From: University of Melbourne
June 2, 2022 -- A new
method to combat malaria which sees the disease turn against itself could offer
an effective treatment for the hundreds of millions of people infected globally
each year, as the efficacy of current antimalarial drugs weakens.
The University of
Melbourne-led research published today in Science has
identified an anti-malarial compound, ML901, which inhibits the malaria
parasite but does not harm mammalian -- human or other mammals' -- cells.
Co-lead author
Professor Leann Tilley, from the Bio21 Institute at the University of
Melbourne, said the ML901 compound effectively made the parasite the agent of
its own demise, underpinning its potency and selectivity.
"ML901 works by an
unusual reaction-hijacking mechanism," Professor Tilley said.
"Imagine a stealth
weapon that can be used to launch a self-destruct attack on your vehicle --
slamming on the brakes and cutting the engine. ML901 finds a particular chink
in the machinery that the malaria parasite uses to generate the proteins needed
to reproduce itself and stops it doing so.
"While there is
much work to be done to fine tune what we've discovered, these results are
really encouraging in the search for new anti-malarials."
In the collaboration
with Takeda Pharmaceuticals, Medicines for Malaria Medicine -- the peak
international body for anti-malarial drug development -- and research labs
across five continents, tests were conducted using molecules provided by
Takeda, during which the ML901 compound was identified.
Once ML901 entered the
parasite, it attached itself to an amino acid and attacked the protein
synthesis machinery from the inside, rapidly grinding the parasite to a halt.
The molecular structure of human cells means they are not susceptible to attack
by ML901.
In tests using both
human blood cultures and an animal model of malaria, the team found ML901
killed malaria parasites that had resistance to currently used drugs and showed
rapid and prolonged action resulting in excellent parasite killing.
Professor Tilley said
the compound showed it was active against all stages of the lifecycle, meaning
it could be used to prevent malaria infections as well as to treat the disease.
"It also shows
potential for preventing infected people from transmitting the disease to
others, which is critical to stop the spread of malaria."
Every year, at least
200 million new malaria infections are diagnosed worldwide, causing more than
600,000 deaths in Africa and Southeast Asia. Over the past 50 years, ever
increasing levels of resistance to anti-malarials has led to an impending
crisis, with breakthrough drugs desperately needed.
Professor Tilley said
based on these findings the team was ready to pursue the development of new anti-malarial
drug candidates.
"We believe this
is just the beginning. We now have the possibility of finding drugs, similar to
ML901, that target a range of deadly infectious diseases, including multi-drug
resistant bacterial infections. The work opens up several new drug discovery
avenues."
https://www.sciencedaily.com/releases/2022/06/220602140849.htm
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