Phylodynamics of HIV-1 Circulating Recombinant Forms 12_BF and 38_BF in Argentina and Uruguay

被引:40
作者
Bello, Gonzalo [1 ]
Aulicino, Paula C. [2 ]
Ruchansky, Dora [3 ]
Guimaraes, Monick L. [1 ]
Lopez-Galindez, Cecilio [4 ]
Casado, Concha [4 ]
Chiparelli, Hector [3 ]
Rocco, Carlos [2 ]
Mangano, Andrea [2 ]
Sen, Luisa [2 ]
Morgado, Mariza G. [1 ]
机构
[1] Fiocruz MS, Lab AIDS & Imunol Mol, Inst Oswaldo Cruz, BR-21045900 Rio De Janeiro, Brazil
[2] Hosp Pediat JP Garrahan, Lab Biol Celular & Retrovirus, CONICET, Buenos Aires, DF, Argentina
[3] MSP, Lab Nacl Referencia VIH SIDA, Serv Nacl, Lab Salud Publ, Montevideo, Uruguay
[4] Inst Salud Carlos III, Serv Virol Mol, Ctr Nacl Microbiol, Madrid, Spain
来源
RETROVIROLOGY | 2010年 / 7卷
关键词
ANTIRETROVIRAL DRUG-RESISTANCE; LENGTH GENOME SEQUENCES; RIO-DE-JANEIRO; BF RECOMBINANTS; EVOLUTIONARY HISTORY; SUBTYPE-B; MOLECULAR CHARACTERISTICS; PHYLOGENETIC INFERENCE; MAXIMUM-LIKELIHOOD; POPULATION HISTORY;
D O I
10.1186/1742-4690-7-22
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Background: Although HIV-1 CRF12_BF and CRF38_BF are two epidemiologically important recombinant lineages circulating in Argentina and Uruguay, little is known about their population dynamics. Methods: A total of 120 "CRF12_BF-like" and 20 "CRF38_BF-like" pol recombinant sequences collected in Argentina and Uruguay from 1997 to 2009 were subjected to phylogenetic and Bayesian coalescent-based analyses to estimate evolutionary and demographic parameters. Results: Phylogenetic analyses revealed that CRF12_BF viruses from Argentina and Uruguay constitute a single epidemic with multiple genetic exchanges among countries; whereas circulation of the CRF38_BF seems to be confined to Uruguay. The mean estimated substitution rate of CRF12_BF at pol gene (2.5 x 10-3 substitutions/site/year) was similar to that previously described for subtype B. According to our estimates, CRF12_BF and CRF38_BF originated at 1983 (1978-1988) and 1986 (1981-1990), respectively. After their emergence, the CRF12_BF and CRF38_BF epidemics seem to have experienced a period of rapid expansion with initial growth rates of around 1.2 year(-1) and 0.9 year(-1), respectively. Later, the rate of spread of these CRFs_BF seems to have slowed down since the mid-1990s. Conclusions: Our results suggest that CRF12_BF and CRF38_BF viruses were generated during the 1980s, shortly after the estimated introduction of subtype F1 in South America (similar to 1975-1980). After an initial phase of fast exponential expansion, the rate of spread of both CRFs_BF epidemics seems to have slowed down, thereby following a demographic pattern that resembles those previously reported for the HIV-1 epidemics in Brazil, USA, and Western Europe.
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