Toxoplasma gondii parasite may alter signaling in the brain

Toxoplasma gondii parasite may alter signaling in the brain
Inhibitory nerve terminals, such as GABA, are shown in red. The right image demonstrates how a Toxoplasma infection alters the inhibitory nerve terminals, compared to the healthy tissue sample in the left image.

It's creepy, it's crawly, and it infects 20 percent of people in the United States. Fortunately, most people who carry the Toxoplasma gondii parasite don't develop the symptoms of the disease it can cause. Only a small fraction of people, typically with compromised immune systems, develop toxoplasmosis.

Toxoplasmosis can lead to abnormal brain function, including seizures, by changing signaling in the diseased central nervous system.  

In a study using a rodent model, scientists from the Virginia Tech Carilion Research Institute and the University at Buffalo found that the parasite-induced infection alters neural pathways specifically related to the neurotransmitter gamma-Aminobutyric acid, better known as GABA.

The researchers recently published their results in the American Society for Microbiology's open-access journal, mBio.

"Toxoplasma can cause a nasty event in the brain of immunocompromised individuals," said Michael Fox, an associate professor at the Virginia Tech Carilion Research Institute and co-corresponding author on the paper. "In this study we show for the first time that the parasite actually alters neural connections. But we still don't understand why or even exactly how. Our study is only the first scratch on the surface of how it affects brain synapses."

The parasite, mostly contracted from , seems to concentrate on the neurotransmitter GABA.

"The parasite can use GABA as a carbon source for metabolic activity and to facilitate its own dissemination through the brain," said Fox, who is also an associate professor of biological sciences in Virginia Tech's College of Science. "This, and other factors, led us to investigate whether GABA-containing synapses were altered in mice infected by Toxoplasma. We were shocked by the severity of the anatomical deficits observed."

The physical abnormalities were so peculiar, Justin Brooks, who conducted the initial experiment while a graduate student, thought it had failed.

"He repeated the experiment many times before we believed the results," Fox said.

The scientists found that a particular enzyme called GAD67 was actually misplaced in rodent brains with toxoplasmosis.

"The misplacement is significant because it results in defects in the synthesis of GABA, said Ira Blader, co-corresponding author on the paper. "Defects in GABA signaling and release from neurons will cause seizures."

Blader is an associate professor of microbiology and immunology at the Jacobs School of Medicine and Biomedical Sciences at the University at Buffalo in New York.

"Our work is the first showing that an infection can alter this enzyme's localization in the brain," said Blader, who earned his undergraduate degree at Virginia Tech. "We don't know how widespread it is, though. It might only occur during toxoplasmosis or in other infections or disorders. Our goal is to translate our basic research finding to improve patient outcomes."

The patient outcomes can be widely varied, and they're particularly devastating in immunocompromised people and fetuses.

In addition to undercooked meat, Toxoplasma can be contracted from feline feces, which is why pregnant women are advised to avoid the chore of scooping the dirty litter box. In a fully matured brain, the infection can wreak havoc. In a developing brain, the effects are even more disastrous.

GABA is an inhibitory neurotransmitter. Neurons will release the chemical as a signal to reduce the activity of other neurons in an effort to calm the central nervous system. Deficits in GABA signaling in the brain lead to seizures.

The research team found that the parasite concentrated itself around the inhibitory nerve terminals that normally release GABA.

"Toxoplasma can express and metabolize GABA, but we don't know if that's why it attacks these neural connections," Fox said. "It's unclear if the nerve terminals are degenerating, or if the parasite causes other cells to consume them. Perhaps the are still present, but the parasitic infection decouples the molecular machinery needed for their normal function." 

While many questions persist about the effects of toxoplasmosis, Fox and Blader are pleased with their results and eager to learn more.

"Our study was the first to find that Toxoplasma alters GABAergic circuitry during a progressed infection," said Fox. "Now, we're beginning to unravel the mystery of how the parasite affects the brain."

Fox and Blader plan to continue their collaboration in an effort to understand the intricate mechanisms of toxoplasmosis.

"We hope the answers to our questions will provide us clues as to the mechanisms underlying Toxoplasma-induced changes in neural circuits," Fox said. "But already, our research sheds novel light on some of the toxoplasmosis-induced neurological symptoms, such as seizures."

More information: Justin M. Brooks et al. Infections Alter GABAergic Synapses and Signaling in the Central Nervous System , mBio (2015). DOI: 10.1128/mBio.01428-15

Journal information: mBio
Provided by Virginia Tech
Citation: Toxoplasma gondii parasite may alter signaling in the brain (2015, December 3) retrieved 24 June 2024 from
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