Leprosy hijacks our immune system, turning an important repair mechanism into one that causes potentially irreparable damage to our nerve cells, according to new research that uses zebrafish to study the disease.
Leprosy is an infectious disease that affects the skin and peripheral nerves and is caused by Mycobacterium leprae and, less commonly, Mycobacterium lepromatosis. According to the World Health Organization, there has been a dramatic decrease in the global disease burden in the past few decades: from 5.2 million people with leprosy in 1985 to 176,176 at the end of 2015.
The bacteria are difficult to grow in culture and there are no good animal models: M. leprae can grow in the footpads of mice, but do not cause nerve damage; the disease causes nerve damage in armadillos, but these animals are rarely used in research.
Now, an international team of researchers have used a new animal model, the zebrafish, to show for the first time how M. leprae damage nerves by infiltrating the very cells that are meant to protect us. Zebrafish are already used to study another species of mycobacteria, to help understand tuberculosis (TB).
Scientists have previously shown that the nerve damage in leprosy is caused by a stripping away of the protective insulation, the myelin sheath, that protects nerve fibres, but it was thought that this process occurred because the bacteria got inside Schwann cells, specialist cells that produce myelin.
In new research published in the journal Cell, researchers used zebrafish that had been genetically modified so that their myelin is fluorescent green; young zebrafish are themselves transparent, and so the researchers could more easily observe what was happening to the nerve cells. When they injected bacteria close to the nerve cells of the zebrafish, they observed that the bacteria settled on the nerve, developing donut-like 'bubbles' of myelin that had dissociated from the myelin sheath.
When they examined these bubbles more closely, they found that they were caused by M. leprae bacteria inside of macrophages - literally 'big eaters', immune cells that consume and destroy foreign bodies and unwanted material within the body. But, as is also often the case with TB, the M. leprae was consumed by the macrophages but not destroyed.
"These 'Pac-Man'-like immune cells swallow the leprosy bacteria, but are not always able to destroy them," explains the auhtor. "Instead, the macrophages -- which should be moving up and down the nerve fibre repairing damage -- slow down and settle in place, destroying the myelin sheath."
Researchers confirmed that this was the case by knocking out the macrophages and showing that when the bacteria sit directly on the nerves, they do not damage the myelin sheath.
The team further demonstrated how this damage occurs. A molecule known as PGL-1 that sits on the surface of M. leprae 'reprograms' the macrophage, causing it to overproduce a potentially destructive form of the chemical nitric oxide that damages mitochondria, the 'batteries' that power nerves.
"The leprosy bacteria are, essentially, hijacking an important repair mechanism and causing it to go awry," says the author. "It then starts spewing out toxic chemicals. Not only does it stop repairing damage, but it creates more damage itself."
"We know that the immune system can lead to nerve damage - and in particular to the myelin sheath - in other diseases, such as multiple sclerosis and Guillain-Barré syndrome," says another author. "Our study appears to place leprosy in the same category of these diseases."
The researchers say it is too early to say whether this study will lead to new treatments. There are several drugs being tested that inhibit the production of nitric oxide, but the key may be to catch the disease at an early enough stage to prevent damage to the nerve cells.
"We need to be thinking about degeneration versus regeneration," author says. "At the moment, leprosy can be treated by a combination of drugs. While these succeed in killing the bacteria, once the nerve damage has been done, it is currently irreversible. We would like to understand how to change that. In other words, are we able to prevent damage to nerve cells in the first place and can we additionally focus on repairing damaged nerve cells?"