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Journal of Clinical Microbiology, August 1998, p. 2349-2352, Vol. 36, No. 8
Departments of
Microbiology,1
Comparative
Medicine,2
Pediatrics,3
Epidemiology,4 and
Medicine,6 University of Washington,
Seattle, Washington 98195, and
Department of Medical
Microbiology, University of Nairobi, Kenya5
Received 30 December 1997/Returned for modification 27 April
1998/Accepted 13 May 1998
An efficient method for the isolation of human immunodeficiency
virus type 1 (HIV-1) nucleic acids from dry cervical swabs was
developed. HIV-1 gag and env were detected in
96% (25 of 26) and 81% (21 of 26), respectively, of the samples
tested by PCR from HIV-1-seropositive women in a Kenyan cohort study.
Eighty-eight percent of the swabs (22 of 25) were positive for
gag RNA, and 85% (17 of 20) were positive for
env RNA. Fewer than 1,000 copies of HIV-1 gag
RNA were detected in four swabs in which a competitive quantitative PCR
assay was used. The method described here may be useful for both
qualitative and quantitative analyses of HIV RNA in mucosal secretions
as well as amplification and cloning of full-length viral genes for
functional studies.
0095-1137/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Efficient Isolation of Human Immunodeficiency Virus
Type 1 RNA from Cervical Swabs

*
Corresponding author. Mailing address: Dept. of
Microbiology, University of Washington, Seattle, WA 98195. Phone: (206)
543-3146. Fax: (206) 543-8297. E-mail:
overbaug{at}u.washington.edu.
Present address: Department of Pediatrics, Oregon Health Sciences
University, Portland, OR 97201.
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