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Malaria continues to claim a significant number of lives worldwide, estimated at ~ 1 million each year. The genome sequence of the most prominent human parasite, Plasmodium falciparum, was published in Nature in 2002. We are now proud to present the genome sequences of two additional human parasites, Plasmodium vivax and Plasmodium knowlesi, along with a Review article discussing the scientific discoveries that have been aided by this information. In addition, we present a collection of papers illustrating highlights in malaria research that were published in recent years.
Malaria parasites must reproduce sexually to transmit to vectors, but very little is understood about their reproductive strategies. This paper details that malaria parasites adjust their sex ratios in response to unrelated conspecifics, as predicted by evolutionary theory.
The evolutionary theory of sex ratios should apply to all creatures, both great and small. Experimental studies of the proportions of male to female sex cells of malaria parasites deliver cheering results.
This study presents the first large scale transcriptional analysis of malaria parasites isolated from human patients, and defines three distinct transcriptional patterns that can be described as active growth, response to starvation and environmental stress response.
Our knowledge of the inner workings of malaria parasites comes largely from lab-based studies. But parasites growing in humans may have greater metabolic flexibility than those growing in Petri dishes.
The infectious form of the malaria parasite has thousands of proteins, making it tough to develop a vaccine for it. Narrowing down which proteins cause protective immune responses may help resolve the problem.
Malaria parasites trigger an increase in intracellular sodium concentration when infecting red blood cells. This effect provides a direct benefit to the parasite, as it uses the resulting gradient to energize the uptake of phosphate.
Through the bio-engineering of Saccharomyces cerevisiae high titres of artemisinic acid were produced using a novel cytochrome P450 monooxygenase. Optimization of this process on an industrial scale may significantly reduce the cost of artemisinin, which could then be used to combat malaria in resource-poor settings.
To remain hidden from its host's immune system, the malaria parasite must vary the proteins on the surface of the infected cell. The genes encoding these proteins are very similar, so how does the parasite express just one at a time?