Abstract
The likelihood of emergence of drug resistance is a function of mutation rate and the number of replicative events. The mutation rate of human immunodeficiency virus (HIV) is presumed to be at least as high as any virus with a single-stranded RNA genome. The number of replicative events in a host infected with HIV are incalculably high as a result of years of persistent replication that is poorly restricted by immune surveillance. Viral chemotherapy in humans has selected for drug-resistant variants of influenza A virus, herpes simplex virus, varicella zoster virus, cytomegalovirus and rhinovirus (Richman 1990). The prospect of drug resistance to zidovudine (AZT) therefore did not appear as a surprise to many.
This work was supported by grants HB-67019, Al-27670, Al-30457, Al-29164 from the National Institutes of Health and by the Research Center for AIDS and HIV Infection of the San Diego Veterans Affairs Medical Center
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© 1992 Springer-Verlag Berlin · Heidelberg
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Richman, D.D. (1992). Selection of Zidovudine-Resistant Variants of Human Immunodeficiency Virus by Therapy. In: Holland, J.J. (eds) Genetic Diversity of RNA Viruses. Current Topics in Microbiology and Immunology, vol 176. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-77011-1_9
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