top of page

WHAT WE STUDY

The Malaria Parasite: Plasmodium

Plasmodium, the causative agent of the infectious disease Malaria, has a complex life cycle spanning two very different hosts: the human and the mosquito.  This unicellular, protozoan parasite is the cause for 500 million infections and over 1 million deaths in the human population per year.

 


 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

The interest of our lab centers on the developmental stages of Plasmodium within the Anopheles mosquito.  For the parasite, the mosquito serves two purposes: it provides a) the environment for the completions of sexual development and reproduction and b) transport to the next human host.  Yet, the mosquito is not a mere inert flying syringe and represents a serious challenge for the parasite.  The environment in the insect is dramatically different from the human blood.  In addition, to be part of a digesting blood meal, the parasite also has to cope with the innate immune response of the mosquito and an expanding bacterial flora - at the same time. Plasmodium therefore, has to reorganize its cell biology in order to survive, mate, develop, and move within the mosquito to ultimately facilitate transmission to the next human host.  One major adaptive change is the switch from an intracellular lifestyle in the human blood to an extracellular lifestyle in the mosquito vector.  This step has the consequence that Plasmodium is now directly exposed to its rather hostile environment, which requires the parasite, in the form of an ookinete, to actively move through and escape the blood meal. It then produces thousands of sporozoites, which invade the salivary glands of the insect.  From here, they will be injected into the next human host.


Antioxidant defense systems of Plasmodium and their role in malaria transmission by Anopheles mosquitoes

How does the malaria parasite survive the hostile environment in the mosquito midgut?  As most aerobic organisms, Plasmodium is exposed to cytotoxic reactive oxygen (ROS) and reactive nitrogen species (RNS).  It therefore possesses, also like most aerobic organisms, potent antioxidant defense mechanisms that guard it against the harmful impact of these compounds.  How these mechanisms help in protecting the parasite while in the mosquito vector is one of the prime objectives of our lab.  Our data suggest that the parasite, once taken up by the mosquito as part of a blood meal, significantly increases expression of numerous antioxidant genes with overlapping functions pointing to the importance of these mechanisms.  We are investigating the regulation of known and putative antioxidant genes that may play key roles in the stress response and thus in the survival of the parasite in the mosquito.  Understanding the molecular mechanisms that help the parasite survive may hold the key for the development of transmission-blocking strategies.


Mitochondrial energy metabolism in the mosquito stages of the malaria parasite

We also investigate the energy metabolism of the malaria parasite while in the mosquito.  In particular, we are interested in the molecular pathways involved in oxidative phosphorylation: the Tricarboxylic acid (TCA-) cycle, the Electron Transport Chain (ETC) and the ATP synthase complex.  All of these components are located in the mitochondrion.  Interestingly, literature indicates that the main role for the parasites’ mitochondrion in the human host is to provide pyrimidine precursor molecules for the production of the DNA nucleotides Thymine and Cytosine rather than for the production of ATP, which for the most part is generated solely via glycolysis. Microscopic observations show that the mitochondrion significantly increases in size and complexity during parasite development in the mosquito suggesting an upregulation of mitochondrial genes indicating a more prominent role for this organelle in these stages.

bottom of page