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两株人类塔纳痘病毒基因组DNA序列的比较遗传分析。

Comparative genetic analysis of genomic DNA sequences of two human isolates of Tanapox virus.

作者信息

Nazarian Steven H, Barrett John W, Frace A Michael, Olsen-Rasmussen Melissa, Khristova Marina, Shaban Mae, Neering Sarah, Li Yu, Damon Inger K, Esposito Joseph J, Essani Karim, McFadden Grant

机构信息

Biotherapeutics Research Group, Robarts Research Institute, and Department of Microbiology and Immunology, University of Western Ontario, London, Ontario N6G 2V4, Canada.

出版信息

Virus Res. 2007 Oct;129(1):11-25. doi: 10.1016/j.virusres.2007.05.001. Epub 2007 Jun 14.

Abstract

Members of the genus Yatapoxvirus, which include Tanapox virus (TPV) and Yaba monkey tumor virus, infect primates including humans. Two strains of TPV isolated 50 years apart from patients infected from the equatorial region of Africa have been sequenced. The original isolate from a human case in the Tana River Valley, Kenya, in 1957 (TPV-Kenya) and an isolate from an infected traveler in the Republic of Congo in 2004 (TPV-RoC). Although isolated 50 years apart the genomes were highly conserved. The genomes differed at only 35 of 144,565 nucleotide positions (99.98% identical). We predict that TPV-RoC encodes 155 ORFs, however a single transversion (at nucleotide 10241) in TPV-Kenya resulted in the coding capacity for two predicted ORFs (11.1L and 11.2L) in comparison to a single ORF (11L) in TPV-RoC. The genomes of TPV are A+T rich (73%) and 96% of the sequence encodes predicted ORFs. Comparative genomic analysis identified several features shared with other chordopoxviruses. A conserved sequence within the terminal inverted repeat region that is also present in the other members of the Yatapoxviruses as well as members of the Capripoxviruses, Swinepox virus and an unclassified Deerpox virus suggests the existence of a conserved near-terminal sequence secondary structure. Two previously unidentified gene families were annotated that are represented by ORF TPV28L, which matched homologues in certain other chordopoxviruses, and TPV42.5L, which is highly conserved among currently reported chordopoxvirus sequences.

摘要

雅塔痘病毒属的成员,包括塔纳痘病毒(TPV)和雅巴猴肿瘤病毒,可感染包括人类在内的灵长类动物。已对从非洲赤道地区感染患者中分离出的相隔50年的两株TPV进行了测序。1957年从肯尼亚塔纳河谷一名人类病例中分离出的原始毒株(TPV-肯尼亚)和2004年从刚果共和国一名受感染旅行者中分离出的毒株(TPV-刚果共和国)。尽管相隔50年分离,但基因组高度保守。基因组在144,565个核苷酸位置中仅35个位置不同(99.98%相同)。我们预测TPV-刚果共和国编码155个开放阅读框(ORF),然而,与TPV-刚果共和国中的单个ORF(11L)相比,TPV-肯尼亚中的一个单碱基颠换(在核苷酸10241处)导致编码两个预测的ORF(11.1L和11.2L)的能力。TPV的基因组富含A+T(73%),96%的序列编码预测的ORF。比较基因组分析确定了与其他脊索痘病毒共有的几个特征。末端反向重复区域内的一个保守序列,也存在于雅塔痘病毒的其他成员以及山羊痘病毒、猪痘病毒和一种未分类的鹿痘病毒的成员中,这表明存在一个保守的近末端序列二级结构。注释了两个以前未鉴定的基因家族,它们分别由与某些其他脊索痘病毒中的同源物匹配的ORF TPV28L和在当前报道的脊索痘病毒序列中高度保守的TPV42.5L代表。

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