Giving Malaria a Deadline

Giving Malaria a Deadline

Here is a beneficial form of genetic tinkering which stands in contrast to the horrible GMOs which in reality are drivers of agro-chemical poison sales. We wiped out screwworm without poisons, and, we can do the same with malaria.

NOTE: this article was originally published to on September 24, 2018. It was written by Nicolas Wade.

Malaria is among the world’s worst scourges.

In 2016 the disease, which is caused by a parasite and transmitted by mosquitoes, infected 194 million people in Africa and caused 445,000 deaths.

But biologists now have developed a way of manipulating mosquito genetics that forces whole populations of the insect to self-destruct. The technique has proved so successful in laboratory tests that its authors envisage malaria could be eliminated from large regions of Africa within two decades.

A team led by Andrea Crisanti, a biologist at Imperial College, London, altered a gene that disrupts the mosquito’s sexual development; the females become infertile but the males remain able to spread the debilitating gene to an ever-dwindling number of progeny. Dr. Crisanti found that laboratory populations of mosquitoes can be driven to extinction within 11 generations, he and colleagues report in Monday’s issue of Nature Biotechnology. Wild populations could be made to crash in about four years, according to computer models.

The technique involves equipping mosquitoes with a gene drive, a genetic mechanism that forces a gene of choice into all of an organism’s offspring. (Normally, sexual reproduction would pass the gene to only half the progeny.) Genes carried by a gene drive therefore can spread very rapidly through a population, which makes the technique both powerful and potentially dangerous. No gene drive has yet been released in the wild.

Previous efforts to reduce mosquito fertility using gene drives have failed because mutations arise in the stretches of DNA targeted by scientists, nullifying the engineered changes. These mutations are heavily favored by natural selection and permit the mosquitoes to escape the genetic trap.

Dr. Crisanti and his colleagues instead found a way to target a stretch of DNA that does not vary from one mosquito to another, presumably because each DNA unit plays so vital a role that any mutations would kill the organism. This invariant DNA sequence occurs in a gene called doublesex, which determines sexual development in the mosquito species Anopheles gambiae, one of the major carriers of the malaria parasite in Africa.

Dr. Crisanti’s team disrupted the doublesex gene in a way that affects only females. These females develop ambiguous sexual features: they cannot bite because they have male-type mouthparts, and they are infertile. But the males are unaffected and continue spreading the disruptive gene until no more eggs are laid.

In the lab, when males with the doublesex gene drive were placed in cages of wild mosquitoes, the populations were driven to extinction in as few as seven to 11 generations. No mutations could be found in the targeted sequence of DNA.

“We are not saying this is 100 percent resistance-proof,” Dr. Crisanti said. “But it looks very promising.”

Kevin Esvelt, who studies the evolution of gene drives at Massachusetts Institute of Technology, indicated that the biological aspects of mosquito control may now be close to solution. “With this achievement, the major barriers to saving lives are arguably no longer mostly technical, but social and diplomatic,” he said.

Launching a gene drive into the wild is risky. Once released, it can’t be recalled or easily disabled should anything go awry. In 2016, the National Academy of Sciences called for extensive tests and public consultation before any gene drive is released.

The theory of how gene drives could be used to control pest populations was laid out in 2003, in an article by Austin Burt, a biologist at Imperial College, London, and a co-author on the new paper. He hopes that a small-scale field trial can be started in Africa in five years.

Implementing such a program would entail releasing just a few hundred drive-carrying mosquitoes in each village. “We wouldn’t have to hit every village, maybe as few as one percent,” Dr. Burt said. Complete eradication isn’t necessary; the malaria parasite can’t maintain its populations once the number of mosquitoes falls below a certain number.

“If there are no unexpected technical or regulatory delays,” Dr. Burt said, “it’s possible to envisage that gene-drive mosquitoes, in combination with other approaches, could have eliminated malaria in significant parts of Africa in 15 years.”

Achieving such a goal likely will require a continentwide agreement, since a gene drive, once released, probably couldn’t be confined to a single country, and biologists want to avoid any unintended consequences. All insects analyzed so far rely on the doublesex gene to direct their sexual development. It could be disastrous if an altered doublesex gene drive somehow jumped from mosquitoes to another insect species, such as bees.

“That’s not possible,” Dr. Crisanti said. He noted that every insect species has its own version of both the doublesex gene and the gene’s highly conserved region, so a gene drive aimed at one species wouldn’t work in any other. For that same reason, the technique potentially could be aimed at a wide range of noxious insects, each targeted individually.

“These sequences might be an Achilles heel present in many insect pests,” Dr. Crisanti’s team writes in their paper.

Dr. Esvelt acknowledged that the new gene drive could possibly spread to other insects but said that, if it did, the most likely host would be other Anopheles mosquito species. “The known harm of malaria greatly outweighs every possible ecological side-effect that has been posited to date, even if all of them occurred at once,” he said.

A version of this article appears in print on Sept. 24, 2018, on Page D6 of the New York edition with the headline: Nudging a Species Toward Self-Destruction

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