Biological Clocks of People and Malaria Parasites Tick in Tune

Research could pave the way to new anti-malarials that work by 鈥渏et-lagging鈥 the parasites that cause the disease.

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Packed with microscopic Plasmodium parasites, this red blood cell (teal) and other infected cells around it will soon burst and spew their contents into the bloodstream, triggering the periodic fevers that are the hallmark of malaria. Credit: NIAID
Duke biology professor Steve Haase studies the biological clocks that tick inside parasites and people when they鈥檙e infected with malaria.

鈥淲hat these results suggest is that the parasite clock and the host clock are talking to each other."

Steve Haase, professor of biology at Duke

The team of researchers at 老牛影视, Florida Atlantic University and the Armed Forces Research Institute of Medical Sciences says the findings could pave the way to new anti-malarial drugs that throw malaria鈥檚 internal clock out of step with its host, essentially 鈥渏et-lagging鈥 the parasites.

鈥淲e have a reason to care about this,鈥 said senior author , professor of biology at Duke. 鈥淲e're on our last line of drugs, artemisinin-based combination therapies, and we鈥檙e already seeing resistance to those in southeast Asia. Exploring some new ideas for fighting malaria makes sense.鈥

When someone has malaria, a deadly loop repeats itself inside their body. The disease鈥檚 recurring fever spikes are caused by microscopic Plasmodium parasites that invade the person鈥檚 red blood cells, multiply, and then burst out in unison, spewing into the bloodstream by the millions to invade other cells and begin the cycle anew.

This cycle repeats itself every 24, 48 or 72 hours depending on the Plasmodium species. Which got scientists wondering: could the parasites be coordinating in some way with the 24-hour circadian rhythms of their hosts?

To find out, the researchers collected blood from 10 people who tested positive for malaria caused by , the predominant species of malaria parasite found in Asia and Latin America.

Then they analyzed the RNA in those samples every three hours over two days to figure out which genes were active as the parasites matured inside their victim鈥檚 red blood cells. Using a technique called RNA sequencing, the research team tracked the expression of more than 1,000 genes in both the patients鈥 immune cells and in the parasites lurking in their blood.

The researchers identified hundreds of genes that follow a clock-like rhythm, ramping up at certain times of day and switching off at others. Using this data, they developed a way to calculate the internal clock time for each patient and also for their parasites. Then they calculated how well the rhythms of gene expression were aligned.

Plasmodium vivax parasites have a life cycle that repeats every 48 hours. Sure enough, for every turn of the parasite clock, the 24-hour body clock of their host went around twice.

The team found that not every patient鈥檚 24-hour internal clock ran on exactly the same schedule. Some had cycles that began earlier in the day; some later. But no matter how a person鈥檚 biological rhythms were shifted, the cycling genes in their malaria parasites were .

Researchers already knew that malaria parasites have their own internal timekeeping mechanism. In a , Haase and colleagues determined that, even when grown outside the body, without cues like their host鈥檚 meals or sleep cycles to help orient them in time, malaria parasites can still keep a beat. Their rhythmicity is thanks an internal metronome that ticks of its own accord and causes the parasite鈥檚 genes to ramp up and down at regular intervals.

But the shows something more. 鈥淲hat these results suggest is that the parasite clock and the host clock are talking to each other,鈥 Haase said.

Scientists still don鈥檛 know what drives malaria parasites to coordinate their rhythms with those of their host. 鈥淭he parasites are likely taking advantage of their host鈥檚 internal rhythms to achieve their own ends,鈥 Haase said, but the nature of the advantage is unclear.

One theory is that the parasites schedule their emergence from red blood cells to avoid  times when their victim鈥檚 immune system is most active, making themselves less vulnerable to attack.

鈥淭hey could also be timing their developmental cycle so they have the proper nutrition,鈥 Haase said. 鈥淲e don't know. So that's a big question.鈥

The United States has been malaria-free for more than , but the disease is still a leading cause of death in poorer and tropical parts of the world, killing in 2021 alone, most of them children.

Part of the reason is malaria鈥檚 ability to evade attack. Medicines for malaria have been around for hundreds of years, but many of the drugs in the existing arsenal are losing their effectiveness as parasite populations in certain parts of the world develop ways around them.

If they can figure out how malaria parasites stay in step in humans, the researchers say it may be possible to develop new drugs that decouple the parasite鈥檚 clock from that of its host, and thereby help the immune system better fight the invaders.

Findings in other host species are promising. In mice, malaria parasites whose rhythms are out of sync with their hosts are half as effective at .

As a next step, the researchers are trying to figure out exactly how the parasite and human clocks 鈥榗ommunicate鈥 with each other so that their cycles line up.

鈥淭here have to be some molecular signals that they're passing back and forth to each other,鈥 Haase said. 鈥淲e don't know what they are, but if we can disrupt them, then we might have a shot at an intervention.鈥

This research was supported by grants from the Defense Advanced Research Projects Agency (D12AP00025), the National Institutes of Health (R01 GM126555-0), and the National Science Foundation (DMS 1847144).

Citation

"The Parasite Intraerythrocytic Cycle and Human Circadian Cycle Are Coupled During Malaria Infection," Francis C. Motta, Kevin McGoff, Robert C. Moseley, Chun-Yi Cho, Christina M. Kelliher, Lauren M. Smith, Michael S. Ortiz, Adam R. Leman, Sophia A. Campione, Nicolas Devos, Suwanna Chaorattanakawee, Nichaphat Uthaimongkol, Worachet Kuntawunginn, Chadin Thongpiam, Chatchadaporn Thamnurak, Montri Arsanok, Mariusz Wojnarski, Pattaraporn Vanchayangkul, Nonlawat Boonyalai, Philip L. Smith, Michele Spring, Krisada Jongsakul, Ilin Chuang, John Harer, Steven B. Haase. Proceedings of the National Academy of Sciences, June 6, 2023. DOI: 10.1073/pnas.2216522120.