We’re not the same when we get sick. Whether it is sneezing when we get a cold, or ferociously biting people when we get rabies, germs change our behavior.
That’s because germs need to transmit from one host to another.
Consequently, host behavior is usually altered in ways that help the pathogen spread.
Rabies, for example, causes infected animals to aggressively bite others because the virus transmits through saliva.
But some microbes are more subtle.
Toxoplasma gondii parasites, which sexually reproduce only in cats but can infect any animal, hijack the brain and affect the host’s behavior.
A Toxoplasma infection occurs by one of the following:
- Eating undercooked, contaminated meat (especially pork, lamb, and venison) or shellfish (for example, oysters, clams or mussels).
- Accidental ingestion of undercooked, contaminated meat or shellfish after handling them and not washing hands thoroughly (Toxoplasma cannot be absorbed through intact skin).
- Eating food that was contaminated by knives, utensils, cutting boards and other foods that have had contact with raw, contaminated meat or shellfish.
- Drinking water contaminated with Toxoplasma gondii.
- Accidentally swallowing the parasite through contact with cat feces that contain Toxoplasma. This might happen by
- Cleaning a cat’s litter box when the cat has shed Toxoplasma in its feces;
- Touching or ingesting anything that has come into contact with cat feces that contain Toxoplasma; or
- Accidentally ingesting contaminated soil (e.g., not washing hands after gardening or eating unwashed fruits or vegetables from a garden).
- Mother-to-child (congenital) transmission.
- Receiving an infected organ transplant or infected blood via transfusion, though this is rare.
Symptoms of the infection vary.
- Most people who become infected with Toxoplasma gondii are not aware of it because they have no symptoms at all.
- Some people who have toxoplasmosis may feel as if they have the “flu” with swollen lymph glands or muscle aches and pains that may last for a month or more.
- Severe toxoplasmosis, causing damage to the brain, eyes, or other organs, can develop from an acute Toxoplasma infection or one that had occurred earlier in life and is now reactivated. Severe toxoplasmosis is more likely in individuals who have weak immune systems, though occasionally, even persons with healthy immune systems may experience eye damage from toxoplasmosis.
- Signs and symptoms of ocular toxoplasmosis can include reduced vision, blurred vision, pain (often with bright light), redness of the eye, and sometimes tearing. Ophthalmologists sometimes prescribe medicine to treat active disease. Whether or not medication is recommended depends on the size of the eye lesion, the location, and the characteristics of the lesion (acute active, versus chronic not progressing). An ophthalmologist will provide the best care for ocular toxoplasmosis.
- Most infants who are infected while still in the womb have no symptoms at birth, but they may develop symptoms later in life. A small percentage of infected newborns have serious eye or brain damage at birth.
How do the people get toxoplasmosis
In a turn of events that would make Charles Darwin smile, rats and mice infected with Toxoplasma behave in ways that make them easy prey for cats – exactly where Toxoplasma wants to go.
The ability of Toxoplasma to disrupt such basic instincts in rodents is alarming when you consider that one-third of humans also carry this parasite’s cysts in their brain.
Latent toxoplasmosis in humans has been associated with serious neurological disorders, including schizophrenia, intermittent explosive (rage) disorder and suicide, but has never been shown to be a direct cause.
Could the parasite be manipulating people as well?
Is there a way we can get rid of this parasite and, if so, would behavior return to normal?
I am a microbiologist who has been studying Toxoplasma for over 20 years.
Not only have I found the parasite’s effects on its host to be endlessly fascinating, I have been trying to identify its vulnerabilities so physicians can better treat this currently incurable lifelong infection.
In a collaboration with biochemist Ronald Wek and neuroscientist Stephen L. Boehm II, we have made the surprising discovery that the parasites may not be directly manipulating its rodent host. Rather, the host’s immune response to the chronic infection may be to blame.
Your brain on Toxoplasma
Toxoplasma is a single-celled parasite that really gets around – it has managed to infiltrate the brains of billions of creatures around the world, from birds to beluga whales.
Of all the species Toxoplasma can infect, though, only cats support its sexual stage.
