Plagemann P G
Department of Microbiology, University of Minnesota Medical School, Minneapolis.
Arch Virol. 1991;120(3-4):165-80. doi: 10.1007/BF01310473.
HepCV is the major cause of NANB PT hepatitis and is also implicated as the cause in a large proportion of sporadic cases of NANBH. Chronic infection with HepCV has also been linked to the development of hepatocellular carcinoma. Chimpanzees and marmosets are the only animals found to be experimentally infectable and the virus has not been propagated in any cell culture system. HepCV is an enveloped virus with a diameter of 30-60 nm and a 10-kb positive-stranded RNA genome. Its genome organization resembles that of the flaviviruses and pestiviruses. A 5'-untranslated segment of 341 nucleotides precedes a continuous ORF of 9030/9033 nucleotides which is followed by a 54 nucleotides long 3'-non-coding segment. Further work is required to resolve the question of whether the genomic RNA possesses a 3'-poly(U) or poly(A) tail. The genome also carries an internal poly(A) segment towards the 5'-end of its ORF. Genomic RNA is probably translated into a single polyprotein of 3010/3011 amino acids which is processed into functional proteins. The viral proteins have not been identified, but on the basis of the predicted amino acid sequences, hydrophobicity plots, location of potential glycosylation sites and similarities of these properties to those of pesti- and flaviviruses, the following genome organization has been predicted. The predicted viral structural proteins, a nucleocapsid protein and two envelope glycoproteins are located at the amino-terminal end of the polyprotein. They are followed by a highly hydrophobic protein and proteins that exhibit proteinase, helicase and replicase domains and thus are probably involved in RNA replication and protein processing. The replicase domain is located close to the carboxy terminus of the polyprotein. Although the overall nucleotide and amino acid homologies between HepCV and pestiviruses are low, a number of similarities exist that point to a closer ancestral relationship to the latter than the flaviviruses. First, the 5'-untranslated segment of the HepCV genome resembles that of the pestivirus genomes in size and presence of several short ORFs and it contains several segments with high nucleotide homology. Second, the two putative envelope glycoproteins of HepCV resemble two of the three putative envelope glycoproteins of the pestiviruses. Because its genome organization and predicted virion structure closely resemble those of the flaviviruses and pestiviruses, HepCV has been proposed to be placed in the family Flaviviridae.(ABSTRACT TRUNCATED AT 400 WORDS)
丙型肝炎病毒(HepCV)是引起非甲非乙型输血后肝炎的主要原因,在很大一部分散发性非甲非乙型肝炎病例中也被认为是病因。丙型肝炎病毒的慢性感染还与肝细胞癌的发生有关。黑猩猩和狨猴是仅有的经实验可感染的动物,该病毒尚未在任何细胞培养系统中增殖。丙型肝炎病毒是一种包膜病毒,直径为30 - 60纳米,基因组为10千碱基的正链RNA。其基因组结构类似于黄病毒属和瘟病毒属。341个核苷酸的5' - 非翻译区位于9030/9033个核苷酸的连续开放阅读框之前,随后是一个54个核苷酸长的3' - 非编码区。还需要进一步研究来解决基因组RNA是否具有3' - 聚(U)或聚(A)尾的问题。基因组在其开放阅读框5' - 端还带有一个内部聚(A)片段。基因组RNA可能被翻译成一个3010/3011个氨基酸的单一多聚蛋白,该多聚蛋白被加工成功能性蛋白质。病毒蛋白尚未被鉴定,但根据预测的氨基酸序列、疏水性图谱、潜在糖基化位点的位置以及这些特性与瘟病毒和黄病毒的相似性,已预测出以下基因组结构。预测的病毒结构蛋白,一个核衣壳蛋白和两个包膜糖蛋白位于多聚蛋白的氨基末端。随后是一个高度疏水的蛋白以及具有蛋白酶、解旋酶和复制酶结构域的蛋白,因此可能参与RNA复制和蛋白质加工。复制酶结构域位于多聚蛋白的羧基末端附近。尽管丙型肝炎病毒与瘟病毒之间的总体核苷酸和氨基酸同源性较低,但存在一些相似之处,表明其与瘟病毒的亲缘关系比黄病毒更近。首先,丙型肝炎病毒基因组的5' - 非翻译区在大小和几个短开放阅读框的存在方面类似于瘟病毒基因组,并且它包含几个具有高核苷酸同源性的片段。其次,丙型肝炎病毒的两个假定包膜糖蛋白类似于瘟病毒的三个假定包膜糖蛋白中的两个。由于其基因组结构和预测的病毒粒子结构与黄病毒属和瘟病毒属非常相似,丙型肝炎病毒已被提议归入黄病毒科。(摘要截选至400字)