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Certainly there is strength in numbers, but only if those numbers can
effectively communicate with one another. Now, a new study finds that
administration of a novel small molecule which effectively disrupts a
key bacterial communication process protects an animal host from
infection. The research, published in the July 31st issue of the journal
Molecular Cell, may lead to more effective treatments for bacterial infection that won't encourage growth of treatment resistant bacteria.
Bacteria use a process called "quorum sensing" to communicate
information about population density and to synchronously engage in
group behaviors that promote bacterial pathogenesis. "Quorum sensing
allows bacteria to collectively carry out tasks that would be
unsuccessful if carried out by an individual bacterium acting alone,"
explains senior study author Dr. Bonnie L. Bassler from the Howard
Hughes Medical Institute and the Department of Molecular Biology at
Princeton University.
During the process of quorum sensing, bacteria communicate via
chemical signals called autoinducers. Autoinducers bind to receptors,
called LuxR-type proteins, located inside the bacteria, or to receptors
called LuxN proteins located in the bacterial membrane. In an earlier
study, Dr. Bassler and colleagues discovered a class of small molecules
that prevented a key autoinducer called acylhomoserine lactone (AHL)
from binding to LuxN. Although LuxN and LuxR are not structurally
similar, Dr. Bassler's team hypothesized that since both bind to AHLs,
both may respond to the small molecule antagonists.
In the current study, the researchers demonstrated that the small
molecule previously shown to block LuxN-type receptors is also a potent
antagonist of LuxR receptors. This finding was somewhat surprising as
these proteins are not evolutionarily related and exhibit vast
differences in receptor localization, structure and signaling
mechanisms. Importantly, the most potent antagonist protected nematode
worms from quorum sensing-mediated killing by Chromobacterium violaceum,
a human pathogen that frequently infects people through lacerated skin.
"Our results make a strong case and provide compelling evidence that
an anti-quorum-sensing strategy is a valid alternative to traditional
antibiotics and that there is merit to pursuing the clinical relevance
of such strategies," offers Dr. Bassler. The work is also significant in
that treatments based on disruption of quorum sensing interfere only
with bacterial signaling and not growth, potentially minimizing the
sometimes devastating development of bacteria that are resistant to
treatment.
The researchers include Lee R. Swem, Princeton University, Princeton,
NJ, Howard Hughes Medical Institute, Chevy Chase, MD; Danielle L. Swem,
Princeton University, Princeton, NJ, Howard Hughes Medical Institute,
Chevy Chase, MD; Colleen T. O'Loughlin, Princeton University, Princeton,
NJ, Ithaca College, Ithaca, NY; Raleene Gatmaitan, Ithaca College,
Ithaca, NY; Bixiao Zhao, Princeton University, Princeton, NJ, Scott M.
Ulrich, Ithaca College, Ithaca, NY; and Bonnie L. Bassler, Princeton
University, Princeton, NJ, Howard Hughes Medical Institute, Chevy Chase,
MD.
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