Related Experiment Video
Updated: Jul 10, 2026

14:23
A Restriction Enzyme Based Cloning Method to Assess the In vitro Replication Capacity of HIV-1 Subtype C Gag-MJ4 Chimeric Viruses
Published on: August 31, 2014
Plasma viral load threshold for sustaining intrahost HIV type 1 evolution.
Gonzalo Bello1, Concepción Casado, Virginia Sandonis
1Laboratorio de AIDS e Imunologia Molecular, Instituto Oswaldo Cruz, FIOCRUZ, Rio de Janeiro, Brazil.
AIDS Research and Human Retroviruses
|October 27, 2007
Summary
Persistent low plasma viremia below 80 copies/ml may halt human immunodeficiency virus type 1 (HIV-1) evolution. This finding suggests ultrasensitive assays can identify a threshold for containing HIV-1 genetic diversity.
Area of Science:
- Virology
- Immunology
- Genetics
Background:
- Long-term nonprogressors (LTNPs) naturally control human immunodeficiency virus type 1 (HIV-1) replication.
- Understanding the factors that prevent HIV-1 evolution in LTNPs is crucial for developing effective treatment strategies.
Purpose of the Study:
- To investigate whether natural suppression of plasma viremia below commercial assay detection limits (50-80 copies HIV-1 RNA/ml) can inhibit HIV-1 evolution.
- To assess the correlation between plasma viral load and intrahost HIV-1 genetic diversity in LTNPs.
Main Methods:
- Assessed HIV-1 quasispecies complexity in peripheral blood mononuclear cell (PBMC) DNA (env gene) at two time points.
- Analyzed plasma HIV-1 RNA viral loads in 14 LTNPs with varying degrees of viremia control.
Main Results:
- Viral evolution was observed in all patients with median plasma viral loads >100 copies/ml.
- Low-level viral evolution was detected in patients with intermittent viremia (>80 copies/ml).
- No significant evolution occurred in LTNPs with persistent viral suppression (<50-80 copies/ml).
- A significant positive correlation (p < 0.001) was found between viral evolution and plasma viral load.
Conclusions:
- Persistent plasma viremia below the detection limit of ultrasensitive assays may prevent intrahost HIV-1 evolution.
- The detection limit of ultrasensitive viremia assays could be a critical threshold for containing HIV-1 genetic diversity.
More Related Videos
Related Concept Videos
Viral Mutations
A mutation is a change in the sequence of bases of DNA or RNA in a genome. Some mutations occur during replication of the genome due to errors made by the polymerase enzymes that replicate DNA or RNA. Unlike DNA polymerase, RNA polymerase is prone to errors because it is not capable of “proofreading” its work. Viruses with RNA-based genomes, like HIV, therefore accrue mutations faster than viruses with DNA-based genomes. Because mutation and recombination provide the raw material for adaptive...
Size and Structure of Viral Genomes
Viral genomes exhibit remarkable diversity in size, structure, and composition, influencing their replication strategies and interactions with host cells. These genomes consist of either DNA or RNA and may be linear or circular. Additionally, they can be single-stranded or double-stranded, with each configuration affecting how the virus propagates within a host. RNA viruses, for instance, generally have smaller genomes than DNA viruses, a factor that contributes to their high mutation rates and...
Retrovirus Life Cycles
Retroviruses have a single-stranded RNA genome that undergoes a special form of replication. Once the retrovirus has entered the host cell, an enzyme called reverse transcriptase synthesizes double-stranded DNA from the retroviral RNA genome. This DNA copy of the genome is then integrated into the host’s genome inside the nucleus via an enzyme called integrase. Consequently, the retroviral genome is transcribed into RNA whenever the host’s genome is transcribed, allowing the retrovirus to...

