Public Release: 

Scientists identify motor that powers parasitic cell invasion

Imperial College London

The development of drugs to combat some of the world's most serious parasitic diseases is a step nearer with the discovery of a widely-shared gene that helps parasites to invade host cells.

The new understanding of the gene's role in the single-celled parasite Toxoplasma gondii gives scientists a target to block that could stop the parasite literally in its tracks.

In experiments reported today in the journal Science, researchers at Imperial College London and the University of Mannheim, Germany show that the motor powering Toxoplasma's invasion of host cells is stopped when the parasite myosin A gene is disrupted.

Myosin A is present in all members of the Apicomplexa family of parasites, which includes Toxoplasma and Plasmodium falciparum, which cause Toxoplasmosis and malaria respectively.

Toxoplasma, mainly transmitted by consumption of contaminated meat or by cat faeces, chronically infects half the world's population. The pathogen is a leading cause of neurological birth defects in children born to mothers who contract the disease during pregnancy and can cause fatal toxoplasmosis encephalitis in immunosuppressed patients.

Scientists hope that understanding the gene's function will aid efforts to develop drugs that target and block the way Apicomplexa parasites penetrate host cells.

Unlike most viruses and bacteria that require host cell participation to attack cells and be engulfed, Apicomplexans actively penetrate cells.

They use a unique gliding motion powered by an actin-myosin system to rapidly spread throughout tissues in the host's body and to invade cells.

"Our research demonstrates for the first time that parasite motility is powered by an unusual motor, which is essential for invading host cells," says research leader Dr Dominique Soldati from Imperial's Department of Biological Sciences.

"The Apicomplexa family of parasites are all strictly dependent on an unusual gliding motion to get into cells. If the parasite can't get in, it can't establish an infection," she says.

Once the parasite docks with the host cell it sends out proteins that bind tightly to host cell receptors and create an indented pocket in the surface of the cell. The parasite's myosin molecules then latch onto the newly formed protein-receptor complexes pulling the myosin along a skeleton of actin and into the cell.

"Myosin A is an extremely fast moving motor, comparable in speed to the myosin responsible for the contraction of muscle in humans. The motor propels the parasite at a speed of five micrometers per second, allowing it to penetrate host cells within 10 to 30 seconds.

"This rapid entry process is essential for Apicomplexan parasites to replicate safely, hidden from the immune system," says Dr Soldati.

Researchers established myosin A's function by knocking out the gene in Toxoplasma gondii and observing the effects on its motility. They used time-lapse microscopy to score the percentage of parasites able to glide and perform normal forms of movement on coated glass slides.

"In optimum conditions freshly released parasites exhibit circular gliding, upright twirling and helical gliding. But with only partial gene function the parasites performed a reduced number or incomplete circles and at a lower speed. With the gene completely shut down the parasites were totally unable to move."

"Toxoplasma remains an important threat to human health with the continual spread of AIDS, while the malaria parasite kills more than 1 million children each year.

"A detailed understanding of the mechanism of host cell invasion by the Apicomplexans is an important and acute goal since such studies will lead to the identification of novel therapeutic targets, which are urgently needed," says Dr Soldati.

The work was funded by the Deutsche Forschungsgemeinschaft.

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Notes to Editors:

Title: "Role of Toxoplasma gondii Myosin A in Powering Parasite Gliding and Host Cell invasion"
Journal: Science
Authors: Markus Meissner (1), Dirk Schluter (2) and Dominique Soldati (1)

    (1) Department of Biological Sciences, Imperial College London, SW7 2AZ
    (2) Institut fur Med. Mikrobiologie und Hygiene, Universtatsklinkum Mannheim, Theodor-Kutzer-Ufer 1-3 68167, Mannheim Germany

About Imperial College London
Consistently rated in the top three UK university institutions, Imperial College London is a world leading science-based university whose reputation for excellence in teaching and research attracts students (10,000) and staff (5,000) of the highest international quality.

Innovative research at the College explores the interface between science, medicine, engineering and management and delivers practical solutions, which enhance the quality of life and the environment - underpinned by a dynamic enterprise culture. Website: www.imperial.ac.uk

Imperial College and University College London
On 14 October 2002 Imperial College London and University College London began to explore the possibility of merger to create a new, globally competitive university committed to teaching, scholarship and research.

Together the two university institutions would form Britain's biggest university with a combined annual turnover in 2001 of £802 million, research income of £407 million, 3200 academic staff and over 28,000 students. A decision on whether to proceed with merger is expected in December 2002.

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