Polymorphism of SARS-CoV Genomes

SHANG Lei , QI Yan , BAO Qi-Yu , TIAN Wei , XU Jian-Cheng , FENG Ming-Guang , YANG Huan-Ming
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引用次数: 5

Abstract

In this work, severe acute respiratory syndrome associated coronavirus (SARS-CoV) genome BJ202 (AY864806) was completely sequenced. The genome was directly accessed from the stool sample of a patient in Beijing. Comparative genomics methods were used to analyze the sequence variations of 116 SARS-CoV genomes (including BJ202) available in the NCBI Gen-Bank. With the genome sequence of GZ02 as the reference, there were 41 polymorphic sites identified in BJ202 and a total of 278 polymorphic sites present in at least two of the 116 genomes. The distribution of the polymorphic sites was biased over the whole genome. Nearly half of the variations (50.4%, 140/278) clustered in the one third of the whole genome at the 3′ end (19.0 kb-29.7 kb). Regions encoding Orf10–11, Orf3/4, E, M and S protein had the highest mutation rates. A total of 15 PCR products (about 6.0 kb of the genome) including 11 fragments containing 12 known polymorphic sites and 4 fragments without identified polymorphic sites were cloned and sequenced. Results showed that 3 unique polymorphic sites of BJ202 (positions 13 804, 15 031 and 20 792) along with 3 other polymorphic sites (26 428, 26 477 and 27 243) all contained 2 kinds of nucleotides. It is interesting to find that position 18379 which has not been identified to be polymorphic in any of the other 115 published SARS-CoV genomes is actually a polymorphic site. The nucleotide composition of this site is A (8) to G (6). Among 116 SARS-CoV genomes, 18 types of deletions and 2 insertions were identified. Most of them were related to a 300 bp region (27 700–28 000) which encodes parts of the putative ORF9 and ORF10–11. A phylogenetic tree illustrating the divergence of whole BJ202 genome from 115 other completely sequenced SARS-CoVs was also constructed. BJ202 was phylogeneticly closer to BJ01 and LLJ-2004.

sars冠状病毒基因组多态性研究
在这项工作中,我们对SARS-CoV基因组BJ202 (AY864806)进行了完全测序。基因组是直接从北京一名患者的粪便样本中获取的。采用比较基因组学方法分析NCBI genbank中116个SARS-CoV基因组(包括BJ202)的序列变异。以GZ02基因组序列为参照,BJ202共鉴定出41个多态性位点,其中至少有2个基因组存在278个多态性位点。多态性位点的分布在整个基因组中存在偏倚。近一半的变异(50.4%,140/278)聚集在全基因组的三分之一的3 '端(19.0 kb-29.7 kb)。编码Orf10-11、Orf3/4、E、M和S蛋白的区域突变率最高。共获得15个PCR产物(约6.0 kb),其中11个片段含有12个已知多态性位点,4个片段未确定多态性位点。结果表明,BJ202的3个独特多态性位点(位置13 804、15 031和20 792)和另外3个多态性位点(位置26 428、26 477和27 243)均含有2种核苷酸。有趣的是,在其他115个已发表的SARS-CoV基因组中未被确定为多态性的位置18379实际上是一个多态性位点。该位点的核苷酸组成为A (8) ~ G(6)。在116个SARS-CoV基因组中,鉴定出18种缺失和2种插入。其中大部分与一个300 bp的区域(27 700-28 000)有关,该区域编码部分推测的ORF9和ORF10-11。构建了BJ202全基因组与其他115种完全测序的sars - cov的进化树。BJ202在系统发育上与BJ01和LLJ-2004较为接近。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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