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We analyzed the association between evolution of the 5' exon of tat and disease progression in a SIV/SHIV macaque model of opiate-dependence and AIDS. We cloned tat sequences using RT-PCR of plasma virus from eight animals at three time points following infection. Six of these monkeys were part of a morphine-dependent cohort, while two served as non-drug using controls. We found a significant inverse correlation between disease progression and tat diversity in plasma by 20 weeks. The morphine cohort segregated into two classifications based on progression: a rapidly progressing group (Group A) and a second set (Group B) that progressed at a rate similar to the two non-morphine controls (Group C). The three animals in Group A exhibited -40% (p = 0.01) and 50% (p = 0.028) less diversity than Group B and C animals, respectively. Group A animals showed prominent re-emergence of the wild-type inoculum tat sequence as illness progressed. This suggests that the virus from the original infection represented the most pathogenic form in these cohorts throughout the first 20 weeks of infection. Our results indicate that in vivo morphine dependence can contribute to the pathogenesis of SIV/SHIV infection and that it may do so in conjunction with the evolution of viral proteins, such as Tat. It is unclear if this is a direct effect of morphine on the virus replication/evolution or if it is mediated indirectly through modulation of the immune response, or through the enhanced vulnerability of a protected compartment such as the CNS. from 2005 International Meeting of The Institute of Human Virology Baltimore, USA, 29 August – 2 September 2005

retrovirology

Higher Virus Replication and Rapid Disease Progression Correlate Inversely With SIV tat exon 1 Evolution in Morphine-addicted SIV/SHIV-infected Macaques