Poster Presenter
Lucifensin, The Key Antimicrobial
Player Of Maggot Therapy And Its Possible Applications
Václav Čerovský, Jiřina Slaninová,
Jan Zdárek, Lenka Monincová, Vladimír Fučík
Czech Republic
From the extracts of various tissues
(gut, salivary glands, fat body, haemolymph) of the green bottle
fly (Lucilia sericata) larvae and from their excretions/secretions
we have recently isolated and characterized novel homolog of insect
defensin designated lucifensin (Lucilia defensin). This
is 40 residues and three intramolecular disulfide bridges peptide
which is very similar to other dipteran defensins. We assume that
lucifensin is the key antimicrobial component that protects the
larvae when they are exposed to the highly infectious environment
of a wound during the medicinal process known as maggot therapy.
We also believe that lucifensin is one of the crucial disinfectants
of the wound produced by the maggots which contributes to the healing
process. Here, we present the total chemical synthesis of lucifensin
by means of the solid phase peptide synthesis method utilizing both
the "step by step" strategy and the segment condensation.
In antimicrobial assay using a set of different bacteria lucifensin
shows activity preferentially against Gram-positive ones including
Staphylococcus aureus. The discovered lucifensin may have
a potential as a new agent for topical therapeutic applications
in the treatment of serious surface infections. A promising aspect
in the treatment of non-healing wounds could be the combination
of conventional antibiotics with lucifensin and/or the use of this
antimicrobial peptide as a supportive mean to bolster the healing
effect of maggot therapy.
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