| Virology Journal | |
| Full sequence analysis and characterization of the South Korean Norovirus GII-4 variant CUK-3 | |
| Soon-Young Paik3  Sangryeol Ryu4  Weon-Hwa Jheong2  Young-Min Lee1  Sung-Geun Lee3  Jeong-Woong Park4  | |
| [1] Department of Microbiology, College of Medicine and Medical Research Institute, Chungbuk National University, Cheongju, Chungcheongbuk-do 361-763, Republic of Korea;Environmental Infrastructure Research Department, National Institute of Environmental Research, Incheon, 404-708, Republic of Korea;Department of Microbiology, College of Medicine, The Catholic University of Korea, Seoul 137-701, Republic of Korea;Department of Food and Animal Biotechnology, Department of Agricultural Biotechnology, Center for Agricultural Biomaterials, and Research Institute for Agriculture and Life Sciences, Seoul National University, Seoul 151-921, Republic of Korea | |
| 关键词: Phylogenetic tree; Sequence; Norovirus; | |
| Others : 1156839 DOI : 10.1186/1743-422X-8-167 |
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| received in 2010-10-28, accepted in 2011-04-14, 发布年份 2011 | |
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【 摘 要 】
Background
Many of researchers have focused on the emerging pathogen, Norovirus, since its first identification as the causing agent of nonbacterial acute gastroenteritis in humans. One of the virulence factors of norovirus, the great genetic diversity attributed to point mutations and recombinations, has brought forth the result of significant changes in the circulating norovirus genotype patterns.
Findings
In recognition of the necessity for tracking and monitoring of genetic diversity, a norovirus variant among the most prevalent genotype GII-4, Norovirus Hu/GII-4/CUK-3/2008/KR (CUK-3), was isolated from stool samples and analyzed on the level of whole genome sequence. Whole genome sequence analysis revealed three ORF composites of the whole genome, ORF1 (5100 bp), ORF2 (1623 bp), and ORF3 (807 bp). Each genetic relationship of CUK-3 variant analysis located the ORF1 (5,100 bp) in Cluster I, ORF2 (1623 bp) in Cluster I (2006b), ORF3 (807 bp) in Cluster I, and the whole genome sequence (about 5.1 kb) in Cluster I in the phylogenetic tree. And the phylogenetic analyses showed the same location of CUK-3 strain with the GII-4/2006b cluster in the phylogenetic tree.
Conclusions
In This study, a first concerning the full-length sequence of a NoV variant in South Korea is meaningful in that it can be used not only as a full-length NoV variant sequence standard for future comparison studies, but also as useful material for the public health field by enabling the diagnosis, vaccine development, and prediction of new emerging variants.
【 授权许可】
2011 Park et al; licensee BioMed Central Ltd.
【 预 览 】
| Files | Size | Format | View |
|---|---|---|---|
| 20150407140644998.pdf | 689KB | ||
| Figure 2. | 89KB | Image | |
| Figure 1. | 63KB | Image |
【 图 表 】
Figure 1.
Figure 2.
【 参考文献 】
- [1]Donaldson EF, Lindesmith LC, Lobue AD, Baric RS: Norovirus pathogenesis: mechanisms of persistence and immune evasion in human populations. Immunol Rev 2008, 225:190-211.
- [2]Yoon JS, Lee SG, Hong SK, Lee SA, Jheong WH, Oh SS, Oh MH, Ko GP, Lee CH, Paik SY: Molecular epidemiology of norovirus infections in children with acute gastroenteritis in South Korea in November 2005 through November 2006. J Clin Microbiol 2008, 46:1474-1477.
- [3]Lee YF, Nomoto A, Detjen BM, Wimmer E: A protein covalently linked topoliovirus genome RNA. Proc Natl Acad Sci USA 1977, 74:59-63.
- [4]Rueckert RR, Wimmer E: Systematic nomenclature of picornavirus proteins. J Virol 1984, 50:957-959.
- [5]Tan M, Huang P, Meller J, Zhong W, Farkas T, Jiang X: Mutations within the P2 domain of norovirus capsid affect binding to human histo-blood group antigens: evidence for a binding pocket. J Virol 2003, 77:12562-12571.
