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Journal of Clinical Microbiology, January 2000, p. 402-405, Vol. 38, No. 1
HIV and Retrovirology Branch, Division of
AIDS, STD, and TB Laboratory Research, National Center for Infectious
Diseases, Centers for Disease Control and Prevention, Atlanta,
Georgia1; Servicio de Enfermedades
Infecciosas, Hospital Carlos III, Instituto de Salud Carlos III,
Madrid, Spain2; and Division of
Infectious Diseases, Department of Medicine, Case Western Reserve
University, Cleveland, Ohio3
Received 11 May 1999/Returned for modification 2 August
1999/Accepted 21 September 1999
We have evaluated the use of an ultrasensitive reverse
transcriptase (RT) activity assay to monitor plasma viremia in two human immunodeficiency virus type 1 (HIV-1) group O-infected patients treated with stavudine, lamivudine, and indinavir. After a initial decline in RT levels observed at 4 weeks of therapy, RT-based plasma
viremia returned to baseline values at 28 or 44 weeks of treatment. The
rebound in levels of RT activity was associated with the detection of
phenotypic resistance to lamivudine and with the Met184Val mutation.
Analysis of RT activity in plasma provides a sequence-independent means
of monitoring virus loads in HIV-1 group O-infected patients.
0095-1137/0/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Quantitation of Human Immunodeficiency Virus Type 1 Group O Load
in Plasma by Measuring Reverse Transcriptase Activity

*
Corresponding author. Mailing address: HIV and
Retrovirology Branch, Centers for Disease Control and Prevention, 1600 Clifton Rd., N.E., MS G-19, Atlanta, GA 30333. Phone: (404) 639-0218. Fax: (404) 639-1174. E-mail: wmh2{at}cdc.gov.
Present address: Centro de Biología Molecular "Severo
Ochoa" (CSIC-UAM), Universidad Autónoma de Madrid, Madrid, Spain.
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