Prevalence of Mutations Associated with Reduced Antiretroviral Drug Susceptibility among Human Immunodeficiency Virus Type 1 Seroconverters in the United States, 1993–1998

To assess the prevalence of mutations associated with decreased antiretroviral drug susceptibility, specimens were tested from persons infected with human immunodeficiency virus (HIV) during 1993–1998. Subjects were drug naive and were attending sexually transmitted disease clinics in 6 US cities. A...

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Published in:The Journal of infectious diseases Vol. 182; no. 1; pp. 330 - 333
Main Authors: Weinstock, Hillard, Respess, Richard, Heneine, Walid, Petropoulos, Christos J., Hellmann, Nicholas S., Luo, Chi-Cheng, Pau, Chou-Pong, Woods, Toni, Gwinn, Marta, Kaplan, Jonathan
Format: Journal Article
Language:English
Published: Chicago, IL The University of Chicago Press 01-07-2000
University of Chicago Press
Oxford University Press
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Summary:To assess the prevalence of mutations associated with decreased antiretroviral drug susceptibility, specimens were tested from persons infected with human immunodeficiency virus (HIV) during 1993–1998. Subjects were drug naive and were attending sexually transmitted disease clinics in 6 US cities. All were enrolled consecutively and had tested negative for HIV during the 2 years before enrollment. Plasma specimens from patients having ⩾1 reverse transcriptase (RT) or primary protease mutation were tested phenol-typically with a recombinant virus assay. Of 99 patients, 6 (6%) had mutations associated with zidovudine resistance, 2 (2%) had mutations associated with non-nucleoside RT inhibitor resistance, and 1 (1%) had a primary protease mutation. Overall, the prevalence of resistance-associated primary mutations was 5%, although high levels of decreased drug susceptibility (IC5Os ⩾10 times that of a reference virus) were observed in just 1%. These findings confirm the transmission of these mutations to drug-naive persons.
Bibliography:ark:/67375/HXZ-588GQS8Z-W
C.J.P and N.S.H. are employed by ViroLogic, Inc., which developed the phenotypic assay described.
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ISSN:0022-1899
1537-6613
DOI:10.1086/315686