Evolutionary dynamics of human retroviruses investigated through full-genome scanning

被引:21
作者
Lemey, P [1 ]
Van Dooren, S [1 ]
Vandamme, AM [1 ]
机构
[1] Katholieke Univ Leuven, Rega Inst Med Res, Louvain, Belgium
关键词
evolutionary rate; HIV; HTLV; natural selection; retrovirus;
D O I
10.1093/molbev/msi078
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
To test hypotheses on the differences in retroviral genetic diversity, we compared the evolutionary dynamics of the human immunodeficiency virus type I (HIV-1) group M and the primate T-cell lymphotropic virus (PTLV) using a full-genome analysis. Evolutionary rates and nonsynonymous/synonymous substitution rate ratios were estimated across the genome using a maximum likelihood sliding window approach, and molecular clock properties were investigated. We confirm a remarkable difference in genetic stability and selective pressure at the interhost level. While there is evidence for adaptive evolution in HIV-1, the evolution of PTLV is almost exclusively characterized by negative selection or nearly neutral processes. For both retroviruses, evolutionary rate estimates across the genome reflect the differential selective constraints. However, based on the relationship between evolutionary rate and selective pressure and based on the comparison of synonymous substitution rates, the differences in rate between HIV-1 and PTLV cannot be explained by selective forces only. Several evolutionary and statistical assumptions, examined using a Bayesian coalescent method, were shown to have little influence on our inference.
引用
收藏
页码:942 / 951
页数:10
相关论文
共 63 条
[1]   Quantification of human T-cell lymphotropic virus type 1 proviral load by quantitative competitive polymerase chain reaction [J].
Albrecht, B ;
Collins, ND ;
Newbound, GC ;
Ratner, L ;
Lairmore, MD .
JOURNAL OF VIROLOGICAL METHODS, 1998, 75 (02) :123-140
[2]   The immune response to HTLV-1 [J].
Bangham, CRM .
CURRENT OPINION IN IMMUNOLOGY, 2000, 12 (04) :397-402
[3]   The immune control and cell-to-cell spread of human T-lymphotropic virus type 1 [J].
Bangham, CRM .
JOURNAL OF GENERAL VIROLOGY, 2003, 84 :3177-3189
[4]   HIV as the cause of AIDS [J].
BarreSinoussi, F .
LANCET, 1996, 348 (9019) :31-35
[5]   ISOLATION OF A T-LYMPHOTROPIC RETROVIRUS FROM A PATIENT AT RISK FOR ACQUIRED IMMUNE-DEFICIENCY SYNDROME (AIDS) [J].
BARRESINOUSSI, F ;
CHERMANN, JC ;
REY, F ;
NUGEYRE, MT ;
CHAMARET, S ;
GRUEST, J ;
DAUGUET, C ;
AXLERBLIN, C ;
VEZINETBRUN, F ;
ROUZIOUX, C ;
ROZENBAUM, W ;
MONTAGNIER, L .
SCIENCE, 1983, 220 (4599) :868-871
[6]   Evaluating hypotheses on the origin and evolution of the New Zealand alpine cicadas (maoricicada) using multiple-comparison tests of tree topology [J].
Buckley, TR ;
Simon, C ;
Shimodaira, H ;
Chambers, GK .
MOLECULAR BIOLOGY AND EVOLUTION, 2001, 18 (02) :223-234
[7]  
CAVALLISFORZA L, 1994, HIST GEOGRAPHY HUMA
[8]  
Cavrois M, 1996, ONCOGENE, V12, P2419
[9]   Persistent oligoclonal expansion of human T-cell leukemia virus type 1 infected circulating cells in patients with Tropical spastic paraparesis HTLV-1 associated myelopathy [J].
Cavrois, M ;
Leclercq, I ;
Gout, O ;
Gessain, A ;
Wain-Hobson, S ;
Wattel, E .
ONCOGENE, 1998, 17 (01) :77-82
[10]  
COFFIN JM, 1990, DEV BIOLOGICALS, V72, P123