Evolutionary rate and genetic heterogeneity of human T-cell lymphotropic virus type II (HTLV-II) using isolates from European injecting drug users

被引:35
作者
Salemi, M
Vandamme, AM
Gradozzi, C
Van Laethem, K
Cattaneo, E
Taylor, G
Casoli, C
Goubau, P
Desmyter, J
Bertazzoni, U
机构
[1] Katholieke Univ Leuven, Rega Inst Med Res, B-3000 Louvain, Belgium
[2] Katholieke Univ Leuven, Univ Hosp, B-3000 Louvain, Belgium
[3] Univ Verona, Ist Biol & Genet, I-37134 Verona, Italy
[4] Univ Pavia, Policlin San Matteo, IRCCS, I-27100 Pavia, Italy
[5] St Marys Hosp, Imperial Coll, Sch Med, London W2 1PG, England
[6] Univ Parma, Ist Patol Med, I-43100 Parma, Italy
关键词
HTLV-II; IIa and IIb subtypes; restriction analysis; phylogenetic analysis; maximum likelihood; neighbour-joining; parsimony; molecular clock; fixation rate;
D O I
10.1007/PL00006340
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Seven new Italian and two new British HTLV-II isolates were obtained from injecting drug users and the entire long terminal repeat (LTR) region was sequenced. Restriction analysis showed that all the Italian isolates are of the IIb subtype, whereas the British isolates are of the IIa subtype. To understand whether the further differentiation of each two principal HTLV-II subtypes in several subgroups could be statistically supported by phylogenetic analysis, the neighbor-joining, parsimony, and maximum likelihood methods were used. The separation between IIa and IIb is very well supported by all three methods. At least two phylogenetic subgroups exist within the HTLV-IIa and at least three within the HTLV-IIb subtype. In the present analysis, no statistical support was obtained for additional phylogroups. Two particular subgroups seem interesting because they include all European and North American injecting drug user strains within the IIa and IIb subtypes, respectively. These data confirm that European HTLV-II infection among drug users is probably derived from North America. They also suggest that though a certain differentiation by restriction analysis in different subgroups is possible, carefully interpreted phylogenetic analyses remain necessary. Using the likelihood ratio test, a molecular clock for the drug user strains was calibrated. A fixation rate between 1.08 x 10(-4) and 2.7 x 10(-5) nucleotide substitutions per site per year was calculated for the IIa and IIb injecting drug user strains. This is the lowest fixation rate so far reported for RNA viruses, including for HIV, which typically range between 10(-2) and 10(-4).
引用
收藏
页码:602 / 611
页数:10
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