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人类T细胞白血病/淋巴瘤病毒I型在体内的低程度基因漂移作为监测古代人类群体病毒传播和迁移的一种手段。

Low degree of human T-cell leukemia/lymphoma virus type I genetic drift in vivo as a means of monitoring viral transmission and movement of ancient human populations.

作者信息

Gessain A, Gallo R C, Franchini G

机构信息

Laboratory of Tumor Cell Biology, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892.

出版信息

J Virol. 1992 Apr;66(4):2288-95. doi: 10.1128/JVI.66.4.2288-2295.1992.

Abstract

We have studied the genetic variation of human T-cell leukemia/lymphoma virus type I (HTLV-I) isolates in the same individuals over time, as well as of HTLV-I isolates from various parts of the world. The viral DNA fragment studied encodes the carboxy terminus of gp46 and almost all of gp21, both of which are envelope glycoproteins. Samples were obtained from native inhabitants of five African countries, two South American countries, China, the French West Indies, and Haiti and included 14 patients with tropical spastic paraparesis/HTLV-I-associated myelopathy, 10 patients with adult T-cell leukemia, 1 patient with T-cell non-Hodgkin's lymphoma, and 3 healthy HTLV-I-seropositive individuals. DNA analyses of HTLV-I sequences demonstrated that (i) little or no genetic variation occurred in vivo in the same individual or in different hosts from the same region carrying the same virus, regardless of their clinical statuses; (ii) changes in nucleotide sequences in some regions of the HTLV-I genome were diagnostic of the geographical origin of the viruses; (iii) HTLV-I sequences from West African countries (Mauritania and Guinea Bissau) and some from the Ivory Coast and Central African Republic were virtually identical to those from the French West Indies, Haiti, French Guyana, and Peru, strongly suggesting that at least some HTLV-I strains were introduced into the New World through infected individuals during the slave trade events; and (iv) the Zairian HTLV-I isolates represent a separate HTLV-I cluster, in which intrastrain variability was also observed, and are more divergent from the other HTLV-I isolates. Because of the low genetic variability of HTLV-I in vivo, the study of the proviral DNA sequence in selected populations of infected individuals will increase our knowledge of the origin and evolution of HTLV-I and might be useful in anthropological studies.

摘要

我们研究了人类I型嗜T细胞白血病/淋巴瘤病毒(HTLV-I)在同一人体内随时间的基因变异情况,以及来自世界不同地区的HTLV-I分离株的基因变异情况。所研究的病毒DNA片段编码gp46的羧基末端和几乎全部的gp21,二者均为包膜糖蛋白。样本取自五个非洲国家、两个南美国家、中国、法属西印度群岛和海地的当地居民,包括14例热带痉挛性截瘫/HTLV-I相关脊髓病患者、10例成人T细胞白血病患者、1例T细胞非霍奇金淋巴瘤患者以及3名健康的HTLV-I血清阳性个体。对HTLV-I序列的DNA分析表明:(i)在同一宿主内或携带相同病毒的同一地区的不同宿主中,无论其临床状态如何,体内几乎没有发生基因变异;(ii)HTLV-I基因组某些区域的核苷酸序列变化可诊断病毒的地理起源;(iii)来自西非国家(毛里塔尼亚和几内亚比绍)以及象牙海岸和中非共和国的一些HTLV-I序列与来自法属西印度群岛、海地、法属圭亚那和秘鲁的序列几乎相同,这强烈表明至少一些HTLV-I毒株是在奴隶贸易时期通过受感染个体传入新大陆的;(iv)扎伊尔的HTLV-I分离株代表一个独立的HTLV-I簇,其中也观察到了株内变异性,并且与其他HTLV-I分离株的差异更大。由于HTLV-I在体内的基因变异性较低,对选定感染个体群体中的前病毒DNA序列进行研究将增加我们对HTLV-I起源和进化的了解,并且可能在人类学研究中有用。

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