A polymerase chain reaction method for the amplification of full-length envelope genes of HIV-1 from DNA samples containing single molecules of HIV-1provirus

Citation
P. Mcclure et al., A polymerase chain reaction method for the amplification of full-length envelope genes of HIV-1 from DNA samples containing single molecules of HIV-1provirus, J VIROL MET, 88(1), 2000, pp. 73-80
Citations number
21
Categorie Soggetti
Microbiology
Journal title
JOURNAL OF VIROLOGICAL METHODS
ISSN journal
01660934 → ACNP
Volume
88
Issue
1
Year of publication
2000
Pages
73 - 80
Database
ISI
SICI code
0166-0934(200007)88:1<73:APCRMF>2.0.ZU;2-C
Abstract
Polymerase chain reaction (PCR) amplification of full-length envelope genes from the human immunodeficiency virus type 1 (HIV-1) directly from uncultu red clinical samples is difficult. This paper describes a comparative asses sment of the performance of three thermostable polymerases in an HIV-1 full -length envelope gene PCR. The PCR method utilising Expand HiFi polymerase was successful when using DNA samples extracted from a variety of sources i ncluding blood, semen and various tissues. This method generated high and s pecific yields of product from samples containing as little as one copy of HIV-1 proviral DNA. The resulting PCR products were suitable for a variety of downstream analytical methods including DNA sequence analysis. (C) 2000 Elsevier Science B.V. All rights reserved.