OREANDA-NEWS  A new genetic fingerprinting technique is the first to show the huge diversity of the malaria parasite, one of nature’s most persistent and successful human pathogens.

The technique validates a previously untestable “strain hypothesis” that was proposed more than 20 years ago and opens up new ways of thinking about how to tackle this cunning killer.

Key to that understanding is changing the way we think about malaria—that it is not so much like the measles and more like the flu.

As reported in the Proceedings of the National Academy of Sciences, researchers collected blood samples from 641 children, aged 1 to 12 years from Bakoumba, a village in Gabon, West Africa and the genetic fingerprints of parasites from 200 infected children. Remarkably, every child was infected with malaria parasites that had a different fingerprint from the parasites in every other child.

In 1994, Professors Sunetra Gupta and Karen Day, both then working at Imperial College London and later the University of Oxford, proposed that the malaria transmission system may be organized into a set of strains based on diversity of the genes that code for the surface coat of the parasite. If true, this strain diversity could explain why people can be re-infected with malaria many times over.

It has taken until now for Day and colleagues to develop and optimize the mathematical and laboratory techniques to finally address the hypothesis.

Infection and re-infection

The malaria parasite is a single-celled microorganism (known as a Plasmodium) that infects red blood cells and is transferred from human to human via mosquitoes. It has been infecting people for tens of thousands of years, and, according to the World Health Organization, in 2015, nearly half of the world’s population remained at risk of malaria.

“Malaria is like flu, but our fingerprinting results show that it is way more complicated.”

Over the past 20 years, Day’s team has developed a way to genetically fingerprint malaria parasites from small amounts of blood based on what are called var genes. Every parasite has approximately 60 of these var genes but only uses one at a time and can switch between the one it uses. The genes encode proteins that coat the surface of the red blood cells that the parasite infects.

The var genes are significant because they determine the ability of the parasite to disguise itself from the human immune system, and contribute to the virulence of the disease.

If the genes that encode the surface coat overlap between two parasites, such as you would expect in siblings that would share a maximum of 50 percent of their genes, then when someone is re-infected, the immune system will recognize these malaria parasites and quickly purge them if they have seen the parent infections. But if there is little or no overlap in these genes, then the immune system won’t recognize the malaria parasite as readily, leading to chronic infection.

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The study shows that “the parasite has evolved this enormous diversity with limited overlap between the sets of var genes likely so it can keep re-infecting the same humans,” says Day, now a professor of population science and dean of science at the University of Melbourne.

Coauthor Mercedes Pascual, an ecologist and professor at the University of Chicago, describes this as “the parasites forming niches by diversifying. They compete with each other for hosts, and distance themselves from each other to invade the same population of humans, a limited resource.”

Current malaria control programs don’t target the diversity of the parasite, Day says.

“With malaria, we attack something that is conserved between all strains, but the problem is if you don’t get rid of all of the malaria parasites with current strategies, you have this enormous diversity that can allow the system to bounce back quickly to pre-control levels. The resilience of the system is coming from the diversity, so you’ve got to monitor how approaches to control attack diversity and not just the parasite per se.”

Interestingly, the theory of malaria control is based on malaria having no diversity and being like measles. You contract measles once and have lifelong immunity, whereas you can get malaria or the flu many times because there are multiple strains circulating.

“Malaria is like flu, but our fingerprinting results show that it is way more complicated,” Day says.

Intense competition

By analyzing the var genes, researchers came up with a unique identifier, or fingerprint, for each malaria strain that they call a var code.

“Every child had a different parasite fingerprint, and importantly, each fingerprint was highly unrelated to all other fingerprints.”

“Looking down the microscope you would have said all of the infections look the same, but when we did the fingerprinting genetically with this variant antigen gene system, we could see that every child had a different parasite fingerprint, and importantly, each fingerprint was highly unrelated to all other fingerprints,” Day says.

This unrelatedness was a surprise, Day says. “Malaria has sex as part of its lifecycle, every time it goes through a mosquito. And so, because the malaria parasite mates you would expect to find related parasites that we might call parents, siblings, cousins, and aunts and uncles in the population.”

“Even with very high levels of sex between parasites, their competition for available hosts can be so intense, that really only very unrelated parasites would be fit enough to survive and here we have a structure where highly related parasites were not detected,” says Yael Artzy-Randrup, a theoretical ecologist from the University of Amsterdam, and a coauthor of the study.

“Malaria is similar to flu in that humans can be infected multiple times by different malaria parasite variants. However, in contrast to the flu, the situation with malaria is much more complex. With malaria, at any given point of time there is a high diversity of variants coexisting even in very small human populations, while in flu, variants usually replace each other, and people will only be infected by one variant at a time.”

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After waiting 20 years to get their results, the researchers suffered a setback in 2012 when Hurricane Sandy cut the power to Day’s laboratory at New York University, destroying samples that represented months of work. The team was eventually able to recover and continue its work. Once the team had assembled all the data, they had to assure their scientific peers—many of whom were skeptical of the strain hypothesis—that the pattern of diversity and unrelatedness they were seeing was not just through random chance.

Researchers tested the results using statistical and computational techniques inspired by the analysis of complex systems in ecology, such as communities of species in ecosystems. They found that the system was non-random, and the relatives were absent from the population.

The project is connected to a central question in ecology: what is the structure of diversity?

“We are asking this question for the ensemble of parasites within a population of Plasmodium falciparum, but it can also be asked for the ensemble of tree species in a rainforest,” Pascual says. “It is an exciting time for bringing together quantitative analyses and deep sampling of biological systems in the field.

“Our findings indicate that the enormous diversity of the parasite is structured and that we need to consider the implications of this structure for intervention, and possibly develop a different way to model transmission in malaria altogether.”

Additional researchers from the University of Melbourne, the University of Chicago, New York University, the University of Michigan, the University of Amsterdam, the University of Montpellier, and the University of Paris Descartes are coauthors of the study.