Probe detects staph infection faster, more cheaply
Date: Feb-03-2014Currently, to test if patients are infected with Staphylococcus bacteria,
commonly known as staph, doctors have to take a biopsy and send it for analysis. Now, researchers
from the University of Iowa have developed an ingenious noninvasive chemical probe
that can detect the presence of a common species of staph in less than an hour.
The probe specifically targets Staphylococcus aureus, a species of staph that is
common both inside hospitals and out in the general community. This species causes skin
infections, and it can spread to the joints and bones and is potentially fatal, particularly in
patients whose immune systems are already weak.
To design the probe, the team made use of the fact S. aureus shreds DNA. They
exploited this feature to make the probe emit a light, which signals to doctors that the
bacterium is present.
Speaking about their study, published in the journal Nature Medicine, first author
and post-doctoral researcher Frank Hernandez says:
"Every year in the US half a million people become infected by S. aureus bacteria, and
20,000 of those who become infected die. We believe that we are significantly improving the
actual methods for detecting bacteria with a simple approach, which we expect to be cheap, fast
and reliable."
Corresponding author James McNamara, assistant professor in internal medicine, adds:
"We've come up with a new way to detect staph bacteria that takes less time than current
diagnostic approaches. It builds on technology that's been around a long time, but with an
important twist that allows our probe to be more specific and to last longer."
Currently, it can take days for doctors to find out if a patient is infected with staph, as
they have to wait for lab results of biopsies. Prof. McNamara says they are "flying blind," and
that it is "the state of medicine at this time."
Probe made of two molecules
The ingenious design of the probe hinges on a unique feature. It is a particle made of two
molecules. One molecule gives off light under certain conditions, and the other molecule blocks that light.
Staph shreds DNA, so the researchers
exploited this feature to make the probe emit a light, which signals to doctors that the
bacterium is present.
As long as the particle stays whole - that is with the light-giving and the light-canceling
molecules attached to each other - then no light is given off.
But if the particle is split,
thus allowing the molecules to go their separate ways, then the light-giving molecule is not
blocked and starts to give off light.
This unique feature is what makes it so useful. When the staph bacterium encounters the
particle, it starts slashing at it like it does with DNA.
It cleaves it in half, releasing
the light-emitting molecule from its light-blocking partner, allowing it to shine and give away the
fact staph is present in the tissue.
The idea is doctors could administer the probe and, with the right equipment, see if it lights up in the infected tissue, to test if staph is present.
Probe uniquely and quickly detects staph
The researchers are not sure why staph behaves as aggressively as it does. They think it could be because it has developed this
as the only way to tackle the sticky environment that DNA creates when it leaks out of infected,
dying cells.
The idea of the chemical probe is not new, but what is new is that this team has produced
one that lasts longer and identifies staph quickly, as Dr. Hernandez explains:
The "sword" that staph wields to shred the DNA is an enzyme called nuclease. Normal healthy
tissue cells have a type of this enzyme as well, but the team has developed the probe so that
only the staph nuclease attacks it and not the normal tissue cells.
They have so far tested it in human serum and mice with muscle infections and found it worked
as they expected. Healthy normal cells did not cleave the probe particle.
Prof. McNamara says this showed the key feature of their chemical probe:
"If the probe gets cleaved by serum nucleases, then our probe would be lit up all over the
bloodstream. But since it's split only by staph nucleases, then we can pinpoint where the staph
bacteria are active."
He and his colleagues, who have already filed a final US patent for the probe, now plan to
fine-tune it for use deeper inside the body. They also want to test how well it works with
catheter infections.
Funds from the National Institutes of Health and the American Heart Association helped
finance the study.
In another study, published in Science in November 2013, researchers at the
University of Chicago revealed how staph circumvents the immune
system and showed that a mutation in the bacterium's nuclease was involved.
Written by Catharine Paddock PhD
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