12:29pm Friday 15 December 2017

Slamming the brakes on the malaria life-cycle

MalariaPlasmodium

The research has uncovered a vital player in the sexual phase of the malaria parasite’s reproduction which could prove an effective target for new treatments to stop the disease in its tracks.

The scientists from The University of Nottingham’s School of Biology, with collaborators from the Universities of Leicester, Oxford, Imperial College London and Leiden in the Netherlands, have just published the results of their work in the journal PLoS Pathogens.

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Biting back

Malaria is a devastating global disease with several hundred million clinical cases and just under a million people die from it every year. The disease is caused by an infection of the red blood cells with a tiny parasite called a Plasmodium, of which there are four important species. These organisms are carried from person to person by the Anopheles mosquito. When it bites an infected person, the mosquito sucks up blood containing the parasite, which may then be passed on to the mosquito’s next victim.

Dr David Guttery, lead scientist of the paper and part of Dr Tewari’s group from The University of Nottingham’s Centre for Genetics and Genomics in the School of Biology said:

“The malaria parasite is a complex organism and to understand how it multiplies is crucial to stopping its transmission. Our study has identified a cell-division cycle gene in the malaria parasite and its role in the development of male sex cells and is hence a good candidate for putting the brakes on its development. We have shown that by deleting this gene, male gametes cannot form and burst out of their host cell (a process called exflagellation). Blocking the formation of these cells can be an important strategy in the prevention of malaria transmission from mosquito to mammalian hosts.” 

New Target

The protein that has been identified is called CDC20 and plays a part in the cell division cycle of the malaria parasite Plasmodium berghei which infects mice and rats. This gene has been shown to have an important role in cell division in many organisms, but up to now nothing has been known about its function in the malaria parasite. The new study provides the first description of the role of CDC20 in Plasmodium cell division and in the development of the malaria parasite’s male sex cells (microgametes), which are essential for parasite transmission between humans and the mosquito carrier. The scientists have discovered that the absence of this gene stops the male sex cell from bursting out of its host cell and fertilising a female cell as they are arrested in their cell division.

The sexual stage of the malaria parasite’s life-cycle occurs within the mosquito after it has fed on malaria-infected blood. This activates the parasite’s sexual phase and during this period, the male sex cell precursor (microgametocyte) rapidly replicates DNA and produces eight male sex cells (gametes). These gametes then burst out of the microgametocyte in a process called exflagellation and seek out a female sex cell to fertilise. By blocking the process of exflagellation, the team have identified a way of slamming the brakes on malaria transmission.

The team of researchers were from the Centre of Genetics and Genomics at The University of Nottingham, the University of Oxford, Imperial College London, Leiden University, the University of Leicester and the MRC National Institute for Medical Research funded by the MRC, Wellcome Trust, and EviMalar.

The group at Nottingham has previously uncovered other major players in the life cycle of the malaria parasite. More details on these can be found in earlier media releases ‘Stopping the spread of malaria’ and ‘Malaria research begins to bite’.

The new paper in PLoS Pathogens can be found online at: http://dx.plos.org/10.1371/journal.ppat.1002554

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Image caption:: A putative cdc20/cdh1 homologue in Plasmodium regulates cytokinesis and subsequent exflagellation in activated male gametocytes.  Activated male gametocytes of ∆cdc20 parasites of Plasmodium berghei arrested prior to cytokinesis and subsequent exflagellation. Parasites were stained and imaged to reveal axoneme formation (anti-α-tubulin antibody, red) and elevated DNA content (DAPI – blue). Staining of α-tubulin in ∆cdc20 parasites revealed normal formation of axonemes and characteristic circling of the nucleus by the axonemes in concentric rings. However, subsequent cytokinesis and exflagellation was completely blocked, effectively abolishing development of microgametes.

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Notes to editors: The University of Nottingham, described by The Sunday Times University Guide 2011

as ‘the embodiment of the modern international university’, has award-winning campuses in the United Kingdom, China and Malaysia. It is ranked in the UK’s Top 10 and the World’s Top 75 universities by the Shanghai Jiao Tong (SJTU) and the QS World University Rankings. It was named ‘the world’s greenest university’ in the UI GreenMetric World University Ranking 2011, a league table of the most environmentally-friendly higher education institutions.

 

 

The University is committed to providing a truly international education for its 40,000 students, producing world-leading research and benefiting the communities around its campuses in the UK and Asia.Impact: The Nottingham Campaign, its biggest ever fund-raising campaign, will deliver the University’s vision to change lives, tackle global issues and shape the future. For more details, visit: www.nottingham.ac.uk/impactcampaign

More than 90 per cent of research at The University of Nottingham is of international quality, according to the most recent Research Assessment Exercise, with almost 60 per cent of all research defined as ‘world-leading’ or ‘internationally excellent’. Research Fortnight analysis of RAE 2008 ranked the University 7th in the UK by research power.

The University’s vision is to be recognised around the world for its signature contributions, especially in global food security, energy & sustainability, and health. The University won a Queen’s Award for Higher and Further Education in 2011, for its research on global food security. More news from the University at: www.nottingham.ac.uk/news

Story credits

More information is available from Dr Rita Tewari on +44 (0)115 823 0362, rita.tewari@nottingham.ac.uk or Dr David Guttery david.guttery@nottingham.ac.uk

Emma Rayner

Emma Rayner – Media Relations Manager

Email: emma.rayner@nottingham.ac.uk Phone: +44 (0)115 951 5793 Location: King’s Meadow Campus


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