After sex in the cat gut, Toxoplasma is packaged into sturdy pods called oocysts that are released into the environment via feces, and can then be ingested or inhaled by other animals.
Infection with Toxoplasma does not usually produce symptoms in humans unless their immune systems are compromised, but the parasites remain in the body for life as latent tissue cysts.
These tissue cysts are commonly found in the brain, heart and skeletal muscle.
The formation of tissue cysts occurs in all infected animals, including many that end up on our dinner plate. Consumption of these tissue cysts in raw or undercooked meat also transmits the infection.
Another way these tissue cysts serve as a vehicle for parasite transmission is through the alteration of host behavior.
Rats and mice with latent toxoplasmosis become hyperactive and lose their instinctual fear of cats, essentially making them a free lunch for felines.
Jennifer Martynowicz, an M.D.-Ph.D. student in my lab, was intrigued by the ability of latent toxoplasmosis to alter the behavior of mice.
It has long been a mystery as to how exactly this little microbe, which seems inert when encased in its tissue cyst wall, manages to pull off such a feat.
It is known that Toxoplasma releases an arsenal of parasite proteins into host cells that can alter gene activity, but how this translates into altering behavior remains unknown.
Previous work in our lab found that guanabenz, an FDA-approved drug used to treat hypertension, significantly reduces the number of brain cysts in an infected strain of mice we call BALB/c. Using this drug, Martynowicz was able to address a fundamental question:
If we reduce the number of parasite cysts in the brain, can we restore normal behavior?
Toxoplasma changes behavior – drug reverses it
Martynowicz administered guanabenz for three weeks to the mice that were hyperactive due to latent toxoplasmosis.
When Martynowicz examined the brains of the treated mice and mice that received no guanabenz, she discovered that cyst counts were lowered about 75% in treated mice, reinforcing the results from prior studies.
In the first demonstration of its kind, Martynowicz then examined whether the reduction in cysts affected activity levels in the mice.
To our delight, the hyperactivity usually seen in mice with latent toxoplasmosis had disappeared.
The animals treated with guanabenz behaved like normal, uninfected mice.
So it looked like our lab’s hypothesis was correct: Brain cysts correlated with behavior changes.
To be certain that the hyperactivity was caused by the cysts, Martynowicz decided to examine the effect of guanabenz in a different mouse strain called C57BL/6, which are more susceptible to Toxoplasma.
In this mouse strain, guanabenz did not lower cyst counts. But it reversed the hyperactive behavior.
These unexpected findings showed that the hyperactivity in infected mice does not correlate with the number of parasite brain cysts after all.
Toxoplasma cyst, green, in a section of brain tissue. The nuclei are stained blue. The image is credited to Jennifer Martynowicz.
To address this puzzling discrepancy, Martynowicz examined the level of inflammation in the brains of these mice.
Other investigators have observed that latent parasite cysts in the brain recruit immune cells, producing a low level of sustained inflammation.
Is brain inflammation changing behavior?
Guanabenz is known to have anti-inflammatory effects.
Decreasing brain inflammation is exactly what it appears to be doing in the brains of both infected mouse strains.
These results suggest that the hyperactivity in infected mice is more likely driven by their immune response rather than a parasite-driven manipulation.
If so, the key to controlling some behavioral changes in infected animals may be modulating their immune response.
We do not yet know how neuroinflammation may lead to hyperactivity.
But it is interesting to note that some emerging studies have also found a link between inflammation and attention-deficit hyperactivity disorder (ADHD), which affects more than 6 million children in the U.S.
If our findings in mice, published in the journal mBio, extend to people, it could have important ramifications for how we currently treat brain infections.
Our results suggest that brain infections may cause neurological consequences only in a subset of people, based on their immune response.
Further studies are needed to determine if anti-inflammatory drugs like guanabenz may be effective at managing these conditions.
Funding: Bill Sullivan works for Indiana University School of Medicine and his research is supported by grants from the National Institutes of Health.ABOUT THIS NEUROSCIENCE RESEARCH ARTICLE
Bill Sullivan – The Conversation
The image is credited to Jennifer Martynowicz.