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Related Concept Videos

Retrovirus Life Cycles01:10

Retrovirus Life Cycles

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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...
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Updated: Aug 13, 2025

Amplifying and Quantifying HIV-1 RNA in HIV Infected Individuals with Viral Loads Below the Limit of Detection by Standard Clinical Assays
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Insights into HIV-1 Transmission Dynamics Using Routinely Collected Data in the Mid-Atlantic United States.

Seble G Kassaye1, Zehava Grossman2,3, Priyanka Vengurlekar1

  • 1Department of Medicine, Georgetown University, Washington, DC 20057, USA.

Viruses
|January 21, 2023
PubMed
Summary
This summary is machine-generated.

Molecular epidemiology of HIV sequences and viral load data reveals transmission clusters. Combining phylogenetic analysis with viral load data enhances HIV contact tracing and prevention efforts.

Keywords:
HIV drug resistanceclinical and phylogenetic data combinedcontact tracing toolmolecular epidemiologyphylogenetic analysisregional transmission dynamicstransmission networks

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Area of Science:

  • Molecular epidemiology
  • Virology
  • Public Health

Background:

  • Molecular epidemiology offers insights into HIV transmission dynamics.
  • Routine clinical data can be leveraged for epidemiological studies.
  • Understanding transmission patterns is crucial for public health interventions.

Purpose of the Study:

  • To assess the utility of analyzing HIV sequences and viral load (VL) data from routine clinical care for characterizing HIV transmission.
  • To identify HIV transmission clusters using phylogenetic methods.
  • To evaluate the combined utility of phylogenetic inference and VL data for enhanced contact tracing.

Main Methods:

  • HIV-1 pol sequences were analyzed using phylogenetic methods (ClustalW, REGA, IQTree, ClusterPicker, BEAST).
  • Transmission clusters were defined by genetic distance (≤3%) and bootstrap support (≥90%).
  • Early HIV infection was indicated by nucleotide ambiguity (≤0.5%).
  • Descriptive statistics and comparative tests (chi-square, t-test) were used.

Main Results:

  • Analysis of 2775 adults (2014-2015) revealed 193 HIV transmission clusters involving 456 individuals.
  • Cluster members were more likely to be male, younger, and have early-stage HIV infection compared to non-cluster individuals.
  • A significant proportion of clusters (22.3%) spanned multiple jurisdictions.
  • Individuals in larger clusters (≥4) and those not in clusters showed higher viral loads compared to individuals in smaller clusters (2-3).

Conclusions:

  • HIV sequence data from clinical care provide valuable insights into regional transmission dynamics.
  • Integrating HIV-1 VL data with phylogenetic analysis enhances contact tracing effectiveness.
  • Trans-jurisdictional collaboration is essential for optimizing HIV prevention and control strategies to end the epidemic.