Malaria is among the world's deadliest diseases. It killed King Tut and Genghis Khan, along with as many as half of all of the people that have ever lived. And despite modern disease management strategies like insecticides, drugs and vaccines, in 2015 malaria still killed nearly half a million people. In fact, malaria infects more people today than it did 50 years ago.
Image: Wikimedia But in recent years, advances in genetic engineering have brought new hope to conquering the disease known by the Romans as the "rage of the Dog Star". In particular, some scientists are experimenting with how they could alter the genetic code of mosquitoes to stop malaria transmission, then use a technique called gene drive to make sure those alterations spread throughout infected mosquito populations. And there's good news: A new modelling study by scientists in the US and UK suggests that this might actually work.
Malaria is a parasite that is carried by several different species of mosquito, and passed on to humans exclusively by female mosquitoes, the only ones that bite. What we know about mosquitoes and malaria suggests three different approaches that could stop the spread of disease: Scientists could alter mosquito genetics to spread a fatal flaw through the entire population, reducing overall numbers; they could modify mosquitoes to produce more male offspring than female offspring, reducing the number of mosquito bites; or they could equip mosquitoes with genes to help them fend off malaria, reducing transmission of the disease within mosquito populations and thus to humans, too. After making changes to a mosquito's DNA, by whatever method, researchers would rely on what's known as a gene drive to circumvent Mendelian inheritance laws, ensuring that their lab-engineered tweaks spread throughout wild mosquito populations. In labs, all three of these approaches have shown early promise.
Researchers from the Institute for Disease Modelling, Oxford and the Imperial College of London decided to use mathematical modelling to test how these methods might fare in the wilds of sub-Saharan Africa, where 90 per cent of malaria-related deaths occur. Relying on epidemiological data such as rainfall, mosquito population and disease transmission rates, they simulated the effect of different types of genetic modifications on both local mosquito populations and malaria transmission. The results were optimistic: "Each approach has a range of successful parameters... that would succeed in removing the transmission potential of the targeted species in even the most challenging settings," they wrote.
In all of their models, under the right conditions, disease-spreading mosquitoes were basically eliminated from wild populations over several years. The modelling also suggested which conditions might give each strategy the best chance of success -- for instance, releasing lab-engineered mosquitoes into the wild at certain times of year.
Gene drives, the study says, have made eliminating malaria a realistic prospect.
"In short," the authors wrote, "malaria elimination would move from aspiration to a rapidly implementable track, saving millions of lives and freeing up many billions of dollars in global health resources to solve other challenges."
Other methods of using genetic engineering to stop mosquito-borne illness are already under way. In the Florida Keys, the British biotech firm Oxitec plans to kill the disease-harbouring pests off over time, by releasing genetically engineered male mosquitoes whose offspring cannot survive to adulthood. But gene drive offers a significant advantage. While Oxitec will have to release tens of thousands of mosquitoes over many years to significantly impact the wild population, in theory, the gene drive automates the spread of any lab-made alteration by relying on "selfish genes" to force desired traits into offspring.
Scientists succeeded in installing the first gene drive in mosquitoes in 2015, and since then there has been significant advancement and investment in the technology as an approach to malaria. Researchers now have a good handle on which genetic modifications are mostly likely to curtail the spread of malaria.
"Gene drives have enormous potential for the control of populations of insect vectors and pests," mosquito researchers Tony Nolan and Andrea Crisanti wrote this week in The Scientist. "They are species-specific, self-sustaining, and have the potential to be long-term and cost-effective."
The hurdles, though, are still significant. There are still many more steps before scientists are ready to test their gene-driven mosquitoes in the wild. And even once they are ready, it isn't clear whether regulators or the public will let them.
What is clear, though, is that the methods we're using to control malaria right now, on their own, are not working. Between 2010 and 2015, malaria have rates decreased by 21 per cent. But less than half of the 91 countries and territories with malaria are on track to meet the World Health Organisation goal of decreasing rates by 40 per cent by 2020. Gene drive just might be the new tool that gets us there.