Leishmania is a microorganism that enters the human body via a sandfly bite. The parasite allows itself to be swallowed up by white blood cells to advance its life cycle. The disease threatens the health of over 500 million people at risk of infection in Africa, Europe, Asia and the Americas.
Leishmaniasis, the disease caused by the parasite, has been on the radar of scientists for a long time, not only because of efforts to find treatment, but because the parasite makes an ideal model for study. Hence, numerous immune mechanisms have been elucidated by researchers. However, the quest for affordable and effective treatment continues. INRS professors Albert Descoteaux and Steven LaPlante have developed a new, cost-effective strategy to rapidly identify molecules capable of eliminating leishmania, a disease which can disfigure, disable, or kill its victims, especially in tropical areas.
“I have been studying this parasite for 30 years, and there is still a lot we do not understand,” says parasitologist Albert Descoteaux, who works to uncover the secrets of leishmania, a genus encompassing some 20 single-celled species. In addition to its human victims, the parasite also targets some 70 other mammal species, according to the World Health Organization. Leishmania moves from one host to another by hitching a ride with tiny phlebotomine sandflies, which transmit the undesirable parasite when they bite.
According to the most recent estimates, 12 million people are currently affected by one form of leishmaniasis or another. There are three main forms: cutaneous, mucocutaneous, and visceral. “These are diseases that destroy lives—when they do not kill outright,” says Professor Descoteaux, adding that the pharmaceutical companies have little interest in developing treatments. “There is little commercial interest in neglected tropical apothekegenerika.de diseases like leishmaniasis,” he says. “It is the second-leading parasitic killer in the world, right behind malaria, yet there has been no real headway made on treatments in decades. There is currently no effective vaccine, and the available treatments all have major shortcomings, including serious side effects, high cost, and problems administering them in endemic areas. Unfortunately, as is the case with many other drugs, the parasite is also developing resistance. That is never good news.”
Albert Descoteaux, who is based at Centre INRS-Institut Armand-Frappier, is one of five INRS professors currently working on leishmaniasis. Their efforts to better understand the fundamental interaction between the parasite and its host account for one-third of all research activity on the disease in Canada, and their work is recognized worldwide.
Professor Steven LaPlante, who has been with INRS since 2015, specializes in drug discovery. With his colleague Albert Descoteaux, he has developed a project to identify new molecules that show promise for treating leishmaniasis. Their innovative approach is raising hopes of finding a more effective tool for developing drugs for leishmaniasis, but also for many other diseases.
The challenge of finding the right target
Having evolved its tactics and molecular machinery over millions of years, leishmaniasis has more than one trick up its sleeve. This is why there are so many obstacles to identifying molecules capable of eliminating the disease. For one thing, unicellular protists like leishmania have more in common with mammal cells than with bacteria and viruses. “Like fungus, yeast, and worms, Leishmania are complex cells with a nucleus, and they have similarities to human cells,” notes the professor. “But they have taken a different evolutionary path, so there are lots of differences we need to identify and understand.”
Second, delivering a useful molecule to the parasite is a challenge. “Before it can kill Leishmania, the drug has to get past all kinds of barriers,” explains LaPlante.” It has to penetrate the infected cell without killing it or being too toxic. Then it has to reach and enter the protist to do its thing. Let’s just say that there are a lot of molecules to test before we find the right one for the job.”
Testing a lot of molecules is the approach used by most researchers in the drug discovery process, but it takes extensive resources. Unfortunately, in the fight against leishmaniasis, there is little financial incentive for funding this kind of work. Yet, given the prevalence of the disease worldwide, there are numerous calls for urgent action to find new treatments.
A promising new approach
This is the context in which the two INRS researchers collaborated, drawing on Descoteaux’s expertise in biology and LaPlante’s in medicinal chemistry. LaPlante has access to a special small-molecule library from which he selected 1,604 molecules that had the best chances of reaching Leishmania in the macrophages and preventing it from completing its life cycle. Compared to the molecule libraries maintained by pharmaceutical companies—which can hold up to 2 million molecules—his library represents a very modest number, but has special properties that make it easily manageable within the confines of a university research lab.
“We dubbed our approach ‘fragment-based phenotypic lead discovery,’ or FPLD,” says Professor LaPlante. “It’s a combination of tried and tested methods that hadn’t previously been adapted for leishmaniasis. We start by administering very small molecules to cultured cells and then observe the impact on the infection.”
In medicinal chemistry, several phases are required to develop a drug with multiple characteristics. The ideal molecule for fighting an infection should be nontoxic to humans, easy to administer, capable of reaching the infectious agent, affordable to produce, and, obviously, effective against the pathogen in question.
Different components of a drug are selected to perform different jobs. The components in question are molecular fragments. The goal of the two INRS professors was to identify which of these could stop leishmania in its tracks. The idea is that effective fragments can be combined with other components serving various purposes—stability, delivery, absorption, and so on—to improve efficacy and end up with a viable drug.
A painstaking job
Yann Ayotte, lead author on the study recently published on the project, systematically observed cultures treated with the fragments under the microscope, counting the number of parasites in the infected cells in order to compare them. The Ph.D. student, who is currently continuing his research in Professor LaPlante’s lab, first joined the project as an intern in Albert Descoteaux’s lab at the end of his undergraduate degree. The two professors are quick to praise his outstanding dedication to his work.
After numerous experiments, the highly targeted screening of a small number of molecules allowed the team to identify two families of molecules showing high efficacy against Leishmania: indole and indazole derivatives. A dozen molecules have shown good potential, a very high number compared to other screening techniques.
Is there a new drug on the horizon? “For now, we are still at the very beginning of the process,” says Professor Descoteaux. “And you can’t skip any steps,” adds LaPlante. First, it’s essential to understand why the molecules have a leishmanicidal effect, a task that will keep Professor Descoteaux busy for a good while yet. In the meantime, the active molecule can be improved upon and “dressed up” with other appendages in order to fulfil all the criteria of an effective treatment—a job for Professor LaPlante and his team.
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