| dc.contributor.author | Jones, Christopher T. |  | 
| dc.contributor.author | Catanese, Maria Teresa |  | 
| dc.contributor.author | Law, Lok Man J. |  | 
| dc.contributor.author | Khetani, Salman R. |  | 
| dc.contributor.author | Syder, Andrew J. |  | 
| dc.contributor.author | Ploss, Alexander |  | 
| dc.contributor.author | Oh, Thomas S. |  | 
| dc.contributor.author | Schoggins, John W. |  | 
| dc.contributor.author | MacDonald, Margaret R. |  | 
| dc.contributor.author | Bhatia, Sangeeta N. |  | 
| dc.contributor.author | Rice, Charles M. |  | 
| dc.date.accessioned | 2012-12-10T19:55:33Z |  | 
| dc.date.available | 2012-12-10T19:55:33Z |  | 
| dc.date.issued | 2010-01 |  | 
| dc.date.submitted | 2009-08 |  | 
| dc.identifier.issn | 1087-0156 |  | 
| dc.identifier.issn | 1546-1696 |  | 
| dc.identifier.uri | http://hdl.handle.net/1721.1/75340 |  | 
| dc.description | Author Manuscript 2010 August 1 | en_US | 
| dc.description.abstract | Hepatitis C virus (HCV), which infects 2–3% of the world population, is a causative agent of chronic hepatitis and the leading indication for liver transplantation1. The ability to propagate HCV in cell culture (HCVcc) is a relatively recent breakthrough and a key tool in the quest for specific antiviral therapeutics. Monitoring HCV infection in culture generally involves bulk population assays, use of genetically modified viruses and/or terminal processing of potentially precious samples. Here we develop a cell-based fluorescent reporter system that allows sensitive distinction of individual HCV-infected cells in live or fixed samples. We demonstrate use of this technology for several previously intractable applications, including live-cell imaging of viral propagation and host response, as well as visualizing infection of primary hepatocyte cultures. Integration of this reporter with modern image-based analysis methods could open new doors for HCV research. | en_US | 
| dc.description.sponsorship | New York (State). Dept. of Health (Empire State Stem Cell Fund Contract C023046) | en_US | 
| dc.description.sponsorship | United States. Public Health Service (Grant R01 DK56966) | en_US | 
| dc.description.sponsorship | National Institutes of Health (U.S.) (Roadmap for Medical Research Grant 1 R01 DK085713-01) | en_US | 
| dc.description.sponsorship | Howard Hughes Medical Institute (Investigator) | en_US | 
| dc.language.iso | en_US |  | 
| dc.publisher | Nature Publishing Group | en_US | 
| dc.relation.isversionof | http://dx.doi.org/10.1038/nbt.1604 | en_US | 
| dc.rights | Creative Commons Attribution-Noncommercial-Share Alike 3.0 | en_US | 
| dc.rights.uri | http://creativecommons.org/licenses/by-nc-sa/3.0/ | en_US | 
| dc.source | PMC | en_US | 
| dc.title | Real-time imaging of hepatitis C virus infection using a fluorescent cell-based reporter system | en_US | 
| dc.type | Article | en_US | 
| dc.identifier.citation | Jones, Christopher T et al. “Real-time Imaging of Hepatitis C Virus Infection Using a Fluorescent Cell-based Reporter System.” Nature Biotechnology 28.2 (2010): 167–171. | en_US | 
| dc.contributor.department | Harvard University--MIT Division of Health Sciences and Technology | en_US | 
| dc.contributor.department | Massachusetts Institute of Technology. Department of Electrical Engineering and Computer Science | en_US | 
| dc.contributor.mitauthor | Khetani, Salman R. |  | 
| dc.contributor.mitauthor | Bhatia, Sangeeta N. |  | 
| dc.relation.journal | Nature Biotechnology | en_US | 
| dc.eprint.version | Author's final manuscript | en_US | 
| dc.type.uri | http://purl.org/eprint/type/JournalArticle | en_US | 
| eprint.status | http://purl.org/eprint/status/PeerReviewed | en_US | 
| dspace.orderedauthors | Jones, Christopher T; Catanese, Maria Teresa; Law, Lok Man J; Khetani, Salman R; Syder, Andrew J; Ploss, Alexander; Oh, Thomas S; Schoggins, John W; MacDonald, Margaret R; Bhatia, Sangeeta N; Rice, Charles M | en | 
| dc.identifier.orcid | https://orcid.org/0000-0002-1293-2097 |  | 
| mit.license | OPEN_ACCESS_POLICY | en_US | 
| mit.metadata.status | Complete |  |