Rapid progress in the areas of molecular virology and molecular epidemiology of human caliciviruses (HuCVs) in recent years highlights the clinical importance and worldwide distribution of HuCVs as a cause of acute gastroenteritis in humans. This renewal builds on the scientific productivity of the past and will initiate new research initiatives based on novel approaches. Our long-term goals are to seak new information about the virology, immunology and pathogenesis of HuCVs and to develop strategies to control and prevent the diseases caused by these viruses. The following four specific aims will be addressed.
Specific aim 1. To define the HuCV antigenic types and develop diagnostic assays for detection and typing using type-common and type-specific antibodies.
Specific aim 2. To characterize the infection status and immunity of children and adults involved in sporadic and outbreak episodes of gastroenteritis using type-common and type-specific assays against HuCVs.
Specific aim 3. To characterize the molecular basis of virus-cell interaction and possible viral receptor(s) using recombinant virus-like particles (VLPs) as a probe.
Specific aim 4. To characterize primate CV (PrCV) replication and attempt to cultivate HuCVs in cell culture using novel approaches learned from animal CVs.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI037093-09
Application #
6768793
Study Section
Experimental Virology Study Section (EVR)
Program Officer
Berard, Diana S
Project Start
1997-04-01
Project End
2007-06-30
Budget Start
2004-07-01
Budget End
2005-06-30
Support Year
9
Fiscal Year
2004
Total Cost
$333,000
Indirect Cost
Name
Cincinnati Children's Hospital Medical Center
Department
Type
DUNS #
071284913
City
Cincinnati
State
OH
Country
United States
Zip Code
45229
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Jin, Miao; Tan, Ming; Xia, Ming et al. (2015) Strain-specific interaction of a GII.10 Norovirus with HBGAs. Virology 476:386-94
Tan, Ming; Jiang, Xi (2014) Histo-blood group antigens: a common niche for norovirus and rotavirus. Expert Rev Mol Med 16:e5
Wei, Chao; Meller, Jarek; Jiang, Xi (2013) Substrate specificity of Tulane virus protease. Virology 436:24-32
Fan, Qiang; Wei, Chao; Xia, Ming et al. (2013) Inhibition of Tulane virus replication in vitro with RNA interference. J Med Virol 85:179-86
Dai, Ying-Chun; Zhang, Xu-Fu; Tan, Ming et al. (2013) A dual chicken IgY against rotavirus and norovirus. Antiviral Res 97:293-300
Fang, Hao; Tan, Ming; Xia, Ming et al. (2013) Norovirus P particle efficiently elicits innate, humoral and cellular immunity. PLoS One 8:e63269
Liu, Yang; Huang, Pengwei; Jiang, Baoming et al. (2013) Poly-LacNAc as an age-specific ligand for rotavirus P[11] in neonates and infants. PLoS One 8:e78113
Yu, Guimei; Zhang, Dongsheng; Guo, Fei et al. (2013) Cryo-EM structure of a novel calicivirus, Tulane virus. PLoS One 8:e59817
Liu, Yang; Huang, Pengwei; Tan, Ming et al. (2012) Rotavirus VP8*: phylogeny, host range, and interaction with histo-blood group antigens. J Virol 86:9899-910

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