Nerurkar V R, Song K J, Bastian I B, Garin B, Franchini G, Yanagihara R
Laboratory of Central Nervous System Studies, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland 20892.
J Infect Dis. 1994 Dec;170(6):1353-60. doi: 10.1093/infdis/170.6.1353.
Sequence variants of human T cell lymphotropic virus type I (HTLV-I), genetically distinct from cosmopolitan strains of HTLV-I from Japan, the Americas, the Caribbean, and Africa, have been discovered among Melanesians in Papua New Guinea and the Solomon Islands and among Australian aboriginals. By using oligonucleotide primer pairs derived from sequences unique to the gp46- and gp21-encoding regions of the env gene of the Melanesian HTLV-I variants, HTLV-I strains from widely separated geographic regions could be grouped into either of two major geographic-specific genotypes or topotypes: Australo-Melanesian and cosmopolitan. These primers did not permit amplification of the corresponding env gene regions in strains of simian T cell lymphotropic virus type I from Asia and Africa. Phylogenetic analysis also supported two distinct lineages, consistent with evolution of HTLV-I in Australia and Melanesia independent from that in other parts of the world.
在巴布亚新几内亚和所罗门群岛的美拉尼西亚人以及澳大利亚原住民中,发现了与来自日本、美洲、加勒比地区和非洲的世界范围的I型人类嗜T细胞病毒(HTLV-I)毒株在基因上不同的HTLV-I序列变体。通过使用源自美拉尼西亚HTLV-I变体env基因的gp46和gp21编码区域独特序列的寡核苷酸引物对,来自广泛分离地理区域的HTLV-I毒株可被归为两种主要的地理特异性基因型或拓扑型之一:澳大拉西亚-美拉尼西亚型和世界范围型。这些引物不能扩增来自亚洲和非洲的I型猿猴嗜T细胞病毒毒株的相应env基因区域。系统发育分析也支持两个不同的谱系,这与HTLV-I在澳大利亚和美拉尼西亚的进化独立于世界其他地区的进化一致。