Literature DB >> 25681527

Single genome amplification and standard bulk PCR yield HIV-1 envelope products with similar genotypic and phenotypic characteristics.

Behzad Etemad1, Melissa Ghulam-Smith1, Oscar Gonzalez1, Laura F White2, Manish Sagar3.   

Abstract

Recent studies suggest that single genome amplification (SGA) as compared to standard bulk PCR and virus stocks from 293T transfection versus short term passage in peripheral blood mononuclear cells (PBMC) yield a less biased representation of HIV-1 envelope characteristics. In 9 different subjects, genetic diversity, divergence, and population structure were not significantly different among SGA or bulk PCR amplified envelope V1-V3 segments. In these subjects, 293T transfection derived virus stocks with SGA or bulk PCR amplified envelopes have similar infectivity, replication kinetics, co-receptor usage, and neutralization susceptibility. While PBMC passage as compared to the 293T derived virus stocks had similar co-receptor usage, PBMC viruses were less neutralization susceptible to some specific antibodies. Our results suggest that the method of envelope sequence amplification, either SGA or bulk PCR, does not have a significant impact on the genotypic and phenotypic properties of the virus envelope quasispecies.
Copyright © 2015 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Diversity; Envelope; HIV-1; Neutralization; Replication; Single genome amplification

Mesh:

Substances:

Year:  2015        PMID: 25681527      PMCID: PMC4394631          DOI: 10.1016/j.jviromet.2015.01.006

Source DB:  PubMed          Journal:  J Virol Methods        ISSN: 0166-0934            Impact factor:   2.014


  36 in total

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