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A
ttaching an antimicrobial drug,
which is activated by light, to a peptide that binds to bacteria
and stops them making toxins, resulted in a treatment that
was highly effective at killing the superbug, methicillin-resistant
Staphylococcus aureus or commonly known as MRSA.
Miss Linda Dekker and colleagues from the UCL Eastman Dental
Institute, University College London presented the work to
the Society for General Microbiology's meeting at Harrogate
April 1.
Photodynamic therapy uses antimicrobial agents, in this case
tin chlorin e6 (SnCe6), which produce free radicals and an
unstable form of oxygen called singlet oxygen when they are
exposed to light at the right wavelength. These damage and
kill bacteria. To improve the effectiveness of treatment and
avoid damage to human cells, the drug was targeted to MRSA
by attaching it to a peptide, RNAIII inhibiting peptide (RIP)
that binds to a molecular receptor on the bacterium's surface.
Photodynamic therapy (PDT) is a treatment that uses a drug,
called a photosensitizer or photosensitizing agent, and a
particular type of light. When photosensitizers are exposed
to a specific wavelength of light, they produce a form of
oxygen that kills nearby cells (1, 2, 3).
Each photosensitizer is activated by light of a specific
wavelength (3, 4). This wavelength determines how far the
light can travel into the body (3, 5). Thus, doctors use specific
photosensitizers and wavelengths of light to treat different
areas of the body with PDT.
99.97% of 10 million MRSA cells were killed using this new
combination, which was 1000 times more effective at killing
MRSA compared to the commercially available SnCe6 when the
same quantity is used. In addition to being far more effective
at killing the bacteria, the new drug has the potential to
prevent bacteria from producing tissue-damaging toxins; the
mechanism of killing also means that it is very unlikely that
bacteria can develop resistance to this treatment.
"The results from laboratory studies are very encouraging
and indicate that this technique might be effective at treating
topical infections such as wound and burn infections,"
said Ms Dekker, "This work will require in vivo trials
before it can be used. Due to the growing resistance of many
organisms to antibiotics, this approach may be the only one
available for use against microbes resistant to all known
antibiotics".
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