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Flesh-eaters make skin creep

06.12.2001


Bacteria (red) persuade skin cells (green)to let them in.
© Nature


Bacteria give skin cells their marching orders.

Bacteria that cause potentially lethal ’flesh-eating’ infections make their entrance by telling skin cells to step aside. The bugs hijack the body’s signal for skin cells to become mobile.

Group A streptococci (GAS) normally infect the surface lining of the throat. But occasionally they penetrate skin or the tissues lining the airways, invading deep into the body and causing life-threatening disease.



Finding out how streptococci enter tissues doesn’t reveal why merely troublesome bacteria sometimes turn lethal. But it may lead to treatments for severe infections, called necrotizing fasciitis, and sore throats.

Michael Wessels and Colette Cywes at Harvard Medical School in Boston find that GAS are covered with a cloak of molecules that mimic a signal that is normally sent to mobilize cells1. "Cells don’t know any better - they think this is a signal to get up and move," says Wessels.

Like mortar being removed from a brick wall, the impenetrable layer of skin cells dissolves, allowing the bacteria in.

"This generates a new dogma," says Lukas Huber, a cell biologist at the Molecular Pathology Research Institute in Vienna, Austria. Invading bacteria normally infect and destroy individual cells. "Clearly [GAS] are much smarter than that," he says.

GAS’ deceitful cloak resembles a signalling chemical called hyaluronic acid. This is released when cells must be rearranged - to heal wounded skin, for example. "The bacteria subvert this normal function," says Wessels.

Hyaluronic acid - or its bacterial doppelganger - binds to a receptor on the cell surface called CD44. When this happens " the junctions [between the cells] just open," says Huber.

Wolf in sheep’s clothing

Wessels and Cywes infected laboratory cultures of human skin with GAS. They saw the skin-cell membranes ’ruffling’, a sign that they had let go of their neighbours. A mutant form of GAS unable to produce the deceptive molecular coat was unable to penetrate skin.

Wessels and Cywes are now working to prevent GAS infection by blocking the CD44 receptors on cells, or interfering with GAS binding. They hope to gain an understanding of why GAS turn nasty, although that may have more to do with the infected individual than the bacteria, Wessels suspects.

"There are host issues that play a big role in who’s going to get the disease," says Elaine Tuomanen, an infectious disease expert at St Jude’s Children’s Research Hospital in Memphis, Tennessee.

In the meantime, Wessel’s team hopes to develop a treatment to prevent throat infections with GAS.

"That’s certainly where the money is," comments Tuomanen.

References

  1. Cywes, C. & Wessels, M. R. Group A Streptococcus tissue invasion by CD44-mediated cell signalling. Nature, 414, 648 - 652, (2001).


TOM CLARKE | © Nature News Service
Further information:
http://www.nature.com/nsu/011206/011206-12.html

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