Frog peptides block HIV in lab study
(30 September 2005: VIDYYA MEDICAL NEWS SERVICE) -- A new weapon in the battle against HIV may come from an unusual source -- a small tropical frog.
Investigators at Vanderbilt University Medical Center reported this month in the Journal of Virology that compounds secreted by frog skin are potent blockers of HIV infection.
The findings could lead to topical treatments for preventing HIV transmission, and they reinforce the value of preserving the Earth's biodiversity.
"We need to protect these species long enough for us to understand their medicinal cabinet," said Louise A. Rollins-Smith, Ph.D., associate professor of Microbiology & Immunology, who has been studying the antimicrobial defenses of frogs for about six years. Frogs, she explained, have specialized granular glands in the skin that produce and store packets of peptides, small protein-like molecules. In response to skin injury or alarm, the frog secretes large amounts of these antimicrobial peptides onto the surface of the skin to combat pathogens like bacteria, fungi and viruses.
Rollins-Smith happens to have the laboratory next door to Derya Unutmaz, M.D., associate professor of Microbiology & Immunology. During a hallway chat one day, the two decided it would be interesting to investigate whether any frog peptides have activity against human viruses, specifically HIV, the focus of Unutmaz's group.
Postdoctoral fellow Scott E. VanCompernolle, Ph.D., screened 15 antimicrobial peptides from a variety of frog species for their ability to block HIV infection of T cells, immune system cells targeted by HIV. He found several that inhibited HIV infection without harming the T cells.
The peptides appear to selectively kill the virus, perhaps by inserting themselves into the HIV outer membrane envelope and creating "holes" that cause the virus particle to fall apart, Unutmaz said.
"We like to call these peptides WMDs -- weapons of membrane destruction," Unutmaz said. It is curious that the antimicrobial peptides do not harm the T cells at concentrations that are effective against the virus, he noted, since HIV's outer membrane is derived from, and therefore essentially identical to, the cellular membrane. The investigators have proposed that the peptides act selectively on the virus in part because of its small size relative to cells.
The ability of the peptides to destroy HIV was enticing, but to be really effective as antimicrobial agents, they need to prevent transmission of HIV from dendritic cells to T cells, Unutmaz said.
Dendritic cells, he explained, are the sentinels of the immune system. They hang out in the mucosal surface tissues, scanning for invading pathogens.
"Their purpose in life is to capture the enemy, bring it to the lymph node -- the command center -- and present it to the general, the T cell, to activate a battle plan," Unutmaz said. "It's a very efficient system that has allowed us to survive many insults, pathogens and viruses."
But HIV is a wily foe. When it is picked up at the mucosal surface by a sentinel dendritic cell, it somehow evades destruction. Instead, it hides inside the cell, waiting to invade the T cell with a Trojan Horse-like mechanism. The ability of HIV to remain hidden in the dendritic cell, avoiding destruction by circulating antibodies and immune system cells, "may explain why after 20 years we don't have a vaccine for this virus," Unutmaz said.
To test the effectiveness of the frog peptides in preventing HIV transmission, VanCompernolle first allowed cultured dendritic cells to capture active HIV. He then incubated the HIV-harboring dendritic cells with antimicrobial peptides, washed the peptides away, and added T cells.
"Normally the dendritic cell passes the virus to the T cell, and we get very efficient infection of the T cell," Unutmaz said. "But when we treated the dendritic cells with peptides, the virus was gone, completely gone.
"This was a great surprise."
The finding was puzzling, he added, since the prevailing notion is that HIV captured by dendritic cells is hidden and protected. The investigators currently are using imaging technologies to test the hypothesis that HIV is actually cycling to the dendritic cell surface.
"We think maybe it's popping its head out, looking around for a T cell, and then going back inside to hide until it cycles out again," Unutmaz said. If peptide is present outside the cell, "it targets the virus that pops up and kills it." Preliminary experiments suggest that the hypothesis is correct.
"This is very exciting, as it suggests that these peptides could be very effective since the virus now has nowhere to hide," Unutmaz said. "And if this cycling is really happening, we may be able to generate a vaccine that will target virus captured by dendritic cells."
The frog peptides are an exceptional tool for probing "what the virus knows about the dendritic cell that we don't know," Unutmaz added. "How does HIV manage to survive and cycle back and forth to the cell membrane? If we can understand that, we'll find the gaps, and that will open a whole new universe of targets for intervention."
The investigators learned this week that the American Foundation for AIDS Research will fund their continuing quest to understand how the frog peptides kill HIV in dendritic cells. Their plans include imaging how the peptides work, screening additional frog peptides for activity, and testing peptides on a mucosal cell system to study the feasibility of developing them as prophylactics against HIV infection.
"If we are able to learn the mechanisms these peptides are using to kill HIV, it might be possible to make small chemical molecules that achieve the same results," Unutmaz said. Such chemicals would be more practical as therapeutic microbicides, he said. "This study is a great example of how collaboration across disciplines leads to big discoveries," Unutmaz said.
Other members of the Department of Microbiology and Immunology assisted the investigators by providing viruses for testing. The team found that membrane-coated viruses were susceptible to destruction by the frog peptides, but non-coated viruses, such as reovirus and adenovirus, were not affected.
R. Jeffery Taylor, Ph.D., Kyra Oswald-Richter, Ph.D., Jiyang Jiang, Ph.D., Bryan E Youree, M.D., Christopher R. Aiken, Ph.D., and Terence S. Dermody, M.D., at Vanderbilt are co-authors of the study. The research was supported by the National Institutes of Health, the Elizabeth B. Lamb Center for Pediatric Research, and the National Science Foundation.
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