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Updated: Jun 3, 2026

Amplification of Near Full-length HIV-1 Proviruses for Next-Generation Sequencing
Published on: October 16, 2018
PCR Amplification and Cloning of Virtually Full-Length HIV-1 Provirus
1Department of Chronic Virus Diseases, National Public Health Institute, Helsinki, Finland.
Abstract:
Molecular analyses of HIV-1 variation, and its impact on the biological properties of the virus have by necessity been restricted by the scarcity of cloned proviruses. Only a handful of full-length clones exist (1), and of these, even a smaller fraction are infectious upon transfection into cell lines. Furthermore, the available infectious clones only represent subtypes B and D (1). The main reasons for the lack of infectious clones are related to the relatively low copy number of proviral DNA especially in primary cultures (8).
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