First-ever video reveals how HIV spreads
March 27th, 2009 - 4:42 pm ICT by ANIWashington, Mar 27 (ANI): A team of researchers at Mount Sinai School of Medicine and the UC Davis Center for Biophotonics Science and Technology has made a breakthrough in understanding how HIV spreads through the human body after capturing the process on camera.
Researchers have recorded the transfer of human immunodeficiency virus (HIV) from infected to uninfected T cells through structures called virological synapses.
The breakthrough study could lead to new methods to block the transmission of HIV, and shows that cell-to-cell may be the predominant mode of HIV transmission in the body.
The research has been published in the March 27 edition of Science.
“Most prior studies of HIV dissemination have focused on free roaming viruses, but this study shows us how direct T cell-to-T cell contact could in fact be the predominant mode of dissemination within the body,” said Dr. Benjamin Chen, Assistant Professor of Medicine, Infectious Diseases, Mount Sinai School of Medicine.
“Direct T cell-to-T cell transfer through virological synapses is a highly efficient avenue of HIV infection. Our recent experiments show that the viral structural protein moves with surprising speed in infected cells and that the cell machinery actively participates in the transport of virus between T cells. This suggests there are many targets for interfering with the process,” said Dr. Chen.
In order to make the HIV virus visible to track on video from cell to cell, researchers at Mount Sinai created a molecular clone of infectious HIV that contains green fluorescent jellyfish protein. With the team at UC Davis, they then used quantitative, high-speed 3D video microscopy to record both viral particle formation and transmission of the virus between T cells.
The resulting images and videos show that, once an infected cell adheres to a healthy cell, the HIV proteins - which appear bright green in the study - migrate within minutes to the contact site. At that point, large packets of virus are simultaneously released by the infected cell and internalized by the recipient cell. This efficient mode of transfer is a distinct pathway from the cell-free infection that has been the focus of most prior HIV studies, and reveals another mechanism by which the virus evades immune responses that can neutralize free virus particles within the body.
“We found that the transfer of HIV is highly coordinated between T cells, and that the transfer is rapid and massive,” said Dr. Chen.
“Future efforts to block HIV transmission may be designed to specifically exploit and block this cell-to-cell mode of infection,” the expert added. (ANI)
- Mechanism T cells use to block HIV discovered - May 18, 2010
- Cellular protein that acts as receptor for Ebola virus identified - May 03, 2011
- Complete structure of HIV's outer shell revealed - Jan 20, 2011
- How 'silent HIV virus' attacks immune system - Sep 21, 2010
- Human trials under way for new HIV vaccine - Jan 03, 2012
- New compound destroys deadly flu virus - Sep 26, 2011
- New research could 'protect newborn babies from HIV infection' - Oct 04, 2010
- Non-stick protein coating in semen cuts HIV infection - Sep 24, 2010
- How interferon-induced genes launch antiviral defenses - Apr 11, 2011
- Target to inhibit HIV infectivity identified - Jan 05, 2010
- Compound that halts poxvirus replication - Jan 04, 2012
- Why retroviruses like HIV get easily acquainted with uninfected neighbours - Jul 28, 2009
- How specific viruses can kill cancer cells - Dec 02, 2010
- Virus that piggybacks on AIDS virus to beat disease developed - Mar 28, 2011
- Fancy a tattoo? Beware of hepatitis virus (July 28 is World Hepatitis Day) - Jul 28, 2011
Tags: breakthrough study, dr benjamin, dr chen, hiv infection, hiv proteins, hiv transmission, hiv virus, human immunodeficiency virus, immunodeficiency virus hiv, infectious hiv, mount sinai school, mount sinai school of medicine, particle formation, predominant mode, speed 3d, t cells, transmission of hiv, uc davis, video microscopy, viral particle