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Related Concept Videos

Inhibitors Of Virion Release01:25

Inhibitors Of Virion Release

Viral replication and dissemination rely on efficient mechanisms for host cell entry, genome replication, assembly, and release. Influenza viruses, such as types A and B, are negative-sense single-stranded RNA viruses with a segmented genome, that depend on two critical surface glycoproteins to carry out these processes: hemagglutinin (HA) and neuraminidase (NA). HA initiates infection by binding to sialic acid residues on the surface of host epithelial cells, facilitating receptor-mediated...
Inhibitors of Virion Maturation and Assembly01:19

Inhibitors of Virion Maturation and Assembly

As part of their replication cycle, certain viruses synthesize long precursor proteins called polyproteins within infected host cells. In human immunodeficiency virus (HIV), two major polyproteins are produced: Gag and Gag-Pol. The Gag polyprotein supplies the structural components of the virus, while Gag-Pol includes essential viral enzymes such as reverse transcriptase, integrase, and protease. After synthesis, these polyproteins move to the host cell membrane, where they assemble into an...
Retrovirus Life Cycles01:10

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...
Inhibitors of Viral Protein Synthesis01:30

Inhibitors of Viral Protein Synthesis

Protein synthesis is indispensable for viral replication, as viruses lack the cellular machinery required for this process and must hijack the host's translational apparatus. In response, host cells deploy a critical innate immune defense involving interferons, specialized cytokines that play a central role in inhibiting viral propagation.Upon viral detection, infected cells release interferons that bind to receptors on adjacent uninfected cells, activating the JAK-STAT signaling pathway and...
Immune Response Against Viral Pathogens01:29

Immune Response Against Viral Pathogens

The immune system's response to viral infections is a complex and coordinated process involving natural killer (NK) cells, T cell-mediated responses, and antibody-mediated responses.
NK Cells
NK cells are a crucial part of our innate immune system, acting as the first line of defense against viral infections. These cells can recognize and kill infected cells without prior exposure to the virus, effectively slowing down the spread of infection. Additionally, NK cells produce proinflammatory...
Retroviruses02:33

Retroviruses

Retroviruses and retrotransposons both insert copies of their genetic elements into the genome of the host cell. Thus, the viral genes are passed on when the host genome is replicated or translated. A typical retroviral DNA sequence contains 3-4 genes that encode the different proteins required for its structural assembly and function as a molecular parasite. This DNA is transcribed into a single mRNA, which is very similar in structure to conventional mRNAs, i.e., it is capped at the 5’...

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Related Experiment Video

Updated: Jun 18, 2026

Single-cell Quantitation of mRNA and Surface Protein Expression in Simian Immunodeficiency Virus-infected CD4+ T Cells Isolated from Rhesus macaques
13:13

Single-cell Quantitation of mRNA and Surface Protein Expression in Simian Immunodeficiency Virus-infected CD4+ T Cells Isolated from Rhesus macaques

Published on: September 25, 2018

Viruses within the Flaviviridae decrease CD4 expression and inhibit HIV replication in human CD4+ cells.

Jinhua Xiang1, James H McLinden, Robert A Rydze

  • 1Department of Internal Medicine, Iowa City Veterans Affairs Medical Center and University of Iowa, Iowa City, IA 52242, USA.

Journal of Immunology (Baltimore, Md. : 1950)
|November 20, 2009
PubMed
Summary
This summary is machine-generated.

Flavivirus NS5 proteins, including from Dengue and Yellow Fever viruses, inhibit HIV replication by reducing CD4 gene expression. This discovery may offer new therapeutic strategies for HIV and immune diseases.

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In Vitro Assay to Evaluate the Impact of Immunoregulatory Pathways on HIV-specific CD4 T Cell Effector Function
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A Restriction Enzyme Based Cloning Method to Assess the In vitro Replication Capacity of HIV-1 Subtype C Gag-MJ4 Chimeric Viruses
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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

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Last Updated: Jun 18, 2026

Single-cell Quantitation of mRNA and Surface Protein Expression in Simian Immunodeficiency Virus-infected CD4+ T Cells Isolated from Rhesus macaques
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Single-cell Quantitation of mRNA and Surface Protein Expression in Simian Immunodeficiency Virus-infected CD4+ T Cells Isolated from Rhesus macaques

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In Vitro Assay to Evaluate the Impact of Immunoregulatory Pathways on HIV-specific CD4 T Cell Effector Function
09:26

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A Restriction Enzyme Based Cloning Method to Assess the In vitro Replication Capacity of HIV-1 Subtype C Gag-MJ4 Chimeric Viruses
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

Area of Science:

  • Virology
  • Immunology
  • Molecular Biology

Background:

  • Viral coinfections can alter host cell functions, impacting immune evasion and microbial replication.
  • Certain flaviviruses, like Dengue virus (DV) and GB virus type C (GBV-C), are linked to reduced HIV replication and improved survival in HIV-infected individuals.

Purpose of the Study:

  • To investigate if the inhibitory effect on HIV replication is conserved across various flaviviruses.
  • To characterize the mechanisms by which flaviviruses, specifically their NS5 proteins, inhibit HIV replication.

Main Methods:

  • Expression of NS5 proteins from GBV-C, DV, Hepatitis C virus, West Nile virus, and Yellow Fever virus (YFV) in CD4(+) T cells.
  • Infection of CD4(+) T cells and macrophages with YFV (17D vaccine strain).
  • Measurement of HIV replication, CD4 mRNA levels, and cell surface CD4 protein expression.

Main Results:

  • All tested flavivirus NS5 proteins inhibited HIV replication in CD4(+) T cells.
  • This inhibition correlated with decreased steady-state CD4 mRNA and reduced cell surface CD4 protein expression.
  • YFV infection also inhibited HIV replication and decreased CD4 gene expression in relevant cell types.

Conclusions:

  • Flavivirus NS5 proteins consistently decrease CD4 gene expression.
  • Flavivirus-mediated CD4 regulation may impact innate and adaptive immunity, contributing to HIV replication inhibition.
  • Understanding these mechanisms could lead to novel therapeutic strategies for HIV and immunological disorders.