Skip to Content

In Africa, Scientists Are Preparing to Use Gene Drives to End Malaria

Mosquitoes that drive themselves out of existence are being bred in labs—but letting them loose in nature is another matter.
A volunteer tests a decidedly lower-tech weapon against malaria - a soap called "Faso Soap" meant to repel mosquitoes.

In Burkina Faso, Mali, and Uganda, the groundwork is being laid for a powerful kind of experiment. A project now under way aims to release mosquitoes that have been genetically programmed to drive themselves and their malaria-causing brethren toward extinction.

As we wrote last year, the program, called Target Malaria, is meant to use a gene drive to drastically reduce the number of mosquitoes that transmit the disease in sub-Saharan Africa, where it kills hundreds of thousands of people a year. Not long ago this was merely theoretical, but modified mosquitoes with gene drives on board are already being bred and tested in labs.

The idea is that a so-called selfish gene with effects that would ultimately doom the population is introduced and then replicates itself at a far higher rate than normal, spreading rapidly. Target Malaria, which is funded by the Bill and Melinda Gates Foundation, is exploring several ways to use this technology. One of the most promising involves altering mosquitoes in such a way that new generations are almost exclusively male. Male mosquitoes don’t bite people, and a population with hardly any females would be unable to reproduce.

There is still a long way to go before gene drive insects are released into the wild, but plans are moving ahead. Apart from further developing the technology, one of the biggest challenges at this stage is making sure people living in the region understand the nature of the work and what’s at stake. As Stat reports, many people in Burkina Faso believe that malaria can be caused by a bad diet rather than mosquito bites. Researchers are canvassing communities as part of a push to educate locals on how the disease works and what Target Malaria entails.

Little is known about the ecological consequences as well. In sub-Saharan Africa, most malaria is transmitted through three types of Anopheles mosquitoes. Target Malaria is focusing on Anopheles gambiae, with the goal of severely reducing or eradicating this type. Out of around 3,500 known species of mosquitoes, eliminating one may not seem like a big deal. But it’s never been done before. And no one knows if a gene drive, once released into the wild, could jump into other species.

What is known is that malaria is a persistent, deadly disease that damages quality of life for millions of people around the world. Gene drives have been proposed as a way to solve many ecological ills, from the decline of rare Hawaiian birds to the excess of invasive mammals in New Zealand. With many questions remaining about how gene drives might work in nature, scientists are understandably cautious about deploying them. But malaria is one of the greatest public health threats on the planet. If we have the power to end it, the real question must be: Why shouldn’t we use it?

(Read more: Stat, “The Extinction Invention,” “With This Genetic Engineering Technology, There’s No Turning Back,” “First Gene Drive in Mammals Could Aid Vast New Zealand Eradication Plan”)

Keep Reading

Most Popular

Geoffrey Hinton tells us why he’s now scared of the tech he helped build

“I have suddenly switched my views on whether these things are going to be more intelligent than us.”

Meet the people who use Notion to plan their whole lives

The workplace tool’s appeal extends far beyond organizing work projects. Many users find it’s just as useful for managing their free time.

Learning to code isn’t enough

Historically, learn-to-code efforts have provided opportunities for the few, but new efforts are aiming to be inclusive.

Deep learning pioneer Geoffrey Hinton has quit Google

Hinton will be speaking at EmTech Digital on Wednesday.

Stay connected

Illustration by Rose Wong

Get the latest updates from
MIT Technology Review

Discover special offers, top stories, upcoming events, and more.

Thank you for submitting your email!

Explore more newsletters

It looks like something went wrong.

We’re having trouble saving your preferences. Try refreshing this page and updating them one more time. If you continue to get this message, reach out to us at with a list of newsletters you’d like to receive.