Developing an in vitro system for HCV propagation
Developing an in vitro system for HCV propagation
批准号:
7657339
负责人:
Ratna B. Ray
金额:
$15.26万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2008
资助国家:
美国
项目状态:
已结题
起止时间:
2008-07-14 至 2012-06-30
关键词:
AddressAntibodiesAntiviral AgentsApplications GrantsAreaBiological AssayCD81 geneCell Culture SystemCell Culture TechniquesCellsComputer Systems DevelopmentDetectionDevelopmentExhibitsFutureGenomeGenotypeGeographic LocationsGoalsGrowthHepatitis CHepatitis C virusHepatocyteHumanImmunofluorescence ImmunologicImmunohistochemistryIn VitroInfectionInfectious hepatitidesInterferon-alphaMolecular CloningMutationPan GenusPharmaceutical PreparationsProductionRNARNA replicationRenilla LuciferasesReporterReporter GenesReportingResearch PersonnelResistanceScreening procedureSerial PassageSerumSystemTherapeuticTitrationsTransfectionVaccinesVariantVirionVirusVirus DiseasesWorkbaseeffective therapyhigh throughput screeningimprovedinhibitor/antagonistnovelparticleprogramspublic health relevancerecombinant virustherapeutic vaccinetoolvaccine evaluationviral RNA
中文摘要
描述(由申请人提供):丙型肝炎病毒(HCV)通常会导致人类长期和持续感染,迫切需要开发高效的治疗和疫苗。不同的HCV基因型和亚型存在于不同的地理位置。HCV基因型1 (a和b亚型)感染在美国很普遍,并且对现有治疗具有相对耐药性。最近,我们和其他研究者报道了HCV在细胞培养中的生长。大部分工作是用HCV基因型2a (JFH1株)在Huh7细胞或其衍生物中完成的。我们已经在永生化人肝细胞(IHH)中培养了HCV基因型1a (H77株)。然而,野生型HCV 1a的产量较低,HCV H77和JFH1之间存在显著的序列差异。虽然可以产生HCV 1a颗粒,但尚未确定病毒在肝细胞中的连续传代生长。因此,有一个强大的细胞培养系统对HCV - 1a生长是极其重要的。此外,基于免疫荧光或免疫组织化学的检测限制了传染性病毒颗粒的滴定。在这项Developmental R21资助申请中,我们计划通过不同方法表征病毒在IHH中的生长来产生高滴度的HCV 1a,并使用报告基因法开发一种方便的病毒感染读数。这项工作的结果将有助于进一步开发新的领域,包括对药物和疫苗发现计划产生巨大影响的抗病毒筛选的高通量测定。公共卫生相关性:丙型肝炎病毒(HCV)经常导致人类长期和持续感染,迫切需要开发高效的治疗方法和疫苗。我们最近在细胞培养中产生了HCV。我们将研究提高这种病毒的体外生长,并开发一种敏感的读数,用于未来的高通量抗病毒筛选和疫苗发现项目。
英文摘要
DESCRIPTION (provided by applicant): Hepatitis C virus (HCV) often causes a prolonged and persistent infection in humans, and there is an urgent need for the development of a highly effective therapy and vaccine. Distinct genotypes and subtypes of HCV exist in different geographic locations. Infection with HCV genotype 1 (subtypes a and b) is prevalent in the USA, and is relatively resistant to available therapies. Recently, HCV growth in cell culture has been reported by us and other investigators. Majority of the work was done with HCV genotype 2a (JFH1 strain) in Huh7 cells or its derivatives. We have developed growth of HCV genotype 1a (H77 strain) in immortalized human hepatocytes (IHH). However, wild type HCV 1a yield is low and a significant sequence variation exists between HCV H77 and JFH1 strains. Although, HCV 1a particles are generated, virus growth from serial passages in hepatocytes has not been established. Therefore, it is extremely important to have a robust cell culture system for HCV 1a growth. Furthermore, titration of infectious virus particles is restricted with immunofluorescence or immunohistochemistry based assay. In this Developmental R21 grant application, we plan to generate a high titer HCV 1a by characterizing virus growth in IHH following different approaches, and develop a convenient readout for virus infection using a reporter assay. The results from the proposed work will help in further developing novel areas, including high throughput assay for antiviral screening with tremendous impact for drug and vaccine discovery programs. PUBLIC HEALTH RELEVANCE: Hepatitis C virus (HCV) often causes a prolonged and persistent infection in humans, and there is an urgent need for the development of highly effective therapy and vaccine. We have recently generated HCV in cell culture. We will study to improve the in vitro growth of this virus and develop a sensitive readout for future use in high throughput antiviral screening and vaccine discovery programs.
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