membrane will elucidate fundamental membrane transport processes. Moreover, identifying the cellular targets that Py co-opts during infection may lead to the development of drugs that allow selective interference. As many of Py's structurally-related viruses are human pathogens, such as the JC, BK, and papilloma viruses, the lessons gleaned from the cellular entry mechanism of Py may be applied to a broader spectrum of human diseases.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI064296-05
Application #
7849541
Study Section
Virology - B Study Section (VIRB)
Program Officer
Park, Eun-Chung
Project Start
2006-06-15
Project End
2011-11-30
Budget Start
2010-06-01
Budget End
2011-11-30
Support Year
5
Fiscal Year
2010
Total Cost
$286,680
Indirect Cost
Name
University of Michigan Ann Arbor
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
073133571
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
Qi, Ling; Tsai, Billy; Arvan, Peter (2017) New Insights into the Physiological Role of Endoplasmic Reticulum-Associated Degradation. Trends Cell Biol 27:430-440
Ravindran, Madhu Sudhan; Engelke, Martin F; Verhey, Kristen J et al. (2017) Exploiting the kinesin-1 molecular motor to generate a virus membrane penetration site. Nat Commun 8:15496
Dupzyk, Allison; Williams, Jeffrey M; Bagchi, Parikshit et al. (2017) SGTA-Dependent Regulation of Hsc70 Promotes Cytosol Entry of Simian Virus 40 from the Endoplasmic Reticulum. J Virol 91:
Inoue, Takamasa; Tsai, Billy (2017) Regulated Erlin-dependent release of the B12 transmembrane J-protein promotes ER membrane penetration of a non-enveloped virus. PLoS Pathog 13:e1006439
Inoue, Takamasa; Tsai, Billy (2016) The Grp170 nucleotide exchange factor executes a key role during ERAD of cellular misfolded clients. Mol Biol Cell 27:1650-62
Williams, Jeffrey M; Tsai, Billy (2016) Intracellular trafficking of bacterial toxins. Curr Opin Cell Biol 41:51-6
Ravindran, Madhu Sudhan; Bagchi, Parikshit; Cunningham, Corey Nathaniel et al. (2016) Opportunistic intruders: how viruses orchestrate ER functions to infect cells. Nat Rev Microbiol 14:407-420
Bagchi, Parikshit; Inoue, Takamasa; Tsai, Billy (2016) EMC1-dependent stabilization drives membrane penetration of a partially destabilized non-enveloped virus. Elife 5:
Bagchi, Parikshit; Walczak, Christopher Paul; Tsai, Billy (2015) The endoplasmic reticulum membrane J protein C18 executes a distinct role in promoting simian virus 40 membrane penetration. J Virol 89:4058-68
Inoue, Takamasa; Tsai, Billy (2015) A nucleotide exchange factor promotes endoplasmic reticulum-to-cytosol membrane penetration of the nonenveloped virus simian virus 40. J Virol 89:4069-79

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