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不同严重程度甲型肝炎患者血清中甲型肝炎病毒的系统发育分析。

Phylogenetic analysis of hepatitis A virus in sera from patients with hepatitis A of various severities.

作者信息

Fujiwara Keiichi, Kojima Hiroshige, Yonemitsu Yutaka, Yasui Shin, Imazeki Fumio, Miki Makoto, Suzuki Kazuyuki, Sakaida Isao, Okita Kiwamu, Tanaka Eiji, Omata Masao, Yokosuka Osamu

机构信息

Department of Medicine and Clinical Oncology, Graduate School of Medicine, Chiba University, Chiba, Japan.

出版信息

Liver Int. 2009 Jul;29(6):838-45. doi: 10.1111/j.1478-3231.2008.01919.x. Epub 2008 Nov 25.

Abstract

BACKGROUND

We analysed the association of the 5' nontranslated region (5'NTR), nonstructural proteins 2B and 2C of the hepatitis A virus (HAV) genome, whose mutations have previously been shown to be important for enhanced replication in cell culture systems, in order to align all our data and examine whether genomic differences in HAV are responsible for the range of clinical severities.

METHODS

Our accumulated HAV strains of 5'NTR [nucleotide(nt) 200 and 500], entire 2B and 2C from 25 Japanese patients with sporadic hepatitis A, consisting of seven patients with fulminant hepatitis (FH), five with severe acute hepatitis (AHs) and 13 with self-limited acute hepatitis (AH), in whom the sequences of all three regions were available, were subjected to phylogenetic analysis.

RESULTS

Fulminant hepatitis patients had fewer nucleotide substitutions in 5'NTR, had a tendency to have more amino acid (aa) substitutions in 2B and had fewer aa substitutions in 2C than AH patients. Four FH and two AHs with a higher viral replication were located in the near parts of the phylogenetic trees, indicating the association between the severity of hepatitis A and genomic variations in 5'NTR, 2B and 2C of HAV.

CONCLUSIONS

Our study suggests that genetic variations in HAV not in one specific region but in 5'NTR, 2B and 2C might cooperatively influence replication of the virus, and thereby affect virulence. Viral factors should be considered and examined when discussing the mechanisms responsible for the severity of hepatitis A.

摘要

背景

我们分析了甲型肝炎病毒(HAV)基因组5'非翻译区(5'NTR)、非结构蛋白2B和2C之间的关联,这些区域的突变先前已被证明对细胞培养系统中增强复制很重要,目的是整合我们所有的数据,并研究HAV的基因组差异是否是临床严重程度范围的原因。

方法

我们收集了25例日本散发性甲型肝炎患者的HAV毒株,这些毒株的5'NTR(核苷酸200和500)、完整的2B和2C区域序列均可用,其中包括7例暴发性肝炎(FH)患者、5例严重急性肝炎(AHs)患者和13例自限性急性肝炎(AH)患者,对这三个区域的序列进行了系统发育分析。

结果

与AH患者相比,暴发性肝炎患者的5'NTR核苷酸替换较少,2B区域的氨基酸(aa)替换有增加的趋势,2C区域的aa替换较少。4例FH患者和2例AHs患者病毒复制较高,位于系统发育树的近端,表明甲型肝炎的严重程度与HAV的5'NTR、2B和2C基因组变异之间存在关联。

结论

我们的研究表明,HAV的遗传变异不是在一个特定区域,而是在5'NTR、2B和2C区域可能协同影响病毒的复制,从而影响毒力。在讨论甲型肝炎严重程度的机制时,应考虑并检查病毒因素。

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