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한국에서 분리된 콕사키 바이러스 B3 cDNA의 클로닝 및 전체 염기서열 분석Cloning and Sequencing Analysis of the Full-length cDNA of Coxsackievirus B3 Isolated in Korea

Authors
정윤석김기순박정구이윤성신수연천두성지영미김문보나병국윤재득이광호송철용
Issue Date
Apr-2000
Publisher
대한바이러스학회
Citation
대한바이러스학회지, v.30, no.1, pp 71 - 81
Pages
11
Journal Title
대한바이러스학회지
Volume
30
Number
1
Start Page
71
End Page
81
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/57696
Abstract
We have determined and analyzed the full-length cDNA sequence of a coxsackievirus B3 (CVB3) Korean isolate (CVB3-Korea/97) which has been known as a general human pathogen. The whole genome contains 7,400 nucleotides and has a single large open reading frame with 6,555 nucleotides that encodes a potential polyprotein precursor of 2,185 amino acids. The genome also contains a 5' non-coding region (NCR) of 741 bases and a 3' NCR of 104 bases followed by poly(A) tail. Sequence homologies of nucleotides and deduced amino acids between the CVB3-Korea/97 strain and the prototype (Nancy strain) were 81.7% and 91.5%, respectively. The genes encoding the functional proteins including viral protease and RNA dependent RNA polymerase showed higher homology than those encoding the structural proteins. We have further analyzed the sequences of 5' NCR, VP1 and VP2 of CVB3-Korea/97, which are known as cardiovirulent determining factors at the nucleotide and amino acid levels. Although the CVB 3-Korea/97 strain was isolated from an aseptic meningitis patient without cardiomyopathy, its 234th nucleotide and 165th amino acid were uracil and Asn as same as those of other cardiovirulent strains one. However, the 155th amino acid of VP1, which closely associated with cardiovirulence, was replaced with Arg^155 by single nucleotide substitution from A^2916 to T^2916. Moreover, additional amino acid substitutions were observed in the flanking region of Asp^155. Taken together, amino acid(s) substitution in VP1 may playa critical role in determining cardiovirulence of the CVB3-Korea/97 strain rather than individual nucleotide replacements in the 5' NCR and/or an amino acid substitution in VP2.
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