Trick identified that aids viral infection
Date:
January 30, 2014
Source:
Washington University in St. Louis
Summary:
Scientists
have identified a way some viruses protect themselves from the immune
system’s efforts to stop infections, a finding that may make new
approaches to treating viral infections possible.
Scientists
have discovered a defense system — built into some viruses — that may
be vulnerable to treatment. The researchers studied alphaviruses similar
to the Eastern equine encephalitis virus, pictured above in red. This
virus is transmitted to humans and horses by mosquito bites.
Credit: Fred Murphy, Sylvia Whitfield/CDC
Scientists
have identified a way some viruses protect themselves from the immune
system's efforts to stop infections, a finding that may make new
approaches to treating viral infections possible.
Viruses
have well-known strategies for slipping past the immune system. These
include faking or stealing a molecular identification badge that
prevents a cell from recognizing a virus.
Scientists at Washington University School of Medicine in St. Louis and elsewhere have found some viruses have another trick. They can block the immune system protein that checks for the identification badge.
The blocking structure is called a stem-loop, found at the beginning of the virus's genetic material. This is the first time scientists have found an immune-fighting mechanism built directly into the genetic material of a virus. They are looking for ways to disable it and searching for similar mechanisms that may be built into the genetic material of other disease-causing microorganisms.
"When the stem-loop is in place and stable, it blocks a host cell immune protein that otherwise would bind to the virus and stop the infectious process," said senior author Michael Diamond, MD, PhD, professor of medicine. "We found that changing a single letter of the virus's genetic code can disable the stem-loop's protective effects and allow the virus to be recognized by the host immune protein. We hope to find ways to weaken the stem-loop structure with drugs or other treatments, restoring the natural virus-fighting capabilities of the cell and stopping or slowing some viral infections."
Most life forms encode their genes in DNA. To use the instructions contained in DNA, though, cells have to translate them into a related genetic material, RNA, that can be read by a cell's protein-making machinery.
Some viruses encode their genes directly in RNA. Examples include West Nile virus and influenza virus, and the viruses that cause sudden acute respiratory syndrome (SARS), yellow fever and polio.
When a virus infects a cell, it co-opts the cell's protein-making machinery to make viral proteins. These proteins allow the virus to replicate. Copies of the virus break into other cells, repeat the process, and the infection spreads.
The researchers studied alphaviruses, a group of RNA viruses that cause fever, encephalitis and infectious arthritis. They showed that a single-letter change in the RNA of an alphavirus strengthened the stem-loop. When the structure was stable, a key immune system protein called Ifit1 was blocked from binding to the viral RNA and the infection continued unchecked. But when the stem-loop was unstable, Ifit1 would bind to the viral RNA and disable it, stopping the infectious process.
"Knowing about this built-in viral defense mechanism gives us a new opportunity to improve treatment of infection," Diamond said. "To control emergent infections, we must continue to look for ways that viruses have antagonized our natural defense mechanisms and discover how to disable them."
Scientists at Washington University School of Medicine in St. Louis and elsewhere have found some viruses have another trick. They can block the immune system protein that checks for the identification badge.
The blocking structure is called a stem-loop, found at the beginning of the virus's genetic material. This is the first time scientists have found an immune-fighting mechanism built directly into the genetic material of a virus. They are looking for ways to disable it and searching for similar mechanisms that may be built into the genetic material of other disease-causing microorganisms.
"When the stem-loop is in place and stable, it blocks a host cell immune protein that otherwise would bind to the virus and stop the infectious process," said senior author Michael Diamond, MD, PhD, professor of medicine. "We found that changing a single letter of the virus's genetic code can disable the stem-loop's protective effects and allow the virus to be recognized by the host immune protein. We hope to find ways to weaken the stem-loop structure with drugs or other treatments, restoring the natural virus-fighting capabilities of the cell and stopping or slowing some viral infections."
Most life forms encode their genes in DNA. To use the instructions contained in DNA, though, cells have to translate them into a related genetic material, RNA, that can be read by a cell's protein-making machinery.
Some viruses encode their genes directly in RNA. Examples include West Nile virus and influenza virus, and the viruses that cause sudden acute respiratory syndrome (SARS), yellow fever and polio.
When a virus infects a cell, it co-opts the cell's protein-making machinery to make viral proteins. These proteins allow the virus to replicate. Copies of the virus break into other cells, repeat the process, and the infection spreads.
The researchers studied alphaviruses, a group of RNA viruses that cause fever, encephalitis and infectious arthritis. They showed that a single-letter change in the RNA of an alphavirus strengthened the stem-loop. When the structure was stable, a key immune system protein called Ifit1 was blocked from binding to the viral RNA and the infection continued unchecked. But when the stem-loop was unstable, Ifit1 would bind to the viral RNA and disable it, stopping the infectious process.
"Knowing about this built-in viral defense mechanism gives us a new opportunity to improve treatment of infection," Diamond said. "To control emergent infections, we must continue to look for ways that viruses have antagonized our natural defense mechanisms and discover how to disable them."
Story Source:
The above story is based on materials provided by Washington University in St. Louis. The original article was written by Michael C. Purdy. Note: Materials may be edited for content and length
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