- [6]Nilssson MK, Hedlund O, Thorhagen M, Larson G, Johansen K, Ekspong A, Svensson L: Evolution of human calicivirus RNA in vivo: accumulation of mutations in the protruding P2 domain of the capsid leads to structural changes and possibly a new phenotype. J Virol 2003, 77:13117-13124.
- [7]Lochridge VP, Jutila KI, Graff JW, Hardy ME: Epitopes in the P2 domain of norovirus VP1 recognized by monoclonal antibodies that block cell interactions. J Gen Virol 2005, 86:2799-2806.
- [8]Glass PJ, White LJ, Bull JM, Leparc-Goffart I, Hardy ME, Estes MK: Norwalk virus open reading frame 3 encodes aminor structural protein. J Virol 2000, 74:6581-6591.
- [9]Bertolotti-Ciariet A, Crawford SE, Hutson AM, Estes MK: The 3' end of Norwalk virus mRNA contains determinants that regulate the expression and stability of the viral capsid protein VP1: a novel function for the VP2 protein. J Virol 2003, 77:11603-11615.
- [10]Kearney K, Menton J, Morgan JG: Carlow virus, a 2002 GII-4 variant norovirus strain from Ireland. Virol J 2007, 4:61. BioMed Central Full Text
- [11]La Rosa G, Pourshaban M, Iaconelli M, Muscillo M: Detection of genogroup IV noroviruses in environmental and clinical samples and partial sequencing through rapid amplification of cDNA ends. Arch Virol 2008, 153:2077-2083.
- [12]Motomura K, Oka T, Yokoyama M, Nakamura H, Mori H, Ode H, Hansman GS, Katayama K, Kanda T, Tanaka T, Takeda N, Sato H: Identification of monomorphic and divergent haplotypes in the 2006-2007 norovirus GII/4 epidemic population by genome wide tracing of evolutionary history. J Virol 2008, 82:11247-11262.
- [13]Hale A, Mattick K, Lewis D, Estes M, Jiang X, Green J, Eglin R, Brown D: Distinct epidemiological patterns of Norwalk-like virus infection. J Med Virol 2000, 62:99-103.
- [14]Glass RI, Parashar UD, Estes MK: Norovirus gastroenteritis. N Engl J Med 2009, 361:1776-1785.
- [15]Lopman B, Vennema H, Kohli E, Pothier P, Sanchez A, Negredo A, Buesa J, Schreier E, Reacher M, Brown D, Gray J, Iturriza M, Gallimore C, Bottiger B, Hedlund KO, Torvén M, von Bonsdorff CH, Maunula L, Poljsak-Prijatelj M, Zimsek J, Reuter G, Szücs G, Melegh B, Svennson L, van Duijnhoven Y, Koopmans M: Increase in viral gastroenteritis outbreaks in Europe and epidemic spread of new norovirus variant. Lancet 2004, 363:682-688.
- [16]Allen DJ, Noad R, Samuel D, Gray JJ, Roy P, Iturriza-Gómara M: Characterisation of a GII-4 norovirus variant-specific surface-exposed site involved in antibody binding. Virol J 2009, 6:150. BioMed Central Full Text
- [17]Chung JY, Han TH, Park SH, Kim SW, Hwang ES: Detection of GII-4/2006b Variant and Recombinant Noroviruses in Children With Acute Gastroenteritis, South Korea. J Med Virol 2010, 82:146-152.
- [18]Ho EC, Cheng PK, Lau AW, Wong AH, Lim WW: A typical norovirus epidemic in Hong Kong during summer of 2006 caused by a new genogroup II/4 variant. J Clin Microbiol 2007, 45:2205-2211.
- [19]Tu ET, Bull RA, Greening GE, Hewitt J, Lyon MJ, Marshall JA, McIver CJ, Rawlinson WD, White PA: Epidemics of gastroenteritis during 2006 were associated with the spread of norovirus GII.4 variants 2006a and 2006b. Clin Infect Dis 2008, 46:413-420.
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